Multi-Year Strategic
2013-17
Plan
Universal Immunization Program
REACHING EVERY CHILD
Contents
Foreword . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Preface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ..
1. INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1.1 UIP as a component of Reproductive, Maternal, Newborn, Child and Adolescent
health (RMNCH+A) in India . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1.2 Purpose of cYMP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1.3 Planning Process . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1.4 Immunization global priorities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2. NATIONAL CONTEXT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2.1 History of immunization program in India . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2.2 National Rural Health Mission (NRHM) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2.3 Burden of vaccine preventable diseases (VPDs) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2.4 Status of vaccine coverage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2.4.1 Vaccine coverage and equity issues . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2.5 Current structure for service delivery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2.5.1 Other stakeholders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ..
2.5.2 Current UIP Schedule in India . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2.6 UIP successes as a child survival strategy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2.7 Barriers for effective programming . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
3. GUIDING PRINCIPLES OF UIP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4. UIP STRATEGIC PLAN: 2013-17 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.1 UIP strategic plan framework . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.2 Impact indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.3 Target population . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Acknowledgment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ..
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M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
5. NATIONAL MONITORING AND EVALUATION PLAN FOR UIP . . . . . . . . . . . . . . . . .. .
5.1 Rationale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
5.2 Objective . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
5.3 Methodology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ...
5.4 Components of National M & E Plan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ...
5.5 Process for National M & E Plan development . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
6. ANNEXURES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
ANNEX 1: List of states showing good performance on immunization coverage and other
parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
ANNEX 2: List of States showing poor performance on immunization coverage and other
parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
ANNEX 3: NCCVMRC concept approved by MoHFW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ..
ANNEX 4: Key Recommendations from Effective Vaccine Management Assessment Report
2013 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ..
ANNEX 5: National Open Vial Policy 2013 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
ANNEX 6: Monitoring Framework . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ..
ANNEX 7: Emergency Preparedness and Response Plan 2011 . . . . . . . . . . . . . . . . . . . . . . . . . .
7. COSTING AND FINANCIAL SUSTAINABILITY OF THE UNIVERSAL
IMMUNIZATION PROGRAM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1. Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2. Summary of Findings on Baseline Expenditures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
3. Details of Baseline Program Cost and Financing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4. Recurrent Costs - Structure and Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.1 Demographic projections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.2 Vaccine and injection supplies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.3 Personnel Costs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.4 Training, Program Management, Disease Surveillance, Social Mobilization, Advocacy
and Communication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.5 Cold Chain . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
5.0. Future Resource Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
6.0. Future Financing and funding gap analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
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Acknowledgment
The comprehensive Multi Year plan (2013-17) was commissioned by the Ministry of Health and
Family Welfare and its development was carried out under the leadership of Ms. Anuradha Gupta,
Additional Secretary and Mission Director NRHM and Dr Rakesh Kumar, Joint Secretary.
We wish to acknowledge the contribution of the following from National Immunization Division,
MoHFW for providing regular guidance and inputs into the document – Dr Ajay Khera, Deputy
Commissioner Child Health and Immunization; Dr M.K. Agarwal, Deputy Commissioner UIP and
Immunization; and Dr Pradeep Haldar, Deputy Commissioner Immunization.
Immunization Technical Support Unit (ITSU) maintained an oversight and coordinated the
development of the plan by a team comprising of Dr Manish Pant, Dr Susmita Chatterjee, Dr Rajeev
Gera, Ms Susmita Roy. Dr Shrihari Dutta from UNICEF India office provided technical inputs on a
regular basis to this team.
Professor Ramanan Laxminarayan, Public Health Foundation of India and Dr Vijay Moses,
Director ITSU were a constant source of support for the ITSU team while drafting the plan.
We are grateful to the following individuals for contributing their time and inputs in preparing this
document.
Dr Brighu Kapuria ITSU
Dr Jyoti Joshi Jain ITSU
Ms. Monica Chaturvedi ITSU
Ms Chaitali Mukherjee ITSU
Dr Prem Singh ITSU
Ms. Amruta Bahulekar ITSU
Mr Nithiyananthan Muthusamy ITSU
Ms Apoorva Sharan ITSU
Mr Arup Deb Roy ITSU
Mr Rajat Jain ITSU
Dr Raveesha R. Mugali, UNICEF India
Dr Satish Gupta UNICEF India
Dr Chandrakant Lahariya WHO India
Dr Pankaj Bhatnagar WHO India
Dr Balwinder Singh WHO India
Dr Satyabrata Routray WHO India
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Abbreviations
AEFI
AES
AFP
ASHA
AVD
AWW
BCG
bOPV
CBHI
CCE
CCL
CFC
cMYP
CRM
CSO
CSSM
DF
DIR
DPT
DTFI
EPC
EPRP
eVIN
EVM
FHW
FIR
FMG
Adverse Events Following Immunization
Acute Encephalitis Syndrome
Acute Flaccid Paralysis
Accredited Social Health Activist
Alternate Vaccine Delivery
Anganwadi Worker
Bacillus Calmette–Guérin
Bivalent Oral Polio Vaccine
Central Bureau of Health Intelligence
Cold Chain Equipment
Cold Chain and Logistics
Chloroflurocarbon
Comprehensive Multi-year Plan
Common Review Mission
Civil Society Organization
Child Survival and Safe Motherhood
Deep Freezer
Detailed Investigation Report
Diphtheria Pertussis Tetanus
District Task Force on Immunization
Evidence to Policy
Empowered Program Committee
Emergency Preparedness and Response Plan
electronic Vaccine Intelligence Network
Effective Vaccine Management
Frontline Health Worker
First Information Report
Financial Management Group
E2P
................................ v i i
M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 v i i i
GMSD
GoI
HepB
HiB
HMIS
HR
ICDS
IDH
IEC
ILR
IMNCI
IMR
IPC
IPC
IPHS
ISP
ITSU
IUCD
JE
JRM
JSSK
JSY
KO
LHV
MCTS
MCV
MDG
MDVP
MIS
MMR
MoHFW
MSG
NBSU
NCCA
NCCMIS
NCCTC
NCCVMRC
Government Medical Store Depot
Government of India
Hepatitis B
Haemophilus influenzae B
Health Management Information system
Human Resources
Integrated Child Development Services
Infectious Diseases Hospital
Information, Education and Communication
Ice-Lined Refrigerator
Integrated Management of Neonatal and Childhood Illnesses
Infant Mortality Rate
Inter-personal Communication
Indian Pharmacopoeia Commission
Indian Public Health Standards
Immunization Strengthening Project
Immunization Technical Support Unit
Intra-Uterine Contraceptive Device
Japanese Encephalitis
Joint Review Mission
Janani Shishu Suraksha Karyakram
Janani SurakshaYojna
Key Objective
Lady Health Visitor
Mother and Child Tracking System
Measles Containing Vaccine
Millennium Development Goal
Multi Dose Vial Policy
Management Information System
Maternal Mortality Rate
Ministry of Health and Family Welfare
Mission Steering Group
Newborn Stabilization Unit
National Cold Chain Assessment
National Cold Chain Management Information System
National Cold Chain Training Center
National Cold Chain Vaccine Management Resource Center
................................
NGO
NIHFW
NNT
NRC
NRHM
NTAGI
OCP
OPV
ORS
OVP
PIP
PIR
RCH
RI
RMNCH+A
RRT
RTI
SBHI
SHTO
SIA
SMS
SNCU
STI
STSC
TFR
tOPV
TT
UIP
UNICEF
UT
VHND
VLM
VMAT
VPD
WHO
WIC
WIF
Non-Governmental Organization
National Institute of Health and Family Welfare
Neonatal Tetanus
Nutrition Rehabilitation Center
National Rural Health Mission
National Technical Advisory Group on Immunization
Oral Contraceptive Pill
Oral Polio Vaccine
Oral Rehydration Salt
Open Vial Policy
Program Implementation Plan
Preliminary Investigation Report
Reproductive and Child Health
Routine Immunization
Reproductive, Maternal, Newborn, Child & Adolescent Health
Rapid Response Team
Reproductive Tract Infection
State Bureau of Health Intelligence
State Health Transport Organization
Supplementary Immunization Activity
Short Message Text
Sick Newborn Care Unit
Sexually Transmitted Infection
Standing Technical Sub-Committee
Total Fertility Rate
Trivalent Oral Polio Vaccine
Tetanus Toxoid
Universal Immunization Program
United Nations Children's Fund
Union Territory
Village Health and Nutrition Day
Vaccines Logistics Management
Vaccine Management Assessment Tool
Vaccine Preventable Disease
World Health Organization
Walk-in Cooler
Walk-in Freezer
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A B B R E V I A T I O N S
Introduction
1.1 UIP as a component of
Reproductive, Maternal, Newborn,
Child and Adolescent Health in
India
There is a growing acknowledgment that over
the years various service packages have been
developed around the Reproductive and Child
Health program that have tended to function
independently. To bring about a greater impact
of the program there is a need to build synergies
between these various packages since they
address different stages of the life cycle. The
'Continuum of Care' approach includes two
dimensions – stages of life cycle and places
where care is provided. This approach
underpins the RMNCH+A strategy that seeks
to provide an integrated set of interventions
through a large cadre of community-based
ASHAs and a three-tiered health system. The
key components of the RMNCH+A
interventions as a 'continuum of care' are given
in Table 1. Immunization is one of the key
1
elements in this strategy.
Table 1: RMNCH+A continuum of care across life cycle and different levels of healthcare
Reproductive care Newborn and childcarePregnancy and child birth care
• Comprehensive abortion
care
• RTI/STI case management,
• Postpartum IUCD and
sterilisation; interval IUCD
procedures
• Adolescent friendly health
services
• Skilled obstetric care and
immediate newborn care
and resuscitation
• Emergency obstetric care
• Preventing Parent to Child
Transmission (PPTCT) of
HIV
• Postpartum sterilisation
• Essential newborn care
• Care of sick newborn (SNCU, NBSU)
• Facility-based care of childhood illnesses (IMNCI)
• Care of children with severe acute malnutrition
(NRC)
• Immunisation
Clinical
• Family planning (including
IUCD insertion, OCP &
condoms)
• Prevention and
management of STIs
• Peri-conception Folic acid
supplenentation
• Full antenatal care
package
• PPTCT
• Early detection and
management of
illnesses in mother and
newborn
• Immunisation
• First level assessment
and care for newborn
and childhood illnesses
• Immunisation
• Micro-nutrient
supplementation
• Weekly IFA
supplementation
• Information and counselling
on sexual reproductive
health and family planning
• Community based
promotion and delivery of
contraceptives
• Menstrual hygiene
• Counselling and
preparation for newborn
care, breast feeding, birth
preparedness
• Demand generation for
pregnancy care and
institutional delivery (JSY,
JSSK)
Antenatal care Postnatal careReproductive health care
• Home-based newborn care and prompt referral
(HBNC scheme)
• Antibiotic for suspected case of newborn sepsis
• Infant and Young Child Feeding (IYCF), including
exclusive breast feeding and complementary feeding,
• Child health screening and early intervention services
(0-18 years)
• Early childhood development
• Danger sign recognition and care-seeking for illness
• Use of ORS and Zinc in case of diarrhoea
Intersectoral: Water, sanitation, hygiene, nutrition, education, education, empowerment
Outreach/SubcentreFamily&Community
Child health care
1
A Strategic Approach to Reproductive, Maternal, Newborn, Child and Adolescent Health in India:
For Healthy Mother and Child. MoHFW, Government of India, 2013.
Adolescence/ Pre-pregnancy Pregnancy Birth Newborn / postnatal Childhood
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0 1................................
0 2M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Immunization is one of the most cost-effective
interventions that prevent needless suffering
through sickness, disability and death. The
benefits of immunization are not restricted to
improvement in health and life expectancy but
also have social and economic impact at both
community and national levels. Moreover, an
effective, equitable immunization program and
its impact on reducing the burden of vaccine-
preventable diseases will greatly contribute to
achieving the Millennium Development Goal
4 (MDG4) that envisages a two-third reduction
in child mortality by 2015.
In the last three decades, India has made
significant progress on sustainable and
inclusive growth. There is now a greater sense
of awareness and expectations from the people
as the country makes further social and
economic progress. Investments on the social
determinants of health have improved
availability and access to health services
though there still remain challenges of inequity
and affordability.
This multi-year strategic plan (2013–17) has
evolved from its first iteration (cMYP 2005–10)
and is underpinned by the Government of
India RMNCH+A 2013 strategy and the
National Vaccine Policy, 2011. The document
mainly seeks to:
a. Provide a broad framework of objectives,
expected results and strategies that cover the
different aspects of Routine Immunization –
program service delivery, system
strengthening, social mobilization and
demand generation, newer vaccines and
technology, epidemiology of vaccine-
preventable diseases and management of
adverse events following immunization.
b. Identify costing and financing requirement
as part of the planning cycle.
c. Propose monitoring and accountability
tracking mechanisms that should lead to
improved program efficiency
d. Explore and expand opportunities to
1.2 Purpose of cMYP
integrate other maternal and child health
interventions such as breast feeding,
Vitamin A supplementation and ORS
through UIP.
The strategic plan had been prepared through a
close collaborative and iterative process
involving national program managers, state
officials, professional associations,
development partners and implementing
agencies, which provide the goals, objectives,
indicators, strategies and costs. As cMYP
(2005–10) was completing its life in March
2010, a supplement to extend it till March 2012
was prepared. Initially, a framework for revised
cMYP was agreed upon by a working group of
national immunization program managers and
development partners where attention was
paid to new developments and initiatives that
had taken place since 2005. These initiatives
included those that have been enacted under
the National Rural Health Mission (NRHM)
and the recommendations of NTAGI in the
recent years. Two regional consultations were
held in New Delhi and Kolkata. These
consultations were attended by senior officials
in the Ministry of Health and Family Welfare
(MoHFW), program managers from the
national immunization division; state, district
and block level immunization officials, and by
representatives of development partners and
other professional organizations and Non-
Government Organizations.
In April 2013, under the guidance of national
immunization division, ITSU facilitated the
process of drafting the next cMYP (2013–17)
and set up a core committee to draft the plan,
comprising of representatives from ITSU,
WHO and UNICEF. The members of the core
committee met and communicated on a regular
basis among themselves to continually refine
the draft plan. Inputs on key objectives and
strategies came through the national
immunization division through regular
meetings with the drafting team. The current
cMYP document went through several
iterations before it was sent to NTAGI for
comments, which were subsequently
1.3 Planning process
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0 3 I N T R O D U C T I O N
to reducing approximately 25 percent to the
2
reduction in child mortality.
WHO has identified priority areas in
immunization for the future to sustain the
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momentum on immunization. These
priorities, which are also reflected in the
national cMYP, include the following:
lstrengthening the Routine Immunization
program,
laccelerating measles control activities,
lintroducing newer vaccines through
evidence-based policies,
lincreasing access to immunization services
through system strengthening.
As the current set of MDGs reach their end in
2015, new global health paradigms will emerge
that will focus on universal health coverage and
sustainable development. A well-functioning
UIP that aims to reach out to every child will
contribute to universal health coverage and
healthier future generation. To achieve this,
UIP will need strong underpinning of good
governance and accountability at all levels.
This will necessarily lead to improved program
efficiency and more children will get
immunized.
incorporated. In addition to the main strategic
component of cMYP, the core committee also
worked on the detailed costing of the program
under the guidance of national immunization
division.
According to WHO, immunization
interventions have proven to be a success across
the globe and today reach out to over 100
million children and prevent 2.5 million deaths
per year. As new global health paradigms
emerge, fresh perspectives and priorities are
emerging in immunization as well. Universal
immunization coverage is an important
element of universal health coverage to achieve
the MDGs by 2015. Despite improved
vaccination coverage there are rising inequities
among different population groups that need to
be addressed for a more meaningful success.
There are at least ten new antigens now
available that can be added to the traditional
EPI interventions including vaccines against
Hepatitis B, Rota virus, Japanese Encephalitis,
and Human Papilloma Virus. Several countries
are now moving beyond the traditional target
population of infants and pregnant women to
include adolescents and adults. WHO expects
that by 2015 immunization should contribute
1.4 Global Priorities on immunization
2
WHO Strategic Plan 2010–15. Department of Immunization, Vaccines and Biologicals
3
Global Action Vaccine Plan 2011–2020. World Health Organization
................................ 0 5
2.1 History of immunization
program in India
The success of smallpox eradication in the 70s
brought attention to the immunization
program globally as well as in India. The
Expanded Program on Immunization (EPI), a
national policy of immunizing all children
during the first year of life with DPT, OPV,
BCG and typhoid–paratyphoid fever vaccines
was launched in 1978. Immunization of
pregnant mothers with TT vaccine was
introduced in 1983. In 1985, the name of EPI
was changed to the Universal Immunization
Program (UIP) with activities phased in to the
entire country by 1990. The stated objectives of
UIP are:
lTo rapidly increase immunization coverage
lTo improve the quality of services
lTo establish a reliable cold chain system to
the health facility level
lTo introduce a district-wise system for
monitoring of performance
lTo achieve self-sufficiency in vaccine
production
UIP was given the status of a one of the five
'National Technology Missions' in 1986.
Subsequently in 1992, UIP became a part of
Child Survival and Safe Motherhood (CSSM)
program and then of Reproductive and Child
Health (RCH) program in 1997. A specific
Immunization Strengthening Project (ISP) was
designed to run from 2000 to 2003, which
included the following main components:
lpolio eradication
lstrengthening routine immunization
lstrategic framework for development.
Immunization is a critical component of the
Government of India's child survival strategy.
In 1997 the MoHFW launched a Reproductive
and Child Health (RCH) program to reduce
IMR, MMR, TFR and to increase
immunization coverage, especially in rural
areas. The second phase of the RCH program
(2005–10) focused on minimizing regional
variations through provision of assured,
equitable, and responsive quality services.
With a view to strengthen public health system
in rural areas, the Government of India
launched the National Rural Health Mission in
2005. The NRHM was established as a single
platform to bring together all of the national
4
health efforts, including RCH. The goal of the
NRHM is to address gaps in the provision of
effective health care to rural population with a
special focus on 18 states, which have weak
5
public health infrastructure. To achieve this
goal the NRHM envisions a shift away from the
vertical health and family welfare programs to
a new architecture in which societies under
different programs are merged and resources
pooled at the district level. NRHM also
provides states with flexibility in making their
own plans in delivering RI interventions. It also
seeks to strengthen local public health
provision with infrastructure and manpower
and facilitate the participation of the not-for-
profit and for-profit sectors in achieving
2.2 National Rural Health Mission
(NRHM)
National Context
2
4
Ministry of Health and Family Welfare (2005): “National Rural Health Mission, Framework for Implementation (2005-12)”
5
The 18 states are Arunachal Pradesh, Assam, Bihar, Chhattisgarh, Himachal Pradesh, Jharkhand, Jammu &
Kashmir, Manipur, Mizoram, Meghalaya, Madhya Pradesh, Nagaland, Odisha, Rajasthan, Sikkim,
Tripura, Uttaranchal and Uttar Pradesh.
0 6M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
desirable health outcomes. In the 12th FYP the
Government of India has proposed a National
Health Mission for improving healthcare in
rural as well as urban areas. UIP is an integral
component of NRHM.
At the national level, the NRHM has a Mission
Steering Group (MSG) headed by the Union
Minister for Health & Family Welfare and an
Empowered Program Committee (EPC)
headed by the Union Secretary for Health &
Family Welfare. EPC implements the Mission
6
under the overall guidance of the MSG.
At the state level, the mission functions under
the overall guidance of the State Health
Mission headed by the Chief Minister of the
6
Source: www.nrhm.gov.in
state and provides oversight to the functioning
of the health system and NRHM activities,
policy inputs for health sector, conducts
intersectoral coordination and advocacy. The
functions under the mission are carried out
through the State Health & Family Welfare
Society led by the Mission Director. Under
NRHM, states have set up State Health
Societies to strengthen health service delivery
infrastructure, financial management,
coordination with NGOs/CSOs/donors and
monitoring of various national programs.
The State Mission and State Society are
interlinked in terms of a common secretariat as
shown in Figure 1 below.
Figure 1: Composite organogram of the State Mission and the State Society
State Health Mission
Governing Body, State Health Society
Program Committees
(Headed by Director/
Director General)
(Optional)
SPMSU
(Headed by Executive
Director/Mission
Director)
Executive Committee, State Health Society
2.3 Burden of vaccine-preventable
diseases (VPDs)
Over the past 20 years, the reported cases of the
main VPDshave declined. However, in recent
yearsthere has been an increasing trend in the
number of reported measles, diphtheria and
pertussis cases as shown in Figure 2. This
increasing trend may be due to an actual
increase in number of cases or can be attributed
to improvements in case detection and the
overall surveillance system strengthening. To
minimize this inconsistency and to stabilize the
reporting trends, improving the surveillance of
VPDs in the countryis urgently needed.It is
estimated that approximately 80,000 children
die annually from measles and associated
complications. Although this figure has
................................
07 N A T I O N A L C O N T E X T
MCV2 six months following the completion of
the campaign. Delhi, Sikkim, Goa and
Puducherry took initiative themselves and
introduced 2nd measles dose through MMR.In
September 2013, India committed to
eliminating measles and controlling
rubella/congenital rubella syndrome (CRS) by
2020 as part of the resolution that was
approved by SEARO's 66th regional
committee.
decreased over the years with improvements in
routine vaccination coverage rates, measles
mortality still remains high. In 2010, the
Government of India decided to introduce a
second dose of measles containing vaccine
(MCV2) in UIP. In 21 states with measles 1st
dose coverage more than 80 percent, MCV2
was introduced directly in their routine
immunization whereas, 14 states were taken up
for measles Supplementary Immunization
Activity (SIA) followed by introduction of
Figure 2: Trends in the reported cases of Measles and Pertussis from 1990–2010 (Source CBHI)
120000
100000
80000
60000
40000
20000
0
1990
1991
1992
1993
1994
1995
1996
1997
1998
1999
2000
2001
2002
2003
2004
2005
2006
2007
2008
2009
2010
Cases
PertusslsMeasles
Burden of VPDs
between geographies and population groups.
These inequities represent gaps in service
delivery that leaves certain groups of children
at a high risk of remaining unvaccinated. As
per NHFS-3 data, nine states are below the
national average for vaccination coverage
including Madhya Pradesh, Uttar Pradesh,
Bihar and Jharkhand. Even within states there
exists a difference in total coverage between
7
different districts as shown in Figure 4.
2.4 Status of vaccine coverage
Though the reported vaccination coverage for
all vaccines has always been higher than
evaluated coverage, the average vaccination
coverage has shown a consistent increase over
the last two decades as shown in Figure 3
below.
However these averages mask the disparities
7
NFHS-3 data
0 8M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
2.4.1 Vaccine coverage and equity
issues
While vaccines under UIP are provided free of
cost through all the public health facilities
across the countries, disparities in coverage
exist for different population groups that need
to be addressed. There are significant inequities
in vaccination coverage in different states based
on various factors related to individual (gender,
birth order), family (area of residence,
wealth,parental education), demography
(religion, caste) and the society (access to
health care, community literacy level)
8
characteristics.
There is a clear gender coverage differential as
reported by different surveys. Boys generally
have a higher vaccination coverage than girls as
reported by most surveys conducted across the
country (Figure 5).
The gap between genders also exists for
individual vaccines such as BCG, DPT and
measles.
Figure 3: Trends in vaccination coverage over the last twenty years as shown in different surveys
Figure 4: District level coverage of fully immunized children between 12 and 23 months of age.
(Source: DLHS 2007–08)
Vaccine coverage70.0%
60.0%
50.0%
40.0%
30.0%
20.0%
10.0%
0.0%
NFHS-1
(1992-93)
NFHS-2
(1998-99)
NFHS-3
(2005-06)
DLHS-1
(1998-99)
DLHS-2
(2002-04)
DLHS-3
(2007-08)
CES
(2009-10)
35.4%
42.0% 43.5%
54.2%
45.9%
53.5%
61.4%
Below 30
30 to 50
50 to 70
70 to 90
Above 90
8
Joseph L Mathew (2012): “Inequity in Childhood Immunization in India: A Systematic Review,” Indian Pediatrics,
Volume 69, March 16, 2012.
................................
0 9
Urban areas have higher vaccination coverage
as compared to rural areas and this gap exists
for all vaccines. Within urban areas, slum
populations have a lower coverage. Migrants
coming to urban areas to have a lower coverage
level as compared to the resident population.
Urban and rural poor populations have a lower
coverage as compared to the wealthier one.
Figure 5: Gender differential in vaccine coverage (Source: HMIS)
13000000
12500000
12000000
11500000
11000000
10500000
10000000
9500000
9000000
2008-09 2009-10 2010-11 2011-12 2012-13
Male Female
Fully Immunized Children
Figure 6: Differentials in vaccine coverage across geography, caste and wealth status
(Source: UNICEF CES 2009)
Percentage of children age 12-23 mfully immunized
Urban Rural Others OBC SC ST Richest
Quintile
Poorest
Quintile
67.4
58.5
66.3
60.6 58.9
49.8 47.3
75.5
Vaccination coverage is also lower amongst
infants coming from scheduled caste (SC),
scheduled tribes (ST) and other backward
castes (see Figure 6).
A comparison of states showing good and poor
performance on immunization coverage is
given in Annex 1 and Annex 2 respectively.
N A T I O N A L C O N T E X T
1 0M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
2.5 Current structure for
immunization service delivery in
the country
The implementation of the UIP is a joint
responsibility of government at all levels,
namely Central, State and Union Territory
Districts and Sub-Districts. The relationships
between central and state immunization
departments and between state and district
immunization officers are critical for efficient
and effective service delivery.
National: The MoHFW comprises of four
departments, each of which is led by a
Secretary to the Government of India. These
include:
lDepartment of Health & Family Welfare;
lDepartment of Ayurveda, Yoga &
Naturopathy, Unani, Siddha and
Homoeopathy;
lDepartment of Health Research; and
lDepartment of AIDS Control.
The MoHFW is responsible for implementing
various national health programs in all states of
India. The Directorate General of Health
Services renders technical advice on all
medical and public health matters and is
involved in the monitoring of implementation
of various health services. The MoHFW is
responsible for funding of various national
programs including immunization program,
providing technical assistance and policy
guidance to the states, and for monitoring and
evaluation. Funding for extra staff and other
health system resources at the state level is
provided by the NRHM, a flexible mechanism
that allows for integration of funds for all the
national schemes while allowing for states to
flexibly allocate funds for system improvement
in a manner that is consistent with their needs
and challenges. All states are required to
submit in advance a Program Implementation
Plan (PIP) for a financial year, along with
complete projections of funds required to
implement the PIP.
To augment technical and managerial support
under UIP for strengthening, revitalization and
successful implementation of RI, the
Immunization Division at MoHFW has set up
an Immunization Technical Support Unit
(ITSU). The ITSU is staffed with technical
officers to support various functions of UIP
under six different pillars:
lStrategic planning and system design,
lMonitoring and evaluation,
lVaccine logistics and cold chain
management,
lAdverse events following immunization
(AEFI) management and vaccine quality
and safety,
lTranslation of evidence to policy, and
lStrategic communication.
Through ITSU,the ministry will facilitate to
harmonize various initiatives being piloted or
implemented in different states by all
immunization partners and provide a single
platform for discussions, development of
strategies and coordination with partners for
scaling up the successful models.
State: At the state level, the Secretary of Health
is responsible for all health-related efforts. The
State Department of Health and Family
Welfare is led by a Director of Health Services
under which the State Directorate of Health
Services serves as the technical wing. Large
states such as Bihar, Madhya Pradesh, Uttar
Pradesh, Andhra Pradesh, and Karnataka have
additional zonal or regional or divisions set-up
between the State Directorate of Health
Ser vices and the District Health
Administration. Most of the states have a
dedicated State EPI Officer; however, at places
Deputy Director-HFW has additional
responsibility of being EPI Officer. Additional
support for UIP at the state level is provided by
a cold chain officer and by data and
administrative support staff. State governments
are responsible for implementation and
supervision of the various programs and for
provision of relevant infrastructure and
curative services in the states including village
outreach sessions for immunization.
District: In the district, under the overall
supervision of Chief Medical and Health
Officer (CMHO) or Civil Surgeon (CS), the
District Immunization Officer (DIO)
................................
1 1
coordinates all the immunization-related
efforts. The responsibility for immunization
also lies with Block Medical Officers and PHC
Medical Officers. The Auxiliary Nurse
Midwife (ANM) delivers the immunization
services to the community.
Immunization services are provided through
the following:
lsub-centers, primary health centers, and
community health centers,
lsub-divisional/taluk/speciality hospitals,
ltertiary hospitals,
lurban health services provided by
municipalities,
lhospitals and dispensaries run by railways,
defense, and public sector undertakings,
lEmployees’ State Insurance Scheme
hospitals
ldispensaries funded by the government
(State and Centre).
Private health sector also provides an estimated
15–20 percent of immunization services.
The Indian Public Health Standards (IPHS) for
immunization has been drafted to improve the
quality of the service and NRHM supports
efforts to improve the quality of service by
strengthening sub-centers and primary health
centers. The funding mechanism for
immunization has also been simplified and
made flexible along with adoption of the
bottom-up planning approach through district
and state Project Implementation Plans (PIPs).
Immunization service delivery in many areas
within a district, i.e. urban areas, especially
slums and peri-urban areas, where migrant
families live; areas in semi-legal situations due
to weak infrastructure; areas which are
managed by different local bodies such as
railways and cantonment have been, and are
still, a major concern.
Civil Society Civil Society Organizations
(CSOs): These organizations offer a wide
range of experience and knowledge essential
for UIP. They can provide insight into gaps in
2.5.1 Other stakeholders
9
Howard D, Roy K. Private care and public health: do vaccination and prenatal care rates differ between users of private vs.
public sector care in India? Health Services Research 2004;49:2013-26
health service delivery and identify practical
and political challenges that must be overcome
to improve the health of citizens. CSOs
therefore play a crucial role to advocate for
policy changes, generate greater transparency
and hold governments and other healthcare
stakeholders to account. At the country level,
Civil Society encompasses a diverse array of
actors, including the following:
lpatient groups, health workers, medical or
health unions and associations,
lfaith-based organizations,
lnon-governmental organizations,
lcommunity-based organizations,
lacademic institutions,
lmedia,
ladvocacy groups,
lmigrants, women, youth and other neglected
or vulnerable groups.
Civil society groups of particular importance
to ensuring that UIP achieves its intended
results are those with expertise in maternal
health, child health, immunizations, nutrition,
health systems and services, monitoring and
evaluation. The MOHFW will engage more
proactively with academia, professional
societies, and other national agencies and
committees and networks like the development
partners forum to ensure a cohesive and
coordinated approach to achieving national
immunization priorities.
Private hospitals and clinics: Private health
sector plays an important role in providing
immunization services and fill gaps in delivery
of RI services through public system. Studies in
India have shown that private sector does
enable increased access to traditional EPI
9
vaccines for those who can afford to pay.
Private sector also plays a role in introducing
newer and underutilized vaccines prior to their
induction in the public program. Private sector
also has a key role to play in supporting the
surveillance system for vaccine-preventable
diseases and adverse events following
immunization by reporting cases that may have
been missed out by the public surveillance
system.
N A T I O N A L C O N T E X T
1 2M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
2.5.2 Current UIP Schedule in India
The current UIP vaccination schedule caters to
pregnant women, infants, children and
adolescents as shown in Table 2 below.
Table 2: Vaccination schedule under UIP in India
*Give TT-2 or Booster doses before 36 weeks of pregnancy. However, give these even if more than 36 weeks have passed. Give TT to a woman in labor, if she has not previously
receivedTT.
**Pentavalent vaccines contain a combination of DPT, HepB and HiB. In the states where it has been introduced, it will replace DPT 1,2& 3 and Hepatitis B 1, 2 & 3. Hepatitis B birth
dose and booster doses of DPTwill continue as before.
*** JE Vaccine (SA14-14-2) is given in select endemic districts, after the campaign is over in that district.
****The 2nd to 9th doses of VitaminAcan be administered to children 1-5 years old during biannual rounds, in collaboration with ICDS.
Vaccine When to give Dose Route Site
0.5 ml
0.5 ml
0.5 ml
0.1ml
(0.05ml until 1
month of age)
0.5 ml
2 drops
2 drops
0.5 ml
0.5 ml
0.5 ml
0.5 ml
0.5 ml
0.5 ml
2 drops
0.5 ml
0.5 ml
0.5 ml.
0.5 ml
Intra-muscular
Intra-muscular
Intra-muscular
Intra-dermal
Intra-muscular
Oral
Oral
Intra-muscular
Intra-muscular
Intra-muscular
Sub-cutaneous
Sub-cutaneous
Intra-muscular
Oral
Sub-cutaneous
Sub-cutaneous
Intra-muscular
Intra-muscular
Early in pregnancy
4 weeks after TT-1*
If received 2 TT doses in a
pregnancy within the last 3 years
At birth or as early as possible till
one year of age
At birth or as early as possible
within 24 hours
At birth or as early as possible
within the first 15 days
At 6 weeks, 10 weeks & 14 weeks
9 completed months-12 months.
(give up to 5 years if not received
at 9-12 months age)
9 completed months
16-24 months
16-24 months
16-24 Months
16-24 months with DPT/OPV
booster
5-6 years
10 years & 16 years
Upper Arm
Upper Arm
Upper Arm
Left Upper Arm
Antero-lateral side
of mid-thigh
Oral
Oral
Antero-lateral side
of mid-thigh
Antero-lateral side
of mid-thigh
Antero-lateral side
of mid-thigh
Right upper Arm
Left Upper Arm
Antero-lateral side
of mid-thigh
Oral
Right upper Arm
Left Upper Arm
Upper Arm
Upper Arm
For Pregnant Women
TT-1
TT-2
TT- Booster
BCG
Hepatitis B
Birth dose
OPV
Zero dose
OPV 1,2 & 3
DPT1,2 & 3
Hepatitis B
1,2 & 3
Hi Bcontaining
Pentavalent
1, 2 & 3**
st
Measles 1
dose
st
JE 1 dose***
st
DPT 1
booster
OPV Booster
Measles
2nd dose
nd
JE 2 dose
DPT
nd
2 Booster
TT
Vitamin A****
For Infants
For Children and Adolescents
................................
1 3
2.6 UIP successes as a child
survival strategy
The Universal Immunization Program (UIP)
in India is one of the largest of its kind in the
world, in terms of the following:
lquantity of vaccines used,
lnumber of beneficiaries reached out to,
lnumber of immunization sessions
organized,
lthe geographical spread and diversity of
areas covered.
It caters to nearly 27 million infants and 30
million pregnant women annually free of cost.
There is a strong political commitment for
achieving universal immunization coverage in
the country along with the eradication and
elimination of the targeted diseases.
As a key element of the national child survival
strategy, UIP has contributed significantly to
reducing mortality and morbidity due to
vaccine-preventable diseases and the infant
mortality rate over the last decade. While
surveillance information for specific VPDs is
limited, the steady fall of IMR from 123 to 50
deaths per 1000 live-births does in part reflect
10
the impact of the UIP.
Since its launch in 1995, the Pulse Polio
campaign aimed at eradicating polio from
India, has begun to show results. Governments
at the national and state levels are
implementing strategies on a scale and
intensity that is unprecedented in the history of
polio eradication. These efforts have brought
India closer to the goal of polio eradication and
there is currently no reported case since
11
January 2011. India has been declared polio
non-endemic country by World Health
Organization in early 2012. Neonatal Tetanus
cases have declined significantly as more
pregnant women received TT vaccine as part of
their ante-natal care. There has been an overall
reduction in the number of cases and deaths
due to diphtheria, pertussis and measles as
well.
Under National Rural Health Mission,
MoHFW has undertaken many initiatives to
improve health systems and immunization
outcomes. Districts have been provided with
more human as well as financial resources to
improve delivery of immunization and other
health services. Introduction of ASHA into the
system as a community link worker has
brought about a major improvement in
community mobilization. Districts have
strengthened their delivery systems and
developed micro-plans for improved efficiency.
The number of vaccine delivery points has
increased along with the cold chain points.
MoHFW also introduced a system for
Alternate Vaccine Delivery (AVD) to provide
vaccines at the outreach session sites.
Innovative technology like auto-disable
syringes are now in use in all states and union
territories. Immunization-related trainings
have led to an increased capacity of frontline
health workers to deliver vaccines at the village
level. Focus in the urban areas has led to an
improved immunization services in slums
areas, though more needs to be done in this
12
area. MoHFW has also initiated Mother and
Child Tracking System (MCTS) to enable the
entry of mother and child data into a central
database.
The year 2012–13 was declared by the
Government of India as the year of
Intensification of RI in India. In this context,
the MoHFW had put in place a few strategic
actions to improve immunization coverage.
These included
limproving health systems,
lpromoting village health and nutrition day
(VHND),
llaunching Immunization Weeks,
llaunching of the “Teeka Express” for
delivery of vaccines to outreach sessions,
lpilot-launching of the National Cold Chain
Management Information System
(NCCMIS) for real-time monitoring and
management of cold chain systems and
lsetting up of the Immunization Technical
10
SRS 2011
11
National Polio Surveillance Program. www.npspindia.org.
12
UIP Review 2004
N A T I O N A L C O N T E X T
1 4M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Support Unit (ITSU) to provide technical
and programmatic support for successful
implementation of the UIP.
India's 'Call to Action on Child Survival and
Development' announced in February 2013,
and led by the MoHFW, the Government of
India, calls for a concerted, convergent and
inter-sectorial approach to achieving the
country's child survival goals by 2017. Based
on composite indicators the Government of
India has identified strengthening efforts in the
184 high priority districts in the country. This
five-year ambitious target will heighten the
importance of 'continuum of care', ensuring
the tight linkage between maternal and
newborn health as outlined in the new strategic
Figure 7: Reasons for low immunization coverage in India (Source – UNICEF CES 2009)
Did not feelneed
Not knowing about vaccines
Not knowing where to go for immunization
Time not convenint
Fear of side effects
Do not have time
Wrong advice by someone
Cannot afford the cost
Vaccine not available
Place not convenient
ANM absent
Long waiting time
Place too far
Service not available
28.2
26.3
10.8
8.9
8.1
6
3
1.2
6.2
3.8
3.9
2.1
2.1
2.1
11.8
0 5 10 15 20 25 30
Percentage
Demand side
issues
Supply side
issues
Others
The performance of immunization program in
India is regularly assessed through UIP review
meetings at national and state levels, Joint
Review Missions (JRM) and Common Review
Missions (CRM) sent by GoI. At least one
national review is conducted every year besides
additional state specific review as per the
program need. The common constraints in
immunization program are summarized
below:
a. Gaps in cold chain and vaccine logistics
management: There is limited cold chain
infrastructure and capacity in many states, even
for routine UIP vaccines. Systematic efforts to
identify gaps and address issues in cold chain
document called RMNCH+A. Strengthening
RI to increase coverage has been identified as a
key intervention in RMNCH+A. Many
different ministries, global and Indian experts,
goodwill ambassadors, private sector, civil
society, media, and faith-based organizations
have pledged to recommit themselves to the
Call to Action.
Overall immunization coverage levels are low
in the country. According to the CES 2009, the
reasons for low immunization coverage pertain
to issues on the demand and supply side as
given in Figure 7 below
2.7 Barriers for effective
programming
................................
1 5
and VLM have been conducted in recent years.
In addition to the 2008 NCCA, a number of
vaccine and cold chain management
assessments (Vaccine Management
Assessment Tool (VMAT)/EVM assessments)
have been conducted in 10 states and one
national UIP store (Government Medical Store
13
Depots (GMSD) – Karnal) between 2007–11.
A recent national-level assessment of EVM
conducted by the Government of India and
UNICEF in 10 states and four GMSDs along
with other studies including deep dive and
KPMG exercises by ITSU have identified the
following constraints:
lInfrastructure issues include poor
infrastructure of vaccine stores and
transportation systems; a lack of standards
for vaccine stores at different levels and
insufficient temperature monitoring system
at all vaccine storage points from GMSDs to
last cold chain point level, state, and regional
stores. There exist difficulties in procuring
the right quality of cold chain equipment on
time with adequate after-sale support. There
is a paucity of repair kits and spares cold
chain technicians and inequitable cold chain
point (last vaccine storage site) distribution.
Cold chain equipment in many states in the
country is old and in many cases broken.
There is also a paucity of available data on
Vaccine Logistics and Cold Chain to devise
national plans and strategies to address
them. .
lHR issues such as lack of a CCL support
unit with experts on cold chain for both the
immunization division of MoHFW and at
the state level; lack of induction training and
a regular educational program for staff
inducted in the Vaccine Logistics and Cold
Chain system; insufficient institutional
training capacity to manage cold chain and
logistics at all levels; shortage of trained
manpower and relevant job-aids for
managing cold chain at all levels (state,
division/regional and district levels); and
lack of HR with capacity for Vaccine
Logistics Management (VLM) at all levels
(national, GMSDs, state, district and
PHCs). The shortage of HR is more acute in
the poor performing states and specifically at
the field level.
lMonitoring and MIS issues such as lack of
realtime vaccine stock status, consumption
patterns, wastage rates, along with a
continuous temperature monitoring system
for cold chain, lack of cold chain inventory
and real-time NCCMIS, no regular review
of CCL system at the state and district level,
and poor documentation and MIS for
vaccine management (standardized
registers, records and procedures).
lVaccine procurement issues are significant
as delay in placement of procurement orders
and irregular supply of vaccines have a direct
impact on vaccine availability affecting
immunization coverage. Moreover, certified
vaccine suppliers are few, and since orders
are always given to the lowest bidder, the
supply of vaccines is often erratic.
These constraints have led to high breakdown
rate of equipment, overstocking and stock-
outs, inadequate monitoring and supervision,
poor management, and the possibility of
AEFIs, thus hampering improved vaccine
coverage.
b. Poor social mobilization: Low levels of
awareness, communication and information-
sharing amongst frontline workers as well as
poor HR capacity for BCC in government
institutions as a whole contributes to the
problem of high left-outs and dropouts. Studies
have shown that insufficient and ineffective
health communication along with lack of
promotion or follow-up of RIs are two of the
main health system constrains behind low
coverage in immunization, preventing parents
from initiating or following through with their
child's vaccination schedule. Given that the
actual rate of immunization is low, the high
dropout rate reduces the number of fully
immunized children in the country. Poor
populations and those with lower levels of
education are most vulnerable to impacts of
low levels of advocacy and communication.
Listed below are some of the system-related
constraints in advocacy and communication
13
National Cold Chain Assessment, India. July 2008. NRHM & UNICEF
N A T I O N A L C O N T E X T
1 6M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
inception of UIP, India has set up a reporting
mechanism from the health center to national
level. In last few years, the country has also
introduced electronic data systems like HMIS
and MCTS to improve reporting, analysis,
monitoring and planning at all levels. However,
there are big gaps in quality of data being
reported, its analysis and use for decision
making and thus leading to inadequate
information to support NTAGI and UIP to
design and implement strategies to improve
immunization quality and coverage. Some of
the main constraints in the area of data
management and evidence generation are
listed below:
lPoor monitoring and evaluation for data
entry, resulting in errors in data entry and
inaccurate data. In recent years, partners'
support and networks have contributed to
increased monitoring and supportive
supervision with visible positive impact in
select states. However, there is a need to
build the capacity of government officials
and strengthen the system to improve
monitoring and supervision by government
officials.
lPoor monitoring and evaluation results in
insufficient data quality and reporting rates.
A vast majority of states have wide gaps in
reported and evaluated coverage data. The
factors for this variation need to be identified
through regular data quality audits and
necessary corrective measures should be
taken.
lInadequate surveillance data quality and
reporting rates result in poor surveillance of
VPDs and AEFIs. While some attention has
been paid to strengthening VPD
surveillance, systemic deficiencies and
bottlenecks such as insufficient laboratory
capacity and limited trained manpower at
the district levels to carry out surveillance,
continue to exist. Inadequate VPDs
reporting results in the inability of UIP to
measure disease burden to make a decision
on the introduction of new antigens and
impact of vaccination on the disease. There
is a felt need for HR capacity building in
that lead to low levels of immunization
coverage.
lThere is weak capacity at the state level and
inadequate HR to generate evidence-based
communication strategies and effective BCC
campaigns
lWeak communication capacities
(spokesperson system) within the
government machinery at national and state
levels in handling AEFIs.
lInformation dissemination is not timely and
often mixed messages are received by
beneficiaries
lWeak counseling and interpersonal
communication (IPC) skills among health
workers and community mobilizers, which
adversely affects dissemination of
communication of messages.
lWeak capacities and counseling skills of
service providers to ensure delivery of
quality care, especially in hard-to-reach
areas.
There is an urgent need to strategically
approach communication, aiming at behavior
change both at the service delivery level and at
the community level to generate demand
among the caregivers. Meeting the shortfall of
health professionals and building their
counseling and communication skills are
imperative to a sustained and holistic response
to the public health concerns in the country.
This requires health care to be addressed not
only from the scientific perspective of what
works, but also from the social and behavioral
perspective of who needs it the most. One also
needs to understand the social norms and
barriers that prevent them from accessing the
services and how to reach the unreached.
c. Poor data management and analysis for
evidence generation: A robust system for data
management and evidence generation is
crucial to support informed decision making
for the creation of realistic goals and strategies
for improvement of current coverage levels and
introduction of new antigens in UIP. Since the
................................
1 7
VPD surveillance, strengthening laboratory
capacity by improving infrastructure and
making reagents available, and building
system for timely reporting and actions.
Similarly surveillance of AEFI cases is poor
and a structured response to reported serious
cases of AEFI is lacking.
lLimited focus on operational research for
immunization and finding locally suitable
solutions. Good quality research is needed
to provide an evidence base for a more
informed decision making and improving
performance.
The successful implementation of HMIS under
NRHM and MCTS under Mission Mode
Project provides a great opportunity to
strengthen data management and evidence
generation to inform decision making in UIP.
With the augmentation of human resource at
national level also provides an opportunity for
coordination between various reporting and
surveillance systems in the country as well as
putting up a system for using information for
decision making.
d. Weak human resource capacity: In a study
of HR needs assessment in UIP by Mavlankar
14
et al (IIM Ahmedabad) the following was
found:
lThere is limited technical and operational
human resource capacity and quality at
various levels in UIP.
lImmunization cells at both the state and the
national level are small and inadequately
staffed.
lKey personnel capacities are spread thin
across multiple areas in day-to-day
management with no focus on priorities.
They are not able to focus on developing
strategic solutions and to organize and
coordinate activities such as introducing
new vaccines, updating technology,
applying for international funding and
support, writing reports and analyzing data.
lThe roles and responsibilities of officials at
the state immunization cells are not well
defined
lState immunization officials have no
financial powers and their titles are not
commensurate with their responsibilities.
The lack of human resource capacity and
poorly defined roles and responsibilities at
various levels have a cascading effect on all
other areas of program performance, including
monitoring and evaluation, supply chain and
logistics management, and strategic
communications. Lower quality of monitoring
and supportive supervision of the program
leads to reduced efficiency and effectiveness of
interventions at all levels of programming and
needs to be addressed seriously.
While UIP is a part of a wider RMNCH+A
strategy of the government, there is a need to
increase the HR capacity and numbers of
immunization managers at all levels. The
Government of India has set up an
Immunization Technical Support Unit (ITSU)
to augment human resource capacity at
national level with focal persons assigned for
specific functions such as cold chain and
vaccine logistics, Evidence to Policy and
surveillance, Strategic Communication,
Monitoring and Evaluation and Adverse
Events Following Immunization (AEFI).
Training immunization staff on relevant topics
will improve program efficiency and
effectiveness as well.
e. Need for a well delineated accountability
systems: A major problem is the lack of
institutionalized and uniform accountability
structures, focused on performance review at
each administrative level i.e. central, state and
district levels. The country has a Multi-Year
Strategic Plan for UIP but its implementation is
not monitored in absence of a monitoring and
accountability structure. Though, there are
review mechanisms in place at all levels, but
these are not followed consistently. Moreover,
in absence of a robust system for data analysis,
N A T I O N A L C O N T E X T
14
Universal Immunization Program in India: A Study on HR Needs Assessment at National and State Levels.
Dr D.V Mavalankar et al, IIM Ahmedabad. Study commissioned by HRD Committee on UIP constituted by GoI.
1 8M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
interventions and follow up, these are not very
effective.
f. Evidence synthesis for informed policy
making: The NTAGI was formed in 2001 and
tasked with advising the MoHFW on issues
related to the program, policy and
implementation of the national immunization
program. Since its inception the NTAGI has
r e c o m m e n d e d e v i d e n c e - b a s e d
recommendations to the UIP, such as the
following:
lintroduction of the Hepatitis B, Pentavalent
and Japanese Encephalitis vaccine
luse of VVM in government vaccine supplies
luse of AD syringes
However, there is great scope for revision and
improvement in the decision-making process
for the introduction of new vaccines in the UIP.
In the light of the current advancements in the
field and the availability of several new
interventions, it is imperative to establish
scientific evidence-based protocols for making
immunization related decisions.
As India considers adding new antigens (e.g.,
rotavirus, pneumococcal, MMR, HPV,
IPV/hexavalent, cholera, typhoid, and JE) as
well as new immunization technologies (e.g.,
updated injection safety devices), the
immunization program also needs to keep
pace. NTAGI is an advisory body with clear
terms of reference for overall guidance but not
day-to-day operations. NTAGI needs a well-
defined secretariat to conduct regular meetings
and a clear scope of work that maintains focus
on making a structured recommendation on
immunization. At the same time, there is an
ever increasing need to develop capacity to
identify and address critical gaps in evidence
base. The health system must be able to
evaluate new vaccines for safety, efficacy,
relevance and cost-effectiveness; accommodate
the new vaccines in its cold chain management
system and vaccine logistics; assess and
respond in real time to roll-out challenges; and
conduct post-marketing surveillance to ensure
that lessons learnt from the roll-out are
incorporated back into the system.
The services provided through the
UIP shall be guided by the following
principles
1. Universal immunization coverage:
Sustaining demand and ensuring that all
pregnant mothers, children and adolescents are
immunized as per national schedule in line
with the principles of universal health
coverage.
2. Equitable access: Ensuring that the
immunizations services reach out to the under-
served, needy and most vulnerable populations
while addressing regional inequalities across
states.
3. High quality services and innovation:
Maintaining highest possible quality in vaccine
Guiding Principles of UIP
................................ 1 9
3
procurement, storage, distribution and delivery
services in an innovative and safe manner.
4. Sustainability and Partnerships:
Committing resources, financial, human and
technical, that sustain immunization benefits
to the people at all times and promoting
partnerships across different sectors and
organizations build synergies and expand the
overall coverage of the program.
5. Governance: Decentralized planning
through a bottoms up approach to improve
operational efficiency
6. Management excellence and
accountability: Implementation, oversight
and accountability of interventions that
optimize efficient use of resources
This comprehensive multi-year strategy plan
seizes on the opportunity to address geographic
and social inequities in immunization coverage
rates, and other immunization-related issues
highlighted in earlier sections. The plan aims to
strengthen immunization infrastructure within
the broader RCH program and offer a platform
for integrating other primary care interventions
and strengthening the public health system at
all levels. UIP offers universal immunization
coverage to all children in the country as per the
national immunization schedule.
This plan derives its essence from the National
Vaccine Policy 2011 and is underpinned by the
goals ascribed in the National Health Policy
2002 and National Rural Health Mission 2005.
The plan framework consists of an overarching
Goal and a set of six Key Objectives (KO) that
4.1 UIP strategic plan framework
Box 1: UIP Goal and Key Objectives
GOAL
KEYOBJECTIVES
Reduce mortality and morbidity due to vaccine-preventable diseases through high quality
immunization services
KO 1: Improve program service delivery for equitable and efficient immunization services by
all districts
KO 2: Increase demand and reduce barriers for people to access immunization services
through improved advocacy at all levels and social mobilization
KO 3: Strengthen and maintain robust surveillance system for vaccine-preventable diseases
(VPDs) and adverse events following immunization (AEFI)
Introduce and expand the use of new and underutilized vaccines and technology in UIP
KO 5: Strengthen health system for immunization program
KO 6: Contribute to global polio eradication, measles, maternal and neonatal tetanus
elimination
KO 4:
................................ 2 1
4
cover different aspects of the immunization
program including - operational efficiency,
epidemiological support, health system
strengthening and demand generation(See Box
1). These Key Objectives are interlinked and
mutually reinforce each other, thus providing
greater focus, structure and flexibility for
developing context-specific strategies and
interventions. Each Key Objective has a set of
Expected Results to be achieved in the medium
term and a set of actionable strategies that can
be contextualized in the State and District
implementation plans. The framework
elements are designed to be simple, feasible,
flexible and relevant to the needs of the people.
As part of providing better governance for the
program, the UIP strategic plan has a
comprehensive monitoring and accountability
tracking framework which consists of a key
indicators, targets, source of information,
assigned responsibility and information
dissemination.
UIP Strategic Plan: 2013-17
2 2M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
4.2 Impact indicators
4.3 Target population
KEY OBJECTIVE 1: Improve program
service delivery for equitable and
efficient immunization services by
all districts
1. Reduction in infant mortality rate
2. Reduction in cases of vaccine-preventable
diseases
RI interventions will be targeted at reaching out
to all eligible children and pregnant women as
per the national schedule. Given the equity
issues, special efforts will be made to ensure
that immunization services reach out to
targeted beneficiaries belonging to the lower
socio-economic strata, those living in urban
slums, rural areas, tribal and other hard-to-
reach areas.
The following section elaborates on the
strategic framework further
Vaccine logistics management is one of the
critical elements in the immunization program
to ensure that all vaccines are available at the
last cold chain point for immunization
sessions. Similarly, a reliable and adequate cold
chain network is essential to ensure that
vaccines are stored within the recommended
temperature ranges, and safe and potent
vaccines are delivered to children. Various
recent studies like Effective Vaccine
Management (EVM 2013), Vaccine Wastage
Study (2008), ITSU deep dive study, KPMG
vaccine logistics study (2013), ICMR Freezing
Study etc. have pointed out issues related to the
existing vaccine logistics system up to the last
cold chain point, and the capacity,
functionality and maintenance of cold chain
equipment at all levels.
Key Performance Indicators (KPI)
1. Number of States/UTs where > 95%
sessions were held as planned
2.%of districts having > 80% full
immunization coverage
3. Number of States/UTs having less than 10%
dropout from DPT1-DPT3 (or Pentavalent)
The indicators will disaggregated by gender,
geography (urban slum, urban, rural) and
socio-economic parameters, where relevant.
Expected Result 1.1: Strengthen the national
cold chain management system:
Maintaining a strong cold chain system is
critical for maximizing the operational
efficiency of UIP. Strategies to achieve this will
focus on capacity building, hardware
management and innovative technology.
Strategies
A national plan for cold chain management is
essential for improving overall UIP program
efficiency. The national cold chain plan shall be
based on various situation analyses on cold
chain and vaccine logistics management in the
country. The major components of the plan
will include:
a) National Standards:
One of the major gaps in cold chain
management is the absence of standards
performance parameters. The national cold
chain plan will include standards for the
following:
lVaccine storage at all levels as per WHO
standards
lCold Chain point expansion guidelines
lCold Chain equipment plan for different
levels of vaccine stores
lQuality maintenance of vaccines
lTemperature monitoring of cold chain
system
lHuman resource for cold chain and vaccine
logistics
lCCE testing lab
1. Develop National Cold Chain
Management action plan:
................................
2 3
b) Specification of equipment and accessories
A specification committee comprising
technical experts from the field, the National
Cold Chain Training Centre (NCCTC),
engineering colleges, IITs, and program experts
will be established to provide guidelines on the
technical specifications of cold chain
equipment and accessories.
c) Procurement guidelines for cold chain
equipment and accessories
Procurement guidelines for cold chain
equipment and accessories shall be developed,
and reviewed periodically by a technical
committee of experts convened by the
MoHFW. The guidelines shall provide
parameters for equipment procurement,
rationale for purchase, quantity, guidelines on
aging etc. The technical committee shall meet
at least once a year.
Stress will be placed on promoting indigenous
cold chain equipment which is contextualized
and adaptable to local needs and environment.
A Management Information System (MIS) for
tracking the working status of cold chain
equipment and spare parts will also be set up.
The plan will also focus on regular retiring of
old and sick cold chain equipment, regular
program reviews with cold chain officers, staff
trainings, maintenance and servicing of cold
chain equipment, implementation of MIS,
logistics and supply chain management.
d) Promote indigenous cold chain equipment
for immunization
To reduce costs and improve overall program
efficiency, the MOHFW will promote the use
of cold chain equipment that is locally
produced and ser viced by Indian
manufacturers. NCCVMRC will organize
consultative meetings with engineering
colleges, industries, IITs, national physical
laboratories, DG S&D to determine the safety
standard, program need and scale of
requirement required to fulfill the needs of UIP.
2. Enhance the capacity of the National
Cold Chain Vaccine Management
Resource Centre (NCCVMRC) and the
National Cold Chain Training Center
(NCCTC) to better manage the Cold
Chain and Vaccine Logistics
Management (VLM) system.
The NCCVMRC has been set up in National
Institute of Health and Family Welfare
(NIHFW) to conduct training and capacity
building activities on cold chain equipment and
vaccine management, including preventive
maintenance and repair, at the state level. The
center provides supportive supervision to states
to promote smooth functioning of cold chain
and vaccine management systems. The center
also undertakes cold chain and vaccine
management assessments and reviews jointly
with the Immunization division MOHFW,
UNICEF, WHO and other partners. It
functions as an extended wing of the
Immunization division (MoHFW) for cold
chain and vaccine management. The
NCCVMRC's needs enhancement in terms of
human resources recruitment, infrastructure
and equipment to be able to function effectively
(See Annex 3).
The NCCTC, which has been set up at SHTO
Pune, is the country's only cold chain training
center. The NCCTC will have its capacity
strengthened to perform the following:
lfunction as a testing lab of equipment
performance,
lexperiment with innovative technologies,
lsupport the MoHFW for procurement by
producing evidence on the specifications of
equipment and their performance,
ldevelop appropriate spare parts for all types
of cold chain equipment enabling local
repair,
ldevelop a training module of Cold Chain
Equipment (CCE) repair and maintenance,
lprovide maintenance support to GMSDs.
The center will be run as an independent body
U I P S T R A T E G I C P L A N F R A M E W O R K
2 4M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Table 4: Cold Chain equipment in the four GMSDs
* Needs 100 percent replacement of cold chain equipment
Kolkata
Chennai
Karnal*
Mumbai
Need 2 more WIC and 2
Need 6 more WIC and 2 more WIF
Need 8 WIC and 4 WIF
Need 6 more WIC and 2 more WIF
more WIF4
2
2
2
2
2
GMSD WIC WIF Future needs (within plan period)
with its own governance and management
structure reporting to the Director, NIHFW.
The National Cold Chain Management
Information System (NCCMIS), which is a
web-based system for tracking cold chain
equipment in real-time, shall be expanded to
cover all states. The system will be hosted on
NIHFW servers with helpline support
provided by NCCVMRC. Key objectives of the
NCCMIS are to provide guidance on:
lcold chain infrastructure up to the lowest
level with performance indicators;
lstock positions of cold chain equipment
spare parts at GMSDs and at the state level,
and specification for local procurement;
ltroubleshooting of cold chain equipment;
lcold chain and vaccine management
practices as per national norms;
lavailable trained HR in cold chain and
upcoming training programs; and
lcold chain space requirements for
introduction of new vaccines.
Currently, there are over 27,000 cold chain
points across the country. All states need to
plan and ensure that one cold chain point caters
to a population of 30,000 in rural areas, up to
50,000 population in urban areas, and 15-
20,000 population in tribal and hard to reach
3. Conduct a nationwide rollout of cold
chain MIS
4. Increase the number of cold chain
points closer to vaccination sites in
selected states and take up repairs and
maintenance work of the existing
equipment
areas, keeping in mind factors such as distance
from and time to travel to session sites.
................................
2 5
In addition to the GMSDs, each of the 39 State
Vaccine Stores need to have 50 percent of their
existing cold chain equipment replaced within
the plan period. Each of these stores should
have at least four WICs and two WIFs of 40
cub mt. which shall be put in place within the
plan period.
Each of the 139 Divisional Vaccine Stores need
to have one WIC of 40 cub mt and one WIF of
20 cub mt, which shall be put in place within
the plan period.
Before the end of the plan period, each District
Vaccine Store should have the following:
lone WIC and six DF in districts with a
population of more than 2 million ,
leight large ILR and four large DF in districts
with a population below 2 million.
Supplies of all non-electrical equipment
15
(vaccine carrier, ice boxes) and accessories
shall be updated as per the needs of every cold
chain point.
India is a vast country and putting a robust cold
chain system in place requires a larger number
of staff at all levels. As recommended in the
Mavalankar report there shall be a position
created for a focal point on cold chain at the
national level. Each state should also make
provision for a cold chain officer along with an
assistant at that level. In addition, each district
should have one Vaccine Logistics Manager
and one Cold Chain Handler. The majority of
issues and barriers related to cold chain and
vaccine logistics pertain to program
management rather than technical faults. All
staff associated with cold chain and vaccine
logistics will be provided training on various
aspects of program management.
6.Enhance management capacity and
numbers of cold chain and vaccine
logistics staff at all levels with the
district being responsible for stock
distribution planning, management and
repair.
7. Promote mentoring and supportive
supervision to ensure that vaccines are
stored within the correct temperature
range
8. Scale up a system for SMS-enabled
real-time temperature monitoring for
cold chain as part of electronic Vaccine
Intelligence Network (eVIN)
9.Enhance capacity of cold chain
handlers and mechanics across the
country
Various models of supportive supervision exist
-using line supervisors, externally hired
monitors or medical college faculty to provide
mentoring and supportive supervision. A
mixed approach will be applied based on state
requirements to ensure that RI sessions use
quality vaccines that have been stored at
appropriate temperatures throughout the cold
chain. Effective cold chain and vaccine
management consultants will be used to review
these improvement plans and vaccine store self-
assessments using standard formats and local
improvement plans from facilities visited
Real-time monitoring of cold chain equipment
along with prompt alerts and corrective action
are critical for the immunization program as all
vaccines under the program are temperature-
sensitive and cannot be used once damaged. As
most cold chain points in the country are
located in remote village settings with limited
facilities, a special SMS-enabled temperature
monitoring system has been developed and is
being currently piloted. The technology will be
further refined to prepare for its expansion to all
cold chain points in the country. As part of the
eVIN strategy, the possibility of unifying
vaccine logistics management, temperature
monitoring and cold chain equipment
inventory management into one system will
also be explored.
The training for vaccine and cold chain
handlers shall be based on standard technical
16
guidelines developed by the government. In
addition to induction training, the cold chain
mechanics and technicians will also be
15
Accessories include voltage stabilizer with every ILR and DF and toolkits for cold chain technicians
16
Handbook for Vaccine and Cold Chain Handlers 2010.Ministry of Health and Family Welfare,
Government of India and UNICEF.
U I P S T R A T E G I C P L A N F R A M E W O R K
2 6M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
provided training on cold chain equipment –
WIC, WIF, DF, ILR, cold chain accessories,
solar and hybrid equipment. Refresher
trainings will be held every three years to
sustain capacity and ensure quality.
Expected Result 1.2: Strengthen vaccine and
syringe logistics management across the
countr y including forecasting and
procurement at central level
A significant challenge in improving RI
coverage is lack of visibility at every levels in
the chain. Managers do not have real-time
vaccine stocks status at all levels, consumption
patterns, wastage rates and so on. Without such
information, it is difficult to hold system
functionaries responsible for lack of
performance, or to generate prompt responses
to breakdowns/bottlenecks in the vaccine
supply chain. Data from the states where
VMAT, EVMs and deep dives were conducted
by UNICEF and ITSU indicate that the
distribution of vaccines is uneven with some
cold chain points holding excess stock levels,
while others have stock-outs within the same
district or division. Even when there are few
stock-outs reported, there is evidence that store
managers are slowing down vaccine
distribution to cold chain points below them, or
to session sites as a means of preventing stock-
outs. This can lead to insufficient vaccines
reaching immunization sessions, thus directly
affecting the immunization coverage.
Strategies
Under the Universal Immunization Program,
vaccines and syringes are centrally procured
and supplied to States and Union Territories
(UTs). The details of vaccines/syringe receipt,
issue, wastage and consumption are
documented in a variety of registers across the
country. Some states have also started
computerized documentation of stock levels,
but only down to the district level. No
nationwide vaccine logistics management and
monitoring system currently exists that
provides real-time visibility of the stock data,
1. Develop a vaccine and syringe
logistics management system in the
country with real-time stock visibility.
consumption patterns, wastage rates etc. In
absence of such a system, a variety of ad hoc
principles and processes are applied in
distributing vaccines. With the potential
introduction of more costly vaccines under the
UIP, a robust vaccine logistics management
system is a dire need.
A vaccine logistics management model is being
developed that can cater to requirements at all
levels i.e. from GMSD to the last vaccine
storage point (last cold chain point). The
product will be field tested and updated to be
made ready for country-wide rollout. When
fully implemented, the system will also provide
better estimates for further procurement and
will outline the effects on the logistics system of
delays in procurement and erratic vaccine
supply patterns. Based on data analysis and the
vaccine supply schedule being followed, new
guidelines for defining minimum and
maximum stocks at different levels will also be
developed.
An effective vaccine logistic management
system must be supplemented by an operations
team that keeps the network operational as well
ensures prompt response based on data. The
government will introduce a position for VLM
at national, state and district levels at least in
the 12 high-priority states. The district-level
VLM will also oversee the functionality of cold
chain equipment in the district and will ensure
swift repair or replacement of cold chain
equipment with support from the district
refrigerator mechanic. These staff will be
provided training on vaccine logistics and cold
chain management.
There is substantial technology upgradation
going on rapidly across the world in the field of
vaccine logistics and cold chain management.
2. Strengthen HR capacity at all levels
for vaccine management, including
effective vaccine store management and
forecasting
3. Pilot new technology for improving
vaccine logistics and cold chain
management with an overall objective to
develop an electronic Vaccine
Intelligence Network (eVIN)
................................
2 7
These interventions can be useful in ensuring
the availability of safe and potent vaccines upto
the last cold chain point. Such technological
interventions will be field-tested for
performance and will be considered for
implementation with the ultimate aim of
developing an electronic Vaccine Intelligence
Network (eVIN).
Computer optimization models, such as
HERMES, will be used for exploring means to
maximize vaccine and syringe logistics
efficiency.
EVMs assessments were conducted in ten
priority states in 2013. These states include
Jammu & Kashmir, Haryana, Rajasthan, UP,
Bihar, Chattisgarh, MP, Karnataka, Kerala and
17
Tripura. The key recommendations from the
EVM assessments will be implemented
through the PIPs of the respective states. These
recommendations are included in Annex 4. A
trained pool of effective cold chain and vaccine
management consultants will review the
progress of PIPs in states that have completed
an EVM assessment and prepared
improvement plans.
Expected Result 1.3: Ensure safer injection
practices and reduced vaccine wastage
Strategies
The disposal of syringes and other waste
associated with immunization sessions shall be
based on the Biomedical Waste Management
and Handling Rules, 1998, and Central
Pollution Control Board (CPCB) Guidelines
for hospital and immunization waste disposal.
Under the NRHM, an Infection Management
and Environment Plan (IMEP) policy
framework has been formed to guide waste
disposal processes. These guidelines will be
widely disseminated and shared during review
meetings. All health facilities will have 'waste
management guidelines' prominently
4. Implement Effective Vaccine
Management (EVM) improvement plans
1. Review existing mechanisms and
policies on waste management
displayed at the site of waste generation.
India had adopted the Multi-Dose Vial Policy
(MDVP) for OPV during SIA campaigns. In
2011, the Multi-Dose Vial Policy was adopted
for the birth dose of the Hepatitis B vaccine,
and the zero dose of the Oral Polio vaccine in
the UIP. Later, in the year 2011, the Multi-Dose
Vial policy was adopted and implemented as
part of RI for the Pentavalent vaccine in two
states. The current open vial policy (OVP)
applies to multi-dose vials of DPT, TT,
Hepatitis B, Oral Polio and Liquid Pentavalent
vaccines (where applicable). This policy does
not apply to Measles, BCG, and Japanese
Encephalitis (JE) vaccines (See Annex 5).
Relevant immunization trainings shall have a
component on the OVP to facilitate the
appropriate use and return of vials and reduce
wastage. The policy of bundling shall be
adopted for all vaccines, AD syringes,
reconstitution syringes, diluents, disposal bags,
and hub cutters to reduce wastage and improve
logistics efficiency, wherever applicable. The
required amount of vaccines for a session will
be packed along with the needed logistics, so as
to ensure that safe injection practices are
adopted.
A vaccine wastage assessment carried out by
UNICEF in 2010 revealed high wastage rates
ranging from 61 percent (for BCG) to 27
18
percent (for DPT). The main causes of
wastage include vaccine expiry, discarding
unused doses, poor reconstitution practices,
exposure to heat, frozen vaccines, missing
inventory and theft.
To reduce vaccine wastage, all categories of
staff shall be trained on this aspect of the
program as part of their regular training
regimen and given job aids on injection safety
and safe waste disposal.
2. Strengthen the implementation of
Open Vial Policy (OVP) and Bundling
Policy to reduce waste at session sites
3. Scale up training on injection safety
and waste disposal guidelines for all
categories of staff
17
National Effective Vaccine Management Plan 2013: Summary Report. UNICEF and MoHFW.
18
Vaccine Wastage Assessment: Field assessment and observations from national stores and five selected states of India.
UNICEF, April 2010.
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4. Expand the availability and use of hub
cutters in all districts and explore other
technological advancements to ensure
safe and appropriate bio-waste handling
1. Conduct risk analysis at state and
district level
2. Provide training to and follow up with
relevant staff on preparing and
implementing RI micro-plans
To ensure safer injection practices, health
workers will be trained on the use of hub cutters
as part of their on-going trainings. In addition,
technological developments in injection safety
and bio-waste management will be explored
and field tested. Based on performance
evaluations, cost considerations, feasibility of
use at the field level etc., the inclusion of these
technologies in the Immunization program
will be considered.
Expected Result 1.4: Ensure that regular
immunization sessions are planned and held
and coverage increased
Strategies
The country has identified high-priority
districts for interventions under RMNCHA+A
where immunization coverage has been
considered a one of the key elements. States
have also identified high-priority district under
Emergency Preparedness and Response Plan
(EPRP) to prevent wild polio virus
importation. Further risk analysis will be done
to identify high risk blocks and urban dwellings
with low coverage.
Continuous training and skill building of
health staff involved in routine immunization
program is required to achieve and sustain
quality and coverage of immunization.
Training modules for frontline health workers,
medical officers and cold chain and vaccine
supply staff have been prepared and states are
using them regularly to train the staff. Ministry
updates these modules on regular interval and
provides to states. These modules include all
relevant components for preparation of plan
for RI and its implementation and monitoring.
However, the Government of India has
identified issues in implementation of training
that varies from state to state resulting in gaps in
performance. The Government of India will
encourage all states to develop a time-bound
schedule for training for all staffs and refresher
trainings at regular intervals. These cycles will
be aligned with annual PIP.
Guidelines for micro-planning and service
delivery have been developed and included in
the immunization handbooks for medical
officers and health workers. Health workers
and other relevant UIP staff will be trained on
preparation of micro-plans that ensure
inclusion of areas with underserved
population, hard-to-reach areas and others.
The efforts will be made to reach the un-
reached population at least four times a year.
The support of the development partners will
be sought for the micro-planning efforts. The
districts should ensure that micro-plans are
available and being used to provide
immunization services in the area.
MoHFW has recommended fixed-day, fixed-
time and fixed-site strategy for outreach
sessions for delivering immunization services
to ensure that communities are aware of the
immunization day that is now being
implemented by all states. Under this strategy,
the Government of India has recommended
that immunization sites be fixed for each
habitation, preferably at sub-centers; in villages
at anganwadi centers, school and panchayat
chaupal, etc. The day of the week and time of
session in a particular location are also fixed.
The immunization session can also be
combined with Village Health and Nutrition
Days (VHNDs) under NRHM to help
maximize the opportunity for community
mobilization and service delivery.
The Government of India is planning to
strengthen health service delivery in urban
areas now. This will be further strengthened
with special focus to reach poor and
underserved populations living especially in
slums, streets and peri-urban areas.
3. Promote fixed-day, fixed time and
fixed site strategy
................................
2 9
4. Fill up gaps in RI coverage through
strengthening alternative vaccine
delivery to provide needs-based
immunization services in difficult to
reach areas
5. Reduce left-outs and missed
opportunities, drop-outs and ensure
booster doses
To ensure improved vaccine and logistics
supply and help ANM to spend more time at
outreach session site and focus on improving
immunization service delivery, the
Government of India has provided funds for
implementing alternate vaccine delivery
(AVD) system. These efforts will be further
strengthened. Under the plan for
intensification of RI, the Government of India
has planned to provide vaccine delivery vans to
high-priority districts and blocks to strengthen
vaccine supply. In this regard, the Government
of India has already provided 120 vehicles in
six districts of five states – Madhya Pradesh,
UP, Haryana, Jammu & Kashmir and
Rajasthan to implement a pilot before
expansion. These vehicles have been branded
“Teeka Express”. These vehicles will be used
not only for vaccine delivery but carrying other
logistics for immunization sessions, promoting
IEC for RI, running mobile health clinic etc.
depending on the need of the district.
The Government of India aims to identify all
areas/populations/opportunities to reduce
left-outs and to improve booster coverage
beyond primary immunization schedule. This
is also important in view of new antigens being
introduced in UIP. To improve the access with
the aim of reducing left-outs the Government
of India has developed guidelines to include all
high risk populations/areas, identified through
polio eradication program, in the routine
immunization micro-plans. The Government
of India has also recommended to use polio
micro-plan to identify all small areas/hamlets
under each sub-center area to be reflected in
micro-plan to improve reach and monitoring. It
will be further strengthened by identifying all
opportunities and places like OPDs and
schools to enquire and vaccinate children..
a) Health facilities: Every contact of health
care system with children of vaccination age
will be used to enquire about the child's
vaccination status. Vaccines will be
administered where applicable, provided the
minimum interval between doses is respected.
Possible reasons for non-vaccination shall be
identified and addressed.
b) Schools: School health programs will be
strengthened. The LHVs will visit every school
with ANMs at least once a year with vaccines
to assess the immunization status of children
and ensure vaccination with DPT of children
aged 5–6 years, and TT vaccination for children
aged 10 and 16 years.
Once a beneficiary is registered, all the efforts
will be made to ensure full utilization of
immunization services for completion of
immunization scheduled. Special efforts will
be made in the areas where immunization
coverage is low and dropout rates are high.
a) Strengthen use of Due List by frontline
health workers for tracking beneficiaries and
improve communication with parents to
reduce drop-outs:
Ensure that states and UTs make available the
standardized Due List to all the FHWs with
appropriate guidelines and trainings for its
effective use.
b) Strengthen Mother and Child Tracking
System (MCTS): The Government of India has
launched Mother and Child Tracking System
to improve registration of pregnant women and
infants and utilization of Ante-Natal Care
(ANC) and immunization services. This is
being implemented as a mission mode project
and all states have implemented this. The
implementation and utilization of MCTS will
be further strengthened to achieve the
objectives.
States will utilize the NRHM framework to
innovate to increase immunization coverage.
The best practices and successful examples will
be disseminated widely for cross learning and
adoption by the states.
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6. Strengthen the RI supervision and
monitoring system
7. Involve private facilities in delivering
RI services
8. Plan and conduct immunization weeks
at regular intervals to improve coverage
level in missed out and hard-to-reach
areas, followed by integration of these
areas under the district RI micro-plans.
1. Conduct bi-annual national level
meetings of state EPI officers
MOHFW will focus on improving program
supervision and monitoring for RI at all levels
using data generated in the program and
through field monitoring. RI partnership in the
country is actively participating in monitoring
of implementation at field level and assisted
states in involving their program managers and
staff in the monitoring. Haryana has developed
a monitoring system by involving independent
monitors using NRHM funds. Other states will
also be encouraged to prepare plans for
monitoring and propose in PIPs.
The involvement should be underpinned by
accountability and quality standards that are
regulated by the state nodal medical authority.
Public and private practitioners providing
vaccination will be provided free of charge
vaccine and immunization cards etc. All
private practitioners, offering vaccination
services, will be expected to maintain
appropriate institutional records, retrievable on
demand. They will also be expected to report
coverage, VPDs, AEFI, and wastage on a
monthly basis. Private sector accountability
and quality issues will be coordinated by the
nodal medical authority providing the vaccines
19
as per the Government of India guidelines.
Necessary efforts will be made to implement
the guidelines for involvement of private
practitioners in immunization program.
Expected Result 1.5: Improve program
coordination at all levels
Strategies
National-level half yearly meetings of all state
EPI officers will be conducted regularly. State
immunization officials will be requested to
conduct regular and quality quarterly review
meetings with district immunization officers to
strengthen the program at ground level.
The Government of India has issued directives
to all states for setting up state and district-level
task force on immunization for improved
program coordination and monitoring. States
will ensure that these task force meetings are
held every month and necessary feedback is
shared with national immunization division.
The ministry recognizes various efforts being
done and the support provided by development
par tners in routine immunization
strengthening both at national and sub-
national level. Efforts will be made to ensure
better coordination between government and
development partners through regular
coordination meetings, partner's forum and
other relevant platforms.
IAG, which has been setup by MoHFW, will
advise and provide technical inputs to the
national immunization division on ways to
improve routine immunization coverage and
issues around newer and underutilized
vaccines.
1. % of caregivers whose child received partial
or no immunization who did not feel the need
for adhering to the schedule of immunization
2. % of caregivers not recalling any of routine
vaccine
The indicators will be disaggregated by gender,
2. Improve coordination with
development partners through regular
meetings and information sharing
3. Promote immunization and related
interventions through Immunization
Action Group (IAG) including academia,
CSOs, political representatives
KEY OBJECTIVE 2: Increase demand
and reduce barriers for people to
access immunization services
through improved social
mobilization.
Key Performance Indicators (KPI)
19
Guidelines for involvement of private practitioners in the universal immunization program (UIP). Government of India,
Ministry of Health and Family Welfare, Immunization Division, 31 August 2009.
................................
3 1
geography (urban slum, urban, rural) and
socio-economic parameters, where relevant.
Expected Result 2.1:Develop and implement a
multi-pronged national communication
strategy with a focus on priority states
Strategies
A national strategic communication plan for
RI will be prepared. States and districts will
also be encouraged to prepare an integrated
communication work plan. This plan will have
focus upon components and strategies for
addressing the issues related to left-outs and
drop-outs, and to increase community
participation in immunization.
The IRI communication guidelines have been
developed by the Government of India to
provide a roadmap to the immunization
program managers and IEC functionaries at
state, district and block level. These guidelines
can be used as a reference while formulation
20
state-specific communication plans.
National and state-level workshops will be
conducted for immunization program
managers and other staff working on
communication. The trainings will focus on
strengthening their communication and
planning skills to better operationalize and
implement IEC interventions. MOFFW will
also conduct regular national and state-level
meetings to monitor the progress, identify gaps
and suggest possible solutions on
communication strategies. In addition,
effective communication activities and best
practices will be documented and shared with
all the stakeholders to be used for inter-state
learning.
Enhanced partnerships with CSOs and NGOs
will promote greater awareness and access to
1. Develop state-specific
Communication Implementation plans,
advocacy and social mobilization plans
2. Strengthen national and state capacity
on behavior change communication
3. Engage with partners to ensure a
wider dissemination of immunization
messages.
RI services. The CSO engagement strategy will
focus on engaging civil society in policy and
advocacy processes. The Government of India
will engage the private sector to work in
immunization program as part of their CSR
utilizing their strengths in communication.
NRHM has provided necessary flexibility to
use funds for activities related to immunization
program. The available funds with districts will
be utilized for health communication. The
untied funds with AWW/ASHA, VHSC and
ANM may also be used for these
communication efforts, if funding from other
sources is not available. States will be
encouraged to prepare a detailed IEC plan for
immunization and funds will allocated to this
activity from NRHM PIP part A
Expected Result 2.2:Effective communication
channels are set up with the community for
better acceptance of vaccines
Strategies
Utilize the widespread network of over
860,000 ASHA workers to conduct social
mobilization for improving immunization
coverage. Interpersonal communication (IPC)
with individuals and families will be strongly
promoted through the frontline health workers
– ASHA, ANM, Anganwadi workers and
other key leaders in the communities.
The Government of India has developed a
training kit to improve IPC skills of frontline
health workers to improve awareness among
parents about need for immunization and
completion of recommended schedule and to
reduce fear of AEFI to reduce drop-outs. All
FHW will be trained on using this kit.
The community members, non-government
organization and interest groups in
4. Ensure adequate funds are available
for communication interventions
1. Use frontline health workers and
community platforms like Village Health
and Nutrition Day to promote RI through
inter-personal communication (IPC)with
families
20
Intensification of Routine Immunization: Communication Operational and Technical Guideline. 2012.
Immunization Division, Ministry of Health and Family Welfare. Government of India.
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immunization like women's self-help groups
will be involved in advocacy for
implementation and increasing demand for
services. Events like VHNDs will be utilized as
opportunities for community mobilization.
Wherever reports of mistrust towards
immunization by community members are
noticed, these should be studied and
appropriate corrective actions need to be taken.
At the community level there is a greater scope
of better social mobilization and reaching local
community leaders through convergence of RI
with ICDS, women self-help groups and
panchayati raj institutions. The program will
also seek to involve local MLAs and MPs to
utilize their funds to ensure that each and every
child in their community is vaccinated. Local
institutions, community networks, and
religious groups will also be reached out in
coordinated way to reach specific groups of
people for dialogue with planned messages.
School children and adolescents will also be
engaged as change agents to dispel myths and
misconceptions related to immunization.
Expected Result 2.3: Evidence based and
contextually relevant communication
messages are disseminated in the community
Strategies
Targeted communication will be needed for
those who have never participated before, or
who are not participating consistently because
of lack of knowledge, doubts and
misconceptions, or frustration with the quality
of health services. The issues and barriers for
the immunization will be addressed in the
integrated communication work plan. The
focus will be on SC, ST population, migratory
2. Promote inter-sectoral synergies
between organizations, communities
and individuals on promoting
immunization
1. Identify issues and barriers for
immunization in hard-to-reach
populations and address them in the
communication plan
population and difficult to access areas. The
reasons for low coverage and level of
knowledge about immunization program will
be regularly assessed. The findings from these
assessments will be a base for communication
and social mobilization plans.
Promote the RI branding with a new logo color
coding and tagline through various media.
New audiovisual communication messages for
TV and radio along with print material will be
developed. The government will also use social
media as a parallel communication channel to
increase visibility about RI with multiple target
audience. The program will strengthen delivery
of interpersonal communication using Polio
SMNet (from UNICEF), school teachers,
student networks, national-level youth
networks to support social mobilization.
Institutions like NSS and NCC will be
mobilized to reach out of school youth and
eligible children in hard-to-reach population
areas
Standard Operating Procedures (SOPs) will be
developed for production of new
communication materials and their
dissemination to the states.
The Government of India will engage all
categories of media – print or electronic
–through regular workshops, meetings and
field visits to advocate for and create an
enabling environment that leads to an
increasing demand for immunization services.
With newer vaccines planned for introduction
in the coming years, all efforts will be made to
educate people and dispel any misinformation.
Communication strategies for newer vaccines
including campaigns will be developed in
consultation with all stakeholders.
2. Develop and disseminate widely, new
communication material on
immunization
3. Increase people's confidence in
vaccine safety through generation and
dissemination of supportive data
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3 3
4. Develop effective communication
response for AEFI crisis management
KEY OBJECTIVE 3:Strengthen and
maintain a robust surveillance
system for vaccine-preventable
diseases (VPDs) and Adverse Events
Following Immunization (AEFI)
To dispel any public misapprehension around
adverse events following immunization the
Government of India will develop
communication guidelines to handle situations
around AEFI.
The burden of diseases preventable by the
vaccines is the most significant factor for
making a decision on introducing relevant
vaccines in the UIP. Therefore, a robust
surveillance system to detect cases and deaths
due to vaccine-preventable diseases is essential
to generate evidence to inform the decision on
introducing the vaccine as well as to measure its
impact on the disease after its introduction.
Besides that, the completeness and quality of
VPD surveillance data is also necessary to
observe the trends in disease incidence and
geographical spread to help plan to strengthen
the immunization program. Reporting of
VPDs has been an integral part of UIP
reporting system. Major challenges for UIP
include the following:
lweak capacity of frontline health workers to
identify cases,
llack of attention in the health system for
VPD reporting,
lpoor coordination between various
surveillance systems
lpoor reporting from private sectors and large
institutions.
This has adversely impacted informed decision
making on newer vaccine introduction and
vaccine impact assessment. Therefore, it is
necessary to
ldevelop the capacity of health workers for
improved detection of VPDs,
lhave regular review of reports and data
limprove coordination among various
surveillance systems
linclude private sectors and other institutions
for improving VPD surveillance in the
country.
The goal of immunization is to protect
individual and the community from vaccine-
preventable diseases (VPD). Although modern
vaccines are safe, no vaccine is entirely without
risk; adverse reactions will occasionally occur
following vaccination. Some people experience
adverse events after immunization ranging
from mild side-effects to rare life-threatening
illnesses. However, in most serious cases these
events are merely coincidences. In others
words, they are caused by the vaccine or by an
error in the administration or handling of the
vaccine. Sometimes there is no causal
relationship between the vaccine and the
adverse effects. Maintaining public trust in
vaccine safety, therefore, is key to the success of
21
all vaccination programs.
Irrespective of the cause, when adverse events
following immunization (AEFI) occur, people
become confused to the extent that they refuse
further immunization of their children, making
the children susceptible to VPDs that are more
disabling and life-threatening. Surveillance of
AEFIs, i.e. systematic collection of data on
events following immunization,
provides valuable information to help plan and
take necessary actions in order to sustain public
confidence and ensure smooth functioning of
the program. The national AEFI surveillance
program supports the effective vaccine
pharmacovigilance function for ensuring use
of safe vaccines. Aggregate data for serious and
non-serious AEFI are currently collected
through routine monthly reporting in the
HMIS but, details of serious AEFIs are also
reported directly using the FIR, PIR and DIR
formats.
Along with the national health programs, such
as HIV and TB, that generate their own
respective data through surveillance, different
surveillance systems in India provide
information of various diseases, including
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Immunization Safety Surveillance: Guidelines for Managers of Immunization Programs on Reporting
and Investigating Adverse Events Following Immunization. WHO Regional Office for Western Pacific. 1999.
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VPDs. These include:
Integrated Disease Surveillance Project
(IDSP): This is a nationwide system that
captures information on outbreaks of diseases
including VPDs, such as diphtheria, pertussis,
measles, AES, AFP, and Hepatitis B.
Central and State Bureaus of Health
Intelligence (CBHI and SBHI):This
nationwide system captures information on
suspected cases through passive surveillance
including that of VPDs that are under the
current UIP.
Health Information Management System
(HIMS): Within the NRHM framework,
HMIS is an electronic data reporting system
that captures data for health service delivery at
health facility level every month to assist health
departments, at all levels, in managing and
planning health programs. HMIS also captures
information on VPD disease burden from sub-
block level on a monthly basis.
WHO supported AFP and Measles outbreak
surveillance through NPSP network: AFP
surveillance is a laboratory-based system for
poliovirus detection in all states. The lab-based
measles surveillance covers 15 states
generating data on measles and rubella
outbreaks. The laboratory assisted joint AFP-
measles surveillance system is planned to cover
all states and UTs by the end of 2014.
Acute Encephalitis Syndrome (AES/JE)
surveillance: This is a facility-based
surveillance system providing information on
AES as per the guidelines under the National
Vector-Borne Disease Control Program with
lab support provided by ICMR.
Multicentre Pneumonia and Meningitis
Surveillance: Sentinel surveillance sites are
functional to identify etiologic diagnosis of
pneumonia and meningitis among children
below two years.
Rotavirus Surveillance Network in India:
The Indian Rotavirus strain surveillance
network is functional in seven regions, four
hospitals and four labs. Children below five
years admitted with acute gastroenteritis and
given rehydration for at least six hours are
enrolled. Sites for sample collection for
Rotavirus surveillance are in following cities:
Delhi, Mumbai, Pune, Vellore, Jabalpur,
Imphal, and Kolkata.
1. % of sentinel sites providing timely and
complete reports on VPDs (including zero
report) on 90% occasions
2. Increase in the number of notified serious
AEFI cases above the 2012 baseline value
The indicators will be disaggregated by gender,
geography (urban slum, urban, rural) and
socio-economic parameters, where relevant.
Expected Result 3.1:Institutionalize and
strengthen surveillance mechanisms for VPDs
Strategies
There is a need to use epidemiological methods
to better measure the impact of the
immunization program. This will involve an
initial landscaping of existing surveillance
systems in the country, efforts will be made for
collating, and analyzing data on VPDs
generated from different surveillance systems
and collate them to provide appropriate
feedback. The following will be analyzed:
ldata on the VPD disease burden,
lemerging trends in the molecular
epidemiology of different VPD antigens,
lseroprevalence of protective antibodies
against the VPDs,
lgeographical variations in VPDs.
MoHFW will work towards developing a
system that facilitates convergence of relevant
data from various surveillance systems, such as
IDSP and NPSP, in the country.
Key Performance Indicators (KPI)
1. Assessment of trends on VPD burden
in context of reported immunization
coverage
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3 5
2. Strengthen and improve coordination
between Health information system
(HMIS) and disease surveillance
systems such as IDSP and NPSP to
gather information on VPDs
3. Involve private sector in reporting of
VPDs to further strengthen surveillance
systems and inform policy making
4. Strengthen laboratories(including
polio and measles lab network) and
epidemiology units at medical colleges
and other institutions for timely
reporting, case investigation and
detailed data analysis
IDSP-based surveillance system, along with
other systems, need to be strengthened from
district onwards to capture information on all
VPDs. The model of District/Municipal
Corporation-based surveillance unit for action
and reporting to the state would be further
strengthened. To better streamline information
sharing on VPD and AEFI occurrence across
the country, MoHFW will strengthen
coordination and data sharing between IDSP
and Immunization Division at national level to
monitor and improve program performance.
Similarly coordination at the state and district
levels will also be promoted to strengthen
DIO's role as focal person for all information
on VPD and AEFI.
In view of the number of patients using private
healthcare, lessons learnt from Kerala will be
used to link surveillance and monitoring
mechanisms with the private sector.
Community reporting of VPDs will also be
encouraged and specific strategies will be
reviewed. Mechanisms for coverage data
collection, compilation and flow from session
sites/sub-centers/private clinics to the district
and then to the State on uniform patterns will
be highlighted. VPD surveillance mechanisms
will attempt to integrate as much as possible
with other surveillance mechanisms, without
losing the required responsiveness for outbreak
response or diluting the focus on AFP
surveillance.
For improved coordination and information
sharing Infectious Diseases Hospitals(IDH)
and super speciality hospitals should be
integrated into IDSP. There is a network of
IDH that needs to strengthen their laboratory
capacity to provide updated information on
outbreaks of existing or potential VPDs. India
has developed a Health Management
Information System (HMIS) for reporting of
all health-related data from field. This tool will
be used for updating VPD surveillance data in
India.
Improve coordination, information sharing
with existing agencies and systems such as
IDSP, ICMR, CBHI and SBHI networks so as
to coordinate, collate and generate robust data
that will guide a more evidence-based policies
and program inter ventions in the
immunization program future.
Expected Result 3.2: Institutionalize and
strengthen surveillance mechanisms for AEFIs
Strategies
The national AEFI guidelines mandate that all
states and districts in the country constitute
AEFI committees at each level, to assist in
streamlining AEFI reporting mechanism,
investigating serious AEFI, and be involved in
causality assessment at state and national level.
An AEFI secretariat for the National AEFI
committee has been set up at ITSU-MoHFW,
New Delhi, to coordinate all AEFI related
activities in India with technical support and
oversight from a leading medical college
(LHMC). In addition Zonal AEFI consultants
are planned to be in place to provide technical
support and oversight to the AEFI Secretariat
in the four zones of the country and enable
timely reporting, investigation and support to
the states.
The National AEFI committee has been
reconstituted to support the program in
reviewing and updating information on tasks
and responsibilities of key stakeholders in the
AEFI system, including the Drug Controller
5. Strengthen sentinel surveillance for
newer antigens
1. Revitalize the institutional framework
and guidelines for AEFI surveillance in
the country
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General of India (DCGI), Indian
Pharmacopoeia Commission (IPC), National
UIP managers and state-level UIP managers.
National AEFI Operational Guidelines, which
were revised in 2010, are being revised and will
22
be published in 2014. These guidelines will be
distributed to all medical officers till Primary
Health Centers and will be used for training the
UIP staff including ASHA and ANMs.
Innovative AEFI reporting models shall be
piloted to enable enhanced AEFI reporting.
The revised guidelines will also be utilized for
trainings of AEFI committee members in the
country. An abridged Standard Operating
Procedure (SOP) for AEFI surveillance and
case investigation version been printed and
23
widely disseminated in 2011. There is well
known poor reporting of minor AEFIs in
India. The efforts will be made to train the field
staff in collecting data on minor AEFIs and
pass this information to the next level.
Since 2010, India has been participating in
WHO Global network of post-marketing
surveillance and the Government of India has
nominated Maharashtra state for uploading
AEFI data into the Uppsala Monitoring Centre
vaccine safety database. The national
immunization division has also started
coordination with the IPC, the coordinating
agency for the National Pharmacovigilance
Program of India to collate and monitor
vaccine safety reports in the country. The
National AEFI Program already shares all data
on vaccine safety with the national regulatory
authority to inform all vaccine safety
stakeholders.
AEFI surveillance data require detailed
analysis on numerous parameters in the
context of the doses distributed and children
vaccinated in the UIP. Currently serious AEFIs
2. Train field level staff on new National
AEFI Guidelines
3. Convergence with vaccine
pharmacovigilance stakeholders and
private sector for AEFI reporting and
analysis
4. Electronic database and reporting
system for AEFI
are reported manually on FIR/PIR and DIR
formats by districts but can be transmitted
electronically to the higher level (state and
national). The government will pilot an
electronic AEFI database and reporting system
that is E2P compliant for AEFI reporting by
2015 in a phased manner.
As UIP evolves, newer antigens, such as
rotavirus, JE, rubella, Pneumococcal and
Pentavalent vaccines, are expected to be
introduced and expanded in the schedule. This
will require a strong epidemiological
underpinning for estimating disease burden in
the country through a robust surveillance
system to be put in place. There will be a need
for improving coordination among different
stakeholders and experts to develop an
evidence-based policy for introducing newer
antigens in the program in the medium term. In
addition to newer antigens, improved service
delivery will require innovations in technology
and approaches.
The choice of newer vaccines to be included in
the UIP will be determined and periodically
reviewed by the MoHFW, taking guidance
from the NTAGI. Basic clinical and
operational studies will be encouraged to
provide inputs for NTAGI. These studies will
provide evidence for decisions on the timing
and selection of new vaccine introduction and
provide guidelines for the use of these new
vaccines. Such analysis will include the major
mortality-causing diseases of children in India,
namely acute diarrheal diseases and acute
respiratory diseases, in anticipation of
rotavirus vaccine and pneumococcal vaccine
becoming available. Disease burden and health
economic analyses will help assess the cost-
benefit ratios of new vaccine introduction. Box
2 captures the key principles that will guide the
inclusion of newer vaccine in UIP as per the
national vaccine policy 2011. However,
introduction of new vaccines would be as per
decision of Mission Steering Group (MSG)
following NTAGI recommendations.
KEY OBJECTIVE 4: Introduce and
expand the use of new and
underutilized vaccines and
technology in UIP
22
Adverse Event Following Immunization (AEFI): Surveillance and Response Operational Guidelines. MoHFW,
Government of India. 2010.
23
Standard Operating Procedures for reporting AEFI. MoHFW, Government of India. 2011.
................................
3 7
Box 2: Principles to guide the inclusion of newer vaccines
• Disease burden (incidence/prevalence, absolute number of morbidity/mortality,
epidemic/pandemic potential);
• Safety and efficacy of the vaccine under consideration;
• Affordability and financial sustainability of the vaccination program, even if the initial introduction is
supported by the external funding agency;
• Program capacity to introduce a new antigen, including cold chain capacity;
• Availability of a domestic or external vaccine production capacity;
• Cost effectiveness of the vaccination program and also of the alternatives other than vaccination
Key Performance Indicators (KPI)
1. Institutionalize mechanisms to guide
the introduction of newer and
underutilized vaccines in the country
1. Number of newer vaccines that have been
reviewed for introduction in UIP by NTAGI
2. Number of States that have introduced
Pentavalent vaccine
The indicators will be disaggregated by gender,
geography (urban slum, urban, rural) and
socio-economic parameters, where relevant.
Expected Result 4.1: Set up and strengthen
institutional mechanisms, framework and
policies for newer and underutilized vaccine
introduction
Strategies
The introduction of new vaccines involves
reviewing all licensed vaccines in different
parts of the world and identifying those that
would be relevant to India in the context of the
burden of disease in the country and
prioritization of target vaccine-preventable
diseases in the country. There are several
vaccines that are popular in the private market,
and many of those are recommended by the
Indian Academy of Pediatrics. Accurate
information on which to base the decision of
introducing a new vaccine to the UIP requires
periodic review and assessment on an objective
scale by all agencies concerned through strong
coordination and collaboration.
In this regard, the immunization decision-
making process has been institutionalized by
the establishment of an independent advisory
body, the National Technical Advisory Group
on Immunization (NTAGI) in 2001,
comprising of independent experts from
diverse fields such has immunology,
community medicine and health economics;
representatives from partner organizations like
WHO, UNICEF, ICMR and DCGI as well as
liaison officers from the government. The
NTAGI has been reconstituted twice in 2008
and again in June 2013. The current
reconstituted NTAGI comprise of a Standing
Technical Sub-Committee (STSC) tasked with
undertaking a detailed technical review of the
issues highlighted above and a broader body
with representations from all organizations
mentioned above. In addition, a secretariat for
this advisory body has been established by
ministry under Immunization Technical
Support Unit to facilitate technical and
managerial support required for continuity and
follow up to this body. However, the mandates
of both the NTAGI and STSC are still work-in-
progress. The spelling out of well-defined
Standard Operating Procedures (SOPs) for the
functioning and decision making of the
U I P S T R A T E G I C P L A N F R A M E W O R K
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NTAGI is necessary to institutionalize the
evidence-based decision-making process for
the introduction of new and underutilized
vaccines in the country. It is also imperative to
adopt and standardize mechanisms to grade
the quality of evidence available, such as
burden of disease, published literature, global
data, cost effectiveness data, for the NTAGI to
r ev i ew a n d m a k e ev i d e n c e - b a s e d
recommendations.
There are several vaccines that are already
licensed and available or soon to be licensed
with expanded indications for particular
groups in India. Unfortunately, access to the
bulk of these vaccines is available only to the
privileged few who have access to private
health care. The NTAGI is the highest advisory
body tasked to review the available evidence
on disease burden, potential impact, safety,
efficacy etc. To assess these vaccines and
prioritize vaccines for inclusion in the program.
Vaccines that can be potentially considered for
review include the Injectable Polio
Vaccine(IPV), rotavirus and pneumococcal
vaccines
The absence of reliable baseline estimates for
the burden of VPDs in India is a major obstacle
in informed policy-making process. Currently,
there are multiple systems to measure different
VPDs including antigen/disease specific
sentinel surveillance network (Indian
Rotavirus Sentinel Surveillance Network,
National Polio Surveillance Program (NPSP)
network and Infectious disease surveillance
eProgram (IDSP). With plans to expand the
range of vaccines in the UIP and improve its
reach (coverage), the surveillance of VPDs will
be intensified and steps will be taken to
establish stronger collaboration between the
already established networks and the
immunization program. At the national level,
2. Identify newer vaccines that will be
introduced and/or expanded to use
during the plan period
3. Assess disease burden for which
vaccine are becoming available or will
become available in the near future
the newly formed STSC of the NTAGI has
been tasked for undertaking critical review of
disease burden data prior to recommending the
introduction of a new vaccine in the UIP. The
NTAGI secretariat at ITSU will collaborate
closely with the disease surveillance centers in
the country to collate the evidence for the
review of the NTAGI and STSC.
Generate evidence for introducing new vaccine
– including areas like vaccine safety, equity,
vaccine ethics and financial sustainability, IPV
as part of post-polio eradication.
Expected Result 4.2: Scale up and sustain the
implementation of JE vaccination in identified
endemic districts as part of Japanese
Encephalitis (JE) control
Strategies
In India there are 175 districts currently
identified as being endemic for JE. Most of the
cases occur in UP and Assam. Though any age
group can be affected by JE, children between 1
and 15 years of age bear the brunt of the
disease. A study carried out in South India
showed JE incidence to be 15/10,000 children
between 5 and 9 years. Mortality due to JE has
been estimated to be between 20 and 30
percent. Recent studies under the WHO
surveillance program in India undertaken in
selected centers (Bellary, Dibrugarh, Madurai
and Burdwan) show that about 10 to 20 percent
of the total Acute Encephalitis Syndrome
(AES) cases are JE.
JE, at present like other vaccines in India's UIP,
is restricted to children but there is an
increasing demand for use of JE vaccine to
protect the adult population in endemic
districts. The NTAGI will discuss the safety
and immunogenicity data of the vaccine for use
in the program. Since JE is a vector-borne
disease, immunizing adult populations will
prove critical in breaking the transmission cycle
and control of the disease.
4. Conduct operational research
1. Identify disease burden and endemic
districts for prioritization
................................
3 9
2. Continue JE campaign in the endemic
districts
3. Expand training and advocacy on JE
vaccination
4. Introduction of JE vaccine in routine
immunization program
ICMR recommends that JE vaccination
program should continue for another five years
in endemic areas. It was suggested, that in view
of low evaluated coverage with JE vaccine, the
strategy in 2010 should be to re-immunization
all children up to 15 years with high vaccine
coverage in a campaign mode. Thereafter
coverage should be sustained by immunization
of children below than 2 years through Routine
24
Immunization.
Coverage survey conducted for JE vaccine
suggests that overall community knowledge on
JE vaccines is low. While some people are not
convinced about the need for JE vaccination,
others do not know where to access the vaccine
from. Some pockets of communities have fear
of side effects or have formed a negative
opinion on the vaccine following some AEFIs
25, 26
in their area.
Information about JE vaccination has been
incorporated in immunization handbooks for
Medical officers and health workers.
Operational guidelines for JE vaccination
program has been prepared and widely
disseminated to ensure correct reporting and
clarification on the role and responsibility of
each health care provider in JE vaccination.
Publicity around the JE vaccination will be
made more intense prior to the campaign dates
and respective states shall ensure that the IEC
material reaches the target users well in in time.
Adverse publicity around the vaccine will need
to be countered through appropriate messages.
The planned strategy was to complete SIAs for
JE vaccine and subsequent introduction of the
JE vaccine routine immunization program of
endemic districts to ensure adequate
vaccination coverage for new birth cohort. As
from April 2013, the Government of India has
already introduced a 2-dose schedule for JE
vaccines in the districts implementing JE
routine immunization. The 1st dose is given at
9 months of age and the 2nd dose at 16 – 24
months of age
In India, currently the SA-14-14-2 imported
from China is being used in the national
immunization program. Efforts will be made
to ensure that JE vaccine is produced
indigenously from local strains and introduced
in the program.
Expected Result 4.3: Streamline and expand
the use of Pentavalent vaccine to cover all the
states
Strategies
As of 2012, the Haemophilus Influenzae b
(HiB) vaccine has been introduced in eight
states of India (Tamil Nadu, Kerala,
Karnataka, Puducherry, Goa, Gujarat, Jammu
and Kashmir and Haryana) in the form of the
combined Pentavalent vaccine (DPT+ Hep B+
HiB). On 23 September 2013 the NTAGI
endorsed the STSC's recommendation for
further scale-up of the vaccine in the remaining
states of India in a logistically structured
manner with simultaneous strengthening of
the AEFI and sentinel surveillance systems in
the country. Preparations for the expansion of
vaccination to the other states are planned. The
operational guidelines on HiB as part of
Pentavalent vaccine have been already been
developed and will be useful for immunization
program managers at state, district and sub-
27
district level.
5. Roll out indigenously produced JE
vaccine
1. Nationwide scale up of Pentavalent
vaccine to introduce HiB vaccine in
other states of the country
24
Minutes of the Meeting of ICMR Core Committee on Vaccines. 2010
25
Japanese Encephalitis Coverage Evaluation Survey Report, 2008. UNICEF and NRHM
26
A coverage evaluation survey of JE vaccination in two districts of Karnataka. Kumar KR et al. Journal of Communicable Diseases.Sep2010;42(3):179-84;
27
Operational Guidelines: Introduction of HaemophilusInfluenzae b (HiB) as Pentavalent Vaccine in Universal
Immunization Program (UIP) in India. MoHFW, Government of India. 2011.
U I P S T R A T E G I C P L A N F R A M E W O R K
4 0M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
2. Conduct a revision of recording and
reporting formats for improved
surveillance and data management
3. Conduct training of FHWs and their
supervisors on newer vaccine
4. Strengthen surveillance system for
HiB and AEFI reporting
Introduction of newer vaccines will
accompany the revision of recording and
reporting formats. Vaccination cards will also
be revised and updated to include newer
vaccines. The reporting system in the country
will also have necessary column to collect
information on newer vaccines.
ANMs and their supervisors will be trained on
newer vaccines and other related aspects
including the vaccine administration and AEFI
reporting as part of regular training. The DIOs
and other Mid-level managers (MLM) will be
specially trained prior to the new vaccine
introduction in their respective states.
The surveillance system for newer vaccines will
be further strengthened and expanded in India.
Eleven sentinel sites for HiB meningitis in six
different states have already started in 2013.
These selected sites for bacterial meningitis
surveillance (including HiB) will monitor the
disease trends to measure impact trends of
vaccination on the study populations. The
surveillance sites for other newer vaccines are
also likely to be introduced to cover additional
states. Model AEFI systems are also being
planned to ensure timely reporting and
management of AEFIs before they snowball
into a crisis.
Expected Result 4.4: Evaluate Rubella antigen
for introduction in RI program
During the 66th SEARO regional committee
meeting in New Delhi in 2013, India has
committed to the elimination of measles and
control of rubella and CRS by 2020.
Strategies
The public health importance of rubella
infection stems from the fact that rubella
infection in pregnancy has the potential to
cause Congenital Rubella Syndrome (CRS) in
the new born. The risk of development of CRS
is highest when infection is in the first trimester
of pregnancy. While there is no hard data on
CRS, the estimated incidence in India from
modelling studies gives a range of around 123
per 100,000 live births. CRS results in a
cumulative burden on the health system and
families of affected children on account of the
chronic sequelae (such as disability of sight,
hearing or cardiovascular systems) and the
economic burden in diagnosis, assessment and
treatment of congenital malformations and
challenges to providing education in an
increasingly nuclear family structure in society.
There are plans at national level to establish
and expand CRS surveillance through partner
agencies and existing surveillance programs.
The surveillance sites will be established in
selected states for observing the trends in CRS,
before and after vaccine introduction.
The strategy for introducing the rubella vaccine
in India's UIP will be planned to fulfil the
commitment the country has made to the
SEARO declaration for control of rubella
disease and CRS burden in the country. Since
immunization program performance differs
across states, expansion of rubella sentinel
surveillance sites is also planned. The strategy
for phase-wise implementation will be chalked
out over the cMYP period. The STSC of the
NTAGI shall play a crucial role in reviewing
and recommending a potential strategy for
implementation. The NTAGI has also
recommended the establishment of a Measles
1. Expansion of Congenital Rubella
Syndrome (CRS) surveillance
2. Introduction and expansion of rubella
vaccine in UIP
................................
4 1
& Rubella- India Expert Advisory Group (MR-
IEAG) on the same lines as polio to develop a
comprehensive strategy and monitor progress
for rubella control and measles elimination in
the country.
Existing measles surveillance system in India
frequently report rubella outbreaks or mixed
measles and rubella outbreaks. The existing
measles network will continue to be utilized for
identifying rubella outbreaks. It is envisaged
that with introduction of rubella vaccine, cases
of rubella will go down and, thereafter, a
possibility and need for case based surveillance
will be explored.
Once CRS surveillance system is established,
the information collected from surveillance
network will be utilized for assessing the trends
in CRS in states and the country. Studies
should be carried out to estimate incidence of
CRS and the social and economic burden
resulting from it.
Expected Result 4.5: Evaluate Rotavirus
antigen for introduction in RI program
Strategies
Diarrheal diseases are one of the largest causes
of childhood (under-5 years) deaths in India
28,29
and rotavirus is the leading cause. WHO
estimates that 23 percent of the annual 527,000
deaths due to rotavirus occur in India. It is
estimated that even with a vaccine with 50
percent effectiveness, a rotavirus vaccination
program in India would prevent 44,000 deaths,
293,000 hospitalizations, and 328,000
outpatient visits annually which would avert
30
$20.6 million in medical treatment costs.
3. Conduct Rubella surveillance through
the existing systems
4. Conduct research on CRS and trends
1. Assess disease burden due to
rotavirus and the potential impact of a
preventive vaccine
2. Strengthen national level surveillance
on rotavirus
3. Develop the vaccine schedule in line
with EPI schedule
KEY OBJECTIVE 5: Strengthen
health system for immunization
program
The Indian Rotavirus Surveillance Network
was set up on 2005 with four laboratories and
ten hospitals in seven different parts of the
31
country. The network provides valuable
information on epidemiology of rotavirus that
will underpin the policy decisions regarding
the introduction of rotavirus vaccine in RI.
NTAGI recommends that assuming several
vaccines will be licensed and recommended for
use in India, it would be preferable for each
child to complete all doses using the same
vaccine formulation. This could be facilitated
by choosing a specific vaccine for national use
or by ensuring that each region or state is
supplied with only one specific rotavirus
32
vaccine.
A strong RI program will contribute to the
overall health system strengthening both in the
urban and rural areas. Four states with large
populations - Uttar Pradesh, Bihar, Madhya
Pradesh and Rajasthan – contribute
approximately to 2/3rd of the unimmunized
children in the country (CES 2009). In addition
there are other states that are not performing up
to the mark as shown in Annex 1. Future
strategies for RI will need to be adapted and
contextualized for these high-priority states to
increase the vaccination coverage levels and
reduce VPD mortality and morbidity.
Following polio eradication the technical
support structures established for polio
eradication, both at the national and sub-
national levels, by WHO, UNICEF and other
partners are now 'transitioning' to provide
support to intensification of routine
immunization from 2012 onwards, based on
the lessons learnt from polio. This feeds into the
28
Causes of neonatal and child mortality in India: A nationally representative mortality survey. The Million Death Study Collaborators.The Lancet.Vol 376, November 27, 2010
29
The Global Enteric Multicenter Study (GEMS) of diarrheal disease in infants and young children in developing countries: epidemiologic and clinical
methods of the case/control study.Kotloff K L, et al. Clinical Infectious Diseases. 2012 Dec;55 Suppl 4:S232-45
30
Projected Impact and Cost-Effectiveness of a Rotavirus Vaccination Program in India.Douglas H. Esposito et al.
Clinical Infectious Diseases.2011:52 (15 January)
31
Multicenter, Hospital-Based Surveillance of Rotavirus Disease and Strains among Indian Children Aged <5 Years.
Gagandeep Kang et al. Journal of Infectious Diseases.2009:200 (Supplement 1)
32
Minutes of NTAGI meeting. 3rd August 2009.
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4 2M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
overall goal of strengthening health systems in
the country.
The indicators will be disaggregated by gender,
geography (urban slum, urban, rural) and
socio-economic parameters, where relevant.
Expected Result 5.1: Increase the pool of
skilled human resources to provide quality
immunization services in an integrated manner
Lack of adequate numbers of trained and
skilled human resources has been a major
barrier in improving the overall quality and
outreach of UIP. The Immunization Division
at MoHFW is small with few technical officers
to manage such a large program. The
Government of India has addressed this
capacity gap by setting up an Immunization
Technical Support Unit (ITSU) in year 2012
with technical officers to support various
components of UIP. In addition to the national
level, the HR capacity on UIP in the states need
to expand. It is important to identify key
functions within the UIP at state level also that
would need full time positions to ensure a
smoother functioning, improve institutional
memory and enhance the overall coverage of
immunization in the state. Under NRHM PIP,
the Government of India has given the
flexibility to the states to propose human
resource augmentation plans at state and
district level.
Strategies
The strength and capacity of the national
immunization division has been enhanced
Key Performance Indicators (KPI)
1. Number of districts with full
immunization coverage rate of >80%
1. Increase the number of technical
managers for immunization at national
and state level and strengthen
organizational capacity to adequately
perform strategic and technical
functions under UIP
with the setting up of ITSU at MoHFW with
recruitment of technical officers for key
functions of UIP such as strategic planning and
system designs, monitoring and evaluation,
cold chain and vaccine logistics, strategic
communication, vaccine safety and AEFI, and
evidence to policy. This unit will help in the
development of policies, procedures and
guidelines to improve program management at
national level. This setup will be further
strengthened to augment the capacity for
operational research and use of more
technology in UIP. Similarly, a state-level
structure is also proposed that includes
recruiting focal points for the program
management, Cold Chain, Vaccine Logistics,
Management Information System (MIS), and
Technology and research etc.
Relevant trainings will be carried out for new
staff working in the immunization cell at all
levels based on the existing training norms and
guidelines under NRHM. Immunization-
specific training norms will also be used, e.g.
cold chain training norms. The training
material for both medical officers and health
workers in routine immunization has been
updated, printed and widely disseminated.
This material is being utilized for conducting
need-based training.
National Institute of Health and Family
Welfare (NIHFW) is the national nodal agency
for training activities including Immunization.
The NIHFW, in coordination with
Immunization and Training Divisions within
MoHFW, will review the training plans from
all states; conduct Training of Trainers courses,
as well as monitor and evaluate the quality of
trainings. The State Institute of Health and
Family Welfare (SIHFW) is nodal agency at
state level to plan, implement, monitor and
evaluate the immunization training activities.
2. Conduct relevant training and
induction programs and develop need-
based immunization training materials
3. Strengthen training infrastructure
................................
4 3
A plan is being instituted to conduct induction
training for new State Immunization Officers
as per the need and refresher trainings on
regular interval.
There is need for strengthening the existing
training infrastructure and also starting new
facilities. The issues of shortage of health
workers and their training needs can be
addressed by institutionalizing training
mechanism for this category of staff. This can
be achieved by:
lOn-the-job refresher training every two years
for every health functionary.
lEach state will identify core district training
teams for each district. This team will move
to each block identifying gaps in knowledge
and train appropriately,
lMonthly block meetings will provide an
opportunity for supervisors to help identify
gaps in knowledge and provide some
training.
NRHM provides for hiring staff on contract
basis. All staff members (medical officers, staff
nurses, health workers including ANMs) hired
on contract basis will also be trained. ANM
and ASHA vacancies will be filled up by the
states on urgent basis.
A stronger immunization program will also be
used as a platform to deliver other child health
services in an integrated manner. Preventive
child health interventions like Vitamin A,
deworming, ORS, growth monitoring can also
be given along with immunization. A well-
functioning RI program will act as a catalyst in
getting more people to use the health facility
and contribute to overall demand generation
and better address equity issues.
4. Hire and train more field level staff
under NRHM
5. Promote integrated delivery of
different health interventions through
UIP
Expected Result 5.2: Ensure that adequate
financial resources are available for UIP.
Strategies
A core team for immunization financing
named Financial Management Group (FMG)
has been established within the MoHFW.
Using tools that are already available, this team
will analyze current and projected
immunization costs factoring in the plan for
scale up and introduction of newer vaccines in
the coming years. These will be compared to
projected finances available and funding gaps
will be highlighted.
The country will be expanding the VPD and
AEFI surveillance, which will require a well-
functioning laboratory network. A mechanism
for the separate budgeting mechanism will be
devised for the strengthening of the laboratory
and surveillance mechanism in the country
Expected Result 5.3: Improve program
accountability, monitoring and reporting at all
levels.
Strategies
Quarterly review meetings will be held at
national and state level; and monthly meetings
at district and block levels to track the progress
in immunization program, to identify
problems, analyze the issues and address them.
State-level meetings will be chaired by State
Secretary/MD-NRHM and district-level
meetings will be chaired by the DM.
1. Prepare a national financial
sustainability plan
2. Provide funding for laboratory
strengthening and surveillance
3. Explore the possibility of setting up a
Vaccine Fund through innovative
financing mechanisms
1. Hold regular program reviews at all
levels
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Comprehensive EPI reviews will be held in the
good and poor performing states to help
prepare state specific action plan.
MoHFW will develop a monitoring and
accountability tracking framework for UIP that
will identify key program indicators and assign
responsibility of delivering results on specific
individual or organizations
At the service-delivery level, more formal,
institutionalized systems for complaint and
redressal should be put in place. They must be
supported by timely emergency response
systems, such as telephone helplines, and
proper managerial authority should be granted
so that structures are in place to rectify acute
challenges related to referral and
transportation or the mistreatment/
exploitation of patients at the facilities. A
formal system to lodge complaints and seek
redress should also provide oversight to help
protect women who register complaints, from
future reprisals. The demonstrated
initiatives/innovation for accountability, for
instance call center for integrated grievance
handling system, can be considered.
The Mother and Child Tracking System
(MCTS) is designed to collate information of
all pregnant women and infants into a central
database to ensure that all pregnant women
and children receive full maternal and
immunization services. This centralized
database will enable functions like data
analysis, report generation, and therefore
contribute to greater strategic decision-making
and need-based allocation of resources. It will
act as a feedback system for health workers like
2. Develop national monitoring and
evaluation plan for immunization
3. Formalize and make accountability
mechanisms system-led as part of
community participation
4. Expand the usage of Mother and Child
Tracking System (MCTS) to all districts
to help reduce the gap between reported
and evaluated coverage
Auxiliary Nurse Midwives and ASHAs and
will enable better health service delivery by
drawing out action plans for health workers for
ante-natal care, pre-natal care and child
immunization. MCTS will also generate
reports such as facility service statistics and
Auxiliary Nurse Midwife monthly action
plans. Currently the states aggregate the
relevant data in a Microsoft Excel template
available on the HMIS portal. MCTS has been
fully operational since April 2010 and has
picked up speed in terms of usage by states and
union territories as of 1 April 2011. Under this
system, SMS alerts are sent to pregnant women
who are nearing the delivery date to remind
them of the need to visit the PHC for pre-natal
check-up and delivery. Women are also
reminded over the cell phone on the due dates
for immunization of their children to ensure
follow through with RI. Bring out annual
reports on UIP as part of a strengthened HMIS
at state and district level.
The scope of the Quality Assurance (QA)
system is now enhanced to include the full
range of RMNCH+A services. For rolling out
QA system, organizational arrangements will
be set up at various levels with clearly defined
roles and responsibilities for each level. These
will include
(1) Central Quality Supervisory Committee;
(2) (2a) StateQuality AssuranceCommittees,
(2b) Quality Assurance Cell and
(2c) Full time quality assessors;
(3) District Quality Assurance Committees;
and
(4) Quality Circles at the District Hospital
level.
The central QA team will comprise technical
officers from the program divisions of the
Ministry of Health and Family Welfare and
5. Introduce the Quality Assurance (QA)
system for immunization services as
part of RMCH+A
................................
4 5
counterparts working with technical support
partners. The QA standards will be defined for
each technical theme, categorized by the level
of health facilities.
Expected Result 5.4: Strengthen RI program
management and service delivery through field
level supportive supervision in high priority
states
To achieve immediate and sustainable
improvement in RI coverage at national level,
the Government of India needs to focus on
high priority states, Rajasthan, Madhya
Pradesh, Uttar Pradesh and Bihar, which have
the maximum number of unimmunized and
partially immunized children. The
RMNCH+A strategic approach recognizes the
need to strengthen supportive supervision of
frontline workers (ASHAs and ANMs) and
service providers (Staff Nurses and Medical
Officers) in order to bring about integration of
primary care services, improve quality,
enhance skills and skill application.
Strategies
To support the implementation and monitor
the activities at the district level, there will be a
State Level Supportive Supervision Team
consisting of officers from the state health
department, partners and students and Staff of
Medical Colleges (Department of Community
Medicine). Each state officers or medical
college team will support and monitor 4 to 5
districts for implementation through regular
visits, and help establish a link between districts
and the state. It will establish State and district
RI supportive supervision team. The mobility
support will come from NRHM.
At the district level the supportive supervision
team will consist of selected medical officers,
senior supervisors, medical college staff to
support PHC/planning unit. Each member of
supportive supervision team including medical
college staff will be responsible for two PHC or
1. Augment HR for supportive
supervision and program management
planning units, and would visit each unit twice
a month (total four visits in a month). S/he will
provide regular supportive supervision services
to the unit as well as the vaccinators in the area.
Skill building of ANMs is required for ensuring
supportive supervision of ASHAs (and
AWWs). While ANMs do perform supervisory
functions informally, their skills in supportive
supervision are limited and need to be
enhanced on this specific issue.
The supportive supervision by Institute of
Child Health in Tamil Nadu has led to
significant improvement in quality of
maternal-newborn care in eight districts. A
similar engagement of Medical College faculty
in other districts and states would be a useful
strategy. The technical expertise available with
the partners will be utilized to impart
knowledge to the state and district level staff.
State-level mechanisms will be strengthened to
monitor the program, and guide the districts to
improve, implement and monitor the program.
a) Quarterly review meeting will be held at the
state for all DIOs and District RI managers
b) Monthly meetings will be held between State
and District Task Force meeting
c) Monthly review meetings will be held at the
district for all block and PHC medical
officers in charge and RI coordinators
d) All supportive supervision checklists will be
collected at the district level, and entered
into software. This data will be sent to the
state for compilation and subsequently the
state will send the data sheets to the national
2. Leverage expertise and experience of
development partners and medical
colleges
3. Establish an institutional mechanism
for program oversight and monitoring
the implementation of supportive
supervision model
U I P S T R A T E G I C P L A N F R A M E W O R K
4 6M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
immunization division.
e) Data will be presented and feedback
provided at all the levels (state, division,
district and block level) for appropriate
action.
State RI cell/RRT members will be trained
through Training of Trainer (ToT) by a
national team once in a year. District RI team
will be trained once a year by the state core
team. District RI team shall be responsible for
training, providing supportive supervision and
implementation of RI activities at the block
and PHC level. On-job regular capacity
building will take during the visits of Support
Team members from the state. District-level
immunization officers from partner
organizations will also contribute to the
capacity building process.
Block and PHC team members will be trained
annually by the team comprising of members
of the district team and one of the facilitators
from the state. They will also receive on-job
training on a regular basis by district
immunization facilitators during their visits
and review meetings.
These guidelines will be developed as part of
the RMNCH+A strategy to further augment
the supportive supervision mechanisms.
Result 5.5: Build institutional capacity to
promote operational and translational research
for successful implementation of UIP
4. Carry out capacity building and on-job
training of staff for strengthening RI
supervision all level
5. Prepare integrated guidelines and
checklists for supportive supervision
linking UIP-MNCH (Universal
Immunization Program and Maternal,
Newborn And Child Health) supervisory
mechanism
Strategies:
Areas for OR could include, but not be limited
to, HR training in immunization, operational
aspects of cold chain system, vaccine freezing,
vaccine wastage, injection safety, barriers to
service access and utilization.
A leading research organization may be
identified to work in collaboration with
immunization division and other stakeholders
Funds will be ear-marked and sufficient
amount will be ensured for operational
research and implementation in UIP.
National immunization cell will seek to avoid
long time lag between conducting research and
translating the findings for advocacy,
communication and UIP interventions.
Technical expertise of partners working on
immunization shall be availed as and when
required.
Key Performance Indicators (KPI)
1. No wild polio virus detected in the country
2. Non Polio AFP rate is maintained or
1. Define areas for Operational Research
and mechanisms for translating
evidence-based approaches into
program service delivery
2. Evolve institutional mechanism for
operational research
3. Ensure sufficient funding for
operational research
4. Ensure adequate knowledge
management and translation for greater
public good
KEY OBJECTIVE 6: Contribute to
global polio eradication, measles
and maternal and neonatal tetanus
elimination and rubella control
................................
4 7
exceeds 2 per 100,000 children under 15
years
3. Reported AFP cases have two adequate
stool specimens collected within 14 days of
onset of paralysis in > 80% cases
4. Number of States with MCV 1 coverage of >
90%
5. Number of States with MCV-2 coverage of>
90%
6. % of districts with >80% TT2 coverage for
pregnant women
The indicators will be disaggregated by gender,
geography (urban slum, urban, rural) and
socio-economic parameters, where relevant.
Expected Result 6.1: Achieve country-wide
certification of polio eradication by 2014
Strategies
The polio eradication program and the polio
endgame strategy shall continue to be guided
by India Expert Advisory Group constituted by
33
the Government of India.
Conduct regular supplementary immunization
activities (SIAs), ensure that the SIAs maintain
good quality and conduct regular
seroprevalence surveys to detect immunity
levels. The plans for SIAs to be conducted in the
coming two years are as below
SIAs for the remainder of 2013
As per current national plans, three large scale
SNIDs with bOPV, targeting all of UP, Bihar,
Delhi and associated high risk areas of
Haryana, Rajasthan, and Uttarakhand, and
migrant/high risk areas in Maharashtra,
Punjab, Gujarat, Jharkhand, and West Bengal.
1. Maintain high level of population
immunity
Polio SIAs in 2014
lTwo NIDs with tOPV in all areas in 1st
quarter of 2014
lThree SNIDs with bOPV, ideally one in each
of quarters 2, 3, and 4 of 2014 targeting all of
UP, Bihar, Delhi, and associated high risk areas
of Haryana, Rajasthan, and Uttarakhand, and
migrant/high risk areas in Maharashtra,
Punjab, Gujarat, Jharkhand, and West Bengal.
Polio SIAs in 2015
lTwo NIDs with tOPV in all areas in 1st
quarter of 2014
lTwo to three SNIDs with bOPV (depending
on global epidemiology) targeting all of UP,
Bihar, Delhi, and associated high risk areas of
Haryana, Rajasthan, and Uttarakhand, and
migrant/high risk areas in Maharashtra,
Punjab, Gujarat, Jharkhand, and West Bengal.
The timing of sub-national rounds should be at
the discretion of the national program and
based on operational and epidemiological
considerations
An extremely high level of vigilance will be
maintained through to global certification of
eradication, and through to cessation of use of
oral poliovirus vaccines; this requires ensuring
that adequate financial and human resources
and attention are devoted to the surveillance
and laboratory systems by the Government of
India and partners.
Regular field reviews of surveillance would
continue to be conducted on a rotational basis
and with particular attention to high risk areas
as determined by epidemiological, surveillance
or immunization indicators.
2. Maintain the quality and effectiveness
of the existing surveillance and
laboratory systems to detect and
respond to outbreaks
33
http://www.npspindia.org/advisory.asp
U I P S T R A T E G I C P L A N F R A M E W O R K
4 8M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Environmental surveillance for detection of
polioviruses in the sewage would be expanded
in other states of the country. All detected
VDPVs would continue to be thoroughly
investigated to determine any risk of
circulation, and appropriate actions taken
based on investigation findings.
The Emergency Preparedness and Response
Plans (EPRPs) at national and state-levels will
be updated annually; the update will include a
full new risk analysis to inform risk mitigation
measures. See Annex 7 for EPRP details.
A simulation exercise ('table top exercise') for
the emergency response plans at national and
selected state levels will be conducted annually
to maintain readiness and sharpness of
response. Government of India will ensure a
rolling stock of 40 million doses of bOPV and
10 million doses of tOPV to enable response to
any wild poliovirus or vaccine derived
poliovirus detection.
Immunization of travelers at land border
crossing points from neighboring countries is
the most significant risk reduction strategy and
will continue until there is no longer an
epidemiological risk. Particular attention
should continue to be paid to border
populations to ensure that they are effectively
covered by SIAs and routine immunization.
The Government of India will strongly
promote implementation of the current WHO
p o l i o i m m u n i z a t i o n a d v i s o r y
3. Augment the current response
capacity by developing a national and
state-level emergency response
preparedness plan and maintain a
rolling stock of bOPV and tOPV
4. Reduce risks of polio importation
based on WHO recommendations for
travelers coming to or from endemic or
infected areas
/recommendations for travelers to and from
endemic or infected areas.
The Government of India will develop the
inventory of all labs holding polio virus(phase
1) and securing the WPV (phase 2).
This includes planning for tOPV/bOPV shift,
IPV introduction process, and operational
assessments of the cold chain system.
These sero-surveys will be conducted in the
traditionally high risk areas of UP and Bihar
and other regions with potential risk of wild
poliovirus importation or emergence of
circulating vaccine derived poliovirus. This will
provide an epidemiological description of the
trends on population immunity and possible
reasons for these trends.
Expected Result 6.2:Achieve measles
elimination and control for rubella/congenital
rubella syndrome (CRS) by 2020
Strategies
The first-dose Measles Containing Vaccine
(MCV1) at 9-12 months is delivered through
Routine Immunization. Efforts will be made to
improve coverage with MCV1 by strengthening
RI services with a target to reach all children. In
addition follow-up campaigns will be
conducted in low coverage areas. It will be
ensured that the coverage in every district is
more than 90 percent and progress is sustained.
5. Work towards the certification
process
6. Develop post-eradication policy in
preparation for the polio endgame
7. Conduct periodic seroprevalence
studies in high priority areas.
1. Increase coverage with the first dose
of measles vaccine for infants (9-12
months)
34
A Guide to Introducing a Second Dose of Measles Vaccine into Routine Immunization Schedules. 2013.
World Health Organization, Measles and Rubella Initiative.
................................
4 9
2. Increase the coverage of second dose
of measles vaccine (at 16–24 months of
age) based on global guidelines
3. Strengthen and expand the laboratory
surveillance for measles and rubella
1. Strengthen service delivery and
improve institutional deliveries
34
Conduct measles SIAs in 14 states where MCV
1 coverage is below 80 percent vaccinating all
children in age group of 9 months to 9 years.
All states where MCV1 coverage was more
than 80 percent have already introduced MCV2
in routine immunization at the time of DPT
booster 1.
Twice yearly state-by-state review of all
measles data will be conducted. The
laboratory-based measles and rubella
surveillance has started in eight states, namely
Andhra Pradesh, Gujarat, Karnataka, Kerala,
Tamil Nadu, West Bengal, Rajasthan, Madhya
Pradesh, Bihar and Assam. The surveillance
laboratory network will be further expanded
with priority being given to the states with
measles morbidity and mortality. In addition,
surveillance data on measles outbreak from
IDSP will also be collated and analyzed for
action.
Expected Result 6.3: Eliminate maternal and
neonatal tetanus by 2015
Strategies
Promote institutional delivery and safe
delivery by skilled birth attendants (SBA)
under NRHM and ensure that TT is offered at
all ante-natal clinics and routine immunization
sessions. Provide twoTT doses for the first
pregnancy (with immunization card) and
further doses according to the national
schedule. The tetanus vaccine for pregnant
mothers will also be ensured in all outreach
sessions being conducted.
Establish MNT as a reportable disease and
report MNT cases from every health facility.
MNT will be included with weekly AFP in
active surveillance and zero reporting. Case
investigations for hospital-based cases and the
cases from low-risk areas are regularly done.
Improve TT coverage through quality RI in all
areas. SIAs may be considered for those areas
where coverage with 2 doses of TT is poor. The
Government of India will take need-based
decision to conduct targeted SIA for
elimination of MNT. The mode and time for
these SIAs will be decided by an expert group.
A national MNT database will be established
with regular review of indicators, identifying
high-risk districts within states. The high-risk
districts within states will be validated for
elimination of MNNT by Lot Quality
Assurance Surveys (LQAS) and districts
prioritized on the basis of this for targeted
corrective action.
In states where MNT has been validated to
have been eliminated, efforts will be made to
maintain the high coverage with TT2, and safe
delivery practices to ensure the elimination
status in those states.
15 states have validated MNT till 2008, and
four more states have conducted MNT
validation exercise in 2013. The remaining
states and UTs will be assessed in 2014–2015.
2. Increased surveillance for tetanus
cases
3. Conduct targeted SIAs
4. Establish national MNT database
5. Maintaining the elimination status
U I P S T R A T E G I C P L A N F R A M E W O R K
5.1 Rationale
lThe Universal Immunization Program
(UIP) in India uses a set of indicators to
measure the performance at national as well
as other levels of program implementation.
For this purpose, the country uses various
data sources that include:
lRoutine administrative reporting,
lReports from various disease surveillance
systems and field level monitoring by
partners,
lPeriodic Coverage Evaluation Surveys
(CESs) at national and sub-national level,
lVarious assessment studies conducted from
time-to-time by different organizations.
Despite the availability of multiple sources of
data, there is no comprehensive independent
UIP Monitoring & Evaluation (M&E) Plan in
the country to
lsystematically identify data needs as well as
data sources to meet dynamic program
requirements,
lreview the process of data gathering,
lconduct Data Quality Assessments (DQAs).
In the absence of this plan, there is also no
mechanism to identify information gaps,
especially to measure process indicators, and
plan targeted studies to inform the program.
Though there are provisions for immunization
program reviews at all levels, these are not
regular and are not effective in the absence of a
real-time quality data.
................................ 5 1
5
5.2 Objective
5.3 Methodology
I. Strengthen routine data reporting
The overall objective of this National
Monitoring and Evaluation (M&E) Plan is to
systematically generate, capture and
disseminate knowledge to guide UIP
implementation monitoring and UIP impact
evaluation.
This monitoring and evaluation plan will work
at three levels:
Currently UIP does not have its own electronic
data management system. The Health
Management Information System (HMIS)
captures immunization data from the health
facility-level and the Mother & Child Tracking
System (MCTS) tracks ante-natal and
immunization services at the individual
pregnant woman and child level. The National
Monitoring and Evaluation Plan will aim to
strengthen these existing data reporting
systems through the following mechanisms:
a) Structured Review Mechanism
There is currently limited use of HMIS and
MCTS data sets for analyzing and reviewing
program implementation and for providing
feedback to the concerned districts or blocks.
The proposed monitoring and evaluation plan
will establish a structured review mechanism in
the country to enhance the use of
immunization data and to further improve data
quality.
National Monitoring And
Evaluation Plan For UIP
5 2M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
b) Human Resource & Capacity Building
A core part of the plan is to improve
monitoring and evaluation human resource
capacity through trainings, supportive
supervision, mentoring, and providing
guidelines and tools.
c) Data Quality Assessments (DQA)
DQAs will be conducted regularly in
coordination with state governments and with
the support of technical and development
partners. State Immunization Managers will
also be trained in conducting these DQAs by
using WHO DQA tools.
d)Feedback to program managers
Data quality will be improved by examining the
immunization information system in operation
at all administrative levels– from data
collection at the point of vaccination, to the
periodic compilation of data at the national
level. Practical feedback will be provided to
managers on how to improve the quality of
their administrative immunization reporting
systems.
Knowledge gaps identified through routine
program monitoring and reporting will be filled
by targeted studies and operational research.
The results from these research activities can
help the UIP in taking ongoing corrective
measures for better outcomes. The monitoring
and evaluation plan will also include regular
audit at facility and service level using WHO
tools and provide feedback to program
managers for strengthening the facilities and
services.
Currently, evaluation surveys conducted in the
country address all MCH services, and the
immunization component is limited only to
antigen-wise and full immunization coverage.
Moreover, these surveys are done every three to
I. Conduct targeted studies and field
assessments to fill knowledge gaps in
the program
II. Plan and conduct coverage evaluation
studies
four years, and do not provide latest coverage
numbers on a yearly basis. The monitoring and
evaluation plan will propose a yearly
evaluation survey for routine immunization,
focusing on outcome and impact indicators of
all RI components. This can be done through
external agencies, in line with NFHS and
DLHS surveys.
MOHFW will guide the development of the
national monitoring and evaluation plan. The
Monitoring and Evaluation division of
Immunization Technical Support Unit (ITSU)
will coordinate the development of the plan.
ITSU will hire a consultant to work on the plan
after consultation with ministry and technical
partners for the scope. The consultant will work
closely with ITSU team and, in consultation
with all stakeholders including states, with the
aim of creating a realistic, expedient and
effective national monitoring and evaluation
plan for the UIP.
The National Monitoring and Evaluation plan
will be developed in line with the cMYP and
five-year plan of the country. The proposed
national monitoring and evaluation plan will
cover all major areas for establishing and
running an effective monitoring and evaluation
system in the country. These include:
lOrganizational structure along with roles
and responsibilities for monitoring and
evaluation at various levels
lPlan for capacity building of monitoring and
evaluation staff on transmission, analysis
and use of data at all levels
lKey coordination mechanisms for the
country
lImmunization monitoring and evaluation
performance and accountability tracking
framework and implementation plan at
national and state level (see Annex 6)
5.4 Process for national M & E Plan
development
5.5 Components of National
Monitoring and Evaluation Plan
................................ 5 3
ANNEXURES
6
................................
5 5
ANNEX 1: List of states showing good performance on immunization coverage and other parameters
States
Andhra Pradesh
Delhi
Goa
Haryana
Himachal Pradesh
Jammu & Kashmir
Karnataka
Kerala
Maharashtra
Punjab
Tamil Nadu
Mizoram
Sikkim
Tripura
Uttarakhand
West Bengal
Full
immunization
coverage (%)
68.0
71.5
87.9
71.7
75.8
66.6
78.0
81.5
78.6
83.6
77.3
73.7
85.3
66.0
71.5
64.9
No. of sub-
centers
without
ANM/HW*
0
0
0
N/A
178
N/A
N/A
0
N/A
N/A
140
N/A
0
0
34
N/A
Mos
trained
(%)
93.7
55.5
93.7
72.8
4.0
7.3
44.8
50.5
51.8
95.8
82.2
48.3
75.0
30.0
19.5
19.7
Sessions
held vs.
planned
(%)**
N/A
92.8
99.2
93.9
98.2
90.5
95.4
N/A
80.2
95.1
99.1
66.7
N/A
92.9
91.8
91.6
Dropout rates
in age
group12-23
months for
BCG- measles
(%)
8.3
6.5
1.4
5.3
2.2
9.4
7.4
8.3
3.7
9.6
0.6
7.3
0.1
7.3
14.2
13.6
No. of severe
AEFI cases
reported***
21
12
4
10
3
N/A
9
1
71
4
5
N/A
N/A
4
1
28
Children aged
12-23 months
having an
immunization
card (%)
64.9
50.7
60.6
42.7
60.3
60
52
78.9
58.8
53.2
44.8
77.9
85.2
75.9
41.1
77.8
* Collated data from state review meetings on immunization obtained from MoHFW, GoI.
* * Data from the HMIS web portal April to October, 2011;
** *Severe AEFI cases reported to the Government of India by the states till mid-December, 2011;
A N N E X U R E S
5 6M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
States
Arunachal Pradesh
Manipur
Meghalaya
Nagaland
Assam
Bihar
Madhya Pradesh
Orissa
Rajasthan
Uttar Pradesh
Chhattisgarh
Gujarat
Jharkhand
Full
immunization
coverage (%)
24.8
51.9
60.8
27.8
59.1
49.0
42.9
59.5
53.8
40.9
57.3
56.6
59.7
No. of sub-
centers
without
ANM/HW*
N/A
N/A
0
0
0
200
119
535
392
1,776
458
488
0
MOs
trained
(%)
43.8
49.4
93.4
40.1
84.7
18.3
32.5
44.9
33.4
32.1
8.7
24.7
36.3
Sessions
held vs.
planned
(%)**
81.5
89.6
80.8
93.7
97.4
95.1
96.1
96.0
113.9
89.8
90.3
97.2
94.4
Dropout rates
in age group
12-23 months
for BCG-
measles (%)
27
12.9%
9.4
11.5
7.2
29.3
24
17.6
20.6
30.9
13.8
8.1
22.8
No. of severe
AEFI cases
reported ***
N/A
N/A
3
N/A
7
19
8
5
3
21
N/A
3
11
Children aged
12-23 months
having an
immunization
card (%)
41.9
55.6
63.8
45
66.9
43.1
45.8
58.3
24
35.9
46.3
49.5
63.1
ANNEX 2: List of States showing poor performance on immunization coverage and other parameters
*Collated data from state review meetings on immunization obtained from MoHFW, GoI.
**Data from the HMIS web portal April to October, 2011;
***Severe AEFI cases reported to the Government of India by the states till mid-December, 2011
adequate space in the unused portion of the
Animal House for the establishment of
NCCVMRC. UNICEF has supported the
establishment by hiring an architect to prepare
the plans and estimates for remodeling of the
existing building of the Animal House.
Immunization Division has provided five tool
kits for the training center. NIHFW has already
conducted a six days pilot Training for Cold
Chain Technicians in Repair and Maintenance
of ILRs and DFs from 17-22 October 2011
using alternate temporary space made
specifically available for the training.
The Resource Centre will be set up to train cold
chain mechanics in repair and maintenance of
all electrical cold chain equipment (ILRs, DFs,
WICs, WIFs and voltage stabilizers). In
addition, it will also conduct trainings related
to vaccine and logistics management for
vaccine and logistics managers in the country.
It is expected to make it a cold chain training
center for other countries in South-east Asia. In
addition to trainings, NCCVMRC will be a
repository of documents such as guidelines,
government orders/notifications and other
resource materials related to cold chain and
Brief about resource centre
Establishment of national cold chain
and vaccine management resource
centre and nihfw, new delhi
BACKGROUND
The Immunization Division, MOHFW, New
Delhi has proposed to establish a National
Cold Chain and Vaccine Management
Resource Centre (NCCVMRC) at NIHFW,
New Delhi and it has been approved by the
competent authority of MoHFW, Government
of India (Annexure A). Further it has been
intimated that NIHFW may utilize any
MOHFW, GoI funds available or the proposal
estimates be provided for necessary approvals
from the competent authority. MOHFW, GoI
shall support the establishment of
NCCVMRC, trainings of officials from
Central/state Governments related to cold
chain equipment, vaccine and logistics
management, etc. and the human resources
needed for the trainings on regular and /or
contractual staff and all other expenses related
to the Training Centre. The necessary technical
support will be provided by UNICEF.
National Institute of Health and Family
Welfare, New Delhi has on its part demarcated
................................
5 7
ANNEX 3: NCCVMRC concept approved by MoHFW
ESTABLISHMENT OF
NATIONAL COLD CHAIN AND VACCINE MANAGEMENT
RESOURCE CENTRE (NCCVMRC)
PROPOSAL ESTIMATES
IMMUNIZATION DIVISION,
MINISTRY OF HEALTH AND FAMILY WELFARE, NEW DELHI
AT NATIONAL INSTITUTE OF HEALTH AND FAMILY WELFARE, NEW DELHI
(With blueprint)
Submitted to
By
National Institute of Health and Family Welfare, New Delhi
A N N E X U R E S
5 8M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
vaccine management. The soft copies will be
on the resource centre website and hard copies
will be maintained in a small library in the
centre.
The resource center will be set in the unused
portion (earlier Primate Section) of the Animal
House. There will be a Lecture Room, a work
lab (for repair of ILRs and DFs) and a room for
housing a Walk in Cooler and a Walk in
Freezer. In addition, there will be an
administrator's room and a facilitator's room as
well as a store room. The ingress will be
separate from the animal House with adequate
accessibility for heavy vehicles (for loading and
unloading of cold chain equipment).
A training coordinator, an assistant and a
support staff are the human resources needed
for the resource center. MoHFW has agreed to
support in hiring of the training coordinator
and support staff from NIHFW can be deputed
to work in the resource center. UNICEF may
also initially support the hiring of technical
staff.
The following are the different types of
trainings to be undertaken at the NCCVMRC,
New Delhi:
1. Training for Cold Chain Technicians in
Repair and Maintenance of ILRs and DFs
2. Training for Cold Chain Technicians in
Repair and Maintenance of WICs and WIFs
3. Training on repair and maintenance of
voltage stabilizers
4. Training on installation and repair of Solar
cold chain equipment.
5. Training for Vaccine and Cold Chain
Handlers
6. Training on Vaccine Management
There are more than 500 cold chain technicians
and vaccine logistics managers in the country.
Some of these are newly inducted have had no
induction training. Many of the older
refrigerator mechanics need refresher trainings
for which such a course will be designed
separately. Therefore the establishment of the
NCCVMRC is justified.
................................
5 9
– Procurement Policy for CCE
– Institutional Capacity Building of NCCTC
and NCCVMRC
– Greater role of NCCTC and NCCVMRC
for CCVLM
– Review Mechanism of CCVLM
lInduction Training of HR engaged for Cold
Chain and VM
lImprovement of management skills of
program managers
lDedicated staffs for CCL at all level (at least
up to district)
lEach GMSD and SVSs need to have VLM
and CCT
lSome of the existing staffs of GMSD can be
profiled for Data management
lCold rooms should have some semiskilled
helpers
lDevelop Training package for the VLMs and
also for the Immunization program
managers and house them in the institution
to overcome attrition
lReview of Knowledge (Training) to skills
transformation barriers
lRegular orientation, at least every 3 years for
all staffs
A.Building
lDedicated stores for State, Division, District
2. Human Resource and capacity
building
3. Infrastructure
The recommendations are categorized in to
five broad categories “Management Policy,
Human Resource and capacity building,
Infrastructure, Planning and Documentation
and improvement in practice and development
of an improvement plan to implement these
recommendations through NRHM state PIPs.
lIntroduce VAR for Vaccine stores up to Sub
National level
lDevelop and implement real time MIS for
Vaccine Logistic Management for 5 levels of
supply chain.
lIntegrate vaccine management MIS with
NCCMIS
lAccelerate NCCMIS implementation for
GMSDs
lSegregate all SVSs attached to RVS and
RVSs attached to DVS: Building,
equipment, documents and Staff.
lDevelop National Cold Chain action Plan
– Develop National standards for:
lVaccine store at all levels as per WHO
standards
lCold Chain point expansion guidelines
lCold Chain Equipment plan for different
level of vaccine stores
lQuality maintenance of vaccine
lTemperature Monitoring of cold chain
system
lHuman resource for Cold Chain and VM
lCCE Testing Lab
1. Management Policy
ANNEX 4: Key Recommendations from Effective Vaccine Management Assessment Report 2013
A N N E X U R E S
6 0M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
and Health Facilities(PHC),
lConsider the future need, national standard
lGreater collaboration with PWD, Electricity
and Municipal corporation/bodies for
regular maintenance
B.Equipment
lEquipment specification as per global
standards
lMinimize variety of equipment to reduce
number of spare parts
lAll WIC/WIF with working hooters
lMapping of spare parts and ensuring
availability to make non-functioning
equipment (Solar, Haier, Blue star,
others)functional
lDefine realistic stock level in months at five
supply chain level
lDefine, print and distribute standard vaccine
stock registers
lVaccine indent and distribution plans based
on the required peak stocks.
lPreventive maintenance plan for technicians
lRegular data uploading in NCCMIS for
performance assessment of CC at all level
lEstablish a system for recording wastage in
vaccine registers
lManual temperature monitoring and
recording to be carried out 2 times daily, for
all 7 days including holidays
lMaintain a service log sheet for each
equipment. This can be done as part of the
4. Planning and Documentation
5. Improvement in Practice
Temperature monitoring booklet.
lDiluents MUST be marked in supply
voucher and should be recorded just like the
vaccines in stock registers.
lAt CHC and PHC the DF must be used
exclusively to prepare ice packs. Vaccines
must never be stored in the same unit. All
vaccines should be kept in ILRs at the CHC
and PHC.
lAlways use standardized Ice Packs after
conditioning
EVM is a diagnostic tool and it assess, 3 Ps like
Process, Practices and Policies of health system
requires for efficient cold chain and vaccine
management.
Improvement Plan(IP )is the intervention for
Strengthening of existing Cold Chain and
Vaccine Logistics System to make it Reliable
,Affordable and Efficient. Issues identified
through EVM needs to be fixed and to be
sustained success of the EVM initiatives lies in
developing an implementable improvement
plan and then actually implementing the IP and
reviewing the IP on the regular basis for
strengthening the Cold chain logistics system.
While EVM is a diagnostic tool, IP lay down
the treatment strategies for the gaps in the CCL
system. Development of an improvement plan
is the key output that comes from the EVM
assessment and its recommendations. While a
skilled facilitation is needed to make sure that
the plan does indeed address key deficiencies, it
should be possible to provide a menu of
innovative approaches and technologies for
consideration, guided by country realities. A
menu of innovations approaches is included in
the Improvement Plan to guide planning for
future system design and to enhance
monitoring of the implementation of the plan.
While planning, guiding principles that need to
be considered for an effective and
implementable IP are:
6. Improvement Plan (IP)
................................
6 1 A N N E X U R E S
lIntegration with other planning processes
lIP template should be adapted by
government to align with existing planning
and budgeting documents
o IP should be consistent with and input into
other planning documents such as cMYP,
national and sub-national annual work
plans, etc.
lDynamic and living document
lPlan that needs regular review and
monitoring for implementations of
recommendations IP need to be prepared
through consultative process and it should
be integrated annual health PIP.
lGovernment ownership
lPlan which need to be reviewed regularly for
progress of implementation
lEngagement of all levels
lDisseminate widely , leveraging existing
mechanisms
lMake IP foundational plan for improving
immunization supply chain performance
o Identifies priority action areas and
establishes accountability for improving
performance
o Takes longer-term view and reflects future
needs (NVI, population growth, etc.)
6 2M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
ANNEX 5: National Open Vial Policy 2013
................................
6 3 A N N E X U R E S
Guidelines for use of open vial in
immunization program
Conditions that must be fulfilled for the
use of open vial policy:
1. This opened vial policy applies to multi-dose
vials of the DPT, TT, Hepatitis B, Oral Polio
Vaccine (OPV) and Liquid Pentavalent
(where applicable). This policy does not
apply to Measles, BCG, Japanese
Encephalitis (JE) vaccines.
2. Use the DPT, TT, Hepatitis B, Oral Polio
vaccine (OPV) and Liquid Pentavalent
(DPT + HepB + HiB) where applicable)
vaccines opened in a fixed or outreach
session can be used at more than one
immunization session up to four weeks
provided that:
a. The expiry date has not passed.
b. The vaccines are stored under appropriate
cold chain conditions both during
transportation and storage in cold chain
storage point.
c. The vaccine vial septum has not been
submerged in water or contaminated in any
way.
d. Aseptic technique has been used to
withdraw all doses.
e. The vaccine vial monitor (VVM), has not
reached the discard point.
3. Discard vaccine vial in case any one of the
following conditions is met:
a. If expiry date has passed.
b. VVM reached discard point (for freeze dried
vaccine, before reconstitution only) or
Vaccine vials without VVM or disfigured
VVM.
c. No label or partially torn label or writing on
label is not legible.
d. Any vial thought to be exposed to non-sterile
procedure for withdrawal.
e. Open vials that have been under water or
vials removed from a vaccine carrier that has
water.
f. If vaccine vial is frozen or contains floccules.
4. Health workers must be able to distinguish
between vials that can be used in subsequent
sessions and vials that must be discarded.
Training and supervision materials should
be revised to reflect the policy change.
5. Maintain temperature of ILR between 20 to
80C for storage of vaccines & diluents and
monitor temperature twice daily regularly.
6. Note the manufacturer, batch and expiry
date of the vaccine and diluent in the stock
register.
7. Proper recording and reporting of vaccine
distribution and usage has to be ensured.
8. Keep stock up to date, don't over-stock or
under-stock vaccines and diluents.
9. Multi-dose vials from which at least one
dose has been removed may be at risk of
contamination of the vial septum. These
vials should therefore, never be allowed to be
submerged in water (from melted ice for
example) and the septum should remain
clean and dry. NOTE: Well-sealed
conditioned ice packs should be used in
vaccine carriers and water should not be
allowed to accumulate where the vials are
stored. Vaccine vials must be transported in a
plastic zipper bag.
10. Keep the “returned, partially used” vials in
a separate box, and label it accordingly.
11.Observe earliest expiry first out (EEFO)
policy for issuing vaccines. If the vaccines
are of same expiry date, the partially used
vaccine vials should be re-issued. The vial
opened earlier, as recorded on the vial label,
should be issued first.
12. Contingency plan has to be in place in case
Cold chain maintenance and vaccine
distribution
6 4M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
of any exigency like power failure,
equipment breakdown, etc.
13. Inspect for and discard vaccine vial with
visible contamination (i.e. checking for any
change in the appearance of vaccine or any
floating particles) or breaches of integrity
(e.g. cracks, leaks).
14. All vaccines vials must be marked with date
& time of opening at first use.
15. Note the manufacturer, batch and expiry
date of the vaccine and diluent in the tally
sheet.
16. Always pierce the septum with a sterile
needle for drawing vaccine from the multi-
dose vials used. Except oral polio vaccine
which is given 2 drops orally, cap needs to be
closed after each use.
17. Ensure that the vaccine vials are returned
inside a vaccine carrier from the session site
to cold chain point immediately after session
ends, using the alternate vaccine delivery
mechanism in the reverse cold chain.
18. Under no circumstance the vaccine
carrier/vaccines will be kept in the field, in
case of such an event, the vaccines in such
vaccine carriers should be discarded and not
used for subsequent sessions.
19. Storage of vaccines at any place other than
a designated cold chain point will not be
At and during the immunization session
After immunization session is over
allowed. No vaccines should be stored at
ANM/LHV or other health worker/ASHA
house.
20.This policy is NOT applicable to opened
reconstituted vials of Measles, BCG and JE
vaccine, which will be used as per following
instructions and discarded immediately
after use:
a. Before reconstitution check that vaccine is
within expiry date and the VVM has not
reached the discard point. Reconstitute the
vial ONLY with diluent provided by
manufacturer for that batch of the vaccine.
b. Date and time of reconstitution must be
mentioned on the label vial at the beginning
of session.
c. Reconstituted vials will only be used for a
single session; they will not be carried from
one session to another, even if the session is
close by.
d. BCG and Measles must be discarded within
four hours of reconstitution or at end of
session whichever is earlier.
e. JE to be discarded after two hours of
reconstitution or at end of session whichever
is earlier.
21. All vaccines are supplied with VVM. Please
note that the VVM has only three status ie (i)
start point (ii) end point (iii) end point
exceeded. The vaccine has to be use before
reaching the end
Specific attention while implementing
open vial policy
End point
Square lighter than circle. If the expiry date has
not passed, USE the vaccine.
Square matches the circle. Do NOT use
the vaccine.
Square darker than the circle. Do NOT
use the vaccine.
End point exceeded
Start point
................................
6 5 A N N E X U R E S
ANNEX6:MonitoringFramework
cMYP(2013-17)-ReachingEveryChild
MonitoringandAccountabilityTrackingFramework
Datawillbedisaggregatedby
district
Fullimmunizationcoverageis
definedasinfantswhohave
receivedallrelevantdosesinthe
firstyearoflife
Numerator:Districtsthatshowfull
immunizationcoveragerates>80%
Denominator:Totaldistrictsinthe
country
Indicatorwilldisaggregatedby
district,gender,geography(urban
slum,urban,rural)andwealth
20(Source:
HMIS201213)
17%
(Source:
DLHS-3)
20(Source:
CES2009)
30
60%
All
States/UTs
(35)
HMIS
HMIS,Periodic
surveysincluding
DLHS,CES
HMIS,Periodic
surveysincluding
DLHS,CES
Monthly
Monthly
Monthly
1.Numberof
States/UTswhere>
95%sessionswere
heldasplanned
2.%ofdistricts
having>80%full
immunization
coverage
3.Numberof
States/UTshaving
lessthan10%
dropoutfrom
DPT1-DPT3(or
Pentavalent)
MoHFW
MoHFW
MoHFW
IndicatorIndicatorDefinition
(&unitofmeasurement)
Baseline
value
TargetDataCollection
Methodsand
Sources
Frequency&
Schedule
Responsibility
GOAL:Reducemortalityandmorbidityduetovaccinepreventablediseasesthroughhighqualityimmunizationservices
KEYOBJECTIVE1:Improveprogramservicedeliveryforequitableandefficientimmunizationservicesbyalldistricts
6 6M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Coldchainsicknessisdefinedas-
coldchainequipmentwhichoutof
orderasapercentageoftotal
equipmentplaced
Self-explanatory
Self-explanatory
Thiswillbeimplementedacrossthe
districtsBiharandUP
Self-explanatory
26
(Source:
NCCMIS
2013/State
reports)
16
(Source:
NIHFWRI
trainingstatus
report)
0
0
0
All
States/UTs
(35)
All
States/UTs
(35)
5
States/UT
110
districts
7
States/UT
NCCMIS
Statetraining
reports
Web-based
temperature
monitoringreport
Web-basedstock
monitoring
system
MoHFW
report/NCCMIS
Monthly
Monthly
Monthly
Monthly
Onetime
MoHFW
SIO
SIO/MoHFW
SIO/MoHFW
MoHFW
IndicatorIndicatorDefinition
(&unitofmeasurement)
Baseline
value
TargetDataCollection
Methodsand
Sources
Frequency&
Schedule
Responsibility
EXPECTEDRESULT1.2:Strengthenvaccineandsyringelogisticsmanagementacrossthecountryincludingforecastingand
procurementatcentrallevel
1.Numberof
States/UTswhere
thecoldchain
sicknessrate
meetsthenational
standardof<2%
2.Numberof
States/UTswhere
allcoldchainstaff
aretrainedincold
chainandvaccine
management
3.Numberof
States/UTwhere
temperature
monitoringisbeing
donewithwireless
dataloggersforall
functionalelectrical
coldchain
equipment
1.Numberof
districtswherereal
timevaccinestock
monitoringsystem
isimplemented
2.Numberof
States/UTsthatare
usingcomputer
simulationmodel
forvaccinesupply
chaincapacity
planning
................................
6 7 A N N E X U R E S
Numerator:Numberofsubcenters
havingafunctionalhubcutter
Denominator:Totalnumberofsun
centerssurveyed
Numerator:Numberofcoldchain
pointshavingafunctionalsafetypit
Denominator:Totalnumberofcold
chainpointssurveyed
PlanningunitisdefinedasPHC,
BlockPHC,CHCorUrbanHealth
Center
Numerator:Numberofplanning
unitswheremicroplansare
available
Denominator:Totalnumberof
planningunitssurveyed
PlanningunitisdefinedasPHC,
BlockPHC,CHCorUrbanHealth
Center
Numerator:Numberofplanning
unitshavingaAVDplan
Denominator:Totalnumberof
planningunitssurveyed
Self-explanatory
NoBaseline
NoBaseline
Nobaseline
NoBaseline
0(in2012)
80%
100%
80%
90%
All
States/UTs
(35)
Coverage
surveys
Statereport
Coverage
surveys
Coverage
surveys
Statereport
Annual
Annual
Annual
Annual
Annual
MoHFW
SIO
MoHFW
MoHFW
MoHFW
IndicatorIndicatorDefinition
(&unitofmeasurement)
Baseline
value
TargetDataCollection
Methodsand
Sources
Frequency&
Schedule
Responsibility
1.%ofsub-centers
withfunctionalhub
cutteravailable
2.%ofcoldchain
pointshaving
functionalsafety
pitsasperthe
CentralPollution
ControlBoard
(CPCB)guidelines
1.%ofplanning
unitswhereRI
microplansare
available
2.%ofplanning
unitswhereAVD
planisapartofRI
microplan
1.Numberof
Stateswherestate
taskforceon
immunizationis
constitutedto
reviewRIprogram
andtake
appropriateaction
EXPECTEDRESULT1.3:Ensuresaferinjectionpracticesandreducedvaccinewastage
EXPECTEDRESULT1.4:Ensurethatregularimmunizationsessionsareplannedandheldandcoverageincreased
EXPECTEDRESULT1.5:Improveprogramcoordinationatalllevels
6 8M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Numerator:Numberofcaregivers
whosechildreceivedpartialorno
immunizationwhodidnotfeelthe
needforadheringtoimmunization
schedule
Denominator:Numberof
caregiverssurveyed
Numerator:Numberofcaregivers
notrecallinganyofroutinevaccine
Denominator:Numberof
caregiverssurveyed
Self-explanatory
Staffshouldincludeprogram
managers(otherthanASHA)
Shouldbestand-aloneBCC
training
Thiswillonlyincluderural
populationandchildrenwhohave
receivedatleastonevaccineprior
tothesurvey
Numerator:Numberofcaregivers
whogotinformationabout
immunizationfromASHA
Denominator:Numberof
caregiverssurveyed
28%
(Source:CES
2009)
12%
(Source:CES
2009)
0(asof2012)
0(asof2012)
EXPECTED
19%
(Source:CES
2009)
<15%
<5%
Allhigh
priority
States
35
(12)
Allhigh
priority
States(12)
>80%
Coveragesurveys
Coveragesurveys
StatePIP
MoHFWreport
EXPECTED
Coveragesurveys
Annual
Annual
Annual
Annual
Annual
MoHFW
MoHFW
State/MoHFW
State/MoHFW
MoHFW
IndicatorIndicatorDefinition
(&unitofmeasurement)
Baseline
value
TargetDataCollection
Methodsand
Sources
Frequency&
Schedule
Responsibility
1.%ofcaregivers
whosechild
receivedpartialor
noimmunization
whodidnotfeelthe
needforadhering
totheimmunization
schedule
2.%ofcaregivers
notrecallinganyof
routinevaccine
1.Numberof
State/UTPIPs
whichhave
communication
actionplanforRI
2.Numberof
Stateswhere80%
ofhealthHRare
trainedonBCC
1.%ofcaregivers
whoreportedthat
theygotinformation
aboutimmunization
fromASHA
KEYOBJECTIVE2:Increasedemandandreducebarriersforpeopletoaccessimmunizationservicesthroughimprovedsocialmobilization
EXPECTEDRESULT2.1:Developandimplementamulti-prongednationalcommunicationstrategywithafocusonprioritystates
EXPECTEDRESULT2.2:Effectivecommunicationchannelsaresetupwiththecommunityforbetteracceptanceofvaccines
35
The 12 States include – Arunachal Pradesh, Assam, Bihar, Chhattisgarh, Gujrat, Jharkhand, Madhya Pradesh, Manipur, Nagaland, Odisha, Rajasthan and UP
................................
6 9 A N N E X U R E S
Self-explanatory
Messagesasrelevantatthetimeof
survey
Numerator:Numberofcaregivers
whocanrecallnewimmunization
messages/tagline
Denominator:Numberof
caregiverssurveyed
Referenceperiod:Timelyreportsas
compliedoverthepreviousone
year.
Numerator:Numberofsentinel
sitesprovidingtimelyandcomplete
reportson90%occasion
Denominator:Allsentinelsites
Self-explanatory
DoesnotincludePolioworkshops
0
0%
0%
(asof2012)
372cases
(sourceFIR
2012-13)
0(asof2012)
All
States/UTs
(35)
40%
80%
>1500
cases
35(States
andUTs)
State
communication
plan
CoverageSurveys
Surveillance
report
FIR,PIR,DIR
VPDSurveillance
report
Annual
Annual
Annual
Annual
Annual
State/MoHFW
MoHFW
MoHFW
DIO,SIO
MoHFW/SIO
IndicatorIndicatorDefinition
(&unitofmeasurement)
Baseline
value
TargetDataCollection
Methodsand
Sources
Frequency&
Schedule
Responsibility
1.Numberof
States/UTsthat
haveadefined
mediatrackingand
assessmentplan.
2.%ofcaregivers
whocanrecallnew
immunization
messages/tagline
1.%ofsentinel
sitesproviding
timelyand
completereports
onVPDs(including
zeroreport)on
90%occasions
2.Increaseinthe
numberofnotified
seriousAEFIcases
abovethe2012
baselinevalue
1.Numberof
Statesthathave
conductedVPD
surveillance
workshops
EXPECTEDRESULT2.3:Evidencebasedandcontextuallyrelevantcommunicationmessagesaredisseminatedinthecommunity
KEYOBJECTIVE3:Strengthenandmaintainrobustsurveillancesystemforvaccinepreventablediseases(VPDs)and
adverseeventsfollowingimmunization(AEFI)
EXPECTEDRESUL3.1:InstitutionalizeandstrengthensurveillancemechanismsforVPDs
7 0M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
NewerantigenincludesHiBand
Rotavirus
Self-explanatory
Timelynotificationisdefinedas
submissionofnotificationform
within48hoursoftheevent
occurringinthefield
Numerator:SeriousAEFIcases
notifiedontime
Denominator:Allnotifiedserious
AEFIcases
Numerator:SeriousAEFIcases
investigatedontime
Denominator:Allnotifiedserious
AEFIcaseswhosePIRisreceived
Numerator:SeriousAEFIcases
classifiedwithin120days
Denominator:Allnotifiedserious
AEFIcases
Vaccinesforreviewinclude,butnot
limitedto,IPV,Pneumococcus,
Rotavirus,Rubella
10
(asofAugust
2013)
9
.
16%
(Source:AEFI
dashboardas
ofJanuary
2013-14)
6%
(Source:AEFI
dashboardas
ofJanuary
2013-14)
64%
(Source:
MoHFWreport
asonApril
2013forcases
uptoDec
2012)
0(asof2013)
30
All
States/UTs
(35)
80%
60%
90%
Atleast2
new
vaccines
MoHFWreport
MoHFWreport
FIR
FIR,PIR
DIR
NTAGIreport
Annual
Annual
Annual
Annual
Annual
6monthly
IndicatorIndicatorDefinition
(&unitofmeasurement)
Baseline
value
TargetDataCollection
Methodsand
Sources
Frequency&
Schedule
Responsibility
2.Numberof
sentinelsitessetup
fornewerantigens
1.Numberof
States/UTswithall
DIOstrainedon
nationalAEFI
guidelines
2.%ofserious
AEFIcasesnotified
inatimelymanner
3.%ofSerious
AEFIcases
investigatedtimely
aspernational
guidelines
4.%ofSerious
AEFIcases
classifiedwithin
120daysof
reportingofthe
case
1.Numberofnewer
vaccinesthathave
beenreviewedfor
introductioninUIP
byNTAGI
EXPECTEDRESUL3.1:InstitutionalizeandstrengthensurveillancemechanismsforVPDs
KEYOBJECTIVE4:IntroduceandexpandtheuseofnewandunderutilizedvaccinesandtechnologyinUIP
ICMR/MoHFW
MoHFW
DIO,SIO
DIO/SIO
SIO,StateAEFI
Committee
NTAGI/MoHFW
................................
7 1 A N N E X U R E S
Self-explanatory
Self-explanatory
Numerator:Numberofnewly
identifiedJE-endemicdistricts
whereJEvaccinehasbeen
introducedinUIP
Denominator:62(newlyidentified
districts)
Fullimmunizationcoverageis
definedasinfantswhohave
receivedallrelevantdosesinthe
firstyearoflife
Numerator:Districtsthatshowfull
immunizationcoveragerates>
80%
Denominator:Totaldistrictsinthe
country
Self-explanatory
9States
(asof
December
2013)
Nobaseline
0
17%
(Source:
DLHS-3)
5States/UTs
(Source:
NIHFWRI
trainingstatus
report)
All
States/UTs
(35)
Atleasttwo
meetings
peryear
100%
60%
30
States/UTs
HMIS
NTAGIminutes
HMIS
HMIS,Periodic
surveysincluding
DLHS,CES

Statetraining
report
Annual
Annual
Annual
Monthly
Annual
IndicatorIndicatorDefinition
(&unitofmeasurement)
Baseline
value
TargetDataCollection
Methodsand
Sources
Frequency&
Schedule
Responsibility
2.Numberof
Statesthathave
introduced
Pentavalent
vaccine
1.Numberof
NTAGImeetingsin
ayear
1.%ofnewly
identified62JE-
endemicdistricts
whereJEvaccine
hasbeen
introducedin
36
UIP
1.Numberof
districtswithfull
immunization
coveragerateof
>80%
1.Numberof
Stateswhereall
MOsaretrainedon
RIMOhandbookin
lastthreeyears
MoHFW
MoHFW
MoHFW
MoHFW
SIO
EXPECTEDRESULT4.1:Setupandstrengtheninstitutionalmechanisms,frameworkandpoliciesfornewerandunderutilizedvaccineintroduction
EXPECTEDRESULT4.2:ScaleupandsustaintheimplementationofJEvaccinationinidentifiedendemicdistrictsaspartofJEcontrol
KEYOBJECTIVE5:Strengthenhealthsystemforimmunizationprogram
EXPECTEDRESULT5.1:Increasethepoolofskilledhumanresourcestoprovidequalityimmunizationservicesinanintegratedmanner
36
The newly identified 62 districts as on 2013
7 2M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Self-explanatory
Self-explanatory
DatawilldisaggregatedbyState
Numerator:Totalnumberofinfants
registeredinMCTS
Denominator:Totalestimated
numberofinfantsintheyear
Self-explanatory
Self-explanatory
2
(Source:
NCCMIS
2013)
7
(Source:
MoHFW
financereport
2011-12)
57%
(Source:
MCTSportal
asonApril
2013)
0
0
0
25
States/UTs
All
States/UTs
(35)
80%
25
States/UTs
0
StatePIP,
NCCMIS
NRHMFMS
StatePIP
Statereports
AFPSurveillance
BulletinIndia
Annual
Annual
Annual
Annual
Annual
IndicatorIndicatorDefinition
(&unitofmeasurement)
Baseline
value
TargetDataCollection
Methodsand
Sources
Frequency&
Schedule
Responsibility
2.Numberof
States/UTswithno
vacantpositionsfor
refrigerator
mechanics
1.Numberof
States/UTsutilizing
>90%ofthe
allocatedfundfor
UIP
1.%ofinfants
registeredinMCTS
1.Numberofstates
whereStateTask
Forceon
Immunization
(STFI)conducted
atleast10monthly
meetingsduringthe
reportingyear
1.Nowildpolio
virusdetectedin
thecountry
SIO
Statemanager
NRHM
States
States
MoHFW
EXPECTEDRESULT5.2:EnsurethatadequatefinancialresourcesareavailableforUIP
EXPECTEDRESULT5.3:Improveprogramaccountability,monitoringandreportingatalllevels
EXPECTEDRESULT5.4:StrengthenRIprogrammanagementandservicedeliverythroughfieldlevelsupportivesupervisioninhighprioritystates
KEYOBJECTIVE6:Contributetoglobalpolioeradication,measles,maternalandneonataltetanuselimination
................................
7 3 A N N E X U R E S
Self-explanatory
Self-explanatory
Datawillbedisaggregatedby
districtlevel
Datawillbedisaggregatedby
districtlevel
Self-explanatory
Self-explanatory
Self-explanatory
>2
>80%
19(Source:
HMIS2012-
13)
2(Source:
HMIS2012-
13)
29States/UTs
(Source:CES
2009)
11
18(Source:
WHOreport
2013
>2
.>80%
AllStates
/Uts(35)
All
States/UTs
(35)
All
States/UTs
(35)
23States
/UTs
All
States/UTs
AFPSurveillance
BulletinIndia
AFPSurveillance
BulletinIndia
HMIS
HMIS
Coveragesurvey
MoHFWreport
MoHFWNNT
validationreport
Annual
Annual
Annual
Annual
Annual
Annual
Annual
IndicatorIndicatorDefinition
(&unitofmeasurement)
Baseline
value
TargetDataCollection
Methodsand
Sources
Frequency&
Schedule
Responsibility
2.NonPolioAFP
rateismaintained
orexceeds2per
100,000children
under15years
3.ReportedAFP
caseshavetwo
adequatestool
specimens
collectedwithin14
daysofonsetof
paralysisin>80%
cases
4.Numberof
StateswithMCV1
coverageof>90%
5.Numberof
StateswithMCV-2
coverageof>90%
6.Numberof
Stateswith>80%
TT2coveragefor
pregnantwomen
1.Numberof
Statesthathave
established
laboratory
supportedmeasles
surveillance
systems
1.Numberof
Statesvalidatedas
NNTeliminated
duringtheplan
MoHFW
MoHFW
MoHFW
MoHFW
MoHFW
MoHFW
MoHFW
EXPECTEDRESULT6.2:Achievemeasleseliminationandcontrolforrubella/congenitalrubellasyndrome(CRS)by2020
EXPECTEDRESULT6.3:Eliminatematernalandneonataltetanusby2015
7 4M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
ANNEX 7: Emergency Preparedness and Response Plan 2011
................................
7 5 A N N E X U R E S
Emergency Preparedness and Response
Plan 2011
1. Background
The Emergency Preparedness and Response
Plan has been developed at the request of the
Minister of Health & Family Welfare to ensure
adequate preparedness and response to an
event of importation of poliovirus anywhere in
India during 2011.
India has made remarkable progress towards
polio eradication in 2010. Only 42 wild
poliovirus (WPV) cases have been detected in
the country, compared to 724 cases detected
during the same period in 2009. The progress in
polio eradication was reviewed during the
India Expert Advisory Group (IEAG) meeting
held in November 2010. At this meeting the
IEAG concluded that “the epidemiologic,
genetic, serologic, operational & technical
evidence show that India is on the right path to
achieve eradication”. However, the IEAG
identified certain risks to the polio eradication
Program in India. One of the major risks
identified includes continued transmission of
poliovirus within the mobile / migrant
populations, resulting in re-introduction and
spread of the virus in Uttar Pradesh (UP) and
Bihar or in areas outside these historically core
endemic states that are at high risk of
importation and further spread of polio. The
IEAG highlighted the fact that as long as virus
transmission continues in any part of India or
elsewhere in the World, the possibility of virus
importation to polio-free areas in India
remains.
In view of these risks, the IEAG recommended
that while intensive efforts should continue to
stop transmission in areas with recent WPV
transmission and the traditionally endemic
areas of UP and Bihar, the program in India
should:
a. make efforts to protect polio-free areas from
importation of virus from within or outside
India
b. rapidly respond to any WPV detected
anywhere in India during 2011 with an
aggressive mop-up vaccination campaign to
stop any further circulation of the virus.
The IEAG recommended that “From now, any
WPV from any source should be considered a
public health emergency and responded to with
urgent mop-ups; government & partners must
deploy additional, highly experienced human
resources to ensure that mop-up rounds are of
the highest quality. Mop-ups should target both
the area of detection of the virus in a case or in
the environment and, if there is a clear genetic
link, the area of origin of the virus”. Thus any
isolation of WPV requires a rapid high quality
mopping-up response as an utmost priority to
stop circulation and spread.
This document is a strategic plan for protecting
the polio-free areas of India from WPV and for
implementing high quality mopping-up
operations with the aim of stopping the final
chains of WPV transmission.
The Government of India will have a “Central
Emergency Preparedness and Response
Group” to ensure adequate preparedness for a
rapid response and manage the actual response
to the detection of a wild poliovirus anywhere
in India during 2011. The group will be chaired
by the Joint Secretary, Health & Family
Welfare, Government of India, and comprise
of senior officials from the Ministry of Health
and Family Welfare (GoI), and representatives
of National Polio Surveillance Project (NPSP)
– WHO, UNICEF and Rotary. The key
responsibilities of the group will include:
lIdentify and train Rapid Response Team
(RRT) members at the national level. The
RRT members will include experienced,
government and partner agency staff from
the fields of epidemiology, public health,
management and communication
(including a media specialist).
lFollow up with state governments to ensure
that a Rapid Response Team, headed by an
officer of the rank of a Principal Secretary, is
constituted in each state. The state RRT should
include at least 2 to 4 well performing Medical
Officers from within the state who have at least
2. Immediate actions - Preparedness for
virus importation and response
2.1 National-level Actions
7 6M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
5 years' experience in dealing with senior
district level officials and a familiarity with the
basic principles of mass vaccination campaign
implementation. The RRT members will be
trained by MoHFW, GoI with assistance from
WHO NPSP and UNICEF. In the event of
WPV detection, it will be necessary to assign
the RRT members full time duty by the state
governments to provide support to mop up
vaccination campaigns.
lDevelop a media response plan to be used in
the event of detection of WPV.
lReview the availability of buffer stocks of
oral polio vaccines to manage mop-up
vaccination campaigns.
Summary of the national actions with the
proposed time frame:
lConstitute the “Central Emergency
Preparedness and Response Group” by mid-
April 2011.
lWrite to state governments and partners, in
the second week of April 2011, for
identification of RRT members in each state
by the end of April 2011.
lOrganize a training of the RRT members
jointly with NPSP and UNICEF by the
second week of May 2011.
lMonitor the identification and training
status of the RRT members.
lProcure sufficient buffer stocks of bOPV,
tOPV and mOPVs to manage the mop-ups.
lDevelop a media response plan by end of
April 2011 that includes mechanisms of
harmonizing messages from union and state
governments to the detection of any polio
cases.
The following states have been identified at a
high or medium risk of importation based on
past epidemiology of polio: Haryana, Delhi,
Uttarakhand, Maharashtra, Punjab,
Rajasthan, West Bengal, Gujarat, Jharkhand,
Madhya Pradesh, Assam, Orissa, Andhra
Pradesh, Himachal Pradesh, Jammu &
Kashmir and
2.2 State level
2.2.1 States at risk of importation
Karnataka.
Endemic states
States at high & medium
risk of importation
States at low risk of importation
lHigh Risk of Importation: 8 or more importations and 5 years or more with importations
lMedium Risk of Importation: 5 or more importations and 3 to 4 years with importations
Risk Categorization of States based on history of polio importations during last fiveyears
................................
7 7 A N N E X U R E S
2.2.2 State Level Actions
Each state at high or medium risk should
undertake the following actions to prepare for
the emergency response:
lConstitute a State Emergency Preparedness
and Response Group chaired by the
Secretary (Health & Family Welfare) and
comprised of senior officials from the State
Government such as the Director Health
Services, State EPI Officer and other
nominated senior government officials.
State representatives of WHO- NPSP,
UNICEF and Rotary International should
also be a part of the group. This group
should monitor the preparedness and
implementation of the mop-up.
lUndertake a risk analysis, in coordination
with WHO- NPSP officials, to identify
districts, blocks or urban areas at high risk of
importation and spread of poliovirus.
This analysis should identify areas that have
had repeated importations of polio viruses
during previous years or a recent clustering
of polio compatible cases in time and space,
or are hard-to-reach areas or have
demographic/ environmental factors that
would facilitate the spread of wild polio
virus following an introduction (such as high
population density, poor sanitation). Special
focus should be on the identification of areas
with low routine immunization coverage
and areas with migratory or mobile
populations in each state as per guidelines
issued by GOI in 2010. This risk analysis
should be completed at the earliest by each
state and the lists of all high-risk areas and
populations shared with GOI.
lUndertake a communication risk analysis in
coordination with UNICEF/ WHO- NPSP
and based on the analysis develop a
communication plan for issues related to
n o n - c o m p l i a n c e / r e s i s t a n c e t o
administration of polio vaccines.
lDevelop a media response plan to be used in
case a virus is detected.
lDevelop and implement a plan to increase
polio SIA coverage and RI coverage in these
high-risk areas/ populations to achieve high
immunity against polioviruses in these
areas, which in turn will prevent spread and
establishment of circulation of any
imported wild polioviruses. These areas
should be targeted for better planning,
training, social mobilization and monitoring
efforts during the SIAs in 2011–12. The
states should also begin the process of
harmonizing the polio microplans with
Routine Immunization plans in the high-risk
areas.
lIdentify and nominate two to four
experienced medical officers to be a part of
the Rapid Response Teams (RRTs).
lReview the surveillance quality in these
areas with the district and block officials in
coordination with NPSP officials to identify
actions to strengthen surveillance sensitivity
in these areas, which in turn will assist with
early detection and response following any
importation.
lAssign senior state government officials to
visit high risk districts and blocks to review
progress in updating and implementing
microplans for improving immunization
coverage and surveillance sensitivity.
Summary of the state actions with the
proposed time frame:
lConstitute a State Emergency Preparedness
and Response group by end of April 2011.
lIdentify RRT members by end of April 2011.
lIdentify high-risk districts and high-risk are
as within districts by mid-May 2011.
lIdentify and assign senior officials to
high-risk districts by third week of May
2011.
lThe above items should be reported back to
the Central Emergency Preparedness and
Response Group by the end of May 2011.
7 8M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
3. Response and actions following the
detection of wild poliovirus
3.1 Key steps in the planning phase of
the mopping up vaccination campaign
3.1.1 National-Level Actions:
lThe Ministry of Health and Family Welfare
will be informed about the detection of the
virus without delay.
lThe Ministry of Health and Family Welfare
will inform the Chief Secretary of the
affected state of the detection of the polio
case in the state.
lThe Central Emergency Preparedness and
Response Group will meet within 24 hours
of receiving the information. The Group
will review and analyze, in detail, the field
epidemiological investigation findings
pertaining to the polio case. Based on the
above findings, the areas and populations at
risk of poliovirus circulation will be
identified and a SIA response within the
broad strategic framework recommended by
the IEAG will be decided. The group will
make specific recommendations on:
§Timing of the response
§Areas to be covered during the response
§Type of vaccine to be used during the
response
§Number of proposed rounds
§Additional investigations and analyses to be
conducted
lMembers from the Central Emergency
Preparedness and Response Group will visit
the concerned state to meet the state health
secretary and other state officials. The
members of the National and State
Emergency Preparedness and Response
groups will subsequently visit the concerned
districts accompanied by the state RRT
members to review planning for an
emergency response.
lThe Central Emergency Preparedness and
Response Group will meet on a weekly basis
to review the planning and implementation
o f t h e r e s p o n s e a n d p r o v i d e
recommendations to the immunization
division and state authorities to make
improvements.
lVaccine will be mobilized to reach the state
or districts undertaking the mop-up at least
three days before the start of the campaign.
lMoHFW shall seek support from other
government departments such as Social
Welfare, Railways, Panchayati Raj, Urban
Development, Education, for the emergency
mop-up operation.
lThe State Emergency Preparedness and
Response Group should be activated within
24 hours of receipt of information to
initiative the following actions:
§Inform the Divisional Commissioners and
the District Magistrates of the areas
undertaking the mop-up within 24 hours of
receipt of information.
§Allocate geographical areas and operational
responsibilities to all RRT members
ensuring an appropriate distribution of
human resource within 72 hours of receipt
of information.
§Assign senior state officials to the districts
and members of the State Emergency
Preparedness and Response Group to visit
and mobilize the districts within 72 hours of
confirmation of case.
lThe currently existing State-level
Steering/Coordination Committee for polio
eradication should be requested to organize
a meeting within five days of case
confirmation to seek support and coordinate
activities with other government
departments and NGOs.
lDistrict-level officials from health and
administration should begin mobilizing
block officials to start preparations within 48
hours of identify the importation.
3.1.2 State level Actions:
3.1.3 District-level Actions:
................................
7 9 A N N E X U R E S
lDistrict Task Force (DTF) meetings should
be organized in the district with RRT
members, NPSP, UNICEF staff and key
government officials to allocate specific
responsibilities within the district and ensure
participation of all sectors for a successful
implementation of the mop-up. The first
DTF to be conducted within five days of
confirmation of the case. Subsequently there
should be a weekly DTF to take stock of the
situation and address requirements of the
response activities.
lDivisional Commissioners should review
the preparedness through participation in
DTFs and field visits.
lTehsil or Block Task force meetings should
be organized at sub-district level in all urban
and rural areas within sevendays of the
confirmation of the case.
lAll existing micro plans should be reviewed
as per operational guide for mop-up with
special emphasis to ensure no areas are
missed and there is high coverage of high
risk areas and migratory populations. All
micro plans should be reviewed and
modified within 10 days of confirmation of
the case.
lAll vaccinators should be retrained on
operational and IPC skills in the week before
the start of the mop-up.
lThe district and block in consultation with
UNICEF and other social mobilization
partners should plan and initiate IEC and
social mobilization measures based on solid
data collected through standardized data
tools.
lDevelop a media response plan to be used in
case a virus is detected.
lIn consultation with the government, NPSP
should develop a monitoring plan for
intensive monitoring and mid course
corrections during the activity. Additional
independent monitors should be deployed
by NPSP in addition to the existing NPSP
and UNICEF staff present in the district.
3.2 Key actions during the mopping up
vaccination campaign
3.2.1 National-level Actions
3.2.2 State-level Actions
3.2.3 District/ Sub District-level Actions:
lMembers from the Central Emergency
Preparedness and Response Group will
monitor the activity in the highest risk
blocks.
lThe Central Emergency Preparedness and
Response Group will meet to review the
feedback from its members, states, RRTs and
provide directions for corrective actions.
lMembers of the State Emergency
Preparedness and Response Group and the
State monitors should visit high risk blocks
to monitor the activity and provide feedback
to the State Principal Secretary (H & FW)
lThe State Emergency Preparedness and
Response Group should meet daily to review
feedback from the districts and plan
corrections.
lThe district should implement the SIA
activity under the direction of the District
Magistrate (DM) and supervision of the
Chief Medical Officer/Civil Surgeon. The
DMs should report on the quality of the
activity to the State Principal Secretary (H &
FW).
lDaily monitoring and review of activity to
plan for corrective actions over subsequent
days
§Senior district-level officials from health and
administration (Divisional Commissioner/
D M / A D M / C M O / D P O / D y
CMO/BDOs) should monitor the
implementation of the activity and attend
evening meetings at the high risk blocks.
§A daily evening review meeting should be
organized at the district under the
chairmanship of the District Magistrate.
8 0M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
4. Key actions at the end of the activity
5. Role of partners
6. States at low risk of importation of
poliovirus
lThe District Magistrate should send a report
of the completed activity to the State
Emergency Preparedness and Response
Group for review and corrective actions.
lThe State Emergency Preparedness and
Response Group should meet to review this
and forward the report to the Central
Emergency Preparedness and Response
Group.
lThe Central Emergency Preparedness and
Response Group will review the activity and
inform the Union Minister who, at his
discretion, will inform the Chief Minister of
the concerned state about the quality of
response activities and ongoing risk
assessment.
Partners should participate in the Central and
State Emergency Preparedness and Response
Groups. The key role of the partners will be as
follows:
lNPSP: Provide surveillance data,
epidemiologic analysis and strategic
planning and other technical support to the
group as well as support monitoring of the
preparedness and response at the district,
state and national levels.
lUNICEF: Provide support to the
communication/ social mobilization and
media strategies and their implementation
and monitor their impact
lRotary International:Provide support to the
advocacy at the state and district levels and
to the communication strategy and social
mobilization activities
lUndertake a risk analysis, in coordination
with WHO-NPSP officials, to identify
districts, blocks, and urban areas at higher
risk of importation and spread of poliovirus.
This analysis should include identification
of areas that have had importations of polio
viruses during previous years or a recent
clustering of compatibles in time and space,
or are hard-to-reach areas or have
demographic or environmental factors that
would facilitate the spread of wild poliovirus
following an introduction (such as low
routine immunization coverage, high
population density, migrant sites, poor
sanitation). Special focus should be on the
identification of areas with migratory or
mobile populations in each state as per
guidelines issued by GOI in 2010. This risk
analysis should be completed at the earliest
and the lists of all high risk areas and
populations shared by each state with GOI.
lThe state should assign Senior State
Government officials to visit high risk
districts and blocks to review progress in
updating and implementing micro plans
prior to the 2011 NIDs for improving
immunization coverage and surveillance
sensitivity.
The basic aim of the mop-up would be to
vaccinate all under-5 children in the mop-up
area. Each household in the mop-up area will
be visited by vaccination teams to vaccinate all
under-5 children. The duration of the
house-to-house (h-t-h) search and vaccination
would be decided by the number of available
vaccination teams in the area. In principle,
there would be a minimum of 2 to 5-day h-t-h
activity in all areas to ensure a rational
workload for each vaccination team.
Additional 1 to 2 days of h-t-h activity will be
undertaken in special areas with lesser number
of available teams e.g. in large urban areas. B
team activity will continue in UP and Bihar.
Transit teams and mobile teams will be
deployed to cover migrant and mobile
populations.
In areas that have used booths during the
SNID/NID, booths will also be setup on day 1
of the mop-up campaign because of their
IEC/SM value.
7. Strategy for mop-ups
................................
8 1 A N N E X U R E S
The mop-ups shall be implemented as per the
Operational Guide for SIAs published by
Government of India in 2006.
The following guidelines as recommended by
the WHA andIEAG should be followed:
lSpeed of response: As early as possible but
no later than two weeks from confirmation
of the case.
lExtent of mop-ups: The response should
consist of at least three large scale,
house-to-house rounds of immunization.
The World Health Assembly Resolution
(59.1) calls for coverage of 2 to 5 million
children in each round. Mop-ups should
cover at a minimum the infected district and
all districts contiguous with it, across state
boundaries if necessary. Where there is a
clear genetic link of the virus to the strains in
another area, the area of origin should also
be included. In the demographic context of
India and considering that this is the final
7.1 General principles for mopping-up
operations
stage of polio eradication, the 18th IEAG
has recommended the appropriate target
population for mop-ups around 5 million
children per round.
o In high risk areas: SNID rounds may
constitute one or more of the three rounds,
but in principle at least one additional round
should be carried out in an appropriate area
using a short interval approach – all rounds
must be of the highest possible quality!
o In non-high risk areas: Mop-ups should
consist of a minimum of three high quality
rounds, using a short interval approach
(minimum interval of two weeks but within
four weeks) – all rounds must be of the
highest possiblequality!
lVaccine of choice for mop-ups is mOPV
appropriate to the local epidemiology or
bOPV; a rolling stockpile of 30 million doses
of bOPV and 10 million doses of mOPV1
should be maintained to allow for rapid
implementation of mopping up vaccination
with the appropriate vaccine.
................................ 8 3
Costing and Financial
Sustainability of the
Universal Immunization
Program
7
................................
8 5
1. Introduction
India is at an important time in the
development of its Universal Immunization
Program (UIP). It is planning several
improvements such as the addition of many
new and underutilized vaccines as well as
adding new staff at different administrative
levels. India will need to secure other sources of
financing as it will probably be graduating from
GAVI support since its high Gross National
1
Income (GNI) per capita will make it ineligible
for support. As a result, information on the
costs and sources of financing for the UIP will
be particularly important for policy-makers to
make informed decisions on phasing-in
strategies and timing of these Program
improvements.
The report on costing and financial
sustainability of the India Immunization
Program was developed during the period June
to December 2013, under the auspices of the
Immunization Technical Support Unit (ITSU)
in India and assisted by the immunization
partners, WHO and UNICEF. The team that
collected and analyzed the data was led by a
research scientist from the Public Health
Foundation of India and consisted of
Government of India officials, and experts
from the Immunization Technical Support
Unit (ITSU-MoHFW) and the immunization
partners. Data was collected from June to
September 2013. Then meetings were held
with ministry officials to go over the
preliminary findings and assumptions to be
made in the analysis. Finally, from September
to December 2013 the data was analyzed and
put into a report.
The main findings of the cost analysis are the
following:
lTotal baseline expenditure was INR 3,446
2
crore ($718 million), including shared
3
personnel costs, and INR 2,131 crore ($444
million) without shared costs.
o Expenditure on the routine Program was
INR 1,253 crore ($261 million) and, on the
supplemental immunization activities
(SIAs), was INR 878 crore ($182 million).
l
2. Summary of Findings on Baseline
Expenditures
Table 1 shows total baseline expenditures
with shared costs and selected indicators on
cost per output and Program financing.
1
Countries' GAVI eligibility for the year 2014 is GNI per capita lower or equal to $1,570.
2
1 crore= ten million (10,000,000)
3
Shared costs include the value of inputs that are not specific to immunization and which are used by different
Programs or activities in the health sector — i.e. their utilization for immunization is less than 100%.
Table 1. Baseline Expenditures and Selected Indicators, 2012.
Total Expenditures (USD)
261,089,884
182,995,523
444,085,407
273,942,919
718,028,326
0.2
14
90
1
2
0.03
Total Expenditures (INR)
12,532,314,431
8,783,785,120
21,316,099,550
13,149,260,100
34,465,359,650
9.6
672
90
1
2
0.03
Baseline Indicators
Routine Immunization only
Campaigns
Total immunization specific expenditure (A)
Total shared cost (B)
Grand Total (A + B)
Per capita
Per DTP3 child
Percentage national funding
Percentage total health expenditures
Percentage govt. health expenditures
Percentage GDP
C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
8 6M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
3. Details of Baseline Program Cost
and Financing
The year 2012 is the baseline for the cost and
financing projections since it has the most
recent complete information. The actual
expenses of the government and the
immunization partners were taken into
account for the baseline cost calculation.
Table 2 shows the baseline cost profile. In 2012,
the total estimated cost of the UIP was INR
3,446 crore ($718 million), including shared
cost. Shared personnel cost (those who spent
less than 100 percent of their time for
immunization) contributed the maximum in
total expenditure (38 percent) while all routine
recurrent cost contributed 36 percent. The
contribution of SIAs was 25 percent in total
cost. The detailed expenditure on shared
personnel cost is provided in Table 3. Vaccines
and injection supplies under routine recurrent
cost are those used for Routine Immunization
only. The amount spent on vaccines and
injection supplies for supplementary
immunization has been provided under SIAs.
Personnel cost includes salaries and benefits for
all who spent 100 percent of their time for
immunization starting from the national level.
Transport cost included the operational cost of
Teeka Express, vaccine handling cost at
GMSD and the petrol, oil, lubricant for vaccine
transport. It was assumed that there were a
total of 700 vaccine vans (250 4WD and 450
2WD) and 120 Teeka Express in 2012. Training
cost included the actual expenditure of the
government on training as well as the training
expenses by immunization partners. The
components and detailed expenditures under
social mobilization, Program management and
other routine recurrent cost are shown in
Tables 4, 5 and 6 respectively.
................................
8 7
Table 2. Baseline Universal Immunization Program Costs, 2012
Routine Recurrent Costs
Vaccines
Injection Supplies
Personnel
Transport
Cold chain maintenance
Training
Social mobilization, advocacy,
communication activities
Disease surveillance
Program management
Other routine recurrent costs
Subtotal
Capital Costs
Cold chain equipment
Subtotal
Total Routine Costs (without
shared costs)
Supplemental Immunization
Activities (SIAs)
Polio
Vaccines and Injection supplies
Operational costs
Total
Measles
Vaccines and Injection supplies
Operational costs
Total
JE
Vaccines and injection supplies
Operational costs
Total
Subtotal SIAs
Shared personnel costs
GRAND TOTAL
2012 (USD million)
59.92
16.46
11.40
27.09
9.24
5.94
50.23
18.97
9.67
37.91
246.81
14.28
14.28
261.09
95.22
53.00
148.21
15.14
13.11
28.25
4.85
1.68
6.54
183.00
273.94
718.03
2012 (INR crore)
287.60
79.00
54.72
130.02
44.34
28.53
241.10
91.04
46.40
181.96
1,184.71
68.52
68.52
1,253.23
457.04
254.37
711.41
72.69
62.91
135.59
23.30
8.08
31.38
878.38
1,314.93
3,446.54
Percent
8.3
2.3
1.6
3.8
1.3
0.8
7.0
2.6
1.3
5.3
34.4
2.0
2.0
36.4
13.2
7.4
20.6
2.1
1.8
3.9
0.7
0.2
0.9
25.5
38.1
100.0
C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
8 8M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Numbers in
2012*
4,833
4,833
24,049
207,578
14,648
16,109
24,049
296,099
Percentage of time
spent on
immunization
10
5
10
33
33
33
5
Shared personnel
MO (in charge) at block level
Data entry operators at block level
MO (in charge) at PHC level
ANM
MPW
LHV
Data entry operators at PHC level
Total
Table 3: Details of shared personnel cost in 2012
Salary per
month (INR)
35,000
8,000
35,000
12,500
12,500
12,500
8,000
INR (crore)
20.30
2.32
101.01
1027.51
72.51
79.74
11.54
1,314.93
USD (million)
4.23
0.48
21.04
214.06
15.11
16.61
2.40
273.94
Table 4: Details of expenditure on social mobilization, advocacy and communication activities in 2012
Cost components
ASHA incentives for social mobilizations
Printed materials (banners, posters, IEC materials) BCC tool
Advocacy and communication (UNICEF)
SMNet (UNICEF)
Total
INR Crore
194.62
24.98
5.73
15.77
241.10
USD million
40.55
5.20
1.19
3.29
50.23
Table 5: Details of Program management expenditure in 2012
Cost components
Evaluations, program reviews and assessment meetings
Office supplies and consumables
Micro planning
Immunization Technical Support Unit (ITSU)
Operational cost of polio and other VPDs (UNICEF)
Operational cost of polio and other VPDs (WHO)
Total
INR Crore
10.97
0.31
2.17
4.77
9.36
18.83
46.40
USD million
2.29
0.06
0.45
0.99
1.95
3.92
9.67
* Source: Rural Health Statistics in India, 2012.
................................
8 9
Table 6: Details of expenditure for other activities under routine immunization in 2012
Cost components
Cost components
Service provision in underserved and hard to reach areas
(including slums)
ASHA Incentives
Planning, supportive supervision and monitoring
Intensification of Routine Immunization (WHO)
Research studies (Govt. + WHO)
Measles, JE control Program (UNICEF)
Other state-specific activities
Total
INR Crore
INR Crore
18.39
132.29
6.56
0.41
4.05
1.92
18.35
181.96
USD million
USD million
3.83
27.56
1.37
0.09
0.84
0.40
3.82
37.91
Figure 1. Baseline Cost Profile (without shared costs), 2012
6%
15% 23%
4%
6%
4%
4%
7%
10%
19%
Vaccines (routine vaccines only)
Injection supplies
Personnel
Transporation
Cold chain maintenance
Training
Social mobilization, advocacy
and communication activites
Disease surveillance
Program management
Other routine recurrent costs
Cold chain equipment
(capital cost)
C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
90%
4%
3% 3%
Govt.
WHO
UNICEF
GAVI
9 0M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Figure 2. Baseline Financing, Indian Immunization Program, 2012
Figure 2 shows the sources of financing in the
baseline year for the UIP. The Government of
India paid for most of the Program
expenditures (90 percent). Other sources of
financing were WHO (4 percent), UNICEF (3
4
percent), and GAVI (3 percent).
4. Recurrent Costs - Structure and
Analysis
4.1 Demographic projections
The calculation of the birth cohort and other
target groups is based on Indian government
estimates and on the latest census of India
(Table 7). The population growth rate is 1
percent and the infant mortality rate is assumed
to decrease from 44 per 1000 in 2012 to 25 per
1000 in 2017.
Demographic Variable
Birth Cohort
Population Growth Rate
Infant Mortality Rate
Childbearing age women
2012
24,676,883
1%
44
15%
2017
26,323,130
1%
25
15%
Table 7. Key Demographic Variables for India, 2012 and 2017
4
WHO and UNICEF are implementing partners and their activities are funded by BMGF, GAVI and other external partners.
................................
9 1
4.2 Vaccine and injection
supplies
The vaccine prices used for the baseline and
projections are shown in Table 8. The costs are
a mixture of GAVI prices as well as prices
obtainable by the government of India. India is
unique since it has many local manufacturers
from which it can purchase vaccines for the
national Program.
Vaccines
BCG
Hep B (birth dose)
OPV
Measles
DTP
TT
JE
DTP-Hib-HepB
(penta)
IPV
MR
Rotavirus
Pneumococcal
Implementation
strategy
Routine
Routine
Routine
Routine
Routine
Routine
Campaign
Roll out to all states
2014 - 11 states
2015 - 16 states
Pan India
Pending NTAGI
endorsement. Start with
campaign (1-15 yr olds)
in 2014. 2015 onwards
under routine at 9
months or 1.5 years old.
Pending NTAGI
Pending NTAGI
Sources of
financing
Govt.
Govt.
Govt.
Govt.
Govt.
Govt.
Govt.
GAVI up to 2015
Govt.
Govt.
Govt.
Govt.
Table 8. Prices per Dose and Expected start year, and Implementation Strategy for Vaccines
Expected
start year
NA
NA
NA
NA
NA
NA
NA
2014-15
2015-16
2014-15
2016-17
2017
Price per
dose
USD 0.05
USD 0.05
USD 0.06
USD 0.16
USD 0.04
USD 0.02
USD 0.18
USD 2.11
USD 1.00
USD 0.50*
USD 1.00
(Bharat)
USD 3.30**
Sources: *MR: http://www.gavialliance.org/library/news/press-releases/2013/over-700-
million-children-in-49-countries-to-be-protected-against-measles-and-rubella/
**Pneumococcal: http://www.pfizer.com/news/press-release/press-release-detail/pfizer signs new agreement with
unicef to supply a total of up to 740 million doses of prevenar 13 for the world's poorest countries through 2025
C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
9 2M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Figure 3 and Table 9 show projected resource
requirements for vaccines from 2013 until
2017. The vaccine wastage rates are given in
Annex Table A.1. During the first four years,
the resource requirements are highest for
pentavalent vaccine as it is scaled up in the
country. However, by 2017, the larger share of
resource requirements will shift to PCV vaccine
if the vaccine is introduced nationwide in 2017.
Introduction of IPV and MR in 2015 will
increase vaccine resource requirements from
INR 633 crore in 2014 to INR 1,455 crore in
2015 (Table 9). Adding rotavirus vaccine in
2016 will increase resource requirements for
vaccines by INR 315 crore while introducing
PCV vaccine in 2017 will double the
requirements for vaccines. It should be noted,
though, that the estimate of resource
requirements in 2017 is probably an over-
estimate since it assumes that PCV will be
introduced nationwide although the vaccine
will probably be phased-in over time.
Another factor that will affect the impact of the
total resource requirements for India is that it
will likely be graduating from GAVI support
during the period of the cMYP. Thus, it will
have to secure a larger proportion of funding
for new vaccines as well as for pentavalent.
Figure 3. Resource requirements for Vaccines, Routine Immunization, 2013–2017
INRCrore
4000
3500
3000
2500
2000
1500
1000
500
0
2013 2014 2015 2016 2017
PCV
Rotavirus
MR
IPV
TT
JE
Measles
Pentavalent
Help B (primary schedule)
DTP3
OPV3
Hep B (Birth dose)
BCG
................................
9 3
Table 9 also shows pentavalent vaccine will be
gradually scaled-up until it is provided
nationwide in 2015. As pentavalent vaccine is
scaled-up, DTP and Hepatitis B (primary
schedule) vaccines will be phased out while the
birth dose of Hepatitis B vaccine will continue.
Resource requirements for pentavalent vaccine
are projected to decrease in 2016 as the price
per dose is assumed to decline from $2.11 to
$1.54. Annex Table A.2 provides the resource
requirements for vaccines in USD.
Table 10 shows the resource requirements for
vaccines for SIAs by antigen and year in INR
crore (see Annex Table A.3 for US$). Polio
SIAs are assumed to take place every year while
measles (monovalent) SIAs end in 2013.
Starting in 2015, as part of the commitments to
reach the target of measles elimination in the
region by 2020, UIP will introduce the measles-
rubella vaccine through SIAs phased between
2015 and 2016. As JE campaign will depend on
the epidemiological situation, we couldn't
project any cost for the same.
2015
15.9
7.1
35.6
858.1
8.0
59.6
6.7
31.1
7.5
230.3
195.1
NA
NA
1,455.1
2016
16.1
8.2
37.7
807.4
NA
64.2
7.1
31.7
NA
203.1
184.0
410.4
NA
1,769.9
2014
15.9
6.1
33.8
459.9
12.7
54.2
6.6
30.5
13.2
NA
NA
NA
NA
632.8
2013
14.9
6.5
37.4
312.7
21.0
53.4
7.6
37.4
19.7
NA
NA
NA
NA
510.6
Table 9. Vaccine Resource Requirements for Routine Immunization by Type and Year, INR Crore, 2013–2017
2017
16.3
9.3
40.7
773.8
NA
68.8
7.1
32.2
NA
203.4
223.0
474.0
1738.8
3,587.1
Vaccines
BCG
Hep B (Birth dose)
OPV
DTP-HepB-Hib (pentavalent)
DTP
Measles
TT
JE
Hep B (primary schedule)
IPV
MR
Rotavirus
PCV
Total
2015
279.2
NA
704.1
983.2
2016
242.4
NA
704.1
946.5
2014
279.2
NA
NA
279.2
2013
315.4
39.7
NA
355.2
2017
242.4
NA
NA
242.4
Vaccines
OPV
Measles
MR
Total
Table 10. Vaccine Resource Requirements for Supplementary Immunization Activities by Type and
Year, INR crore, 2013-2017
C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
9 4M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
4.3 Personnel Costs
Resource requirements for health care staff are
projected based on assumptions about salary
ranges, the percentage of time spent on
immunization, increase in number of staff per
year and annual increases in salary levels. The
assumptions on staffing are shown in annex
Tables A.4 to A.6. The assumptions about the
need for new staffing are based on the findings
and recommendations of the 2011 HR Needs
Assessment Study (GoI 2011). The study found
inadequacies in staffing for the UIP at the
national and state levels. Thus, the estimates
include recommended additional staff at
MOH level (three deputy commissioners and
12 assistant commissioners) and at state level
(two Program officers; one MIS officer; one
administrative and finance officers; one data
analyst; two cold chain / vaccine handler and
vaccine store technicians in each state). At the
state level, the estimates also include some new
immunization staff such as cold chain/vaccine
handler and vaccine store technicians.
Apart from full-time staff, there are shared
personnel who work for immunization. Figure
4 shows that resource requirements on shared
personnel are much higher than those of full-
time staff and are increasing due to annual
salary increments and additions to the number
of total staff. The amount spent on full-time
personnel will increase from INR 55 crore in
2012 to INR 101 crore in 2017 if all new staff
are hired as per assumptions given in annex
tables. On the other hand, the shared personnel
cost will increase from INR 1,315 crore in 2012
to INR 2,509 crore in 2017 (Tables 2 and 11).
Figure 4. Personnel Costs, 2012-2017, INR Crore
INRCrore
2012 2013 2014 2015 2016 2017
3000
2000
1000
0
Baseline Full time personnel
Shared personnel
4.4 Training, Program Management,
Disease Surveillance, Social
Mobilization, Advocacy and
Communication
Training: The government is the main source
of funding for trainings (Figure 5). However,
the immunization partners such as WHO and
UNICEF also implement some training
programs on immunization. The amount spent
by the government on training will increase from
INR 21 crore in 2012 to INR 42 crore in 2017.
The resource requirements are projected to
double by 2017 because of the increased need for
trainings due to recruitment of health workers,
new vaccine introduction and planned SIAs.
................................
9 5
Program management: Expenditure under
this category includes evaluations and meeting
related expenses, micro planning, office
supplies and consumables, operational cost of
immunization technical support unit (ITSU)
and operational cost of different vaccine
preventable diseases. Much of the Program
management is supported through the ITSU.
The Ministry of Health and Family Welfare
(MoHFW) and the Public Health Foundation
of India (PHFI) established ITSU in April 2012
with support from the Bill & Melinda Gates
Foundation (BMGF). The primary mandate of
ITSU has been to strengthen human resource
capacity for the UIP and to provide technical
and managerial support to MoHFW for
revitalizing, and successfully implementing
India's UIP. ITSU is currently focusing its
efforts towards improving immunization
coverage in four states of India: Bihar, Madhya
Pradesh, Rajasthan and Uttar Pradesh, which
have been identified as high priority states with
low immunization coverage.
Figure 6 shows the baseline costs for Program
management in 2012 as well as the projected
resource requirements for 2013-2017. The
projected resource requirements for Program
management increase rapidly from 2013-2016
due to increased funding under GAVI HSS.
The GAVI HSS grant which has been
channeled to UNDP from 2013-14 is projected
to be taken over by the government in 2017.
This will result an increase in government
spending on Program management from INR
12 crore in 2012 to INR 183 crore in 2017.
Figure 5. Training Costs, 2012-2017, INR Crore
60
50
40
30
20
10
0
Baseline
2012 2013 2014 2015 2016 2017
Govt.
WHO
UNICEF
INRCrore
Figure 6. Program Management Costs, 2012–2017, INR Crore
Baseline
INRCrore
3000
250
200
150
100
50
0
2012 2013 2014 2015 2016 2017
GAVI HSS
BMGF
UNICEF
WHO
Govt.
C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
9 6M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Disease Surveillance: WHO is the
implementer of the disease surveillance
activities. Resource requirements for disease
surveillance activities are expected to more
than double by 2017, due to introduction of
new vaccines. The requirements for
surveillance will increase from INR 132 crore
in 2013 to INR 259 crore in 2017 and will be
fully financed by WHO (2013-2016 as "secure"
funding; whereas 2017 is set as "probable"
funding). Donor funding in this area will be
phasing out and the government will need to
increase its investment in disease surveillance.
Social Mobilization, Advocacy and
Communication Activities: Under this
category, we considered ASHA incentives for
social mobilization, government expenditure
for printing materials such as banners, and
posters, and advocacy, communication
activities and SMNet cost for UNICEF. The
government is the main source of financing for
social mobilization activities and is projected to
double its spending by 2017 (Figure 7). In
2012, the actual expenditure of the government
under this head was INR 220 crore which is
projected to be INR 451 crore in 2017.
Figure 7. Social Mobilization, Advocacy and Communication Activities Costs, 2012-2017, INR Crore
Baseline
INRCrore
600
500
400
300
200
100
0
2012 2013 2014 2015 2016 2017
Govt.
UNICEF
Other Routine Recurrent Cost: We considered
service provision in underserved / hard-to-
reach areas (including slums), ASHA
incentives for complete immunization,
planning, supportive supervision and
monitoring activities, intensification of routine
immunization, research related expenses and
different state specific activities under this
category. The government is the main source of
funding for these activities while WHO and
UNICEF also support some of these (Figure
8). Government expenditure under this
category will increase from INR 173 crore in
2012 to INR 270 crore in 2017.
................................
9 7
4.5 Cold Chain
The cold chain related projections are based on
the current assessment of cold chain situation
in India and future needs. The assumptions are
shown in Annex Table A.7. It should be noted
that the number of existing cold chain
equipment includes both the government
purchases as well as those purchased through
partner support (UNICEF). It should also be
noted that KFW is providing 180 crore for cold
chain equipment in 2014-15. We present the
cold chain maintenance related expenditure in
Figure 9. Government finances the most for
cold chain maintenance and the requirement
increases from INR 39 crore in 2012 to INR
218 crore if all assumptions related to cold
chain requirement in India are fulfilled.
Figure 8: Other Routine Recurrent Costs, 2012-2017, INR Crore
Baseline
INRCrore
350
300
250
200
150
100
50
0
2012 2013 2014 2015 2016 2017
Govt.
WHO
UNICEF
Figure 9: Cold Chain Maintenance Costs, 2012-2017, INR Crore
Baseline
INRCrore
250
200
150
100
50
0
2012 2013 2014 2015 2016 2017
Govt.
UNICEF
C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
9 8M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
5.0. Future Resource Requirements
Table 11 and Figure 10 show the future resource
requirements for the routine immunization
Program by Program components. Total
requirement for the five-year period is INR
34,336 crore ($5,282 million). Resource
requirements for vaccines increase rapidly from
INR 510 crore in 2013 to INR 3,587 crore in
2017 as new vaccines are assumed to be
introduced in the Program. The amount in
USD is presented in Annex Table A.8.
Cost Category
Vaccines (routine vaccines only)
Injection supplies
Personnel
Transportation
Cold chain and
other capital equipment
maintenance
Training
Social mobilization /
advocacy / communication
activities
Disease surveillance
Program management
Other routine recurrent costs
Cold chain equipment
Supplemental Immunization
Activities
Shared personnel costs
Total
2013
510.6
71.8
78.7
203.4
116.3
30.8
284.1
132.9
94.1
219.3
131.4
789.6
1,907.1
4,570.0
Table 11. Resource Requirements for India National Immunization Program, INR crore, 2013-2017
2014
632.8
72.3
84.7
234.9
149.4
36.5
373.8
161.4
225.5
248.4
198.2
740.6
2,042.5
5,201.0
2015
1,455.1
89.7
89.9
271.3
175.9
41.5
421.3
186.4
215.4
266.3
269.2
1,520.7
2,187.5
7,190.2
2016
1,769.9
84.7
95.5
313.3
207.0
47.4
467.9
215.3
231.7
282.0
343.6
1,522.6
2,342.8
7,923.9
2017
3,587.1
102.9
101.4
361.9
220.9
54.1
483.1
248.7
248.5
300.2
419.7
813.5
2,509.1
9,451.0
Total
7,955.5
421.4
450.2
1,384.8
869.4
210.3
2,030.3
944.7
1,015.2
1,316.3
1,362.1
5,386.9
10,989.0
34,336.1
................................
9 9
6.0. Future Financing and funding gap
analysis
Figure 11 shows the future secure financing
and gaps in financing for 2013-2017. This
figure does not include other financing that is
5
probable. The largest source of financing for
UIP is the government. The financing gap
increases from INR 56 crore in 2013 to 815
crore in 2015 and further to INR 3,537 crore in
2017 and reflects the fact that funding has not
yet been secured for the new vaccines to be
introduced during those years.
Figure 10. Total Resource Requirements for UIP, 2013-2017, INR CroreINRCrore
10000
9000
8000
7000
6000
5000
4000
3000
2000
1000
0
2013 2014 2015 2016 2017
Shared personnel costs
Supplemental Immunization Activities
Cold chain equipment
Other routine recurrent costs
Program managememt
Disease surveillance
Social mobilization / advocacy /
communication activities
Training
Cold chain and other capital
equipment maintenance
Personnel
Injection supplies
Vaccines (routine vaccines only)
Transportation
5
cMYP costing & financing tool has two categories of funding:
1.Secure funding refers to projected future financing available in the short term, that is considered assured;
2.Probable funding refers to all other funding that is not assured but is likely to be made available in the short and medium term.
C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
Figure 11. Future Secure Financing and Funding Gaps, 2013-2017, INR Crore
INRCrore
10000
8000
6000
4000
2000
0
2013 2014 2015 2016 2017
Funding Gap
GAVI HSS
BMGF (ITSU)
GAVI
UNICEF
WHO
Govt.
100M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Figure 12 shows the Program financing with
probable as well as secure funding. In this
scenario, the government and GAVI will
provide financing for the new vaccines. As can
be seen, if probable funding is included,
funding gap is insignificant.
Figure 12. Future Secure and Probable Financing and Funding Gaps, 2013-2017, INR Crore
INRCrore
10000
9000
8000
7000
6000
5000
4000
3000
2000
1000
0
2013 2014 2015 2016 2017
Funding gap
GAVI HSS
BMGF (ITSU)
GAVI
UNICEF
WHO
Govt.
Conclusion
Total UIP cost in 2012 was:
• INR 3,446 crore ($718 million), including
shared health systems costs
• INR 2,131 crore ($444 million) without
shared costs.
Expenditure on the routine program was INR
1,253 crore ($261 million) and, on the
supplemental immunization activities, was
INR 878 crore ($182 million). The cost per
capita for the Program was INR 9.6 ($0.2) and
cost per DTP3 child was INR 672 ($14).
The total projected resource requirement for
2013-2017 is INR 34,336 crore ($5,282
million). The resource requirement will
increase from INR 4,570 crore in 2013 to INR
9,451 crore in 2017 due to the new vaccine
i n t r o d u c t i o n a n d o t h e r P r o g r a m
improvements. Supplementary immunization
activities are projected to cost INR 5,387 crore
($829 million) during the five-year period.
However, it should be noted that the vaccine
requirement in 2017 is overestimated as we
assumed PCV will be introduced throughout
the country in 2017 while probably it will be
introduced in a phased manner. Secondly, the
total resource requirement is under estimated
as we couldn't project anything for JE
campaign in coming years as the campaign will
depend on the epidemiological situation.
The majority of the UIP resource requirement
is financed by the Government of India.
External partners do, however, provide critical
funding support to technical partners such as
WHO and UNICEF for training, disease
surveillance, IEC/social mobilization. As the
total resource requirement increases steadily,
the funding gap also increases and in order to
fill this gap, the government health budget
needs to increase in the coming years. The
projected increase of government health
expenditure for immunization is from 2.5% in
2013 to 3.3% in 2017.
The UIP could improve its financial
sustainability by improving Program efficiency
through the following:
• reviewing immunization expenditure
annually;
• monitoring Program performance and input
productivity;
• reducing wastage, and
• introducing less resource-intensive means of
service delivery.
The Program should investigate some potential
strategies to improve Program efficiency,
particularly since India will be taking over
more of the costs of the Program after the
funding from GAVI and other donors ends.
................................
101 C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
Annexures
A.1 Wastage rates
Proposed wastage rates for single and ten dose vials are in line with WHO/UNICEF
recommendations and others are as per government wastage rate calculations.
Vaccine
BCG
Hep B (birth dose)
OPV
DTP-Hep B- Hib (Penta)
DTP3
Measles
MR
Hepatitis B
IPV
JE
TT
Table A.1. Assumptions on Wastage Rates by Antigen
2013 (percentage)
50
15
25
25
25
25
25
25
30
25
25
2017 (percentage)
10
10
25
10
30
10
Table A.2. Vaccine Resource Requirements for Routine Immunization by Type and Year, US$ millions, 2013-2017
Vaccines
BCG
Hep B (Birth dose)
OPV3
DTP-Hep B-Hib (Pentavalent)
DTP
Measles
TT
JE
Hep B (primary schedule)
IPV
MR
Rotavirus
PCV
Total
2013
2.3
1.0
5.8
48.1
3.2
8.2
1.2
5.8
3.0
NA
NA
NA
NA
78.5
2014
2.4
0.9
5.2
70.8
1.9
8.3
1.0
4.7
2.0
NA
NA
NA
NA
97.4
2015
2.4
1.1
5.5
132.0
1.2
9.2
1.0
4.8
1.2
35.4
30.0
N
N
223.9
2016
2.5
1.3
5.8
124.2
0.0
9.9
1.1
4.9
NA
31.3
28.3
63.1
NA
272.3
2017
2.5
1.4
6.3
119.0
0.0
10.6
1.1
4.9
NA
31.3
34.3
72.9
267.5
551.9
................................
103 C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
Vaccine
OPV
Measles
MR
Total
Table A.3. Vaccine resource requirements for supplementary immunization activities by type and
year, USD (million), 2013-2017
2013
48.5
6.1
NA
54.6
2014
42.9
NA
NA
42.9
2015
42.9
NA
108.3
151.2
2016
37.3
NA
108.3
145.6
2017
37.3
NA
NA
37.3
Table A.4. Assumptions on health staff on salaries, annual increases in number and salary,
and time spent on immunization
Salary range
Rs. 1,0000 to Rs. 15,000
per month
Rs. 35,000 to Rs. 45,000
per month
Rs. 40,000 to Rs. 50,000
per month
Rs. 30,000 to Rs. 40,000
per month
Rs. 8,000 to Rs. 15,000 per
month
Rs. 12,500 per month
991,200 per
annum (Total)
Rs. 637,700 per
annum (Total)
Rs. 50,130 per month
Rs. 22,355 per month
Rs. 12,496 per month
Rs. 75,000 per month
Percentage
time spent on
immunization
33
10
100
100
Based on
sessions
5
100
15 staff (100%)
(including
contract staff)
8 staff (100%)
100
100
100
100
Increase in
number per
year
2%
2%
NA
NA
2% increase
in sessions
per year
Salary
increase
per year
5%
5%
5%
5%
5%
5%
5%
5%
5%
5%
5%
5%
Staff category
ANM, MPW, LHV
Mos
SIO / DIO
State cold chain officer
ASHAs
Data entry operators
from PHC to block
level
Cold chain technician
At Ministry
At Ministry (Partner
support)
Research consultant
Data analyst
Admin staff
NRHM consultants
AEFI related staff (from 2013-14)
................................
105 C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
Staff category
District vaccine logistics
manager
Cold chain / vaccine
handler
Divisional Vaccine logistics
manager
State HEMR unit with
engineers supported by state
vaccine store technician
WIC/WIF handler in govt.
medical store depot (in shift)
Refrigerator technician at
Govt. medical store depot
State vaccine logistics
manager
Vaccine logistics manager at
GMSD
Salary range
Rs. 15,000 to
Rs. 22,000 per month
Rs. 15,000 to
Rs. 22,000 per month
Rs. 35,000 per month
Rs. 30,000 per month
Rs. 8,000 per month
Rs. 12,500 per month
Rs. 35,000 per month
Rs. 45,000 per month
Table A.5. Assumptions on new immunization staff
Where posted
One in each district
Two in each state
vaccine store
One handles four
districts
Two in large states -
population 40 million
and above;one in small
states
Four in each depot
(semi- skilled helper)
One in each depot
One in each state
One each at GMSD
Year of
recruitment
2014-15
2014-15
2014-15
2014-15
2014-15
2014-15
2014-15
2014-15
Staff category
Deputy commissioners at ministry (3)
Assistant commissioners at ministry (12)
State Program officer (immunization) (2 in each state)
State logistics manager (immunization) (1 in each state)
State MIS manager (immunization) (1 in each state)
Administration and Finance officer (immunization) (1 in each state)
State immunization technology and research officer (1 in each state)
Quality control and AEFI officer (immunization) (1 in each state)
IEC officer (immunization) (1 in each state)
Assistant cold chain officer (1 in each state)
Store officer (immunization) (1 in each state)
Data analyst (1 in each state)
Gross salary per month
Rs. 200,000
Rs. 150,000
Rs. 35,000 - Rs. 45,000
Rs. 35,000 - Rs. 45,000
Rs. 35,000 - Rs. 45,000
Rs. 35,000 - Rs. 45,000
Rs. 35,000 - Rs. 45,000
Rs. 35,000 - Rs. 45,000
Rs. 35,000 - Rs. 45,000
Rs. 30,000 - Rs. 35,000
Rs. 30,000 - Rs. 35,000
Rs. 15,000 - Rs. 18,000
Table A.6. New proposed staff in Mavalankar report (these positions will be started filling up from 2014
onwards in a phased manner)
106M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Number of cold chain points
(existing)
Cold chain points required
Total cold chain points
required
New cold chain points
required
Present number of ILR in
cold chain points
Present number of DF in
cold chain points
Existing ILR/DF needs
replacement
New ILR / DF required at
cold chain points
Cold chain points need
solar or hybrid
.
Existing solar or hybrid
Solar or hybrid
At GMSD level
Present number of WIC at
GMSD
Present number of WIF at
GMSD
Required WICs/WIFs
27,000
One cold chain point per 30,000
population (2011 census)
40,340
28,238
27,000 (assuming one in each
cold chain point)
27,000 (assuming one in each
cold chain point)
50% (27,000) needs immediate
replacement - should be replaced
within 2-3 years
The required number (56,476) will
be procured within 3 years
30% of all PHCs will have less
than 8 hours electricity; hence
need solar or hybrid
50% of these will be hybrid where
there is supply for 4-6 hours
Solar - 270; Hybrid - 300.
The required number (Solar -
5,781; hybrid - 5,751) will be
procured in 2-3 years
At each GMSD, 8 WIC of 40 cub.
Mt; 4 WIF to accommodate
rotavirus / IPV vaccine
8
6
Required number at GMSD level
(22 WICs / 10 WIFs) will be
available in 2 years
State report NCCMIS
CCO meeting minutes
CCO meeting minutes
CCO meeting minutes
CCO meeting minutes +
standard assumptions
CCO meeting minutes +
standard assumptions
Based on NCCMIS of
ageing and useful life of 10
years
Based on NCCMIS of
ageing and useful life of
10 years
NCCMIS
.
State CCO Report
NCCMIS
National EVM, 2013
National EVM, 2013
National EVM, 2013
National EVM, 2013
Table A.7 Cold chain related assumptions
Assumptions Sources
................................
107 C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
At state vaccine store level
WIC/WIF needs
replacement at state
vaccine store level
At divisional vaccine store
level
WIC/WIF required
replacement at divisional
store level
At district vaccines stores
.
WIC/WIF/ILR/DF required
replacement at district store
level
Cold boxes (large and
small) at cold chain points
Cold boxes need
replacement
Cold boxes at state /
divisional vaccine stores
Cold boxes need
replacement
Cold boxes at district
vaccine stores
Cold boxes need
replacement
At each vaccine store, at least 4
WIC and 2 WIF of 40 cu. Mt
50% of the total needs
replacement (117 nos.) - should
be replaced within 2-3 years
At each store, at least 4 WIC of
40 cu. mt and 2 WIF of 20 cu. mt
50% of the total needs
replacement (62 nos. each) - to
be replaced within 2-3 years
District with population more than
20 lakh, one WIC and 6 DFs are
required
Districts with population less than
20 lakh, 8 large ILR and 4 large
DF
231 WICs; 1,386 DFs; 3,272 ILRs
and 1,636 large DFs need
replacement within 2-3 years
Every cold chain points (30,000
population) should have two 20 lit
cold boxes; and four 5 lit cold
boxes
30% (40,340 large; 80,680 small)
needs immediate replacement -
should be replaced within 2-3
years
for 30000 population, 2 large cold
boxes
30% (1,034) needs immediate
replacement - should be replaced
within 2-3 years
Per store, 20 large cold boxes are
required
30% (6,400) need immediate
replacement - should be replaced
within 2-3 years
National EVM, 2013
NCCMIS
Personal discussion with
UNICEF and ministry
Personal discussion with
UNICEF and ministry
Personal discussion with
UNICEF and ministry
.
NCCMIS
CCO Meeting minutes
NCCMIS
Personal discussion with
UNICEF and ministry
NCCMIS
Personal discussion with
UNICEF and ministry
Personal discussion with
UNICEF and ministry
Assumptions Sources
108M U L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7
Cold boxes at GMSD level
Cold boxes need
replacement
Vaccine carrier
Carriers replacement
Ice packs
Ice packs replacement
Voltage stabilizer
Stabilizer needs
replacement
Tool kit
Total number of technicians
/ toolkit
Toolkit supplied by UNICEF
Toolkit to be procured
Temperature monitoring
device
Total number required
Spare parts
Wireless data logger
required
UNICEF supply
Wireless data logger
Assumptions
50 large cold boxes are required
at the GMSD level
30% (100) need immediate
replacement - should be replaced
within 2-3 years
Each ANM should have 2 vaccine
carriers
20% every 3 years (presently
103,789 need replacement).
Should be replaced within 2-3
years
Each vaccine carrier should have
four ice packs
Every 2 years, 50% ice packs
should be replaced. (830,312
needs immediate replacement -
should be replaced within 2
years)
Every ILR/DF will have its own
stabilizer
50% (31,385) needs immediate
replacement - will be replaced
within 2-3 years
Each technician will have one
toolkit - should be replaced within
3-5 years
427
.200
227 (To be procured within 2
years)
Every ILR/DF should have one
temperature monitoring device -
should be replaced in 5 years
75,615; should be procured within
2-3 years
Every year 2 million dollar -
presently supplied by UNICEF
One each in each WIC / WIF -
total required - 743.
54
The required number 689 will be
procured in 3 years
Sources
Personal discussion with
UNICEF and ministry
Personal discussion with
UNICEF and ministry
Personal discussion with
UNICEF and ministry
Personal discussion with
UNICEF and ministry
Personal discussion with
UNICEF and ministry
Personal discussion with
UNICEF and ministry
NCCMIS
NCCMIS
NCCMIS
NCCMIS
NCCMIS
NCCMIS
Personal discussion with
UNICEF and ministry
Personal discussion with
UNICEF and ministry
Personal discussion with
UNICEF and ministry
NCCMIS / NEVM
UNICEF
Personal discussion with
UNICEF and ministry
................................
109 C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
Table A.8. Resource requirements for India Universal Immunization Program, USD (millions), 2013–2017
Cost Category
Vaccines (routine vaccines only)
Injection supplies
Personnel
Transportation
Cold chain and other capital equipment
maintenance
Training
Social mobilization / advocacy /
communication activities
Disease surveillance
Program management
Other routine recurrent costs
Cold chain equipment
Supplemental Immunization Activities
Shared personnel costs
Total
2013
78.5
11.0
12.1
31.3
17.9
4.7
43.7
20.4
14.5
33.7
20.2
121.5
293.4
703.1
2014
97.4
11.1
13.0
36.1
23.0
5.6
57.5
24.8
34.7
38.2
30.5
113.9
314.2
800.2
2015
223.9
13.8
13.8
41.7
27.1
6.4
64.8
28.7
33.1
41.0
41.4
234.0
336.5
1,106.2
2016
272.3
13.0
14.7
48.2
31.8
7.3
72.0
33.1
35.7
43.4
52.9
234.2
360.4
1,219.1
2017
551.9
15.8
15.6
55.7
34.0
8.3
74.3
38.3
38.2
46.2
64.6
125.1
386.0
1,454.0
Total
1,223.9
64.8
69.3
213.0
133.8
32.3
312.3
145.3
156.2
202.5
209.6
828.8
1,690.6
5,282.5
Other cold chain related assumptions
• Price of ILR or DF (large): Rs. 50,000
• Price of ILR or DF (small): Rs. 40,000
• Price of solar: Rs. 200,000
• Price of hybrid: Rs. 13, 00,000 (this is an
alternative source of power – supports entire
PHC with a load of 2.5 KVA including cold
chain equipment)
• Price of WIC / WIF of 40 cu. Mt: Rs. 18,
00,000 (including procurement, installation
and 5 years CMC)
• Price of WIF of 20 cu. Mt: Rs. 15, 00,000
(including procurement, installation and 5
years CMC)
• Price of large cold box (20 lit.): Rs. 7,350
• Price of small cold box (5 lit): Rs. 5,000
• Price of vaccine carrier: Rs. 1,000
• Price of ice packs: Rs. 35
• Price of voltage stabilizer: Rs. 5,000
• Price of toolkit: Rs. 115,500
• Price of temperature monitoring device: Rs.
10,100 (including installation) (30 percent
reduction of price for bulk purchase)
• WIC/WIF wireless data logger: 1 lakh
including equipment, installation, internet,
AMC, and CMC for 5 years
• ILR, DF, WIC and WIF: 10 years
• Cold boxes and tool kit: 5 years
• Voltage stabilizer and vaccine carrier: 3 years
• Ice packs: 2 years
The following numbers of buildings need to be
built over the cMYP period:
• At the district level, 64 percent of the
buildings (410 buildings) (Source: National
EVM Assessment Report 2013)
• At the state level, 75 percent of the buildings
(29 buildings)
• At the divisional level, 75 percent of the
buildings (92 buildings)
Building construction costs:
• In districts with 20 lakh population: 22–25
lakh
• At state and divisional level: 50 lakh
Price increase over the years: 10
percent
Useful life
Building
Comprehensive Multi-year Plan - Universal Immunization Program Reaching Every Child
Comprehensive Multi-year Plan - Universal Immunization Program Reaching Every Child

Comprehensive Multi-year Plan - Universal Immunization Program Reaching Every Child

  • 2.
  • 4.
    Contents Foreword . .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Preface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 1. INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.1 UIP as a component of Reproductive, Maternal, Newborn, Child and Adolescent health (RMNCH+A) in India . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.2 Purpose of cYMP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.3 Planning Process . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.4 Immunization global priorities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2. NATIONAL CONTEXT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.1 History of immunization program in India . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.2 National Rural Health Mission (NRHM) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.3 Burden of vaccine preventable diseases (VPDs) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.4 Status of vaccine coverage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.4.1 Vaccine coverage and equity issues . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5 Current structure for service delivery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5.1 Other stakeholders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 2.5.2 Current UIP Schedule in India . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.6 UIP successes as a child survival strategy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.7 Barriers for effective programming . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3. GUIDING PRINCIPLES OF UIP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4. UIP STRATEGIC PLAN: 2013-17 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.1 UIP strategic plan framework . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.2 Impact indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.3 Target population . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Acknowledgment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. i iii v vii 1 1 2 2 3 5 5 5 6 7 8 10 11 12 13 14 19 21 21 22 22
  • 5.
    M U LT I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 5. NATIONAL MONITORING AND EVALUATION PLAN FOR UIP . . . . . . . . . . . . . . . . .. . 5.1 Rationale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.2 Objective . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.3 Methodology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ... 5.4 Components of National M & E Plan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ... 5.5 Process for National M & E Plan development . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6. ANNEXURES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ANNEX 1: List of states showing good performance on immunization coverage and other parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ANNEX 2: List of States showing poor performance on immunization coverage and other parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ANNEX 3: NCCVMRC concept approved by MoHFW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. ANNEX 4: Key Recommendations from Effective Vaccine Management Assessment Report 2013 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. ANNEX 5: National Open Vial Policy 2013 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ANNEX 6: Monitoring Framework . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. ANNEX 7: Emergency Preparedness and Response Plan 2011 . . . . . . . . . . . . . . . . . . . . . . . . . . 7. COSTING AND FINANCIAL SUSTAINABILITY OF THE UNIVERSAL IMMUNIZATION PROGRAM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1. Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2. Summary of Findings on Baseline Expenditures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3. Details of Baseline Program Cost and Financing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4. Recurrent Costs - Structure and Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.1 Demographic projections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.2 Vaccine and injection supplies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.3 Personnel Costs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.4 Training, Program Management, Disease Surveillance, Social Mobilization, Advocacy and Communication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.5 Cold Chain . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.0. Future Resource Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6.0. Future Financing and funding gap analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51 51 51 51 52 52 53 55 56 57 59 62 65 74 83 85 85 86 90 90 91 94 94 97 98 99
  • 8.
  • 10.
    Acknowledgment The comprehensive MultiYear plan (2013-17) was commissioned by the Ministry of Health and Family Welfare and its development was carried out under the leadership of Ms. Anuradha Gupta, Additional Secretary and Mission Director NRHM and Dr Rakesh Kumar, Joint Secretary. We wish to acknowledge the contribution of the following from National Immunization Division, MoHFW for providing regular guidance and inputs into the document – Dr Ajay Khera, Deputy Commissioner Child Health and Immunization; Dr M.K. Agarwal, Deputy Commissioner UIP and Immunization; and Dr Pradeep Haldar, Deputy Commissioner Immunization. Immunization Technical Support Unit (ITSU) maintained an oversight and coordinated the development of the plan by a team comprising of Dr Manish Pant, Dr Susmita Chatterjee, Dr Rajeev Gera, Ms Susmita Roy. Dr Shrihari Dutta from UNICEF India office provided technical inputs on a regular basis to this team. Professor Ramanan Laxminarayan, Public Health Foundation of India and Dr Vijay Moses, Director ITSU were a constant source of support for the ITSU team while drafting the plan. We are grateful to the following individuals for contributing their time and inputs in preparing this document. Dr Brighu Kapuria ITSU Dr Jyoti Joshi Jain ITSU Ms. Monica Chaturvedi ITSU Ms Chaitali Mukherjee ITSU Dr Prem Singh ITSU Ms. Amruta Bahulekar ITSU Mr Nithiyananthan Muthusamy ITSU Ms Apoorva Sharan ITSU Mr Arup Deb Roy ITSU Mr Rajat Jain ITSU Dr Raveesha R. Mugali, UNICEF India Dr Satish Gupta UNICEF India Dr Chandrakant Lahariya WHO India Dr Pankaj Bhatnagar WHO India Dr Balwinder Singh WHO India Dr Satyabrata Routray WHO India v
  • 12.
    Abbreviations AEFI AES AFP ASHA AVD AWW BCG bOPV CBHI CCE CCL CFC cMYP CRM CSO CSSM DF DIR DPT DTFI EPC EPRP eVIN EVM FHW FIR FMG Adverse Events FollowingImmunization Acute Encephalitis Syndrome Acute Flaccid Paralysis Accredited Social Health Activist Alternate Vaccine Delivery Anganwadi Worker Bacillus Calmette–Guérin Bivalent Oral Polio Vaccine Central Bureau of Health Intelligence Cold Chain Equipment Cold Chain and Logistics Chloroflurocarbon Comprehensive Multi-year Plan Common Review Mission Civil Society Organization Child Survival and Safe Motherhood Deep Freezer Detailed Investigation Report Diphtheria Pertussis Tetanus District Task Force on Immunization Evidence to Policy Empowered Program Committee Emergency Preparedness and Response Plan electronic Vaccine Intelligence Network Effective Vaccine Management Frontline Health Worker First Information Report Financial Management Group E2P ................................ v i i
  • 13.
    M U LT I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 v i i i GMSD GoI HepB HiB HMIS HR ICDS IDH IEC ILR IMNCI IMR IPC IPC IPHS ISP ITSU IUCD JE JRM JSSK JSY KO LHV MCTS MCV MDG MDVP MIS MMR MoHFW MSG NBSU NCCA NCCMIS NCCTC NCCVMRC Government Medical Store Depot Government of India Hepatitis B Haemophilus influenzae B Health Management Information system Human Resources Integrated Child Development Services Infectious Diseases Hospital Information, Education and Communication Ice-Lined Refrigerator Integrated Management of Neonatal and Childhood Illnesses Infant Mortality Rate Inter-personal Communication Indian Pharmacopoeia Commission Indian Public Health Standards Immunization Strengthening Project Immunization Technical Support Unit Intra-Uterine Contraceptive Device Japanese Encephalitis Joint Review Mission Janani Shishu Suraksha Karyakram Janani SurakshaYojna Key Objective Lady Health Visitor Mother and Child Tracking System Measles Containing Vaccine Millennium Development Goal Multi Dose Vial Policy Management Information System Maternal Mortality Rate Ministry of Health and Family Welfare Mission Steering Group Newborn Stabilization Unit National Cold Chain Assessment National Cold Chain Management Information System National Cold Chain Training Center National Cold Chain Vaccine Management Resource Center
  • 14.
    ................................ NGO NIHFW NNT NRC NRHM NTAGI OCP OPV ORS OVP PIP PIR RCH RI RMNCH+A RRT RTI SBHI SHTO SIA SMS SNCU STI STSC TFR tOPV TT UIP UNICEF UT VHND VLM VMAT VPD WHO WIC WIF Non-Governmental Organization National Instituteof Health and Family Welfare Neonatal Tetanus Nutrition Rehabilitation Center National Rural Health Mission National Technical Advisory Group on Immunization Oral Contraceptive Pill Oral Polio Vaccine Oral Rehydration Salt Open Vial Policy Program Implementation Plan Preliminary Investigation Report Reproductive and Child Health Routine Immunization Reproductive, Maternal, Newborn, Child & Adolescent Health Rapid Response Team Reproductive Tract Infection State Bureau of Health Intelligence State Health Transport Organization Supplementary Immunization Activity Short Message Text Sick Newborn Care Unit Sexually Transmitted Infection Standing Technical Sub-Committee Total Fertility Rate Trivalent Oral Polio Vaccine Tetanus Toxoid Universal Immunization Program United Nations Children's Fund Union Territory Village Health and Nutrition Day Vaccines Logistics Management Vaccine Management Assessment Tool Vaccine Preventable Disease World Health Organization Walk-in Cooler Walk-in Freezer i x A B B R E V I A T I O N S
  • 16.
    Introduction 1.1 UIP asa component of Reproductive, Maternal, Newborn, Child and Adolescent Health in India There is a growing acknowledgment that over the years various service packages have been developed around the Reproductive and Child Health program that have tended to function independently. To bring about a greater impact of the program there is a need to build synergies between these various packages since they address different stages of the life cycle. The 'Continuum of Care' approach includes two dimensions – stages of life cycle and places where care is provided. This approach underpins the RMNCH+A strategy that seeks to provide an integrated set of interventions through a large cadre of community-based ASHAs and a three-tiered health system. The key components of the RMNCH+A interventions as a 'continuum of care' are given in Table 1. Immunization is one of the key 1 elements in this strategy. Table 1: RMNCH+A continuum of care across life cycle and different levels of healthcare Reproductive care Newborn and childcarePregnancy and child birth care • Comprehensive abortion care • RTI/STI case management, • Postpartum IUCD and sterilisation; interval IUCD procedures • Adolescent friendly health services • Skilled obstetric care and immediate newborn care and resuscitation • Emergency obstetric care • Preventing Parent to Child Transmission (PPTCT) of HIV • Postpartum sterilisation • Essential newborn care • Care of sick newborn (SNCU, NBSU) • Facility-based care of childhood illnesses (IMNCI) • Care of children with severe acute malnutrition (NRC) • Immunisation Clinical • Family planning (including IUCD insertion, OCP & condoms) • Prevention and management of STIs • Peri-conception Folic acid supplenentation • Full antenatal care package • PPTCT • Early detection and management of illnesses in mother and newborn • Immunisation • First level assessment and care for newborn and childhood illnesses • Immunisation • Micro-nutrient supplementation • Weekly IFA supplementation • Information and counselling on sexual reproductive health and family planning • Community based promotion and delivery of contraceptives • Menstrual hygiene • Counselling and preparation for newborn care, breast feeding, birth preparedness • Demand generation for pregnancy care and institutional delivery (JSY, JSSK) Antenatal care Postnatal careReproductive health care • Home-based newborn care and prompt referral (HBNC scheme) • Antibiotic for suspected case of newborn sepsis • Infant and Young Child Feeding (IYCF), including exclusive breast feeding and complementary feeding, • Child health screening and early intervention services (0-18 years) • Early childhood development • Danger sign recognition and care-seeking for illness • Use of ORS and Zinc in case of diarrhoea Intersectoral: Water, sanitation, hygiene, nutrition, education, education, empowerment Outreach/SubcentreFamily&Community Child health care 1 A Strategic Approach to Reproductive, Maternal, Newborn, Child and Adolescent Health in India: For Healthy Mother and Child. MoHFW, Government of India, 2013. Adolescence/ Pre-pregnancy Pregnancy Birth Newborn / postnatal Childhood 1 0 1................................
  • 17.
    0 2M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Immunization is one of the most cost-effective interventions that prevent needless suffering through sickness, disability and death. The benefits of immunization are not restricted to improvement in health and life expectancy but also have social and economic impact at both community and national levels. Moreover, an effective, equitable immunization program and its impact on reducing the burden of vaccine- preventable diseases will greatly contribute to achieving the Millennium Development Goal 4 (MDG4) that envisages a two-third reduction in child mortality by 2015. In the last three decades, India has made significant progress on sustainable and inclusive growth. There is now a greater sense of awareness and expectations from the people as the country makes further social and economic progress. Investments on the social determinants of health have improved availability and access to health services though there still remain challenges of inequity and affordability. This multi-year strategic plan (2013–17) has evolved from its first iteration (cMYP 2005–10) and is underpinned by the Government of India RMNCH+A 2013 strategy and the National Vaccine Policy, 2011. The document mainly seeks to: a. Provide a broad framework of objectives, expected results and strategies that cover the different aspects of Routine Immunization – program service delivery, system strengthening, social mobilization and demand generation, newer vaccines and technology, epidemiology of vaccine- preventable diseases and management of adverse events following immunization. b. Identify costing and financing requirement as part of the planning cycle. c. Propose monitoring and accountability tracking mechanisms that should lead to improved program efficiency d. Explore and expand opportunities to 1.2 Purpose of cMYP integrate other maternal and child health interventions such as breast feeding, Vitamin A supplementation and ORS through UIP. The strategic plan had been prepared through a close collaborative and iterative process involving national program managers, state officials, professional associations, development partners and implementing agencies, which provide the goals, objectives, indicators, strategies and costs. As cMYP (2005–10) was completing its life in March 2010, a supplement to extend it till March 2012 was prepared. Initially, a framework for revised cMYP was agreed upon by a working group of national immunization program managers and development partners where attention was paid to new developments and initiatives that had taken place since 2005. These initiatives included those that have been enacted under the National Rural Health Mission (NRHM) and the recommendations of NTAGI in the recent years. Two regional consultations were held in New Delhi and Kolkata. These consultations were attended by senior officials in the Ministry of Health and Family Welfare (MoHFW), program managers from the national immunization division; state, district and block level immunization officials, and by representatives of development partners and other professional organizations and Non- Government Organizations. In April 2013, under the guidance of national immunization division, ITSU facilitated the process of drafting the next cMYP (2013–17) and set up a core committee to draft the plan, comprising of representatives from ITSU, WHO and UNICEF. The members of the core committee met and communicated on a regular basis among themselves to continually refine the draft plan. Inputs on key objectives and strategies came through the national immunization division through regular meetings with the drafting team. The current cMYP document went through several iterations before it was sent to NTAGI for comments, which were subsequently 1.3 Planning process
  • 18.
    ................................ 0 3 IN T R O D U C T I O N to reducing approximately 25 percent to the 2 reduction in child mortality. WHO has identified priority areas in immunization for the future to sustain the 3 momentum on immunization. These priorities, which are also reflected in the national cMYP, include the following: lstrengthening the Routine Immunization program, laccelerating measles control activities, lintroducing newer vaccines through evidence-based policies, lincreasing access to immunization services through system strengthening. As the current set of MDGs reach their end in 2015, new global health paradigms will emerge that will focus on universal health coverage and sustainable development. A well-functioning UIP that aims to reach out to every child will contribute to universal health coverage and healthier future generation. To achieve this, UIP will need strong underpinning of good governance and accountability at all levels. This will necessarily lead to improved program efficiency and more children will get immunized. incorporated. In addition to the main strategic component of cMYP, the core committee also worked on the detailed costing of the program under the guidance of national immunization division. According to WHO, immunization interventions have proven to be a success across the globe and today reach out to over 100 million children and prevent 2.5 million deaths per year. As new global health paradigms emerge, fresh perspectives and priorities are emerging in immunization as well. Universal immunization coverage is an important element of universal health coverage to achieve the MDGs by 2015. Despite improved vaccination coverage there are rising inequities among different population groups that need to be addressed for a more meaningful success. There are at least ten new antigens now available that can be added to the traditional EPI interventions including vaccines against Hepatitis B, Rota virus, Japanese Encephalitis, and Human Papilloma Virus. Several countries are now moving beyond the traditional target population of infants and pregnant women to include adolescents and adults. WHO expects that by 2015 immunization should contribute 1.4 Global Priorities on immunization 2 WHO Strategic Plan 2010–15. Department of Immunization, Vaccines and Biologicals 3 Global Action Vaccine Plan 2011–2020. World Health Organization
  • 20.
    ................................ 0 5 2.1History of immunization program in India The success of smallpox eradication in the 70s brought attention to the immunization program globally as well as in India. The Expanded Program on Immunization (EPI), a national policy of immunizing all children during the first year of life with DPT, OPV, BCG and typhoid–paratyphoid fever vaccines was launched in 1978. Immunization of pregnant mothers with TT vaccine was introduced in 1983. In 1985, the name of EPI was changed to the Universal Immunization Program (UIP) with activities phased in to the entire country by 1990. The stated objectives of UIP are: lTo rapidly increase immunization coverage lTo improve the quality of services lTo establish a reliable cold chain system to the health facility level lTo introduce a district-wise system for monitoring of performance lTo achieve self-sufficiency in vaccine production UIP was given the status of a one of the five 'National Technology Missions' in 1986. Subsequently in 1992, UIP became a part of Child Survival and Safe Motherhood (CSSM) program and then of Reproductive and Child Health (RCH) program in 1997. A specific Immunization Strengthening Project (ISP) was designed to run from 2000 to 2003, which included the following main components: lpolio eradication lstrengthening routine immunization lstrategic framework for development. Immunization is a critical component of the Government of India's child survival strategy. In 1997 the MoHFW launched a Reproductive and Child Health (RCH) program to reduce IMR, MMR, TFR and to increase immunization coverage, especially in rural areas. The second phase of the RCH program (2005–10) focused on minimizing regional variations through provision of assured, equitable, and responsive quality services. With a view to strengthen public health system in rural areas, the Government of India launched the National Rural Health Mission in 2005. The NRHM was established as a single platform to bring together all of the national 4 health efforts, including RCH. The goal of the NRHM is to address gaps in the provision of effective health care to rural population with a special focus on 18 states, which have weak 5 public health infrastructure. To achieve this goal the NRHM envisions a shift away from the vertical health and family welfare programs to a new architecture in which societies under different programs are merged and resources pooled at the district level. NRHM also provides states with flexibility in making their own plans in delivering RI interventions. It also seeks to strengthen local public health provision with infrastructure and manpower and facilitate the participation of the not-for- profit and for-profit sectors in achieving 2.2 National Rural Health Mission (NRHM) National Context 2 4 Ministry of Health and Family Welfare (2005): “National Rural Health Mission, Framework for Implementation (2005-12)” 5 The 18 states are Arunachal Pradesh, Assam, Bihar, Chhattisgarh, Himachal Pradesh, Jharkhand, Jammu & Kashmir, Manipur, Mizoram, Meghalaya, Madhya Pradesh, Nagaland, Odisha, Rajasthan, Sikkim, Tripura, Uttaranchal and Uttar Pradesh.
  • 21.
    0 6M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 desirable health outcomes. In the 12th FYP the Government of India has proposed a National Health Mission for improving healthcare in rural as well as urban areas. UIP is an integral component of NRHM. At the national level, the NRHM has a Mission Steering Group (MSG) headed by the Union Minister for Health & Family Welfare and an Empowered Program Committee (EPC) headed by the Union Secretary for Health & Family Welfare. EPC implements the Mission 6 under the overall guidance of the MSG. At the state level, the mission functions under the overall guidance of the State Health Mission headed by the Chief Minister of the 6 Source: www.nrhm.gov.in state and provides oversight to the functioning of the health system and NRHM activities, policy inputs for health sector, conducts intersectoral coordination and advocacy. The functions under the mission are carried out through the State Health & Family Welfare Society led by the Mission Director. Under NRHM, states have set up State Health Societies to strengthen health service delivery infrastructure, financial management, coordination with NGOs/CSOs/donors and monitoring of various national programs. The State Mission and State Society are interlinked in terms of a common secretariat as shown in Figure 1 below. Figure 1: Composite organogram of the State Mission and the State Society State Health Mission Governing Body, State Health Society Program Committees (Headed by Director/ Director General) (Optional) SPMSU (Headed by Executive Director/Mission Director) Executive Committee, State Health Society 2.3 Burden of vaccine-preventable diseases (VPDs) Over the past 20 years, the reported cases of the main VPDshave declined. However, in recent yearsthere has been an increasing trend in the number of reported measles, diphtheria and pertussis cases as shown in Figure 2. This increasing trend may be due to an actual increase in number of cases or can be attributed to improvements in case detection and the overall surveillance system strengthening. To minimize this inconsistency and to stabilize the reporting trends, improving the surveillance of VPDs in the countryis urgently needed.It is estimated that approximately 80,000 children die annually from measles and associated complications. Although this figure has
  • 22.
    ................................ 07 N AT I O N A L C O N T E X T MCV2 six months following the completion of the campaign. Delhi, Sikkim, Goa and Puducherry took initiative themselves and introduced 2nd measles dose through MMR.In September 2013, India committed to eliminating measles and controlling rubella/congenital rubella syndrome (CRS) by 2020 as part of the resolution that was approved by SEARO's 66th regional committee. decreased over the years with improvements in routine vaccination coverage rates, measles mortality still remains high. In 2010, the Government of India decided to introduce a second dose of measles containing vaccine (MCV2) in UIP. In 21 states with measles 1st dose coverage more than 80 percent, MCV2 was introduced directly in their routine immunization whereas, 14 states were taken up for measles Supplementary Immunization Activity (SIA) followed by introduction of Figure 2: Trends in the reported cases of Measles and Pertussis from 1990–2010 (Source CBHI) 120000 100000 80000 60000 40000 20000 0 1990 1991 1992 1993 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 Cases PertusslsMeasles Burden of VPDs between geographies and population groups. These inequities represent gaps in service delivery that leaves certain groups of children at a high risk of remaining unvaccinated. As per NHFS-3 data, nine states are below the national average for vaccination coverage including Madhya Pradesh, Uttar Pradesh, Bihar and Jharkhand. Even within states there exists a difference in total coverage between 7 different districts as shown in Figure 4. 2.4 Status of vaccine coverage Though the reported vaccination coverage for all vaccines has always been higher than evaluated coverage, the average vaccination coverage has shown a consistent increase over the last two decades as shown in Figure 3 below. However these averages mask the disparities 7 NFHS-3 data
  • 23.
    0 8M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 2.4.1 Vaccine coverage and equity issues While vaccines under UIP are provided free of cost through all the public health facilities across the countries, disparities in coverage exist for different population groups that need to be addressed. There are significant inequities in vaccination coverage in different states based on various factors related to individual (gender, birth order), family (area of residence, wealth,parental education), demography (religion, caste) and the society (access to health care, community literacy level) 8 characteristics. There is a clear gender coverage differential as reported by different surveys. Boys generally have a higher vaccination coverage than girls as reported by most surveys conducted across the country (Figure 5). The gap between genders also exists for individual vaccines such as BCG, DPT and measles. Figure 3: Trends in vaccination coverage over the last twenty years as shown in different surveys Figure 4: District level coverage of fully immunized children between 12 and 23 months of age. (Source: DLHS 2007–08) Vaccine coverage70.0% 60.0% 50.0% 40.0% 30.0% 20.0% 10.0% 0.0% NFHS-1 (1992-93) NFHS-2 (1998-99) NFHS-3 (2005-06) DLHS-1 (1998-99) DLHS-2 (2002-04) DLHS-3 (2007-08) CES (2009-10) 35.4% 42.0% 43.5% 54.2% 45.9% 53.5% 61.4% Below 30 30 to 50 50 to 70 70 to 90 Above 90 8 Joseph L Mathew (2012): “Inequity in Childhood Immunization in India: A Systematic Review,” Indian Pediatrics, Volume 69, March 16, 2012.
  • 24.
    ................................ 0 9 Urban areashave higher vaccination coverage as compared to rural areas and this gap exists for all vaccines. Within urban areas, slum populations have a lower coverage. Migrants coming to urban areas to have a lower coverage level as compared to the resident population. Urban and rural poor populations have a lower coverage as compared to the wealthier one. Figure 5: Gender differential in vaccine coverage (Source: HMIS) 13000000 12500000 12000000 11500000 11000000 10500000 10000000 9500000 9000000 2008-09 2009-10 2010-11 2011-12 2012-13 Male Female Fully Immunized Children Figure 6: Differentials in vaccine coverage across geography, caste and wealth status (Source: UNICEF CES 2009) Percentage of children age 12-23 mfully immunized Urban Rural Others OBC SC ST Richest Quintile Poorest Quintile 67.4 58.5 66.3 60.6 58.9 49.8 47.3 75.5 Vaccination coverage is also lower amongst infants coming from scheduled caste (SC), scheduled tribes (ST) and other backward castes (see Figure 6). A comparison of states showing good and poor performance on immunization coverage is given in Annex 1 and Annex 2 respectively. N A T I O N A L C O N T E X T
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    1 0M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 2.5 Current structure for immunization service delivery in the country The implementation of the UIP is a joint responsibility of government at all levels, namely Central, State and Union Territory Districts and Sub-Districts. The relationships between central and state immunization departments and between state and district immunization officers are critical for efficient and effective service delivery. National: The MoHFW comprises of four departments, each of which is led by a Secretary to the Government of India. These include: lDepartment of Health & Family Welfare; lDepartment of Ayurveda, Yoga & Naturopathy, Unani, Siddha and Homoeopathy; lDepartment of Health Research; and lDepartment of AIDS Control. The MoHFW is responsible for implementing various national health programs in all states of India. The Directorate General of Health Services renders technical advice on all medical and public health matters and is involved in the monitoring of implementation of various health services. The MoHFW is responsible for funding of various national programs including immunization program, providing technical assistance and policy guidance to the states, and for monitoring and evaluation. Funding for extra staff and other health system resources at the state level is provided by the NRHM, a flexible mechanism that allows for integration of funds for all the national schemes while allowing for states to flexibly allocate funds for system improvement in a manner that is consistent with their needs and challenges. All states are required to submit in advance a Program Implementation Plan (PIP) for a financial year, along with complete projections of funds required to implement the PIP. To augment technical and managerial support under UIP for strengthening, revitalization and successful implementation of RI, the Immunization Division at MoHFW has set up an Immunization Technical Support Unit (ITSU). The ITSU is staffed with technical officers to support various functions of UIP under six different pillars: lStrategic planning and system design, lMonitoring and evaluation, lVaccine logistics and cold chain management, lAdverse events following immunization (AEFI) management and vaccine quality and safety, lTranslation of evidence to policy, and lStrategic communication. Through ITSU,the ministry will facilitate to harmonize various initiatives being piloted or implemented in different states by all immunization partners and provide a single platform for discussions, development of strategies and coordination with partners for scaling up the successful models. State: At the state level, the Secretary of Health is responsible for all health-related efforts. The State Department of Health and Family Welfare is led by a Director of Health Services under which the State Directorate of Health Services serves as the technical wing. Large states such as Bihar, Madhya Pradesh, Uttar Pradesh, Andhra Pradesh, and Karnataka have additional zonal or regional or divisions set-up between the State Directorate of Health Ser vices and the District Health Administration. Most of the states have a dedicated State EPI Officer; however, at places Deputy Director-HFW has additional responsibility of being EPI Officer. Additional support for UIP at the state level is provided by a cold chain officer and by data and administrative support staff. State governments are responsible for implementation and supervision of the various programs and for provision of relevant infrastructure and curative services in the states including village outreach sessions for immunization. District: In the district, under the overall supervision of Chief Medical and Health Officer (CMHO) or Civil Surgeon (CS), the District Immunization Officer (DIO)
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    ................................ 1 1 coordinates allthe immunization-related efforts. The responsibility for immunization also lies with Block Medical Officers and PHC Medical Officers. The Auxiliary Nurse Midwife (ANM) delivers the immunization services to the community. Immunization services are provided through the following: lsub-centers, primary health centers, and community health centers, lsub-divisional/taluk/speciality hospitals, ltertiary hospitals, lurban health services provided by municipalities, lhospitals and dispensaries run by railways, defense, and public sector undertakings, lEmployees’ State Insurance Scheme hospitals ldispensaries funded by the government (State and Centre). Private health sector also provides an estimated 15–20 percent of immunization services. The Indian Public Health Standards (IPHS) for immunization has been drafted to improve the quality of the service and NRHM supports efforts to improve the quality of service by strengthening sub-centers and primary health centers. The funding mechanism for immunization has also been simplified and made flexible along with adoption of the bottom-up planning approach through district and state Project Implementation Plans (PIPs). Immunization service delivery in many areas within a district, i.e. urban areas, especially slums and peri-urban areas, where migrant families live; areas in semi-legal situations due to weak infrastructure; areas which are managed by different local bodies such as railways and cantonment have been, and are still, a major concern. Civil Society Civil Society Organizations (CSOs): These organizations offer a wide range of experience and knowledge essential for UIP. They can provide insight into gaps in 2.5.1 Other stakeholders 9 Howard D, Roy K. Private care and public health: do vaccination and prenatal care rates differ between users of private vs. public sector care in India? Health Services Research 2004;49:2013-26 health service delivery and identify practical and political challenges that must be overcome to improve the health of citizens. CSOs therefore play a crucial role to advocate for policy changes, generate greater transparency and hold governments and other healthcare stakeholders to account. At the country level, Civil Society encompasses a diverse array of actors, including the following: lpatient groups, health workers, medical or health unions and associations, lfaith-based organizations, lnon-governmental organizations, lcommunity-based organizations, lacademic institutions, lmedia, ladvocacy groups, lmigrants, women, youth and other neglected or vulnerable groups. Civil society groups of particular importance to ensuring that UIP achieves its intended results are those with expertise in maternal health, child health, immunizations, nutrition, health systems and services, monitoring and evaluation. The MOHFW will engage more proactively with academia, professional societies, and other national agencies and committees and networks like the development partners forum to ensure a cohesive and coordinated approach to achieving national immunization priorities. Private hospitals and clinics: Private health sector plays an important role in providing immunization services and fill gaps in delivery of RI services through public system. Studies in India have shown that private sector does enable increased access to traditional EPI 9 vaccines for those who can afford to pay. Private sector also plays a role in introducing newer and underutilized vaccines prior to their induction in the public program. Private sector also has a key role to play in supporting the surveillance system for vaccine-preventable diseases and adverse events following immunization by reporting cases that may have been missed out by the public surveillance system. N A T I O N A L C O N T E X T
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    1 2M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 2.5.2 Current UIP Schedule in India The current UIP vaccination schedule caters to pregnant women, infants, children and adolescents as shown in Table 2 below. Table 2: Vaccination schedule under UIP in India *Give TT-2 or Booster doses before 36 weeks of pregnancy. However, give these even if more than 36 weeks have passed. Give TT to a woman in labor, if she has not previously receivedTT. **Pentavalent vaccines contain a combination of DPT, HepB and HiB. In the states where it has been introduced, it will replace DPT 1,2& 3 and Hepatitis B 1, 2 & 3. Hepatitis B birth dose and booster doses of DPTwill continue as before. *** JE Vaccine (SA14-14-2) is given in select endemic districts, after the campaign is over in that district. ****The 2nd to 9th doses of VitaminAcan be administered to children 1-5 years old during biannual rounds, in collaboration with ICDS. Vaccine When to give Dose Route Site 0.5 ml 0.5 ml 0.5 ml 0.1ml (0.05ml until 1 month of age) 0.5 ml 2 drops 2 drops 0.5 ml 0.5 ml 0.5 ml 0.5 ml 0.5 ml 0.5 ml 2 drops 0.5 ml 0.5 ml 0.5 ml. 0.5 ml Intra-muscular Intra-muscular Intra-muscular Intra-dermal Intra-muscular Oral Oral Intra-muscular Intra-muscular Intra-muscular Sub-cutaneous Sub-cutaneous Intra-muscular Oral Sub-cutaneous Sub-cutaneous Intra-muscular Intra-muscular Early in pregnancy 4 weeks after TT-1* If received 2 TT doses in a pregnancy within the last 3 years At birth or as early as possible till one year of age At birth or as early as possible within 24 hours At birth or as early as possible within the first 15 days At 6 weeks, 10 weeks & 14 weeks 9 completed months-12 months. (give up to 5 years if not received at 9-12 months age) 9 completed months 16-24 months 16-24 months 16-24 Months 16-24 months with DPT/OPV booster 5-6 years 10 years & 16 years Upper Arm Upper Arm Upper Arm Left Upper Arm Antero-lateral side of mid-thigh Oral Oral Antero-lateral side of mid-thigh Antero-lateral side of mid-thigh Antero-lateral side of mid-thigh Right upper Arm Left Upper Arm Antero-lateral side of mid-thigh Oral Right upper Arm Left Upper Arm Upper Arm Upper Arm For Pregnant Women TT-1 TT-2 TT- Booster BCG Hepatitis B Birth dose OPV Zero dose OPV 1,2 & 3 DPT1,2 & 3 Hepatitis B 1,2 & 3 Hi Bcontaining Pentavalent 1, 2 & 3** st Measles 1 dose st JE 1 dose*** st DPT 1 booster OPV Booster Measles 2nd dose nd JE 2 dose DPT nd 2 Booster TT Vitamin A**** For Infants For Children and Adolescents
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    ................................ 1 3 2.6 UIPsuccesses as a child survival strategy The Universal Immunization Program (UIP) in India is one of the largest of its kind in the world, in terms of the following: lquantity of vaccines used, lnumber of beneficiaries reached out to, lnumber of immunization sessions organized, lthe geographical spread and diversity of areas covered. It caters to nearly 27 million infants and 30 million pregnant women annually free of cost. There is a strong political commitment for achieving universal immunization coverage in the country along with the eradication and elimination of the targeted diseases. As a key element of the national child survival strategy, UIP has contributed significantly to reducing mortality and morbidity due to vaccine-preventable diseases and the infant mortality rate over the last decade. While surveillance information for specific VPDs is limited, the steady fall of IMR from 123 to 50 deaths per 1000 live-births does in part reflect 10 the impact of the UIP. Since its launch in 1995, the Pulse Polio campaign aimed at eradicating polio from India, has begun to show results. Governments at the national and state levels are implementing strategies on a scale and intensity that is unprecedented in the history of polio eradication. These efforts have brought India closer to the goal of polio eradication and there is currently no reported case since 11 January 2011. India has been declared polio non-endemic country by World Health Organization in early 2012. Neonatal Tetanus cases have declined significantly as more pregnant women received TT vaccine as part of their ante-natal care. There has been an overall reduction in the number of cases and deaths due to diphtheria, pertussis and measles as well. Under National Rural Health Mission, MoHFW has undertaken many initiatives to improve health systems and immunization outcomes. Districts have been provided with more human as well as financial resources to improve delivery of immunization and other health services. Introduction of ASHA into the system as a community link worker has brought about a major improvement in community mobilization. Districts have strengthened their delivery systems and developed micro-plans for improved efficiency. The number of vaccine delivery points has increased along with the cold chain points. MoHFW also introduced a system for Alternate Vaccine Delivery (AVD) to provide vaccines at the outreach session sites. Innovative technology like auto-disable syringes are now in use in all states and union territories. Immunization-related trainings have led to an increased capacity of frontline health workers to deliver vaccines at the village level. Focus in the urban areas has led to an improved immunization services in slums areas, though more needs to be done in this 12 area. MoHFW has also initiated Mother and Child Tracking System (MCTS) to enable the entry of mother and child data into a central database. The year 2012–13 was declared by the Government of India as the year of Intensification of RI in India. In this context, the MoHFW had put in place a few strategic actions to improve immunization coverage. These included limproving health systems, lpromoting village health and nutrition day (VHND), llaunching Immunization Weeks, llaunching of the “Teeka Express” for delivery of vaccines to outreach sessions, lpilot-launching of the National Cold Chain Management Information System (NCCMIS) for real-time monitoring and management of cold chain systems and lsetting up of the Immunization Technical 10 SRS 2011 11 National Polio Surveillance Program. www.npspindia.org. 12 UIP Review 2004 N A T I O N A L C O N T E X T
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    1 4M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Support Unit (ITSU) to provide technical and programmatic support for successful implementation of the UIP. India's 'Call to Action on Child Survival and Development' announced in February 2013, and led by the MoHFW, the Government of India, calls for a concerted, convergent and inter-sectorial approach to achieving the country's child survival goals by 2017. Based on composite indicators the Government of India has identified strengthening efforts in the 184 high priority districts in the country. This five-year ambitious target will heighten the importance of 'continuum of care', ensuring the tight linkage between maternal and newborn health as outlined in the new strategic Figure 7: Reasons for low immunization coverage in India (Source – UNICEF CES 2009) Did not feelneed Not knowing about vaccines Not knowing where to go for immunization Time not convenint Fear of side effects Do not have time Wrong advice by someone Cannot afford the cost Vaccine not available Place not convenient ANM absent Long waiting time Place too far Service not available 28.2 26.3 10.8 8.9 8.1 6 3 1.2 6.2 3.8 3.9 2.1 2.1 2.1 11.8 0 5 10 15 20 25 30 Percentage Demand side issues Supply side issues Others The performance of immunization program in India is regularly assessed through UIP review meetings at national and state levels, Joint Review Missions (JRM) and Common Review Missions (CRM) sent by GoI. At least one national review is conducted every year besides additional state specific review as per the program need. The common constraints in immunization program are summarized below: a. Gaps in cold chain and vaccine logistics management: There is limited cold chain infrastructure and capacity in many states, even for routine UIP vaccines. Systematic efforts to identify gaps and address issues in cold chain document called RMNCH+A. Strengthening RI to increase coverage has been identified as a key intervention in RMNCH+A. Many different ministries, global and Indian experts, goodwill ambassadors, private sector, civil society, media, and faith-based organizations have pledged to recommit themselves to the Call to Action. Overall immunization coverage levels are low in the country. According to the CES 2009, the reasons for low immunization coverage pertain to issues on the demand and supply side as given in Figure 7 below 2.7 Barriers for effective programming
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    ................................ 1 5 and VLMhave been conducted in recent years. In addition to the 2008 NCCA, a number of vaccine and cold chain management assessments (Vaccine Management Assessment Tool (VMAT)/EVM assessments) have been conducted in 10 states and one national UIP store (Government Medical Store 13 Depots (GMSD) – Karnal) between 2007–11. A recent national-level assessment of EVM conducted by the Government of India and UNICEF in 10 states and four GMSDs along with other studies including deep dive and KPMG exercises by ITSU have identified the following constraints: lInfrastructure issues include poor infrastructure of vaccine stores and transportation systems; a lack of standards for vaccine stores at different levels and insufficient temperature monitoring system at all vaccine storage points from GMSDs to last cold chain point level, state, and regional stores. There exist difficulties in procuring the right quality of cold chain equipment on time with adequate after-sale support. There is a paucity of repair kits and spares cold chain technicians and inequitable cold chain point (last vaccine storage site) distribution. Cold chain equipment in many states in the country is old and in many cases broken. There is also a paucity of available data on Vaccine Logistics and Cold Chain to devise national plans and strategies to address them. . lHR issues such as lack of a CCL support unit with experts on cold chain for both the immunization division of MoHFW and at the state level; lack of induction training and a regular educational program for staff inducted in the Vaccine Logistics and Cold Chain system; insufficient institutional training capacity to manage cold chain and logistics at all levels; shortage of trained manpower and relevant job-aids for managing cold chain at all levels (state, division/regional and district levels); and lack of HR with capacity for Vaccine Logistics Management (VLM) at all levels (national, GMSDs, state, district and PHCs). The shortage of HR is more acute in the poor performing states and specifically at the field level. lMonitoring and MIS issues such as lack of realtime vaccine stock status, consumption patterns, wastage rates, along with a continuous temperature monitoring system for cold chain, lack of cold chain inventory and real-time NCCMIS, no regular review of CCL system at the state and district level, and poor documentation and MIS for vaccine management (standardized registers, records and procedures). lVaccine procurement issues are significant as delay in placement of procurement orders and irregular supply of vaccines have a direct impact on vaccine availability affecting immunization coverage. Moreover, certified vaccine suppliers are few, and since orders are always given to the lowest bidder, the supply of vaccines is often erratic. These constraints have led to high breakdown rate of equipment, overstocking and stock- outs, inadequate monitoring and supervision, poor management, and the possibility of AEFIs, thus hampering improved vaccine coverage. b. Poor social mobilization: Low levels of awareness, communication and information- sharing amongst frontline workers as well as poor HR capacity for BCC in government institutions as a whole contributes to the problem of high left-outs and dropouts. Studies have shown that insufficient and ineffective health communication along with lack of promotion or follow-up of RIs are two of the main health system constrains behind low coverage in immunization, preventing parents from initiating or following through with their child's vaccination schedule. Given that the actual rate of immunization is low, the high dropout rate reduces the number of fully immunized children in the country. Poor populations and those with lower levels of education are most vulnerable to impacts of low levels of advocacy and communication. Listed below are some of the system-related constraints in advocacy and communication 13 National Cold Chain Assessment, India. July 2008. NRHM & UNICEF N A T I O N A L C O N T E X T
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    1 6M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 inception of UIP, India has set up a reporting mechanism from the health center to national level. In last few years, the country has also introduced electronic data systems like HMIS and MCTS to improve reporting, analysis, monitoring and planning at all levels. However, there are big gaps in quality of data being reported, its analysis and use for decision making and thus leading to inadequate information to support NTAGI and UIP to design and implement strategies to improve immunization quality and coverage. Some of the main constraints in the area of data management and evidence generation are listed below: lPoor monitoring and evaluation for data entry, resulting in errors in data entry and inaccurate data. In recent years, partners' support and networks have contributed to increased monitoring and supportive supervision with visible positive impact in select states. However, there is a need to build the capacity of government officials and strengthen the system to improve monitoring and supervision by government officials. lPoor monitoring and evaluation results in insufficient data quality and reporting rates. A vast majority of states have wide gaps in reported and evaluated coverage data. The factors for this variation need to be identified through regular data quality audits and necessary corrective measures should be taken. lInadequate surveillance data quality and reporting rates result in poor surveillance of VPDs and AEFIs. While some attention has been paid to strengthening VPD surveillance, systemic deficiencies and bottlenecks such as insufficient laboratory capacity and limited trained manpower at the district levels to carry out surveillance, continue to exist. Inadequate VPDs reporting results in the inability of UIP to measure disease burden to make a decision on the introduction of new antigens and impact of vaccination on the disease. There is a felt need for HR capacity building in that lead to low levels of immunization coverage. lThere is weak capacity at the state level and inadequate HR to generate evidence-based communication strategies and effective BCC campaigns lWeak communication capacities (spokesperson system) within the government machinery at national and state levels in handling AEFIs. lInformation dissemination is not timely and often mixed messages are received by beneficiaries lWeak counseling and interpersonal communication (IPC) skills among health workers and community mobilizers, which adversely affects dissemination of communication of messages. lWeak capacities and counseling skills of service providers to ensure delivery of quality care, especially in hard-to-reach areas. There is an urgent need to strategically approach communication, aiming at behavior change both at the service delivery level and at the community level to generate demand among the caregivers. Meeting the shortfall of health professionals and building their counseling and communication skills are imperative to a sustained and holistic response to the public health concerns in the country. This requires health care to be addressed not only from the scientific perspective of what works, but also from the social and behavioral perspective of who needs it the most. One also needs to understand the social norms and barriers that prevent them from accessing the services and how to reach the unreached. c. Poor data management and analysis for evidence generation: A robust system for data management and evidence generation is crucial to support informed decision making for the creation of realistic goals and strategies for improvement of current coverage levels and introduction of new antigens in UIP. Since the
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    ................................ 1 7 VPD surveillance,strengthening laboratory capacity by improving infrastructure and making reagents available, and building system for timely reporting and actions. Similarly surveillance of AEFI cases is poor and a structured response to reported serious cases of AEFI is lacking. lLimited focus on operational research for immunization and finding locally suitable solutions. Good quality research is needed to provide an evidence base for a more informed decision making and improving performance. The successful implementation of HMIS under NRHM and MCTS under Mission Mode Project provides a great opportunity to strengthen data management and evidence generation to inform decision making in UIP. With the augmentation of human resource at national level also provides an opportunity for coordination between various reporting and surveillance systems in the country as well as putting up a system for using information for decision making. d. Weak human resource capacity: In a study of HR needs assessment in UIP by Mavlankar 14 et al (IIM Ahmedabad) the following was found: lThere is limited technical and operational human resource capacity and quality at various levels in UIP. lImmunization cells at both the state and the national level are small and inadequately staffed. lKey personnel capacities are spread thin across multiple areas in day-to-day management with no focus on priorities. They are not able to focus on developing strategic solutions and to organize and coordinate activities such as introducing new vaccines, updating technology, applying for international funding and support, writing reports and analyzing data. lThe roles and responsibilities of officials at the state immunization cells are not well defined lState immunization officials have no financial powers and their titles are not commensurate with their responsibilities. The lack of human resource capacity and poorly defined roles and responsibilities at various levels have a cascading effect on all other areas of program performance, including monitoring and evaluation, supply chain and logistics management, and strategic communications. Lower quality of monitoring and supportive supervision of the program leads to reduced efficiency and effectiveness of interventions at all levels of programming and needs to be addressed seriously. While UIP is a part of a wider RMNCH+A strategy of the government, there is a need to increase the HR capacity and numbers of immunization managers at all levels. The Government of India has set up an Immunization Technical Support Unit (ITSU) to augment human resource capacity at national level with focal persons assigned for specific functions such as cold chain and vaccine logistics, Evidence to Policy and surveillance, Strategic Communication, Monitoring and Evaluation and Adverse Events Following Immunization (AEFI). Training immunization staff on relevant topics will improve program efficiency and effectiveness as well. e. Need for a well delineated accountability systems: A major problem is the lack of institutionalized and uniform accountability structures, focused on performance review at each administrative level i.e. central, state and district levels. The country has a Multi-Year Strategic Plan for UIP but its implementation is not monitored in absence of a monitoring and accountability structure. Though, there are review mechanisms in place at all levels, but these are not followed consistently. Moreover, in absence of a robust system for data analysis, N A T I O N A L C O N T E X T 14 Universal Immunization Program in India: A Study on HR Needs Assessment at National and State Levels. Dr D.V Mavalankar et al, IIM Ahmedabad. Study commissioned by HRD Committee on UIP constituted by GoI.
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    1 8M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 interventions and follow up, these are not very effective. f. Evidence synthesis for informed policy making: The NTAGI was formed in 2001 and tasked with advising the MoHFW on issues related to the program, policy and implementation of the national immunization program. Since its inception the NTAGI has r e c o m m e n d e d e v i d e n c e - b a s e d recommendations to the UIP, such as the following: lintroduction of the Hepatitis B, Pentavalent and Japanese Encephalitis vaccine luse of VVM in government vaccine supplies luse of AD syringes However, there is great scope for revision and improvement in the decision-making process for the introduction of new vaccines in the UIP. In the light of the current advancements in the field and the availability of several new interventions, it is imperative to establish scientific evidence-based protocols for making immunization related decisions. As India considers adding new antigens (e.g., rotavirus, pneumococcal, MMR, HPV, IPV/hexavalent, cholera, typhoid, and JE) as well as new immunization technologies (e.g., updated injection safety devices), the immunization program also needs to keep pace. NTAGI is an advisory body with clear terms of reference for overall guidance but not day-to-day operations. NTAGI needs a well- defined secretariat to conduct regular meetings and a clear scope of work that maintains focus on making a structured recommendation on immunization. At the same time, there is an ever increasing need to develop capacity to identify and address critical gaps in evidence base. The health system must be able to evaluate new vaccines for safety, efficacy, relevance and cost-effectiveness; accommodate the new vaccines in its cold chain management system and vaccine logistics; assess and respond in real time to roll-out challenges; and conduct post-marketing surveillance to ensure that lessons learnt from the roll-out are incorporated back into the system.
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    The services providedthrough the UIP shall be guided by the following principles 1. Universal immunization coverage: Sustaining demand and ensuring that all pregnant mothers, children and adolescents are immunized as per national schedule in line with the principles of universal health coverage. 2. Equitable access: Ensuring that the immunizations services reach out to the under- served, needy and most vulnerable populations while addressing regional inequalities across states. 3. High quality services and innovation: Maintaining highest possible quality in vaccine Guiding Principles of UIP ................................ 1 9 3 procurement, storage, distribution and delivery services in an innovative and safe manner. 4. Sustainability and Partnerships: Committing resources, financial, human and technical, that sustain immunization benefits to the people at all times and promoting partnerships across different sectors and organizations build synergies and expand the overall coverage of the program. 5. Governance: Decentralized planning through a bottoms up approach to improve operational efficiency 6. Management excellence and accountability: Implementation, oversight and accountability of interventions that optimize efficient use of resources
  • 36.
    This comprehensive multi-yearstrategy plan seizes on the opportunity to address geographic and social inequities in immunization coverage rates, and other immunization-related issues highlighted in earlier sections. The plan aims to strengthen immunization infrastructure within the broader RCH program and offer a platform for integrating other primary care interventions and strengthening the public health system at all levels. UIP offers universal immunization coverage to all children in the country as per the national immunization schedule. This plan derives its essence from the National Vaccine Policy 2011 and is underpinned by the goals ascribed in the National Health Policy 2002 and National Rural Health Mission 2005. The plan framework consists of an overarching Goal and a set of six Key Objectives (KO) that 4.1 UIP strategic plan framework Box 1: UIP Goal and Key Objectives GOAL KEYOBJECTIVES Reduce mortality and morbidity due to vaccine-preventable diseases through high quality immunization services KO 1: Improve program service delivery for equitable and efficient immunization services by all districts KO 2: Increase demand and reduce barriers for people to access immunization services through improved advocacy at all levels and social mobilization KO 3: Strengthen and maintain robust surveillance system for vaccine-preventable diseases (VPDs) and adverse events following immunization (AEFI) Introduce and expand the use of new and underutilized vaccines and technology in UIP KO 5: Strengthen health system for immunization program KO 6: Contribute to global polio eradication, measles, maternal and neonatal tetanus elimination KO 4: ................................ 2 1 4 cover different aspects of the immunization program including - operational efficiency, epidemiological support, health system strengthening and demand generation(See Box 1). These Key Objectives are interlinked and mutually reinforce each other, thus providing greater focus, structure and flexibility for developing context-specific strategies and interventions. Each Key Objective has a set of Expected Results to be achieved in the medium term and a set of actionable strategies that can be contextualized in the State and District implementation plans. The framework elements are designed to be simple, feasible, flexible and relevant to the needs of the people. As part of providing better governance for the program, the UIP strategic plan has a comprehensive monitoring and accountability tracking framework which consists of a key indicators, targets, source of information, assigned responsibility and information dissemination. UIP Strategic Plan: 2013-17
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    2 2M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 4.2 Impact indicators 4.3 Target population KEY OBJECTIVE 1: Improve program service delivery for equitable and efficient immunization services by all districts 1. Reduction in infant mortality rate 2. Reduction in cases of vaccine-preventable diseases RI interventions will be targeted at reaching out to all eligible children and pregnant women as per the national schedule. Given the equity issues, special efforts will be made to ensure that immunization services reach out to targeted beneficiaries belonging to the lower socio-economic strata, those living in urban slums, rural areas, tribal and other hard-to- reach areas. The following section elaborates on the strategic framework further Vaccine logistics management is one of the critical elements in the immunization program to ensure that all vaccines are available at the last cold chain point for immunization sessions. Similarly, a reliable and adequate cold chain network is essential to ensure that vaccines are stored within the recommended temperature ranges, and safe and potent vaccines are delivered to children. Various recent studies like Effective Vaccine Management (EVM 2013), Vaccine Wastage Study (2008), ITSU deep dive study, KPMG vaccine logistics study (2013), ICMR Freezing Study etc. have pointed out issues related to the existing vaccine logistics system up to the last cold chain point, and the capacity, functionality and maintenance of cold chain equipment at all levels. Key Performance Indicators (KPI) 1. Number of States/UTs where > 95% sessions were held as planned 2.%of districts having > 80% full immunization coverage 3. Number of States/UTs having less than 10% dropout from DPT1-DPT3 (or Pentavalent) The indicators will disaggregated by gender, geography (urban slum, urban, rural) and socio-economic parameters, where relevant. Expected Result 1.1: Strengthen the national cold chain management system: Maintaining a strong cold chain system is critical for maximizing the operational efficiency of UIP. Strategies to achieve this will focus on capacity building, hardware management and innovative technology. Strategies A national plan for cold chain management is essential for improving overall UIP program efficiency. The national cold chain plan shall be based on various situation analyses on cold chain and vaccine logistics management in the country. The major components of the plan will include: a) National Standards: One of the major gaps in cold chain management is the absence of standards performance parameters. The national cold chain plan will include standards for the following: lVaccine storage at all levels as per WHO standards lCold Chain point expansion guidelines lCold Chain equipment plan for different levels of vaccine stores lQuality maintenance of vaccines lTemperature monitoring of cold chain system lHuman resource for cold chain and vaccine logistics lCCE testing lab 1. Develop National Cold Chain Management action plan:
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    ................................ 2 3 b) Specificationof equipment and accessories A specification committee comprising technical experts from the field, the National Cold Chain Training Centre (NCCTC), engineering colleges, IITs, and program experts will be established to provide guidelines on the technical specifications of cold chain equipment and accessories. c) Procurement guidelines for cold chain equipment and accessories Procurement guidelines for cold chain equipment and accessories shall be developed, and reviewed periodically by a technical committee of experts convened by the MoHFW. The guidelines shall provide parameters for equipment procurement, rationale for purchase, quantity, guidelines on aging etc. The technical committee shall meet at least once a year. Stress will be placed on promoting indigenous cold chain equipment which is contextualized and adaptable to local needs and environment. A Management Information System (MIS) for tracking the working status of cold chain equipment and spare parts will also be set up. The plan will also focus on regular retiring of old and sick cold chain equipment, regular program reviews with cold chain officers, staff trainings, maintenance and servicing of cold chain equipment, implementation of MIS, logistics and supply chain management. d) Promote indigenous cold chain equipment for immunization To reduce costs and improve overall program efficiency, the MOHFW will promote the use of cold chain equipment that is locally produced and ser viced by Indian manufacturers. NCCVMRC will organize consultative meetings with engineering colleges, industries, IITs, national physical laboratories, DG S&D to determine the safety standard, program need and scale of requirement required to fulfill the needs of UIP. 2. Enhance the capacity of the National Cold Chain Vaccine Management Resource Centre (NCCVMRC) and the National Cold Chain Training Center (NCCTC) to better manage the Cold Chain and Vaccine Logistics Management (VLM) system. The NCCVMRC has been set up in National Institute of Health and Family Welfare (NIHFW) to conduct training and capacity building activities on cold chain equipment and vaccine management, including preventive maintenance and repair, at the state level. The center provides supportive supervision to states to promote smooth functioning of cold chain and vaccine management systems. The center also undertakes cold chain and vaccine management assessments and reviews jointly with the Immunization division MOHFW, UNICEF, WHO and other partners. It functions as an extended wing of the Immunization division (MoHFW) for cold chain and vaccine management. The NCCVMRC's needs enhancement in terms of human resources recruitment, infrastructure and equipment to be able to function effectively (See Annex 3). The NCCTC, which has been set up at SHTO Pune, is the country's only cold chain training center. The NCCTC will have its capacity strengthened to perform the following: lfunction as a testing lab of equipment performance, lexperiment with innovative technologies, lsupport the MoHFW for procurement by producing evidence on the specifications of equipment and their performance, ldevelop appropriate spare parts for all types of cold chain equipment enabling local repair, ldevelop a training module of Cold Chain Equipment (CCE) repair and maintenance, lprovide maintenance support to GMSDs. The center will be run as an independent body U I P S T R A T E G I C P L A N F R A M E W O R K
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    2 4M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Table 4: Cold Chain equipment in the four GMSDs * Needs 100 percent replacement of cold chain equipment Kolkata Chennai Karnal* Mumbai Need 2 more WIC and 2 Need 6 more WIC and 2 more WIF Need 8 WIC and 4 WIF Need 6 more WIC and 2 more WIF more WIF4 2 2 2 2 2 GMSD WIC WIF Future needs (within plan period) with its own governance and management structure reporting to the Director, NIHFW. The National Cold Chain Management Information System (NCCMIS), which is a web-based system for tracking cold chain equipment in real-time, shall be expanded to cover all states. The system will be hosted on NIHFW servers with helpline support provided by NCCVMRC. Key objectives of the NCCMIS are to provide guidance on: lcold chain infrastructure up to the lowest level with performance indicators; lstock positions of cold chain equipment spare parts at GMSDs and at the state level, and specification for local procurement; ltroubleshooting of cold chain equipment; lcold chain and vaccine management practices as per national norms; lavailable trained HR in cold chain and upcoming training programs; and lcold chain space requirements for introduction of new vaccines. Currently, there are over 27,000 cold chain points across the country. All states need to plan and ensure that one cold chain point caters to a population of 30,000 in rural areas, up to 50,000 population in urban areas, and 15- 20,000 population in tribal and hard to reach 3. Conduct a nationwide rollout of cold chain MIS 4. Increase the number of cold chain points closer to vaccination sites in selected states and take up repairs and maintenance work of the existing equipment areas, keeping in mind factors such as distance from and time to travel to session sites.
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    ................................ 2 5 In additionto the GMSDs, each of the 39 State Vaccine Stores need to have 50 percent of their existing cold chain equipment replaced within the plan period. Each of these stores should have at least four WICs and two WIFs of 40 cub mt. which shall be put in place within the plan period. Each of the 139 Divisional Vaccine Stores need to have one WIC of 40 cub mt and one WIF of 20 cub mt, which shall be put in place within the plan period. Before the end of the plan period, each District Vaccine Store should have the following: lone WIC and six DF in districts with a population of more than 2 million , leight large ILR and four large DF in districts with a population below 2 million. Supplies of all non-electrical equipment 15 (vaccine carrier, ice boxes) and accessories shall be updated as per the needs of every cold chain point. India is a vast country and putting a robust cold chain system in place requires a larger number of staff at all levels. As recommended in the Mavalankar report there shall be a position created for a focal point on cold chain at the national level. Each state should also make provision for a cold chain officer along with an assistant at that level. In addition, each district should have one Vaccine Logistics Manager and one Cold Chain Handler. The majority of issues and barriers related to cold chain and vaccine logistics pertain to program management rather than technical faults. All staff associated with cold chain and vaccine logistics will be provided training on various aspects of program management. 6.Enhance management capacity and numbers of cold chain and vaccine logistics staff at all levels with the district being responsible for stock distribution planning, management and repair. 7. Promote mentoring and supportive supervision to ensure that vaccines are stored within the correct temperature range 8. Scale up a system for SMS-enabled real-time temperature monitoring for cold chain as part of electronic Vaccine Intelligence Network (eVIN) 9.Enhance capacity of cold chain handlers and mechanics across the country Various models of supportive supervision exist -using line supervisors, externally hired monitors or medical college faculty to provide mentoring and supportive supervision. A mixed approach will be applied based on state requirements to ensure that RI sessions use quality vaccines that have been stored at appropriate temperatures throughout the cold chain. Effective cold chain and vaccine management consultants will be used to review these improvement plans and vaccine store self- assessments using standard formats and local improvement plans from facilities visited Real-time monitoring of cold chain equipment along with prompt alerts and corrective action are critical for the immunization program as all vaccines under the program are temperature- sensitive and cannot be used once damaged. As most cold chain points in the country are located in remote village settings with limited facilities, a special SMS-enabled temperature monitoring system has been developed and is being currently piloted. The technology will be further refined to prepare for its expansion to all cold chain points in the country. As part of the eVIN strategy, the possibility of unifying vaccine logistics management, temperature monitoring and cold chain equipment inventory management into one system will also be explored. The training for vaccine and cold chain handlers shall be based on standard technical 16 guidelines developed by the government. In addition to induction training, the cold chain mechanics and technicians will also be 15 Accessories include voltage stabilizer with every ILR and DF and toolkits for cold chain technicians 16 Handbook for Vaccine and Cold Chain Handlers 2010.Ministry of Health and Family Welfare, Government of India and UNICEF. U I P S T R A T E G I C P L A N F R A M E W O R K
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    2 6M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 provided training on cold chain equipment – WIC, WIF, DF, ILR, cold chain accessories, solar and hybrid equipment. Refresher trainings will be held every three years to sustain capacity and ensure quality. Expected Result 1.2: Strengthen vaccine and syringe logistics management across the countr y including forecasting and procurement at central level A significant challenge in improving RI coverage is lack of visibility at every levels in the chain. Managers do not have real-time vaccine stocks status at all levels, consumption patterns, wastage rates and so on. Without such information, it is difficult to hold system functionaries responsible for lack of performance, or to generate prompt responses to breakdowns/bottlenecks in the vaccine supply chain. Data from the states where VMAT, EVMs and deep dives were conducted by UNICEF and ITSU indicate that the distribution of vaccines is uneven with some cold chain points holding excess stock levels, while others have stock-outs within the same district or division. Even when there are few stock-outs reported, there is evidence that store managers are slowing down vaccine distribution to cold chain points below them, or to session sites as a means of preventing stock- outs. This can lead to insufficient vaccines reaching immunization sessions, thus directly affecting the immunization coverage. Strategies Under the Universal Immunization Program, vaccines and syringes are centrally procured and supplied to States and Union Territories (UTs). The details of vaccines/syringe receipt, issue, wastage and consumption are documented in a variety of registers across the country. Some states have also started computerized documentation of stock levels, but only down to the district level. No nationwide vaccine logistics management and monitoring system currently exists that provides real-time visibility of the stock data, 1. Develop a vaccine and syringe logistics management system in the country with real-time stock visibility. consumption patterns, wastage rates etc. In absence of such a system, a variety of ad hoc principles and processes are applied in distributing vaccines. With the potential introduction of more costly vaccines under the UIP, a robust vaccine logistics management system is a dire need. A vaccine logistics management model is being developed that can cater to requirements at all levels i.e. from GMSD to the last vaccine storage point (last cold chain point). The product will be field tested and updated to be made ready for country-wide rollout. When fully implemented, the system will also provide better estimates for further procurement and will outline the effects on the logistics system of delays in procurement and erratic vaccine supply patterns. Based on data analysis and the vaccine supply schedule being followed, new guidelines for defining minimum and maximum stocks at different levels will also be developed. An effective vaccine logistic management system must be supplemented by an operations team that keeps the network operational as well ensures prompt response based on data. The government will introduce a position for VLM at national, state and district levels at least in the 12 high-priority states. The district-level VLM will also oversee the functionality of cold chain equipment in the district and will ensure swift repair or replacement of cold chain equipment with support from the district refrigerator mechanic. These staff will be provided training on vaccine logistics and cold chain management. There is substantial technology upgradation going on rapidly across the world in the field of vaccine logistics and cold chain management. 2. Strengthen HR capacity at all levels for vaccine management, including effective vaccine store management and forecasting 3. Pilot new technology for improving vaccine logistics and cold chain management with an overall objective to develop an electronic Vaccine Intelligence Network (eVIN)
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    ................................ 2 7 These interventionscan be useful in ensuring the availability of safe and potent vaccines upto the last cold chain point. Such technological interventions will be field-tested for performance and will be considered for implementation with the ultimate aim of developing an electronic Vaccine Intelligence Network (eVIN). Computer optimization models, such as HERMES, will be used for exploring means to maximize vaccine and syringe logistics efficiency. EVMs assessments were conducted in ten priority states in 2013. These states include Jammu & Kashmir, Haryana, Rajasthan, UP, Bihar, Chattisgarh, MP, Karnataka, Kerala and 17 Tripura. The key recommendations from the EVM assessments will be implemented through the PIPs of the respective states. These recommendations are included in Annex 4. A trained pool of effective cold chain and vaccine management consultants will review the progress of PIPs in states that have completed an EVM assessment and prepared improvement plans. Expected Result 1.3: Ensure safer injection practices and reduced vaccine wastage Strategies The disposal of syringes and other waste associated with immunization sessions shall be based on the Biomedical Waste Management and Handling Rules, 1998, and Central Pollution Control Board (CPCB) Guidelines for hospital and immunization waste disposal. Under the NRHM, an Infection Management and Environment Plan (IMEP) policy framework has been formed to guide waste disposal processes. These guidelines will be widely disseminated and shared during review meetings. All health facilities will have 'waste management guidelines' prominently 4. Implement Effective Vaccine Management (EVM) improvement plans 1. Review existing mechanisms and policies on waste management displayed at the site of waste generation. India had adopted the Multi-Dose Vial Policy (MDVP) for OPV during SIA campaigns. In 2011, the Multi-Dose Vial Policy was adopted for the birth dose of the Hepatitis B vaccine, and the zero dose of the Oral Polio vaccine in the UIP. Later, in the year 2011, the Multi-Dose Vial policy was adopted and implemented as part of RI for the Pentavalent vaccine in two states. The current open vial policy (OVP) applies to multi-dose vials of DPT, TT, Hepatitis B, Oral Polio and Liquid Pentavalent vaccines (where applicable). This policy does not apply to Measles, BCG, and Japanese Encephalitis (JE) vaccines (See Annex 5). Relevant immunization trainings shall have a component on the OVP to facilitate the appropriate use and return of vials and reduce wastage. The policy of bundling shall be adopted for all vaccines, AD syringes, reconstitution syringes, diluents, disposal bags, and hub cutters to reduce wastage and improve logistics efficiency, wherever applicable. The required amount of vaccines for a session will be packed along with the needed logistics, so as to ensure that safe injection practices are adopted. A vaccine wastage assessment carried out by UNICEF in 2010 revealed high wastage rates ranging from 61 percent (for BCG) to 27 18 percent (for DPT). The main causes of wastage include vaccine expiry, discarding unused doses, poor reconstitution practices, exposure to heat, frozen vaccines, missing inventory and theft. To reduce vaccine wastage, all categories of staff shall be trained on this aspect of the program as part of their regular training regimen and given job aids on injection safety and safe waste disposal. 2. Strengthen the implementation of Open Vial Policy (OVP) and Bundling Policy to reduce waste at session sites 3. Scale up training on injection safety and waste disposal guidelines for all categories of staff 17 National Effective Vaccine Management Plan 2013: Summary Report. UNICEF and MoHFW. 18 Vaccine Wastage Assessment: Field assessment and observations from national stores and five selected states of India. UNICEF, April 2010. U I P S T R A T E G I C P L A N F R A M E W O R K
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    2 8M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 4. Expand the availability and use of hub cutters in all districts and explore other technological advancements to ensure safe and appropriate bio-waste handling 1. Conduct risk analysis at state and district level 2. Provide training to and follow up with relevant staff on preparing and implementing RI micro-plans To ensure safer injection practices, health workers will be trained on the use of hub cutters as part of their on-going trainings. In addition, technological developments in injection safety and bio-waste management will be explored and field tested. Based on performance evaluations, cost considerations, feasibility of use at the field level etc., the inclusion of these technologies in the Immunization program will be considered. Expected Result 1.4: Ensure that regular immunization sessions are planned and held and coverage increased Strategies The country has identified high-priority districts for interventions under RMNCHA+A where immunization coverage has been considered a one of the key elements. States have also identified high-priority district under Emergency Preparedness and Response Plan (EPRP) to prevent wild polio virus importation. Further risk analysis will be done to identify high risk blocks and urban dwellings with low coverage. Continuous training and skill building of health staff involved in routine immunization program is required to achieve and sustain quality and coverage of immunization. Training modules for frontline health workers, medical officers and cold chain and vaccine supply staff have been prepared and states are using them regularly to train the staff. Ministry updates these modules on regular interval and provides to states. These modules include all relevant components for preparation of plan for RI and its implementation and monitoring. However, the Government of India has identified issues in implementation of training that varies from state to state resulting in gaps in performance. The Government of India will encourage all states to develop a time-bound schedule for training for all staffs and refresher trainings at regular intervals. These cycles will be aligned with annual PIP. Guidelines for micro-planning and service delivery have been developed and included in the immunization handbooks for medical officers and health workers. Health workers and other relevant UIP staff will be trained on preparation of micro-plans that ensure inclusion of areas with underserved population, hard-to-reach areas and others. The efforts will be made to reach the un- reached population at least four times a year. The support of the development partners will be sought for the micro-planning efforts. The districts should ensure that micro-plans are available and being used to provide immunization services in the area. MoHFW has recommended fixed-day, fixed- time and fixed-site strategy for outreach sessions for delivering immunization services to ensure that communities are aware of the immunization day that is now being implemented by all states. Under this strategy, the Government of India has recommended that immunization sites be fixed for each habitation, preferably at sub-centers; in villages at anganwadi centers, school and panchayat chaupal, etc. The day of the week and time of session in a particular location are also fixed. The immunization session can also be combined with Village Health and Nutrition Days (VHNDs) under NRHM to help maximize the opportunity for community mobilization and service delivery. The Government of India is planning to strengthen health service delivery in urban areas now. This will be further strengthened with special focus to reach poor and underserved populations living especially in slums, streets and peri-urban areas. 3. Promote fixed-day, fixed time and fixed site strategy
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    ................................ 2 9 4. Fillup gaps in RI coverage through strengthening alternative vaccine delivery to provide needs-based immunization services in difficult to reach areas 5. Reduce left-outs and missed opportunities, drop-outs and ensure booster doses To ensure improved vaccine and logistics supply and help ANM to spend more time at outreach session site and focus on improving immunization service delivery, the Government of India has provided funds for implementing alternate vaccine delivery (AVD) system. These efforts will be further strengthened. Under the plan for intensification of RI, the Government of India has planned to provide vaccine delivery vans to high-priority districts and blocks to strengthen vaccine supply. In this regard, the Government of India has already provided 120 vehicles in six districts of five states – Madhya Pradesh, UP, Haryana, Jammu & Kashmir and Rajasthan to implement a pilot before expansion. These vehicles have been branded “Teeka Express”. These vehicles will be used not only for vaccine delivery but carrying other logistics for immunization sessions, promoting IEC for RI, running mobile health clinic etc. depending on the need of the district. The Government of India aims to identify all areas/populations/opportunities to reduce left-outs and to improve booster coverage beyond primary immunization schedule. This is also important in view of new antigens being introduced in UIP. To improve the access with the aim of reducing left-outs the Government of India has developed guidelines to include all high risk populations/areas, identified through polio eradication program, in the routine immunization micro-plans. The Government of India has also recommended to use polio micro-plan to identify all small areas/hamlets under each sub-center area to be reflected in micro-plan to improve reach and monitoring. It will be further strengthened by identifying all opportunities and places like OPDs and schools to enquire and vaccinate children.. a) Health facilities: Every contact of health care system with children of vaccination age will be used to enquire about the child's vaccination status. Vaccines will be administered where applicable, provided the minimum interval between doses is respected. Possible reasons for non-vaccination shall be identified and addressed. b) Schools: School health programs will be strengthened. The LHVs will visit every school with ANMs at least once a year with vaccines to assess the immunization status of children and ensure vaccination with DPT of children aged 5–6 years, and TT vaccination for children aged 10 and 16 years. Once a beneficiary is registered, all the efforts will be made to ensure full utilization of immunization services for completion of immunization scheduled. Special efforts will be made in the areas where immunization coverage is low and dropout rates are high. a) Strengthen use of Due List by frontline health workers for tracking beneficiaries and improve communication with parents to reduce drop-outs: Ensure that states and UTs make available the standardized Due List to all the FHWs with appropriate guidelines and trainings for its effective use. b) Strengthen Mother and Child Tracking System (MCTS): The Government of India has launched Mother and Child Tracking System to improve registration of pregnant women and infants and utilization of Ante-Natal Care (ANC) and immunization services. This is being implemented as a mission mode project and all states have implemented this. The implementation and utilization of MCTS will be further strengthened to achieve the objectives. States will utilize the NRHM framework to innovate to increase immunization coverage. The best practices and successful examples will be disseminated widely for cross learning and adoption by the states. U I P S T R A T E G I C P L A N F R A M E W O R K
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    3 0M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 6. Strengthen the RI supervision and monitoring system 7. Involve private facilities in delivering RI services 8. Plan and conduct immunization weeks at regular intervals to improve coverage level in missed out and hard-to-reach areas, followed by integration of these areas under the district RI micro-plans. 1. Conduct bi-annual national level meetings of state EPI officers MOHFW will focus on improving program supervision and monitoring for RI at all levels using data generated in the program and through field monitoring. RI partnership in the country is actively participating in monitoring of implementation at field level and assisted states in involving their program managers and staff in the monitoring. Haryana has developed a monitoring system by involving independent monitors using NRHM funds. Other states will also be encouraged to prepare plans for monitoring and propose in PIPs. The involvement should be underpinned by accountability and quality standards that are regulated by the state nodal medical authority. Public and private practitioners providing vaccination will be provided free of charge vaccine and immunization cards etc. All private practitioners, offering vaccination services, will be expected to maintain appropriate institutional records, retrievable on demand. They will also be expected to report coverage, VPDs, AEFI, and wastage on a monthly basis. Private sector accountability and quality issues will be coordinated by the nodal medical authority providing the vaccines 19 as per the Government of India guidelines. Necessary efforts will be made to implement the guidelines for involvement of private practitioners in immunization program. Expected Result 1.5: Improve program coordination at all levels Strategies National-level half yearly meetings of all state EPI officers will be conducted regularly. State immunization officials will be requested to conduct regular and quality quarterly review meetings with district immunization officers to strengthen the program at ground level. The Government of India has issued directives to all states for setting up state and district-level task force on immunization for improved program coordination and monitoring. States will ensure that these task force meetings are held every month and necessary feedback is shared with national immunization division. The ministry recognizes various efforts being done and the support provided by development par tners in routine immunization strengthening both at national and sub- national level. Efforts will be made to ensure better coordination between government and development partners through regular coordination meetings, partner's forum and other relevant platforms. IAG, which has been setup by MoHFW, will advise and provide technical inputs to the national immunization division on ways to improve routine immunization coverage and issues around newer and underutilized vaccines. 1. % of caregivers whose child received partial or no immunization who did not feel the need for adhering to the schedule of immunization 2. % of caregivers not recalling any of routine vaccine The indicators will be disaggregated by gender, 2. Improve coordination with development partners through regular meetings and information sharing 3. Promote immunization and related interventions through Immunization Action Group (IAG) including academia, CSOs, political representatives KEY OBJECTIVE 2: Increase demand and reduce barriers for people to access immunization services through improved social mobilization. Key Performance Indicators (KPI) 19 Guidelines for involvement of private practitioners in the universal immunization program (UIP). Government of India, Ministry of Health and Family Welfare, Immunization Division, 31 August 2009.
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    ................................ 3 1 geography (urbanslum, urban, rural) and socio-economic parameters, where relevant. Expected Result 2.1:Develop and implement a multi-pronged national communication strategy with a focus on priority states Strategies A national strategic communication plan for RI will be prepared. States and districts will also be encouraged to prepare an integrated communication work plan. This plan will have focus upon components and strategies for addressing the issues related to left-outs and drop-outs, and to increase community participation in immunization. The IRI communication guidelines have been developed by the Government of India to provide a roadmap to the immunization program managers and IEC functionaries at state, district and block level. These guidelines can be used as a reference while formulation 20 state-specific communication plans. National and state-level workshops will be conducted for immunization program managers and other staff working on communication. The trainings will focus on strengthening their communication and planning skills to better operationalize and implement IEC interventions. MOFFW will also conduct regular national and state-level meetings to monitor the progress, identify gaps and suggest possible solutions on communication strategies. In addition, effective communication activities and best practices will be documented and shared with all the stakeholders to be used for inter-state learning. Enhanced partnerships with CSOs and NGOs will promote greater awareness and access to 1. Develop state-specific Communication Implementation plans, advocacy and social mobilization plans 2. Strengthen national and state capacity on behavior change communication 3. Engage with partners to ensure a wider dissemination of immunization messages. RI services. The CSO engagement strategy will focus on engaging civil society in policy and advocacy processes. The Government of India will engage the private sector to work in immunization program as part of their CSR utilizing their strengths in communication. NRHM has provided necessary flexibility to use funds for activities related to immunization program. The available funds with districts will be utilized for health communication. The untied funds with AWW/ASHA, VHSC and ANM may also be used for these communication efforts, if funding from other sources is not available. States will be encouraged to prepare a detailed IEC plan for immunization and funds will allocated to this activity from NRHM PIP part A Expected Result 2.2:Effective communication channels are set up with the community for better acceptance of vaccines Strategies Utilize the widespread network of over 860,000 ASHA workers to conduct social mobilization for improving immunization coverage. Interpersonal communication (IPC) with individuals and families will be strongly promoted through the frontline health workers – ASHA, ANM, Anganwadi workers and other key leaders in the communities. The Government of India has developed a training kit to improve IPC skills of frontline health workers to improve awareness among parents about need for immunization and completion of recommended schedule and to reduce fear of AEFI to reduce drop-outs. All FHW will be trained on using this kit. The community members, non-government organization and interest groups in 4. Ensure adequate funds are available for communication interventions 1. Use frontline health workers and community platforms like Village Health and Nutrition Day to promote RI through inter-personal communication (IPC)with families 20 Intensification of Routine Immunization: Communication Operational and Technical Guideline. 2012. Immunization Division, Ministry of Health and Family Welfare. Government of India. U I P S T R A T E G I C P L A N F R A M E W O R K
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    3 2M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 immunization like women's self-help groups will be involved in advocacy for implementation and increasing demand for services. Events like VHNDs will be utilized as opportunities for community mobilization. Wherever reports of mistrust towards immunization by community members are noticed, these should be studied and appropriate corrective actions need to be taken. At the community level there is a greater scope of better social mobilization and reaching local community leaders through convergence of RI with ICDS, women self-help groups and panchayati raj institutions. The program will also seek to involve local MLAs and MPs to utilize their funds to ensure that each and every child in their community is vaccinated. Local institutions, community networks, and religious groups will also be reached out in coordinated way to reach specific groups of people for dialogue with planned messages. School children and adolescents will also be engaged as change agents to dispel myths and misconceptions related to immunization. Expected Result 2.3: Evidence based and contextually relevant communication messages are disseminated in the community Strategies Targeted communication will be needed for those who have never participated before, or who are not participating consistently because of lack of knowledge, doubts and misconceptions, or frustration with the quality of health services. The issues and barriers for the immunization will be addressed in the integrated communication work plan. The focus will be on SC, ST population, migratory 2. Promote inter-sectoral synergies between organizations, communities and individuals on promoting immunization 1. Identify issues and barriers for immunization in hard-to-reach populations and address them in the communication plan population and difficult to access areas. The reasons for low coverage and level of knowledge about immunization program will be regularly assessed. The findings from these assessments will be a base for communication and social mobilization plans. Promote the RI branding with a new logo color coding and tagline through various media. New audiovisual communication messages for TV and radio along with print material will be developed. The government will also use social media as a parallel communication channel to increase visibility about RI with multiple target audience. The program will strengthen delivery of interpersonal communication using Polio SMNet (from UNICEF), school teachers, student networks, national-level youth networks to support social mobilization. Institutions like NSS and NCC will be mobilized to reach out of school youth and eligible children in hard-to-reach population areas Standard Operating Procedures (SOPs) will be developed for production of new communication materials and their dissemination to the states. The Government of India will engage all categories of media – print or electronic –through regular workshops, meetings and field visits to advocate for and create an enabling environment that leads to an increasing demand for immunization services. With newer vaccines planned for introduction in the coming years, all efforts will be made to educate people and dispel any misinformation. Communication strategies for newer vaccines including campaigns will be developed in consultation with all stakeholders. 2. Develop and disseminate widely, new communication material on immunization 3. Increase people's confidence in vaccine safety through generation and dissemination of supportive data
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    ................................ 3 3 4. Developeffective communication response for AEFI crisis management KEY OBJECTIVE 3:Strengthen and maintain a robust surveillance system for vaccine-preventable diseases (VPDs) and Adverse Events Following Immunization (AEFI) To dispel any public misapprehension around adverse events following immunization the Government of India will develop communication guidelines to handle situations around AEFI. The burden of diseases preventable by the vaccines is the most significant factor for making a decision on introducing relevant vaccines in the UIP. Therefore, a robust surveillance system to detect cases and deaths due to vaccine-preventable diseases is essential to generate evidence to inform the decision on introducing the vaccine as well as to measure its impact on the disease after its introduction. Besides that, the completeness and quality of VPD surveillance data is also necessary to observe the trends in disease incidence and geographical spread to help plan to strengthen the immunization program. Reporting of VPDs has been an integral part of UIP reporting system. Major challenges for UIP include the following: lweak capacity of frontline health workers to identify cases, llack of attention in the health system for VPD reporting, lpoor coordination between various surveillance systems lpoor reporting from private sectors and large institutions. This has adversely impacted informed decision making on newer vaccine introduction and vaccine impact assessment. Therefore, it is necessary to ldevelop the capacity of health workers for improved detection of VPDs, lhave regular review of reports and data limprove coordination among various surveillance systems linclude private sectors and other institutions for improving VPD surveillance in the country. The goal of immunization is to protect individual and the community from vaccine- preventable diseases (VPD). Although modern vaccines are safe, no vaccine is entirely without risk; adverse reactions will occasionally occur following vaccination. Some people experience adverse events after immunization ranging from mild side-effects to rare life-threatening illnesses. However, in most serious cases these events are merely coincidences. In others words, they are caused by the vaccine or by an error in the administration or handling of the vaccine. Sometimes there is no causal relationship between the vaccine and the adverse effects. Maintaining public trust in vaccine safety, therefore, is key to the success of 21 all vaccination programs. Irrespective of the cause, when adverse events following immunization (AEFI) occur, people become confused to the extent that they refuse further immunization of their children, making the children susceptible to VPDs that are more disabling and life-threatening. Surveillance of AEFIs, i.e. systematic collection of data on events following immunization, provides valuable information to help plan and take necessary actions in order to sustain public confidence and ensure smooth functioning of the program. The national AEFI surveillance program supports the effective vaccine pharmacovigilance function for ensuring use of safe vaccines. Aggregate data for serious and non-serious AEFI are currently collected through routine monthly reporting in the HMIS but, details of serious AEFIs are also reported directly using the FIR, PIR and DIR formats. Along with the national health programs, such as HIV and TB, that generate their own respective data through surveillance, different surveillance systems in India provide information of various diseases, including 21 Immunization Safety Surveillance: Guidelines for Managers of Immunization Programs on Reporting and Investigating Adverse Events Following Immunization. WHO Regional Office for Western Pacific. 1999. U I P S T R A T E G I C P L A N F R A M E W O R K
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    3 4M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 VPDs. These include: Integrated Disease Surveillance Project (IDSP): This is a nationwide system that captures information on outbreaks of diseases including VPDs, such as diphtheria, pertussis, measles, AES, AFP, and Hepatitis B. Central and State Bureaus of Health Intelligence (CBHI and SBHI):This nationwide system captures information on suspected cases through passive surveillance including that of VPDs that are under the current UIP. Health Information Management System (HIMS): Within the NRHM framework, HMIS is an electronic data reporting system that captures data for health service delivery at health facility level every month to assist health departments, at all levels, in managing and planning health programs. HMIS also captures information on VPD disease burden from sub- block level on a monthly basis. WHO supported AFP and Measles outbreak surveillance through NPSP network: AFP surveillance is a laboratory-based system for poliovirus detection in all states. The lab-based measles surveillance covers 15 states generating data on measles and rubella outbreaks. The laboratory assisted joint AFP- measles surveillance system is planned to cover all states and UTs by the end of 2014. Acute Encephalitis Syndrome (AES/JE) surveillance: This is a facility-based surveillance system providing information on AES as per the guidelines under the National Vector-Borne Disease Control Program with lab support provided by ICMR. Multicentre Pneumonia and Meningitis Surveillance: Sentinel surveillance sites are functional to identify etiologic diagnosis of pneumonia and meningitis among children below two years. Rotavirus Surveillance Network in India: The Indian Rotavirus strain surveillance network is functional in seven regions, four hospitals and four labs. Children below five years admitted with acute gastroenteritis and given rehydration for at least six hours are enrolled. Sites for sample collection for Rotavirus surveillance are in following cities: Delhi, Mumbai, Pune, Vellore, Jabalpur, Imphal, and Kolkata. 1. % of sentinel sites providing timely and complete reports on VPDs (including zero report) on 90% occasions 2. Increase in the number of notified serious AEFI cases above the 2012 baseline value The indicators will be disaggregated by gender, geography (urban slum, urban, rural) and socio-economic parameters, where relevant. Expected Result 3.1:Institutionalize and strengthen surveillance mechanisms for VPDs Strategies There is a need to use epidemiological methods to better measure the impact of the immunization program. This will involve an initial landscaping of existing surveillance systems in the country, efforts will be made for collating, and analyzing data on VPDs generated from different surveillance systems and collate them to provide appropriate feedback. The following will be analyzed: ldata on the VPD disease burden, lemerging trends in the molecular epidemiology of different VPD antigens, lseroprevalence of protective antibodies against the VPDs, lgeographical variations in VPDs. MoHFW will work towards developing a system that facilitates convergence of relevant data from various surveillance systems, such as IDSP and NPSP, in the country. Key Performance Indicators (KPI) 1. Assessment of trends on VPD burden in context of reported immunization coverage
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    ................................ 3 5 2. Strengthenand improve coordination between Health information system (HMIS) and disease surveillance systems such as IDSP and NPSP to gather information on VPDs 3. Involve private sector in reporting of VPDs to further strengthen surveillance systems and inform policy making 4. Strengthen laboratories(including polio and measles lab network) and epidemiology units at medical colleges and other institutions for timely reporting, case investigation and detailed data analysis IDSP-based surveillance system, along with other systems, need to be strengthened from district onwards to capture information on all VPDs. The model of District/Municipal Corporation-based surveillance unit for action and reporting to the state would be further strengthened. To better streamline information sharing on VPD and AEFI occurrence across the country, MoHFW will strengthen coordination and data sharing between IDSP and Immunization Division at national level to monitor and improve program performance. Similarly coordination at the state and district levels will also be promoted to strengthen DIO's role as focal person for all information on VPD and AEFI. In view of the number of patients using private healthcare, lessons learnt from Kerala will be used to link surveillance and monitoring mechanisms with the private sector. Community reporting of VPDs will also be encouraged and specific strategies will be reviewed. Mechanisms for coverage data collection, compilation and flow from session sites/sub-centers/private clinics to the district and then to the State on uniform patterns will be highlighted. VPD surveillance mechanisms will attempt to integrate as much as possible with other surveillance mechanisms, without losing the required responsiveness for outbreak response or diluting the focus on AFP surveillance. For improved coordination and information sharing Infectious Diseases Hospitals(IDH) and super speciality hospitals should be integrated into IDSP. There is a network of IDH that needs to strengthen their laboratory capacity to provide updated information on outbreaks of existing or potential VPDs. India has developed a Health Management Information System (HMIS) for reporting of all health-related data from field. This tool will be used for updating VPD surveillance data in India. Improve coordination, information sharing with existing agencies and systems such as IDSP, ICMR, CBHI and SBHI networks so as to coordinate, collate and generate robust data that will guide a more evidence-based policies and program inter ventions in the immunization program future. Expected Result 3.2: Institutionalize and strengthen surveillance mechanisms for AEFIs Strategies The national AEFI guidelines mandate that all states and districts in the country constitute AEFI committees at each level, to assist in streamlining AEFI reporting mechanism, investigating serious AEFI, and be involved in causality assessment at state and national level. An AEFI secretariat for the National AEFI committee has been set up at ITSU-MoHFW, New Delhi, to coordinate all AEFI related activities in India with technical support and oversight from a leading medical college (LHMC). In addition Zonal AEFI consultants are planned to be in place to provide technical support and oversight to the AEFI Secretariat in the four zones of the country and enable timely reporting, investigation and support to the states. The National AEFI committee has been reconstituted to support the program in reviewing and updating information on tasks and responsibilities of key stakeholders in the AEFI system, including the Drug Controller 5. Strengthen sentinel surveillance for newer antigens 1. Revitalize the institutional framework and guidelines for AEFI surveillance in the country U I P S T R A T E G I C P L A N F R A M E W O R K
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    3 6M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 General of India (DCGI), Indian Pharmacopoeia Commission (IPC), National UIP managers and state-level UIP managers. National AEFI Operational Guidelines, which were revised in 2010, are being revised and will 22 be published in 2014. These guidelines will be distributed to all medical officers till Primary Health Centers and will be used for training the UIP staff including ASHA and ANMs. Innovative AEFI reporting models shall be piloted to enable enhanced AEFI reporting. The revised guidelines will also be utilized for trainings of AEFI committee members in the country. An abridged Standard Operating Procedure (SOP) for AEFI surveillance and case investigation version been printed and 23 widely disseminated in 2011. There is well known poor reporting of minor AEFIs in India. The efforts will be made to train the field staff in collecting data on minor AEFIs and pass this information to the next level. Since 2010, India has been participating in WHO Global network of post-marketing surveillance and the Government of India has nominated Maharashtra state for uploading AEFI data into the Uppsala Monitoring Centre vaccine safety database. The national immunization division has also started coordination with the IPC, the coordinating agency for the National Pharmacovigilance Program of India to collate and monitor vaccine safety reports in the country. The National AEFI Program already shares all data on vaccine safety with the national regulatory authority to inform all vaccine safety stakeholders. AEFI surveillance data require detailed analysis on numerous parameters in the context of the doses distributed and children vaccinated in the UIP. Currently serious AEFIs 2. Train field level staff on new National AEFI Guidelines 3. Convergence with vaccine pharmacovigilance stakeholders and private sector for AEFI reporting and analysis 4. Electronic database and reporting system for AEFI are reported manually on FIR/PIR and DIR formats by districts but can be transmitted electronically to the higher level (state and national). The government will pilot an electronic AEFI database and reporting system that is E2P compliant for AEFI reporting by 2015 in a phased manner. As UIP evolves, newer antigens, such as rotavirus, JE, rubella, Pneumococcal and Pentavalent vaccines, are expected to be introduced and expanded in the schedule. This will require a strong epidemiological underpinning for estimating disease burden in the country through a robust surveillance system to be put in place. There will be a need for improving coordination among different stakeholders and experts to develop an evidence-based policy for introducing newer antigens in the program in the medium term. In addition to newer antigens, improved service delivery will require innovations in technology and approaches. The choice of newer vaccines to be included in the UIP will be determined and periodically reviewed by the MoHFW, taking guidance from the NTAGI. Basic clinical and operational studies will be encouraged to provide inputs for NTAGI. These studies will provide evidence for decisions on the timing and selection of new vaccine introduction and provide guidelines for the use of these new vaccines. Such analysis will include the major mortality-causing diseases of children in India, namely acute diarrheal diseases and acute respiratory diseases, in anticipation of rotavirus vaccine and pneumococcal vaccine becoming available. Disease burden and health economic analyses will help assess the cost- benefit ratios of new vaccine introduction. Box 2 captures the key principles that will guide the inclusion of newer vaccine in UIP as per the national vaccine policy 2011. However, introduction of new vaccines would be as per decision of Mission Steering Group (MSG) following NTAGI recommendations. KEY OBJECTIVE 4: Introduce and expand the use of new and underutilized vaccines and technology in UIP 22 Adverse Event Following Immunization (AEFI): Surveillance and Response Operational Guidelines. MoHFW, Government of India. 2010. 23 Standard Operating Procedures for reporting AEFI. MoHFW, Government of India. 2011.
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    ................................ 3 7 Box 2:Principles to guide the inclusion of newer vaccines • Disease burden (incidence/prevalence, absolute number of morbidity/mortality, epidemic/pandemic potential); • Safety and efficacy of the vaccine under consideration; • Affordability and financial sustainability of the vaccination program, even if the initial introduction is supported by the external funding agency; • Program capacity to introduce a new antigen, including cold chain capacity; • Availability of a domestic or external vaccine production capacity; • Cost effectiveness of the vaccination program and also of the alternatives other than vaccination Key Performance Indicators (KPI) 1. Institutionalize mechanisms to guide the introduction of newer and underutilized vaccines in the country 1. Number of newer vaccines that have been reviewed for introduction in UIP by NTAGI 2. Number of States that have introduced Pentavalent vaccine The indicators will be disaggregated by gender, geography (urban slum, urban, rural) and socio-economic parameters, where relevant. Expected Result 4.1: Set up and strengthen institutional mechanisms, framework and policies for newer and underutilized vaccine introduction Strategies The introduction of new vaccines involves reviewing all licensed vaccines in different parts of the world and identifying those that would be relevant to India in the context of the burden of disease in the country and prioritization of target vaccine-preventable diseases in the country. There are several vaccines that are popular in the private market, and many of those are recommended by the Indian Academy of Pediatrics. Accurate information on which to base the decision of introducing a new vaccine to the UIP requires periodic review and assessment on an objective scale by all agencies concerned through strong coordination and collaboration. In this regard, the immunization decision- making process has been institutionalized by the establishment of an independent advisory body, the National Technical Advisory Group on Immunization (NTAGI) in 2001, comprising of independent experts from diverse fields such has immunology, community medicine and health economics; representatives from partner organizations like WHO, UNICEF, ICMR and DCGI as well as liaison officers from the government. The NTAGI has been reconstituted twice in 2008 and again in June 2013. The current reconstituted NTAGI comprise of a Standing Technical Sub-Committee (STSC) tasked with undertaking a detailed technical review of the issues highlighted above and a broader body with representations from all organizations mentioned above. In addition, a secretariat for this advisory body has been established by ministry under Immunization Technical Support Unit to facilitate technical and managerial support required for continuity and follow up to this body. However, the mandates of both the NTAGI and STSC are still work-in- progress. The spelling out of well-defined Standard Operating Procedures (SOPs) for the functioning and decision making of the U I P S T R A T E G I C P L A N F R A M E W O R K
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    3 8M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 NTAGI is necessary to institutionalize the evidence-based decision-making process for the introduction of new and underutilized vaccines in the country. It is also imperative to adopt and standardize mechanisms to grade the quality of evidence available, such as burden of disease, published literature, global data, cost effectiveness data, for the NTAGI to r ev i ew a n d m a k e ev i d e n c e - b a s e d recommendations. There are several vaccines that are already licensed and available or soon to be licensed with expanded indications for particular groups in India. Unfortunately, access to the bulk of these vaccines is available only to the privileged few who have access to private health care. The NTAGI is the highest advisory body tasked to review the available evidence on disease burden, potential impact, safety, efficacy etc. To assess these vaccines and prioritize vaccines for inclusion in the program. Vaccines that can be potentially considered for review include the Injectable Polio Vaccine(IPV), rotavirus and pneumococcal vaccines The absence of reliable baseline estimates for the burden of VPDs in India is a major obstacle in informed policy-making process. Currently, there are multiple systems to measure different VPDs including antigen/disease specific sentinel surveillance network (Indian Rotavirus Sentinel Surveillance Network, National Polio Surveillance Program (NPSP) network and Infectious disease surveillance eProgram (IDSP). With plans to expand the range of vaccines in the UIP and improve its reach (coverage), the surveillance of VPDs will be intensified and steps will be taken to establish stronger collaboration between the already established networks and the immunization program. At the national level, 2. Identify newer vaccines that will be introduced and/or expanded to use during the plan period 3. Assess disease burden for which vaccine are becoming available or will become available in the near future the newly formed STSC of the NTAGI has been tasked for undertaking critical review of disease burden data prior to recommending the introduction of a new vaccine in the UIP. The NTAGI secretariat at ITSU will collaborate closely with the disease surveillance centers in the country to collate the evidence for the review of the NTAGI and STSC. Generate evidence for introducing new vaccine – including areas like vaccine safety, equity, vaccine ethics and financial sustainability, IPV as part of post-polio eradication. Expected Result 4.2: Scale up and sustain the implementation of JE vaccination in identified endemic districts as part of Japanese Encephalitis (JE) control Strategies In India there are 175 districts currently identified as being endemic for JE. Most of the cases occur in UP and Assam. Though any age group can be affected by JE, children between 1 and 15 years of age bear the brunt of the disease. A study carried out in South India showed JE incidence to be 15/10,000 children between 5 and 9 years. Mortality due to JE has been estimated to be between 20 and 30 percent. Recent studies under the WHO surveillance program in India undertaken in selected centers (Bellary, Dibrugarh, Madurai and Burdwan) show that about 10 to 20 percent of the total Acute Encephalitis Syndrome (AES) cases are JE. JE, at present like other vaccines in India's UIP, is restricted to children but there is an increasing demand for use of JE vaccine to protect the adult population in endemic districts. The NTAGI will discuss the safety and immunogenicity data of the vaccine for use in the program. Since JE is a vector-borne disease, immunizing adult populations will prove critical in breaking the transmission cycle and control of the disease. 4. Conduct operational research 1. Identify disease burden and endemic districts for prioritization
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    ................................ 3 9 2. ContinueJE campaign in the endemic districts 3. Expand training and advocacy on JE vaccination 4. Introduction of JE vaccine in routine immunization program ICMR recommends that JE vaccination program should continue for another five years in endemic areas. It was suggested, that in view of low evaluated coverage with JE vaccine, the strategy in 2010 should be to re-immunization all children up to 15 years with high vaccine coverage in a campaign mode. Thereafter coverage should be sustained by immunization of children below than 2 years through Routine 24 Immunization. Coverage survey conducted for JE vaccine suggests that overall community knowledge on JE vaccines is low. While some people are not convinced about the need for JE vaccination, others do not know where to access the vaccine from. Some pockets of communities have fear of side effects or have formed a negative opinion on the vaccine following some AEFIs 25, 26 in their area. Information about JE vaccination has been incorporated in immunization handbooks for Medical officers and health workers. Operational guidelines for JE vaccination program has been prepared and widely disseminated to ensure correct reporting and clarification on the role and responsibility of each health care provider in JE vaccination. Publicity around the JE vaccination will be made more intense prior to the campaign dates and respective states shall ensure that the IEC material reaches the target users well in in time. Adverse publicity around the vaccine will need to be countered through appropriate messages. The planned strategy was to complete SIAs for JE vaccine and subsequent introduction of the JE vaccine routine immunization program of endemic districts to ensure adequate vaccination coverage for new birth cohort. As from April 2013, the Government of India has already introduced a 2-dose schedule for JE vaccines in the districts implementing JE routine immunization. The 1st dose is given at 9 months of age and the 2nd dose at 16 – 24 months of age In India, currently the SA-14-14-2 imported from China is being used in the national immunization program. Efforts will be made to ensure that JE vaccine is produced indigenously from local strains and introduced in the program. Expected Result 4.3: Streamline and expand the use of Pentavalent vaccine to cover all the states Strategies As of 2012, the Haemophilus Influenzae b (HiB) vaccine has been introduced in eight states of India (Tamil Nadu, Kerala, Karnataka, Puducherry, Goa, Gujarat, Jammu and Kashmir and Haryana) in the form of the combined Pentavalent vaccine (DPT+ Hep B+ HiB). On 23 September 2013 the NTAGI endorsed the STSC's recommendation for further scale-up of the vaccine in the remaining states of India in a logistically structured manner with simultaneous strengthening of the AEFI and sentinel surveillance systems in the country. Preparations for the expansion of vaccination to the other states are planned. The operational guidelines on HiB as part of Pentavalent vaccine have been already been developed and will be useful for immunization program managers at state, district and sub- 27 district level. 5. Roll out indigenously produced JE vaccine 1. Nationwide scale up of Pentavalent vaccine to introduce HiB vaccine in other states of the country 24 Minutes of the Meeting of ICMR Core Committee on Vaccines. 2010 25 Japanese Encephalitis Coverage Evaluation Survey Report, 2008. UNICEF and NRHM 26 A coverage evaluation survey of JE vaccination in two districts of Karnataka. Kumar KR et al. Journal of Communicable Diseases.Sep2010;42(3):179-84; 27 Operational Guidelines: Introduction of HaemophilusInfluenzae b (HiB) as Pentavalent Vaccine in Universal Immunization Program (UIP) in India. MoHFW, Government of India. 2011. U I P S T R A T E G I C P L A N F R A M E W O R K
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    4 0M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 2. Conduct a revision of recording and reporting formats for improved surveillance and data management 3. Conduct training of FHWs and their supervisors on newer vaccine 4. Strengthen surveillance system for HiB and AEFI reporting Introduction of newer vaccines will accompany the revision of recording and reporting formats. Vaccination cards will also be revised and updated to include newer vaccines. The reporting system in the country will also have necessary column to collect information on newer vaccines. ANMs and their supervisors will be trained on newer vaccines and other related aspects including the vaccine administration and AEFI reporting as part of regular training. The DIOs and other Mid-level managers (MLM) will be specially trained prior to the new vaccine introduction in their respective states. The surveillance system for newer vaccines will be further strengthened and expanded in India. Eleven sentinel sites for HiB meningitis in six different states have already started in 2013. These selected sites for bacterial meningitis surveillance (including HiB) will monitor the disease trends to measure impact trends of vaccination on the study populations. The surveillance sites for other newer vaccines are also likely to be introduced to cover additional states. Model AEFI systems are also being planned to ensure timely reporting and management of AEFIs before they snowball into a crisis. Expected Result 4.4: Evaluate Rubella antigen for introduction in RI program During the 66th SEARO regional committee meeting in New Delhi in 2013, India has committed to the elimination of measles and control of rubella and CRS by 2020. Strategies The public health importance of rubella infection stems from the fact that rubella infection in pregnancy has the potential to cause Congenital Rubella Syndrome (CRS) in the new born. The risk of development of CRS is highest when infection is in the first trimester of pregnancy. While there is no hard data on CRS, the estimated incidence in India from modelling studies gives a range of around 123 per 100,000 live births. CRS results in a cumulative burden on the health system and families of affected children on account of the chronic sequelae (such as disability of sight, hearing or cardiovascular systems) and the economic burden in diagnosis, assessment and treatment of congenital malformations and challenges to providing education in an increasingly nuclear family structure in society. There are plans at national level to establish and expand CRS surveillance through partner agencies and existing surveillance programs. The surveillance sites will be established in selected states for observing the trends in CRS, before and after vaccine introduction. The strategy for introducing the rubella vaccine in India's UIP will be planned to fulfil the commitment the country has made to the SEARO declaration for control of rubella disease and CRS burden in the country. Since immunization program performance differs across states, expansion of rubella sentinel surveillance sites is also planned. The strategy for phase-wise implementation will be chalked out over the cMYP period. The STSC of the NTAGI shall play a crucial role in reviewing and recommending a potential strategy for implementation. The NTAGI has also recommended the establishment of a Measles 1. Expansion of Congenital Rubella Syndrome (CRS) surveillance 2. Introduction and expansion of rubella vaccine in UIP
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    ................................ 4 1 & Rubella-India Expert Advisory Group (MR- IEAG) on the same lines as polio to develop a comprehensive strategy and monitor progress for rubella control and measles elimination in the country. Existing measles surveillance system in India frequently report rubella outbreaks or mixed measles and rubella outbreaks. The existing measles network will continue to be utilized for identifying rubella outbreaks. It is envisaged that with introduction of rubella vaccine, cases of rubella will go down and, thereafter, a possibility and need for case based surveillance will be explored. Once CRS surveillance system is established, the information collected from surveillance network will be utilized for assessing the trends in CRS in states and the country. Studies should be carried out to estimate incidence of CRS and the social and economic burden resulting from it. Expected Result 4.5: Evaluate Rotavirus antigen for introduction in RI program Strategies Diarrheal diseases are one of the largest causes of childhood (under-5 years) deaths in India 28,29 and rotavirus is the leading cause. WHO estimates that 23 percent of the annual 527,000 deaths due to rotavirus occur in India. It is estimated that even with a vaccine with 50 percent effectiveness, a rotavirus vaccination program in India would prevent 44,000 deaths, 293,000 hospitalizations, and 328,000 outpatient visits annually which would avert 30 $20.6 million in medical treatment costs. 3. Conduct Rubella surveillance through the existing systems 4. Conduct research on CRS and trends 1. Assess disease burden due to rotavirus and the potential impact of a preventive vaccine 2. Strengthen national level surveillance on rotavirus 3. Develop the vaccine schedule in line with EPI schedule KEY OBJECTIVE 5: Strengthen health system for immunization program The Indian Rotavirus Surveillance Network was set up on 2005 with four laboratories and ten hospitals in seven different parts of the 31 country. The network provides valuable information on epidemiology of rotavirus that will underpin the policy decisions regarding the introduction of rotavirus vaccine in RI. NTAGI recommends that assuming several vaccines will be licensed and recommended for use in India, it would be preferable for each child to complete all doses using the same vaccine formulation. This could be facilitated by choosing a specific vaccine for national use or by ensuring that each region or state is supplied with only one specific rotavirus 32 vaccine. A strong RI program will contribute to the overall health system strengthening both in the urban and rural areas. Four states with large populations - Uttar Pradesh, Bihar, Madhya Pradesh and Rajasthan – contribute approximately to 2/3rd of the unimmunized children in the country (CES 2009). In addition there are other states that are not performing up to the mark as shown in Annex 1. Future strategies for RI will need to be adapted and contextualized for these high-priority states to increase the vaccination coverage levels and reduce VPD mortality and morbidity. Following polio eradication the technical support structures established for polio eradication, both at the national and sub- national levels, by WHO, UNICEF and other partners are now 'transitioning' to provide support to intensification of routine immunization from 2012 onwards, based on the lessons learnt from polio. This feeds into the 28 Causes of neonatal and child mortality in India: A nationally representative mortality survey. The Million Death Study Collaborators.The Lancet.Vol 376, November 27, 2010 29 The Global Enteric Multicenter Study (GEMS) of diarrheal disease in infants and young children in developing countries: epidemiologic and clinical methods of the case/control study.Kotloff K L, et al. Clinical Infectious Diseases. 2012 Dec;55 Suppl 4:S232-45 30 Projected Impact and Cost-Effectiveness of a Rotavirus Vaccination Program in India.Douglas H. Esposito et al. Clinical Infectious Diseases.2011:52 (15 January) 31 Multicenter, Hospital-Based Surveillance of Rotavirus Disease and Strains among Indian Children Aged <5 Years. Gagandeep Kang et al. Journal of Infectious Diseases.2009:200 (Supplement 1) 32 Minutes of NTAGI meeting. 3rd August 2009. U I P S T R A T E G I C P L A N F R A M E W O R K
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    4 2M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 overall goal of strengthening health systems in the country. The indicators will be disaggregated by gender, geography (urban slum, urban, rural) and socio-economic parameters, where relevant. Expected Result 5.1: Increase the pool of skilled human resources to provide quality immunization services in an integrated manner Lack of adequate numbers of trained and skilled human resources has been a major barrier in improving the overall quality and outreach of UIP. The Immunization Division at MoHFW is small with few technical officers to manage such a large program. The Government of India has addressed this capacity gap by setting up an Immunization Technical Support Unit (ITSU) in year 2012 with technical officers to support various components of UIP. In addition to the national level, the HR capacity on UIP in the states need to expand. It is important to identify key functions within the UIP at state level also that would need full time positions to ensure a smoother functioning, improve institutional memory and enhance the overall coverage of immunization in the state. Under NRHM PIP, the Government of India has given the flexibility to the states to propose human resource augmentation plans at state and district level. Strategies The strength and capacity of the national immunization division has been enhanced Key Performance Indicators (KPI) 1. Number of districts with full immunization coverage rate of >80% 1. Increase the number of technical managers for immunization at national and state level and strengthen organizational capacity to adequately perform strategic and technical functions under UIP with the setting up of ITSU at MoHFW with recruitment of technical officers for key functions of UIP such as strategic planning and system designs, monitoring and evaluation, cold chain and vaccine logistics, strategic communication, vaccine safety and AEFI, and evidence to policy. This unit will help in the development of policies, procedures and guidelines to improve program management at national level. This setup will be further strengthened to augment the capacity for operational research and use of more technology in UIP. Similarly, a state-level structure is also proposed that includes recruiting focal points for the program management, Cold Chain, Vaccine Logistics, Management Information System (MIS), and Technology and research etc. Relevant trainings will be carried out for new staff working in the immunization cell at all levels based on the existing training norms and guidelines under NRHM. Immunization- specific training norms will also be used, e.g. cold chain training norms. The training material for both medical officers and health workers in routine immunization has been updated, printed and widely disseminated. This material is being utilized for conducting need-based training. National Institute of Health and Family Welfare (NIHFW) is the national nodal agency for training activities including Immunization. The NIHFW, in coordination with Immunization and Training Divisions within MoHFW, will review the training plans from all states; conduct Training of Trainers courses, as well as monitor and evaluate the quality of trainings. The State Institute of Health and Family Welfare (SIHFW) is nodal agency at state level to plan, implement, monitor and evaluate the immunization training activities. 2. Conduct relevant training and induction programs and develop need- based immunization training materials 3. Strengthen training infrastructure
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    ................................ 4 3 A planis being instituted to conduct induction training for new State Immunization Officers as per the need and refresher trainings on regular interval. There is need for strengthening the existing training infrastructure and also starting new facilities. The issues of shortage of health workers and their training needs can be addressed by institutionalizing training mechanism for this category of staff. This can be achieved by: lOn-the-job refresher training every two years for every health functionary. lEach state will identify core district training teams for each district. This team will move to each block identifying gaps in knowledge and train appropriately, lMonthly block meetings will provide an opportunity for supervisors to help identify gaps in knowledge and provide some training. NRHM provides for hiring staff on contract basis. All staff members (medical officers, staff nurses, health workers including ANMs) hired on contract basis will also be trained. ANM and ASHA vacancies will be filled up by the states on urgent basis. A stronger immunization program will also be used as a platform to deliver other child health services in an integrated manner. Preventive child health interventions like Vitamin A, deworming, ORS, growth monitoring can also be given along with immunization. A well- functioning RI program will act as a catalyst in getting more people to use the health facility and contribute to overall demand generation and better address equity issues. 4. Hire and train more field level staff under NRHM 5. Promote integrated delivery of different health interventions through UIP Expected Result 5.2: Ensure that adequate financial resources are available for UIP. Strategies A core team for immunization financing named Financial Management Group (FMG) has been established within the MoHFW. Using tools that are already available, this team will analyze current and projected immunization costs factoring in the plan for scale up and introduction of newer vaccines in the coming years. These will be compared to projected finances available and funding gaps will be highlighted. The country will be expanding the VPD and AEFI surveillance, which will require a well- functioning laboratory network. A mechanism for the separate budgeting mechanism will be devised for the strengthening of the laboratory and surveillance mechanism in the country Expected Result 5.3: Improve program accountability, monitoring and reporting at all levels. Strategies Quarterly review meetings will be held at national and state level; and monthly meetings at district and block levels to track the progress in immunization program, to identify problems, analyze the issues and address them. State-level meetings will be chaired by State Secretary/MD-NRHM and district-level meetings will be chaired by the DM. 1. Prepare a national financial sustainability plan 2. Provide funding for laboratory strengthening and surveillance 3. Explore the possibility of setting up a Vaccine Fund through innovative financing mechanisms 1. Hold regular program reviews at all levels U I P S T R A T E G I C P L A N F R A M E W O R K
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    4 4M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Comprehensive EPI reviews will be held in the good and poor performing states to help prepare state specific action plan. MoHFW will develop a monitoring and accountability tracking framework for UIP that will identify key program indicators and assign responsibility of delivering results on specific individual or organizations At the service-delivery level, more formal, institutionalized systems for complaint and redressal should be put in place. They must be supported by timely emergency response systems, such as telephone helplines, and proper managerial authority should be granted so that structures are in place to rectify acute challenges related to referral and transportation or the mistreatment/ exploitation of patients at the facilities. A formal system to lodge complaints and seek redress should also provide oversight to help protect women who register complaints, from future reprisals. The demonstrated initiatives/innovation for accountability, for instance call center for integrated grievance handling system, can be considered. The Mother and Child Tracking System (MCTS) is designed to collate information of all pregnant women and infants into a central database to ensure that all pregnant women and children receive full maternal and immunization services. This centralized database will enable functions like data analysis, report generation, and therefore contribute to greater strategic decision-making and need-based allocation of resources. It will act as a feedback system for health workers like 2. Develop national monitoring and evaluation plan for immunization 3. Formalize and make accountability mechanisms system-led as part of community participation 4. Expand the usage of Mother and Child Tracking System (MCTS) to all districts to help reduce the gap between reported and evaluated coverage Auxiliary Nurse Midwives and ASHAs and will enable better health service delivery by drawing out action plans for health workers for ante-natal care, pre-natal care and child immunization. MCTS will also generate reports such as facility service statistics and Auxiliary Nurse Midwife monthly action plans. Currently the states aggregate the relevant data in a Microsoft Excel template available on the HMIS portal. MCTS has been fully operational since April 2010 and has picked up speed in terms of usage by states and union territories as of 1 April 2011. Under this system, SMS alerts are sent to pregnant women who are nearing the delivery date to remind them of the need to visit the PHC for pre-natal check-up and delivery. Women are also reminded over the cell phone on the due dates for immunization of their children to ensure follow through with RI. Bring out annual reports on UIP as part of a strengthened HMIS at state and district level. The scope of the Quality Assurance (QA) system is now enhanced to include the full range of RMNCH+A services. For rolling out QA system, organizational arrangements will be set up at various levels with clearly defined roles and responsibilities for each level. These will include (1) Central Quality Supervisory Committee; (2) (2a) StateQuality AssuranceCommittees, (2b) Quality Assurance Cell and (2c) Full time quality assessors; (3) District Quality Assurance Committees; and (4) Quality Circles at the District Hospital level. The central QA team will comprise technical officers from the program divisions of the Ministry of Health and Family Welfare and 5. Introduce the Quality Assurance (QA) system for immunization services as part of RMCH+A
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    ................................ 4 5 counterparts workingwith technical support partners. The QA standards will be defined for each technical theme, categorized by the level of health facilities. Expected Result 5.4: Strengthen RI program management and service delivery through field level supportive supervision in high priority states To achieve immediate and sustainable improvement in RI coverage at national level, the Government of India needs to focus on high priority states, Rajasthan, Madhya Pradesh, Uttar Pradesh and Bihar, which have the maximum number of unimmunized and partially immunized children. The RMNCH+A strategic approach recognizes the need to strengthen supportive supervision of frontline workers (ASHAs and ANMs) and service providers (Staff Nurses and Medical Officers) in order to bring about integration of primary care services, improve quality, enhance skills and skill application. Strategies To support the implementation and monitor the activities at the district level, there will be a State Level Supportive Supervision Team consisting of officers from the state health department, partners and students and Staff of Medical Colleges (Department of Community Medicine). Each state officers or medical college team will support and monitor 4 to 5 districts for implementation through regular visits, and help establish a link between districts and the state. It will establish State and district RI supportive supervision team. The mobility support will come from NRHM. At the district level the supportive supervision team will consist of selected medical officers, senior supervisors, medical college staff to support PHC/planning unit. Each member of supportive supervision team including medical college staff will be responsible for two PHC or 1. Augment HR for supportive supervision and program management planning units, and would visit each unit twice a month (total four visits in a month). S/he will provide regular supportive supervision services to the unit as well as the vaccinators in the area. Skill building of ANMs is required for ensuring supportive supervision of ASHAs (and AWWs). While ANMs do perform supervisory functions informally, their skills in supportive supervision are limited and need to be enhanced on this specific issue. The supportive supervision by Institute of Child Health in Tamil Nadu has led to significant improvement in quality of maternal-newborn care in eight districts. A similar engagement of Medical College faculty in other districts and states would be a useful strategy. The technical expertise available with the partners will be utilized to impart knowledge to the state and district level staff. State-level mechanisms will be strengthened to monitor the program, and guide the districts to improve, implement and monitor the program. a) Quarterly review meeting will be held at the state for all DIOs and District RI managers b) Monthly meetings will be held between State and District Task Force meeting c) Monthly review meetings will be held at the district for all block and PHC medical officers in charge and RI coordinators d) All supportive supervision checklists will be collected at the district level, and entered into software. This data will be sent to the state for compilation and subsequently the state will send the data sheets to the national 2. Leverage expertise and experience of development partners and medical colleges 3. Establish an institutional mechanism for program oversight and monitoring the implementation of supportive supervision model U I P S T R A T E G I C P L A N F R A M E W O R K
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    4 6M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 immunization division. e) Data will be presented and feedback provided at all the levels (state, division, district and block level) for appropriate action. State RI cell/RRT members will be trained through Training of Trainer (ToT) by a national team once in a year. District RI team will be trained once a year by the state core team. District RI team shall be responsible for training, providing supportive supervision and implementation of RI activities at the block and PHC level. On-job regular capacity building will take during the visits of Support Team members from the state. District-level immunization officers from partner organizations will also contribute to the capacity building process. Block and PHC team members will be trained annually by the team comprising of members of the district team and one of the facilitators from the state. They will also receive on-job training on a regular basis by district immunization facilitators during their visits and review meetings. These guidelines will be developed as part of the RMNCH+A strategy to further augment the supportive supervision mechanisms. Result 5.5: Build institutional capacity to promote operational and translational research for successful implementation of UIP 4. Carry out capacity building and on-job training of staff for strengthening RI supervision all level 5. Prepare integrated guidelines and checklists for supportive supervision linking UIP-MNCH (Universal Immunization Program and Maternal, Newborn And Child Health) supervisory mechanism Strategies: Areas for OR could include, but not be limited to, HR training in immunization, operational aspects of cold chain system, vaccine freezing, vaccine wastage, injection safety, barriers to service access and utilization. A leading research organization may be identified to work in collaboration with immunization division and other stakeholders Funds will be ear-marked and sufficient amount will be ensured for operational research and implementation in UIP. National immunization cell will seek to avoid long time lag between conducting research and translating the findings for advocacy, communication and UIP interventions. Technical expertise of partners working on immunization shall be availed as and when required. Key Performance Indicators (KPI) 1. No wild polio virus detected in the country 2. Non Polio AFP rate is maintained or 1. Define areas for Operational Research and mechanisms for translating evidence-based approaches into program service delivery 2. Evolve institutional mechanism for operational research 3. Ensure sufficient funding for operational research 4. Ensure adequate knowledge management and translation for greater public good KEY OBJECTIVE 6: Contribute to global polio eradication, measles and maternal and neonatal tetanus elimination and rubella control
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    ................................ 4 7 exceeds 2per 100,000 children under 15 years 3. Reported AFP cases have two adequate stool specimens collected within 14 days of onset of paralysis in > 80% cases 4. Number of States with MCV 1 coverage of > 90% 5. Number of States with MCV-2 coverage of> 90% 6. % of districts with >80% TT2 coverage for pregnant women The indicators will be disaggregated by gender, geography (urban slum, urban, rural) and socio-economic parameters, where relevant. Expected Result 6.1: Achieve country-wide certification of polio eradication by 2014 Strategies The polio eradication program and the polio endgame strategy shall continue to be guided by India Expert Advisory Group constituted by 33 the Government of India. Conduct regular supplementary immunization activities (SIAs), ensure that the SIAs maintain good quality and conduct regular seroprevalence surveys to detect immunity levels. The plans for SIAs to be conducted in the coming two years are as below SIAs for the remainder of 2013 As per current national plans, three large scale SNIDs with bOPV, targeting all of UP, Bihar, Delhi and associated high risk areas of Haryana, Rajasthan, and Uttarakhand, and migrant/high risk areas in Maharashtra, Punjab, Gujarat, Jharkhand, and West Bengal. 1. Maintain high level of population immunity Polio SIAs in 2014 lTwo NIDs with tOPV in all areas in 1st quarter of 2014 lThree SNIDs with bOPV, ideally one in each of quarters 2, 3, and 4 of 2014 targeting all of UP, Bihar, Delhi, and associated high risk areas of Haryana, Rajasthan, and Uttarakhand, and migrant/high risk areas in Maharashtra, Punjab, Gujarat, Jharkhand, and West Bengal. Polio SIAs in 2015 lTwo NIDs with tOPV in all areas in 1st quarter of 2014 lTwo to three SNIDs with bOPV (depending on global epidemiology) targeting all of UP, Bihar, Delhi, and associated high risk areas of Haryana, Rajasthan, and Uttarakhand, and migrant/high risk areas in Maharashtra, Punjab, Gujarat, Jharkhand, and West Bengal. The timing of sub-national rounds should be at the discretion of the national program and based on operational and epidemiological considerations An extremely high level of vigilance will be maintained through to global certification of eradication, and through to cessation of use of oral poliovirus vaccines; this requires ensuring that adequate financial and human resources and attention are devoted to the surveillance and laboratory systems by the Government of India and partners. Regular field reviews of surveillance would continue to be conducted on a rotational basis and with particular attention to high risk areas as determined by epidemiological, surveillance or immunization indicators. 2. Maintain the quality and effectiveness of the existing surveillance and laboratory systems to detect and respond to outbreaks 33 http://www.npspindia.org/advisory.asp U I P S T R A T E G I C P L A N F R A M E W O R K
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    4 8M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Environmental surveillance for detection of polioviruses in the sewage would be expanded in other states of the country. All detected VDPVs would continue to be thoroughly investigated to determine any risk of circulation, and appropriate actions taken based on investigation findings. The Emergency Preparedness and Response Plans (EPRPs) at national and state-levels will be updated annually; the update will include a full new risk analysis to inform risk mitigation measures. See Annex 7 for EPRP details. A simulation exercise ('table top exercise') for the emergency response plans at national and selected state levels will be conducted annually to maintain readiness and sharpness of response. Government of India will ensure a rolling stock of 40 million doses of bOPV and 10 million doses of tOPV to enable response to any wild poliovirus or vaccine derived poliovirus detection. Immunization of travelers at land border crossing points from neighboring countries is the most significant risk reduction strategy and will continue until there is no longer an epidemiological risk. Particular attention should continue to be paid to border populations to ensure that they are effectively covered by SIAs and routine immunization. The Government of India will strongly promote implementation of the current WHO p o l i o i m m u n i z a t i o n a d v i s o r y 3. Augment the current response capacity by developing a national and state-level emergency response preparedness plan and maintain a rolling stock of bOPV and tOPV 4. Reduce risks of polio importation based on WHO recommendations for travelers coming to or from endemic or infected areas /recommendations for travelers to and from endemic or infected areas. The Government of India will develop the inventory of all labs holding polio virus(phase 1) and securing the WPV (phase 2). This includes planning for tOPV/bOPV shift, IPV introduction process, and operational assessments of the cold chain system. These sero-surveys will be conducted in the traditionally high risk areas of UP and Bihar and other regions with potential risk of wild poliovirus importation or emergence of circulating vaccine derived poliovirus. This will provide an epidemiological description of the trends on population immunity and possible reasons for these trends. Expected Result 6.2:Achieve measles elimination and control for rubella/congenital rubella syndrome (CRS) by 2020 Strategies The first-dose Measles Containing Vaccine (MCV1) at 9-12 months is delivered through Routine Immunization. Efforts will be made to improve coverage with MCV1 by strengthening RI services with a target to reach all children. In addition follow-up campaigns will be conducted in low coverage areas. It will be ensured that the coverage in every district is more than 90 percent and progress is sustained. 5. Work towards the certification process 6. Develop post-eradication policy in preparation for the polio endgame 7. Conduct periodic seroprevalence studies in high priority areas. 1. Increase coverage with the first dose of measles vaccine for infants (9-12 months)
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    34 A Guide toIntroducing a Second Dose of Measles Vaccine into Routine Immunization Schedules. 2013. World Health Organization, Measles and Rubella Initiative. ................................ 4 9 2. Increase the coverage of second dose of measles vaccine (at 16–24 months of age) based on global guidelines 3. Strengthen and expand the laboratory surveillance for measles and rubella 1. Strengthen service delivery and improve institutional deliveries 34 Conduct measles SIAs in 14 states where MCV 1 coverage is below 80 percent vaccinating all children in age group of 9 months to 9 years. All states where MCV1 coverage was more than 80 percent have already introduced MCV2 in routine immunization at the time of DPT booster 1. Twice yearly state-by-state review of all measles data will be conducted. The laboratory-based measles and rubella surveillance has started in eight states, namely Andhra Pradesh, Gujarat, Karnataka, Kerala, Tamil Nadu, West Bengal, Rajasthan, Madhya Pradesh, Bihar and Assam. The surveillance laboratory network will be further expanded with priority being given to the states with measles morbidity and mortality. In addition, surveillance data on measles outbreak from IDSP will also be collated and analyzed for action. Expected Result 6.3: Eliminate maternal and neonatal tetanus by 2015 Strategies Promote institutional delivery and safe delivery by skilled birth attendants (SBA) under NRHM and ensure that TT is offered at all ante-natal clinics and routine immunization sessions. Provide twoTT doses for the first pregnancy (with immunization card) and further doses according to the national schedule. The tetanus vaccine for pregnant mothers will also be ensured in all outreach sessions being conducted. Establish MNT as a reportable disease and report MNT cases from every health facility. MNT will be included with weekly AFP in active surveillance and zero reporting. Case investigations for hospital-based cases and the cases from low-risk areas are regularly done. Improve TT coverage through quality RI in all areas. SIAs may be considered for those areas where coverage with 2 doses of TT is poor. The Government of India will take need-based decision to conduct targeted SIA for elimination of MNT. The mode and time for these SIAs will be decided by an expert group. A national MNT database will be established with regular review of indicators, identifying high-risk districts within states. The high-risk districts within states will be validated for elimination of MNNT by Lot Quality Assurance Surveys (LQAS) and districts prioritized on the basis of this for targeted corrective action. In states where MNT has been validated to have been eliminated, efforts will be made to maintain the high coverage with TT2, and safe delivery practices to ensure the elimination status in those states. 15 states have validated MNT till 2008, and four more states have conducted MNT validation exercise in 2013. The remaining states and UTs will be assessed in 2014–2015. 2. Increased surveillance for tetanus cases 3. Conduct targeted SIAs 4. Establish national MNT database 5. Maintaining the elimination status U I P S T R A T E G I C P L A N F R A M E W O R K
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    5.1 Rationale lThe UniversalImmunization Program (UIP) in India uses a set of indicators to measure the performance at national as well as other levels of program implementation. For this purpose, the country uses various data sources that include: lRoutine administrative reporting, lReports from various disease surveillance systems and field level monitoring by partners, lPeriodic Coverage Evaluation Surveys (CESs) at national and sub-national level, lVarious assessment studies conducted from time-to-time by different organizations. Despite the availability of multiple sources of data, there is no comprehensive independent UIP Monitoring & Evaluation (M&E) Plan in the country to lsystematically identify data needs as well as data sources to meet dynamic program requirements, lreview the process of data gathering, lconduct Data Quality Assessments (DQAs). In the absence of this plan, there is also no mechanism to identify information gaps, especially to measure process indicators, and plan targeted studies to inform the program. Though there are provisions for immunization program reviews at all levels, these are not regular and are not effective in the absence of a real-time quality data. ................................ 5 1 5 5.2 Objective 5.3 Methodology I. Strengthen routine data reporting The overall objective of this National Monitoring and Evaluation (M&E) Plan is to systematically generate, capture and disseminate knowledge to guide UIP implementation monitoring and UIP impact evaluation. This monitoring and evaluation plan will work at three levels: Currently UIP does not have its own electronic data management system. The Health Management Information System (HMIS) captures immunization data from the health facility-level and the Mother & Child Tracking System (MCTS) tracks ante-natal and immunization services at the individual pregnant woman and child level. The National Monitoring and Evaluation Plan will aim to strengthen these existing data reporting systems through the following mechanisms: a) Structured Review Mechanism There is currently limited use of HMIS and MCTS data sets for analyzing and reviewing program implementation and for providing feedback to the concerned districts or blocks. The proposed monitoring and evaluation plan will establish a structured review mechanism in the country to enhance the use of immunization data and to further improve data quality. National Monitoring And Evaluation Plan For UIP
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    5 2M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 b) Human Resource & Capacity Building A core part of the plan is to improve monitoring and evaluation human resource capacity through trainings, supportive supervision, mentoring, and providing guidelines and tools. c) Data Quality Assessments (DQA) DQAs will be conducted regularly in coordination with state governments and with the support of technical and development partners. State Immunization Managers will also be trained in conducting these DQAs by using WHO DQA tools. d)Feedback to program managers Data quality will be improved by examining the immunization information system in operation at all administrative levels– from data collection at the point of vaccination, to the periodic compilation of data at the national level. Practical feedback will be provided to managers on how to improve the quality of their administrative immunization reporting systems. Knowledge gaps identified through routine program monitoring and reporting will be filled by targeted studies and operational research. The results from these research activities can help the UIP in taking ongoing corrective measures for better outcomes. The monitoring and evaluation plan will also include regular audit at facility and service level using WHO tools and provide feedback to program managers for strengthening the facilities and services. Currently, evaluation surveys conducted in the country address all MCH services, and the immunization component is limited only to antigen-wise and full immunization coverage. Moreover, these surveys are done every three to I. Conduct targeted studies and field assessments to fill knowledge gaps in the program II. Plan and conduct coverage evaluation studies four years, and do not provide latest coverage numbers on a yearly basis. The monitoring and evaluation plan will propose a yearly evaluation survey for routine immunization, focusing on outcome and impact indicators of all RI components. This can be done through external agencies, in line with NFHS and DLHS surveys. MOHFW will guide the development of the national monitoring and evaluation plan. The Monitoring and Evaluation division of Immunization Technical Support Unit (ITSU) will coordinate the development of the plan. ITSU will hire a consultant to work on the plan after consultation with ministry and technical partners for the scope. The consultant will work closely with ITSU team and, in consultation with all stakeholders including states, with the aim of creating a realistic, expedient and effective national monitoring and evaluation plan for the UIP. The National Monitoring and Evaluation plan will be developed in line with the cMYP and five-year plan of the country. The proposed national monitoring and evaluation plan will cover all major areas for establishing and running an effective monitoring and evaluation system in the country. These include: lOrganizational structure along with roles and responsibilities for monitoring and evaluation at various levels lPlan for capacity building of monitoring and evaluation staff on transmission, analysis and use of data at all levels lKey coordination mechanisms for the country lImmunization monitoring and evaluation performance and accountability tracking framework and implementation plan at national and state level (see Annex 6) 5.4 Process for national M & E Plan development 5.5 Components of National Monitoring and Evaluation Plan
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    ................................ 5 5 ANNEX 1:List of states showing good performance on immunization coverage and other parameters States Andhra Pradesh Delhi Goa Haryana Himachal Pradesh Jammu & Kashmir Karnataka Kerala Maharashtra Punjab Tamil Nadu Mizoram Sikkim Tripura Uttarakhand West Bengal Full immunization coverage (%) 68.0 71.5 87.9 71.7 75.8 66.6 78.0 81.5 78.6 83.6 77.3 73.7 85.3 66.0 71.5 64.9 No. of sub- centers without ANM/HW* 0 0 0 N/A 178 N/A N/A 0 N/A N/A 140 N/A 0 0 34 N/A Mos trained (%) 93.7 55.5 93.7 72.8 4.0 7.3 44.8 50.5 51.8 95.8 82.2 48.3 75.0 30.0 19.5 19.7 Sessions held vs. planned (%)** N/A 92.8 99.2 93.9 98.2 90.5 95.4 N/A 80.2 95.1 99.1 66.7 N/A 92.9 91.8 91.6 Dropout rates in age group12-23 months for BCG- measles (%) 8.3 6.5 1.4 5.3 2.2 9.4 7.4 8.3 3.7 9.6 0.6 7.3 0.1 7.3 14.2 13.6 No. of severe AEFI cases reported*** 21 12 4 10 3 N/A 9 1 71 4 5 N/A N/A 4 1 28 Children aged 12-23 months having an immunization card (%) 64.9 50.7 60.6 42.7 60.3 60 52 78.9 58.8 53.2 44.8 77.9 85.2 75.9 41.1 77.8 * Collated data from state review meetings on immunization obtained from MoHFW, GoI. * * Data from the HMIS web portal April to October, 2011; ** *Severe AEFI cases reported to the Government of India by the states till mid-December, 2011; A N N E X U R E S
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    5 6M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 States Arunachal Pradesh Manipur Meghalaya Nagaland Assam Bihar Madhya Pradesh Orissa Rajasthan Uttar Pradesh Chhattisgarh Gujarat Jharkhand Full immunization coverage (%) 24.8 51.9 60.8 27.8 59.1 49.0 42.9 59.5 53.8 40.9 57.3 56.6 59.7 No. of sub- centers without ANM/HW* N/A N/A 0 0 0 200 119 535 392 1,776 458 488 0 MOs trained (%) 43.8 49.4 93.4 40.1 84.7 18.3 32.5 44.9 33.4 32.1 8.7 24.7 36.3 Sessions held vs. planned (%)** 81.5 89.6 80.8 93.7 97.4 95.1 96.1 96.0 113.9 89.8 90.3 97.2 94.4 Dropout rates in age group 12-23 months for BCG- measles (%) 27 12.9% 9.4 11.5 7.2 29.3 24 17.6 20.6 30.9 13.8 8.1 22.8 No. of severe AEFI cases reported *** N/A N/A 3 N/A 7 19 8 5 3 21 N/A 3 11 Children aged 12-23 months having an immunization card (%) 41.9 55.6 63.8 45 66.9 43.1 45.8 58.3 24 35.9 46.3 49.5 63.1 ANNEX 2: List of States showing poor performance on immunization coverage and other parameters *Collated data from state review meetings on immunization obtained from MoHFW, GoI. **Data from the HMIS web portal April to October, 2011; ***Severe AEFI cases reported to the Government of India by the states till mid-December, 2011
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    adequate space inthe unused portion of the Animal House for the establishment of NCCVMRC. UNICEF has supported the establishment by hiring an architect to prepare the plans and estimates for remodeling of the existing building of the Animal House. Immunization Division has provided five tool kits for the training center. NIHFW has already conducted a six days pilot Training for Cold Chain Technicians in Repair and Maintenance of ILRs and DFs from 17-22 October 2011 using alternate temporary space made specifically available for the training. The Resource Centre will be set up to train cold chain mechanics in repair and maintenance of all electrical cold chain equipment (ILRs, DFs, WICs, WIFs and voltage stabilizers). In addition, it will also conduct trainings related to vaccine and logistics management for vaccine and logistics managers in the country. It is expected to make it a cold chain training center for other countries in South-east Asia. In addition to trainings, NCCVMRC will be a repository of documents such as guidelines, government orders/notifications and other resource materials related to cold chain and Brief about resource centre Establishment of national cold chain and vaccine management resource centre and nihfw, new delhi BACKGROUND The Immunization Division, MOHFW, New Delhi has proposed to establish a National Cold Chain and Vaccine Management Resource Centre (NCCVMRC) at NIHFW, New Delhi and it has been approved by the competent authority of MoHFW, Government of India (Annexure A). Further it has been intimated that NIHFW may utilize any MOHFW, GoI funds available or the proposal estimates be provided for necessary approvals from the competent authority. MOHFW, GoI shall support the establishment of NCCVMRC, trainings of officials from Central/state Governments related to cold chain equipment, vaccine and logistics management, etc. and the human resources needed for the trainings on regular and /or contractual staff and all other expenses related to the Training Centre. The necessary technical support will be provided by UNICEF. National Institute of Health and Family Welfare, New Delhi has on its part demarcated ................................ 5 7 ANNEX 3: NCCVMRC concept approved by MoHFW ESTABLISHMENT OF NATIONAL COLD CHAIN AND VACCINE MANAGEMENT RESOURCE CENTRE (NCCVMRC) PROPOSAL ESTIMATES IMMUNIZATION DIVISION, MINISTRY OF HEALTH AND FAMILY WELFARE, NEW DELHI AT NATIONAL INSTITUTE OF HEALTH AND FAMILY WELFARE, NEW DELHI (With blueprint) Submitted to By National Institute of Health and Family Welfare, New Delhi A N N E X U R E S
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    5 8M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 vaccine management. The soft copies will be on the resource centre website and hard copies will be maintained in a small library in the centre. The resource center will be set in the unused portion (earlier Primate Section) of the Animal House. There will be a Lecture Room, a work lab (for repair of ILRs and DFs) and a room for housing a Walk in Cooler and a Walk in Freezer. In addition, there will be an administrator's room and a facilitator's room as well as a store room. The ingress will be separate from the animal House with adequate accessibility for heavy vehicles (for loading and unloading of cold chain equipment). A training coordinator, an assistant and a support staff are the human resources needed for the resource center. MoHFW has agreed to support in hiring of the training coordinator and support staff from NIHFW can be deputed to work in the resource center. UNICEF may also initially support the hiring of technical staff. The following are the different types of trainings to be undertaken at the NCCVMRC, New Delhi: 1. Training for Cold Chain Technicians in Repair and Maintenance of ILRs and DFs 2. Training for Cold Chain Technicians in Repair and Maintenance of WICs and WIFs 3. Training on repair and maintenance of voltage stabilizers 4. Training on installation and repair of Solar cold chain equipment. 5. Training for Vaccine and Cold Chain Handlers 6. Training on Vaccine Management There are more than 500 cold chain technicians and vaccine logistics managers in the country. Some of these are newly inducted have had no induction training. Many of the older refrigerator mechanics need refresher trainings for which such a course will be designed separately. Therefore the establishment of the NCCVMRC is justified.
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    ................................ 5 9 – ProcurementPolicy for CCE – Institutional Capacity Building of NCCTC and NCCVMRC – Greater role of NCCTC and NCCVMRC for CCVLM – Review Mechanism of CCVLM lInduction Training of HR engaged for Cold Chain and VM lImprovement of management skills of program managers lDedicated staffs for CCL at all level (at least up to district) lEach GMSD and SVSs need to have VLM and CCT lSome of the existing staffs of GMSD can be profiled for Data management lCold rooms should have some semiskilled helpers lDevelop Training package for the VLMs and also for the Immunization program managers and house them in the institution to overcome attrition lReview of Knowledge (Training) to skills transformation barriers lRegular orientation, at least every 3 years for all staffs A.Building lDedicated stores for State, Division, District 2. Human Resource and capacity building 3. Infrastructure The recommendations are categorized in to five broad categories “Management Policy, Human Resource and capacity building, Infrastructure, Planning and Documentation and improvement in practice and development of an improvement plan to implement these recommendations through NRHM state PIPs. lIntroduce VAR for Vaccine stores up to Sub National level lDevelop and implement real time MIS for Vaccine Logistic Management for 5 levels of supply chain. lIntegrate vaccine management MIS with NCCMIS lAccelerate NCCMIS implementation for GMSDs lSegregate all SVSs attached to RVS and RVSs attached to DVS: Building, equipment, documents and Staff. lDevelop National Cold Chain action Plan – Develop National standards for: lVaccine store at all levels as per WHO standards lCold Chain point expansion guidelines lCold Chain Equipment plan for different level of vaccine stores lQuality maintenance of vaccine lTemperature Monitoring of cold chain system lHuman resource for Cold Chain and VM lCCE Testing Lab 1. Management Policy ANNEX 4: Key Recommendations from Effective Vaccine Management Assessment Report 2013 A N N E X U R E S
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    6 0M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 and Health Facilities(PHC), lConsider the future need, national standard lGreater collaboration with PWD, Electricity and Municipal corporation/bodies for regular maintenance B.Equipment lEquipment specification as per global standards lMinimize variety of equipment to reduce number of spare parts lAll WIC/WIF with working hooters lMapping of spare parts and ensuring availability to make non-functioning equipment (Solar, Haier, Blue star, others)functional lDefine realistic stock level in months at five supply chain level lDefine, print and distribute standard vaccine stock registers lVaccine indent and distribution plans based on the required peak stocks. lPreventive maintenance plan for technicians lRegular data uploading in NCCMIS for performance assessment of CC at all level lEstablish a system for recording wastage in vaccine registers lManual temperature monitoring and recording to be carried out 2 times daily, for all 7 days including holidays lMaintain a service log sheet for each equipment. This can be done as part of the 4. Planning and Documentation 5. Improvement in Practice Temperature monitoring booklet. lDiluents MUST be marked in supply voucher and should be recorded just like the vaccines in stock registers. lAt CHC and PHC the DF must be used exclusively to prepare ice packs. Vaccines must never be stored in the same unit. All vaccines should be kept in ILRs at the CHC and PHC. lAlways use standardized Ice Packs after conditioning EVM is a diagnostic tool and it assess, 3 Ps like Process, Practices and Policies of health system requires for efficient cold chain and vaccine management. Improvement Plan(IP )is the intervention for Strengthening of existing Cold Chain and Vaccine Logistics System to make it Reliable ,Affordable and Efficient. Issues identified through EVM needs to be fixed and to be sustained success of the EVM initiatives lies in developing an implementable improvement plan and then actually implementing the IP and reviewing the IP on the regular basis for strengthening the Cold chain logistics system. While EVM is a diagnostic tool, IP lay down the treatment strategies for the gaps in the CCL system. Development of an improvement plan is the key output that comes from the EVM assessment and its recommendations. While a skilled facilitation is needed to make sure that the plan does indeed address key deficiencies, it should be possible to provide a menu of innovative approaches and technologies for consideration, guided by country realities. A menu of innovations approaches is included in the Improvement Plan to guide planning for future system design and to enhance monitoring of the implementation of the plan. While planning, guiding principles that need to be considered for an effective and implementable IP are: 6. Improvement Plan (IP)
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    ................................ 6 1 AN N E X U R E S lIntegration with other planning processes lIP template should be adapted by government to align with existing planning and budgeting documents o IP should be consistent with and input into other planning documents such as cMYP, national and sub-national annual work plans, etc. lDynamic and living document lPlan that needs regular review and monitoring for implementations of recommendations IP need to be prepared through consultative process and it should be integrated annual health PIP. lGovernment ownership lPlan which need to be reviewed regularly for progress of implementation lEngagement of all levels lDisseminate widely , leveraging existing mechanisms lMake IP foundational plan for improving immunization supply chain performance o Identifies priority action areas and establishes accountability for improving performance o Takes longer-term view and reflects future needs (NVI, population growth, etc.)
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    6 2M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 ANNEX 5: National Open Vial Policy 2013
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    ................................ 6 3 AN N E X U R E S Guidelines for use of open vial in immunization program Conditions that must be fulfilled for the use of open vial policy: 1. This opened vial policy applies to multi-dose vials of the DPT, TT, Hepatitis B, Oral Polio Vaccine (OPV) and Liquid Pentavalent (where applicable). This policy does not apply to Measles, BCG, Japanese Encephalitis (JE) vaccines. 2. Use the DPT, TT, Hepatitis B, Oral Polio vaccine (OPV) and Liquid Pentavalent (DPT + HepB + HiB) where applicable) vaccines opened in a fixed or outreach session can be used at more than one immunization session up to four weeks provided that: a. The expiry date has not passed. b. The vaccines are stored under appropriate cold chain conditions both during transportation and storage in cold chain storage point. c. The vaccine vial septum has not been submerged in water or contaminated in any way. d. Aseptic technique has been used to withdraw all doses. e. The vaccine vial monitor (VVM), has not reached the discard point. 3. Discard vaccine vial in case any one of the following conditions is met: a. If expiry date has passed. b. VVM reached discard point (for freeze dried vaccine, before reconstitution only) or Vaccine vials without VVM or disfigured VVM. c. No label or partially torn label or writing on label is not legible. d. Any vial thought to be exposed to non-sterile procedure for withdrawal. e. Open vials that have been under water or vials removed from a vaccine carrier that has water. f. If vaccine vial is frozen or contains floccules. 4. Health workers must be able to distinguish between vials that can be used in subsequent sessions and vials that must be discarded. Training and supervision materials should be revised to reflect the policy change. 5. Maintain temperature of ILR between 20 to 80C for storage of vaccines & diluents and monitor temperature twice daily regularly. 6. Note the manufacturer, batch and expiry date of the vaccine and diluent in the stock register. 7. Proper recording and reporting of vaccine distribution and usage has to be ensured. 8. Keep stock up to date, don't over-stock or under-stock vaccines and diluents. 9. Multi-dose vials from which at least one dose has been removed may be at risk of contamination of the vial septum. These vials should therefore, never be allowed to be submerged in water (from melted ice for example) and the septum should remain clean and dry. NOTE: Well-sealed conditioned ice packs should be used in vaccine carriers and water should not be allowed to accumulate where the vials are stored. Vaccine vials must be transported in a plastic zipper bag. 10. Keep the “returned, partially used” vials in a separate box, and label it accordingly. 11.Observe earliest expiry first out (EEFO) policy for issuing vaccines. If the vaccines are of same expiry date, the partially used vaccine vials should be re-issued. The vial opened earlier, as recorded on the vial label, should be issued first. 12. Contingency plan has to be in place in case Cold chain maintenance and vaccine distribution
  • 79.
    6 4M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 of any exigency like power failure, equipment breakdown, etc. 13. Inspect for and discard vaccine vial with visible contamination (i.e. checking for any change in the appearance of vaccine or any floating particles) or breaches of integrity (e.g. cracks, leaks). 14. All vaccines vials must be marked with date & time of opening at first use. 15. Note the manufacturer, batch and expiry date of the vaccine and diluent in the tally sheet. 16. Always pierce the septum with a sterile needle for drawing vaccine from the multi- dose vials used. Except oral polio vaccine which is given 2 drops orally, cap needs to be closed after each use. 17. Ensure that the vaccine vials are returned inside a vaccine carrier from the session site to cold chain point immediately after session ends, using the alternate vaccine delivery mechanism in the reverse cold chain. 18. Under no circumstance the vaccine carrier/vaccines will be kept in the field, in case of such an event, the vaccines in such vaccine carriers should be discarded and not used for subsequent sessions. 19. Storage of vaccines at any place other than a designated cold chain point will not be At and during the immunization session After immunization session is over allowed. No vaccines should be stored at ANM/LHV or other health worker/ASHA house. 20.This policy is NOT applicable to opened reconstituted vials of Measles, BCG and JE vaccine, which will be used as per following instructions and discarded immediately after use: a. Before reconstitution check that vaccine is within expiry date and the VVM has not reached the discard point. Reconstitute the vial ONLY with diluent provided by manufacturer for that batch of the vaccine. b. Date and time of reconstitution must be mentioned on the label vial at the beginning of session. c. Reconstituted vials will only be used for a single session; they will not be carried from one session to another, even if the session is close by. d. BCG and Measles must be discarded within four hours of reconstitution or at end of session whichever is earlier. e. JE to be discarded after two hours of reconstitution or at end of session whichever is earlier. 21. All vaccines are supplied with VVM. Please note that the VVM has only three status ie (i) start point (ii) end point (iii) end point exceeded. The vaccine has to be use before reaching the end Specific attention while implementing open vial policy End point Square lighter than circle. If the expiry date has not passed, USE the vaccine. Square matches the circle. Do NOT use the vaccine. Square darker than the circle. Do NOT use the vaccine. End point exceeded Start point
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    ................................ 6 5 AN N E X U R E S ANNEX6:MonitoringFramework cMYP(2013-17)-ReachingEveryChild MonitoringandAccountabilityTrackingFramework Datawillbedisaggregatedby district Fullimmunizationcoverageis definedasinfantswhohave receivedallrelevantdosesinthe firstyearoflife Numerator:Districtsthatshowfull immunizationcoveragerates>80% Denominator:Totaldistrictsinthe country Indicatorwilldisaggregatedby district,gender,geography(urban slum,urban,rural)andwealth 20(Source: HMIS201213) 17% (Source: DLHS-3) 20(Source: CES2009) 30 60% All States/UTs (35) HMIS HMIS,Periodic surveysincluding DLHS,CES HMIS,Periodic surveysincluding DLHS,CES Monthly Monthly Monthly 1.Numberof States/UTswhere> 95%sessionswere heldasplanned 2.%ofdistricts having>80%full immunization coverage 3.Numberof States/UTshaving lessthan10% dropoutfrom DPT1-DPT3(or Pentavalent) MoHFW MoHFW MoHFW IndicatorIndicatorDefinition (&unitofmeasurement) Baseline value TargetDataCollection Methodsand Sources Frequency& Schedule Responsibility GOAL:Reducemortalityandmorbidityduetovaccinepreventablediseasesthroughhighqualityimmunizationservices KEYOBJECTIVE1:Improveprogramservicedeliveryforequitableandefficientimmunizationservicesbyalldistricts
  • 81.
    6 6M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Coldchainsicknessisdefinedas- coldchainequipmentwhichoutof orderasapercentageoftotal equipmentplaced Self-explanatory Self-explanatory Thiswillbeimplementedacrossthe districtsBiharandUP Self-explanatory 26 (Source: NCCMIS 2013/State reports) 16 (Source: NIHFWRI trainingstatus report) 0 0 0 All States/UTs (35) All States/UTs (35) 5 States/UT 110 districts 7 States/UT NCCMIS Statetraining reports Web-based temperature monitoringreport Web-basedstock monitoring system MoHFW report/NCCMIS Monthly Monthly Monthly Monthly Onetime MoHFW SIO SIO/MoHFW SIO/MoHFW MoHFW IndicatorIndicatorDefinition (&unitofmeasurement) Baseline value TargetDataCollection Methodsand Sources Frequency& Schedule Responsibility EXPECTEDRESULT1.2:Strengthenvaccineandsyringelogisticsmanagementacrossthecountryincludingforecastingand procurementatcentrallevel 1.Numberof States/UTswhere thecoldchain sicknessrate meetsthenational standardof<2% 2.Numberof States/UTswhere allcoldchainstaff aretrainedincold chainandvaccine management 3.Numberof States/UTwhere temperature monitoringisbeing donewithwireless dataloggersforall functionalelectrical coldchain equipment 1.Numberof districtswherereal timevaccinestock monitoringsystem isimplemented 2.Numberof States/UTsthatare usingcomputer simulationmodel forvaccinesupply chaincapacity planning
  • 82.
    ................................ 6 7 AN N E X U R E S Numerator:Numberofsubcenters havingafunctionalhubcutter Denominator:Totalnumberofsun centerssurveyed Numerator:Numberofcoldchain pointshavingafunctionalsafetypit Denominator:Totalnumberofcold chainpointssurveyed PlanningunitisdefinedasPHC, BlockPHC,CHCorUrbanHealth Center Numerator:Numberofplanning unitswheremicroplansare available Denominator:Totalnumberof planningunitssurveyed PlanningunitisdefinedasPHC, BlockPHC,CHCorUrbanHealth Center Numerator:Numberofplanning unitshavingaAVDplan Denominator:Totalnumberof planningunitssurveyed Self-explanatory NoBaseline NoBaseline Nobaseline NoBaseline 0(in2012) 80% 100% 80% 90% All States/UTs (35) Coverage surveys Statereport Coverage surveys Coverage surveys Statereport Annual Annual Annual Annual Annual MoHFW SIO MoHFW MoHFW MoHFW IndicatorIndicatorDefinition (&unitofmeasurement) Baseline value TargetDataCollection Methodsand Sources Frequency& Schedule Responsibility 1.%ofsub-centers withfunctionalhub cutteravailable 2.%ofcoldchain pointshaving functionalsafety pitsasperthe CentralPollution ControlBoard (CPCB)guidelines 1.%ofplanning unitswhereRI microplansare available 2.%ofplanning unitswhereAVD planisapartofRI microplan 1.Numberof Stateswherestate taskforceon immunizationis constitutedto reviewRIprogram andtake appropriateaction EXPECTEDRESULT1.3:Ensuresaferinjectionpracticesandreducedvaccinewastage EXPECTEDRESULT1.4:Ensurethatregularimmunizationsessionsareplannedandheldandcoverageincreased EXPECTEDRESULT1.5:Improveprogramcoordinationatalllevels
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    6 8M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Numerator:Numberofcaregivers whosechildreceivedpartialorno immunizationwhodidnotfeelthe needforadheringtoimmunization schedule Denominator:Numberof caregiverssurveyed Numerator:Numberofcaregivers notrecallinganyofroutinevaccine Denominator:Numberof caregiverssurveyed Self-explanatory Staffshouldincludeprogram managers(otherthanASHA) Shouldbestand-aloneBCC training Thiswillonlyincluderural populationandchildrenwhohave receivedatleastonevaccineprior tothesurvey Numerator:Numberofcaregivers whogotinformationabout immunizationfromASHA Denominator:Numberof caregiverssurveyed 28% (Source:CES 2009) 12% (Source:CES 2009) 0(asof2012) 0(asof2012) EXPECTED 19% (Source:CES 2009) <15% <5% Allhigh priority States 35 (12) Allhigh priority States(12) >80% Coveragesurveys Coveragesurveys StatePIP MoHFWreport EXPECTED Coveragesurveys Annual Annual Annual Annual Annual MoHFW MoHFW State/MoHFW State/MoHFW MoHFW IndicatorIndicatorDefinition (&unitofmeasurement) Baseline value TargetDataCollection Methodsand Sources Frequency& Schedule Responsibility 1.%ofcaregivers whosechild receivedpartialor noimmunization whodidnotfeelthe needforadhering totheimmunization schedule 2.%ofcaregivers notrecallinganyof routinevaccine 1.Numberof State/UTPIPs whichhave communication actionplanforRI 2.Numberof Stateswhere80% ofhealthHRare trainedonBCC 1.%ofcaregivers whoreportedthat theygotinformation aboutimmunization fromASHA KEYOBJECTIVE2:Increasedemandandreducebarriersforpeopletoaccessimmunizationservicesthroughimprovedsocialmobilization EXPECTEDRESULT2.1:Developandimplementamulti-prongednationalcommunicationstrategywithafocusonprioritystates EXPECTEDRESULT2.2:Effectivecommunicationchannelsaresetupwiththecommunityforbetteracceptanceofvaccines 35 The 12 States include – Arunachal Pradesh, Assam, Bihar, Chhattisgarh, Gujrat, Jharkhand, Madhya Pradesh, Manipur, Nagaland, Odisha, Rajasthan and UP
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    ................................ 6 9 AN N E X U R E S Self-explanatory Messagesasrelevantatthetimeof survey Numerator:Numberofcaregivers whocanrecallnewimmunization messages/tagline Denominator:Numberof caregiverssurveyed Referenceperiod:Timelyreportsas compliedoverthepreviousone year. Numerator:Numberofsentinel sitesprovidingtimelyandcomplete reportson90%occasion Denominator:Allsentinelsites Self-explanatory DoesnotincludePolioworkshops 0 0% 0% (asof2012) 372cases (sourceFIR 2012-13) 0(asof2012) All States/UTs (35) 40% 80% >1500 cases 35(States andUTs) State communication plan CoverageSurveys Surveillance report FIR,PIR,DIR VPDSurveillance report Annual Annual Annual Annual Annual State/MoHFW MoHFW MoHFW DIO,SIO MoHFW/SIO IndicatorIndicatorDefinition (&unitofmeasurement) Baseline value TargetDataCollection Methodsand Sources Frequency& Schedule Responsibility 1.Numberof States/UTsthat haveadefined mediatrackingand assessmentplan. 2.%ofcaregivers whocanrecallnew immunization messages/tagline 1.%ofsentinel sitesproviding timelyand completereports onVPDs(including zeroreport)on 90%occasions 2.Increaseinthe numberofnotified seriousAEFIcases abovethe2012 baselinevalue 1.Numberof Statesthathave conductedVPD surveillance workshops EXPECTEDRESULT2.3:Evidencebasedandcontextuallyrelevantcommunicationmessagesaredisseminatedinthecommunity KEYOBJECTIVE3:Strengthenandmaintainrobustsurveillancesystemforvaccinepreventablediseases(VPDs)and adverseeventsfollowingimmunization(AEFI) EXPECTEDRESUL3.1:InstitutionalizeandstrengthensurveillancemechanismsforVPDs
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    7 0M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 NewerantigenincludesHiBand Rotavirus Self-explanatory Timelynotificationisdefinedas submissionofnotificationform within48hoursoftheevent occurringinthefield Numerator:SeriousAEFIcases notifiedontime Denominator:Allnotifiedserious AEFIcases Numerator:SeriousAEFIcases investigatedontime Denominator:Allnotifiedserious AEFIcaseswhosePIRisreceived Numerator:SeriousAEFIcases classifiedwithin120days Denominator:Allnotifiedserious AEFIcases Vaccinesforreviewinclude,butnot limitedto,IPV,Pneumococcus, Rotavirus,Rubella 10 (asofAugust 2013) 9 . 16% (Source:AEFI dashboardas ofJanuary 2013-14) 6% (Source:AEFI dashboardas ofJanuary 2013-14) 64% (Source: MoHFWreport asonApril 2013forcases uptoDec 2012) 0(asof2013) 30 All States/UTs (35) 80% 60% 90% Atleast2 new vaccines MoHFWreport MoHFWreport FIR FIR,PIR DIR NTAGIreport Annual Annual Annual Annual Annual 6monthly IndicatorIndicatorDefinition (&unitofmeasurement) Baseline value TargetDataCollection Methodsand Sources Frequency& Schedule Responsibility 2.Numberof sentinelsitessetup fornewerantigens 1.Numberof States/UTswithall DIOstrainedon nationalAEFI guidelines 2.%ofserious AEFIcasesnotified inatimelymanner 3.%ofSerious AEFIcases investigatedtimely aspernational guidelines 4.%ofSerious AEFIcases classifiedwithin 120daysof reportingofthe case 1.Numberofnewer vaccinesthathave beenreviewedfor introductioninUIP byNTAGI EXPECTEDRESUL3.1:InstitutionalizeandstrengthensurveillancemechanismsforVPDs KEYOBJECTIVE4:IntroduceandexpandtheuseofnewandunderutilizedvaccinesandtechnologyinUIP ICMR/MoHFW MoHFW DIO,SIO DIO/SIO SIO,StateAEFI Committee NTAGI/MoHFW
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    ................................ 7 1 AN N E X U R E S Self-explanatory Self-explanatory Numerator:Numberofnewly identifiedJE-endemicdistricts whereJEvaccinehasbeen introducedinUIP Denominator:62(newlyidentified districts) Fullimmunizationcoverageis definedasinfantswhohave receivedallrelevantdosesinthe firstyearoflife Numerator:Districtsthatshowfull immunizationcoveragerates> 80% Denominator:Totaldistrictsinthe country Self-explanatory 9States (asof December 2013) Nobaseline 0 17% (Source: DLHS-3) 5States/UTs (Source: NIHFWRI trainingstatus report) All States/UTs (35) Atleasttwo meetings peryear 100% 60% 30 States/UTs HMIS NTAGIminutes HMIS HMIS,Periodic surveysincluding DLHS,CES Statetraining report Annual Annual Annual Monthly Annual IndicatorIndicatorDefinition (&unitofmeasurement) Baseline value TargetDataCollection Methodsand Sources Frequency& Schedule Responsibility 2.Numberof Statesthathave introduced Pentavalent vaccine 1.Numberof NTAGImeetingsin ayear 1.%ofnewly identified62JE- endemicdistricts whereJEvaccine hasbeen introducedin 36 UIP 1.Numberof districtswithfull immunization coveragerateof >80% 1.Numberof Stateswhereall MOsaretrainedon RIMOhandbookin lastthreeyears MoHFW MoHFW MoHFW MoHFW SIO EXPECTEDRESULT4.1:Setupandstrengtheninstitutionalmechanisms,frameworkandpoliciesfornewerandunderutilizedvaccineintroduction EXPECTEDRESULT4.2:ScaleupandsustaintheimplementationofJEvaccinationinidentifiedendemicdistrictsaspartofJEcontrol KEYOBJECTIVE5:Strengthenhealthsystemforimmunizationprogram EXPECTEDRESULT5.1:Increasethepoolofskilledhumanresourcestoprovidequalityimmunizationservicesinanintegratedmanner 36 The newly identified 62 districts as on 2013
  • 87.
    7 2M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Self-explanatory Self-explanatory DatawilldisaggregatedbyState Numerator:Totalnumberofinfants registeredinMCTS Denominator:Totalestimated numberofinfantsintheyear Self-explanatory Self-explanatory 2 (Source: NCCMIS 2013) 7 (Source: MoHFW financereport 2011-12) 57% (Source: MCTSportal asonApril 2013) 0 0 0 25 States/UTs All States/UTs (35) 80% 25 States/UTs 0 StatePIP, NCCMIS NRHMFMS StatePIP Statereports AFPSurveillance BulletinIndia Annual Annual Annual Annual Annual IndicatorIndicatorDefinition (&unitofmeasurement) Baseline value TargetDataCollection Methodsand Sources Frequency& Schedule Responsibility 2.Numberof States/UTswithno vacantpositionsfor refrigerator mechanics 1.Numberof States/UTsutilizing >90%ofthe allocatedfundfor UIP 1.%ofinfants registeredinMCTS 1.Numberofstates whereStateTask Forceon Immunization (STFI)conducted atleast10monthly meetingsduringthe reportingyear 1.Nowildpolio virusdetectedin thecountry SIO Statemanager NRHM States States MoHFW EXPECTEDRESULT5.2:EnsurethatadequatefinancialresourcesareavailableforUIP EXPECTEDRESULT5.3:Improveprogramaccountability,monitoringandreportingatalllevels EXPECTEDRESULT5.4:StrengthenRIprogrammanagementandservicedeliverythroughfieldlevelsupportivesupervisioninhighprioritystates KEYOBJECTIVE6:Contributetoglobalpolioeradication,measles,maternalandneonataltetanuselimination
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    ................................ 7 3 AN N E X U R E S Self-explanatory Self-explanatory Datawillbedisaggregatedby districtlevel Datawillbedisaggregatedby districtlevel Self-explanatory Self-explanatory Self-explanatory >2 >80% 19(Source: HMIS2012- 13) 2(Source: HMIS2012- 13) 29States/UTs (Source:CES 2009) 11 18(Source: WHOreport 2013 >2 .>80% AllStates /Uts(35) All States/UTs (35) All States/UTs (35) 23States /UTs All States/UTs AFPSurveillance BulletinIndia AFPSurveillance BulletinIndia HMIS HMIS Coveragesurvey MoHFWreport MoHFWNNT validationreport Annual Annual Annual Annual Annual Annual Annual IndicatorIndicatorDefinition (&unitofmeasurement) Baseline value TargetDataCollection Methodsand Sources Frequency& Schedule Responsibility 2.NonPolioAFP rateismaintained orexceeds2per 100,000children under15years 3.ReportedAFP caseshavetwo adequatestool specimens collectedwithin14 daysofonsetof paralysisin>80% cases 4.Numberof StateswithMCV1 coverageof>90% 5.Numberof StateswithMCV-2 coverageof>90% 6.Numberof Stateswith>80% TT2coveragefor pregnantwomen 1.Numberof Statesthathave established laboratory supportedmeasles surveillance systems 1.Numberof Statesvalidatedas NNTeliminated duringtheplan MoHFW MoHFW MoHFW MoHFW MoHFW MoHFW MoHFW EXPECTEDRESULT6.2:Achievemeasleseliminationandcontrolforrubella/congenitalrubellasyndrome(CRS)by2020 EXPECTEDRESULT6.3:Eliminatematernalandneonataltetanusby2015
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    7 4M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 ANNEX 7: Emergency Preparedness and Response Plan 2011
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    ................................ 7 5 AN N E X U R E S Emergency Preparedness and Response Plan 2011 1. Background The Emergency Preparedness and Response Plan has been developed at the request of the Minister of Health & Family Welfare to ensure adequate preparedness and response to an event of importation of poliovirus anywhere in India during 2011. India has made remarkable progress towards polio eradication in 2010. Only 42 wild poliovirus (WPV) cases have been detected in the country, compared to 724 cases detected during the same period in 2009. The progress in polio eradication was reviewed during the India Expert Advisory Group (IEAG) meeting held in November 2010. At this meeting the IEAG concluded that “the epidemiologic, genetic, serologic, operational & technical evidence show that India is on the right path to achieve eradication”. However, the IEAG identified certain risks to the polio eradication Program in India. One of the major risks identified includes continued transmission of poliovirus within the mobile / migrant populations, resulting in re-introduction and spread of the virus in Uttar Pradesh (UP) and Bihar or in areas outside these historically core endemic states that are at high risk of importation and further spread of polio. The IEAG highlighted the fact that as long as virus transmission continues in any part of India or elsewhere in the World, the possibility of virus importation to polio-free areas in India remains. In view of these risks, the IEAG recommended that while intensive efforts should continue to stop transmission in areas with recent WPV transmission and the traditionally endemic areas of UP and Bihar, the program in India should: a. make efforts to protect polio-free areas from importation of virus from within or outside India b. rapidly respond to any WPV detected anywhere in India during 2011 with an aggressive mop-up vaccination campaign to stop any further circulation of the virus. The IEAG recommended that “From now, any WPV from any source should be considered a public health emergency and responded to with urgent mop-ups; government & partners must deploy additional, highly experienced human resources to ensure that mop-up rounds are of the highest quality. Mop-ups should target both the area of detection of the virus in a case or in the environment and, if there is a clear genetic link, the area of origin of the virus”. Thus any isolation of WPV requires a rapid high quality mopping-up response as an utmost priority to stop circulation and spread. This document is a strategic plan for protecting the polio-free areas of India from WPV and for implementing high quality mopping-up operations with the aim of stopping the final chains of WPV transmission. The Government of India will have a “Central Emergency Preparedness and Response Group” to ensure adequate preparedness for a rapid response and manage the actual response to the detection of a wild poliovirus anywhere in India during 2011. The group will be chaired by the Joint Secretary, Health & Family Welfare, Government of India, and comprise of senior officials from the Ministry of Health and Family Welfare (GoI), and representatives of National Polio Surveillance Project (NPSP) – WHO, UNICEF and Rotary. The key responsibilities of the group will include: lIdentify and train Rapid Response Team (RRT) members at the national level. The RRT members will include experienced, government and partner agency staff from the fields of epidemiology, public health, management and communication (including a media specialist). lFollow up with state governments to ensure that a Rapid Response Team, headed by an officer of the rank of a Principal Secretary, is constituted in each state. The state RRT should include at least 2 to 4 well performing Medical Officers from within the state who have at least 2. Immediate actions - Preparedness for virus importation and response 2.1 National-level Actions
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    7 6M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 5 years' experience in dealing with senior district level officials and a familiarity with the basic principles of mass vaccination campaign implementation. The RRT members will be trained by MoHFW, GoI with assistance from WHO NPSP and UNICEF. In the event of WPV detection, it will be necessary to assign the RRT members full time duty by the state governments to provide support to mop up vaccination campaigns. lDevelop a media response plan to be used in the event of detection of WPV. lReview the availability of buffer stocks of oral polio vaccines to manage mop-up vaccination campaigns. Summary of the national actions with the proposed time frame: lConstitute the “Central Emergency Preparedness and Response Group” by mid- April 2011. lWrite to state governments and partners, in the second week of April 2011, for identification of RRT members in each state by the end of April 2011. lOrganize a training of the RRT members jointly with NPSP and UNICEF by the second week of May 2011. lMonitor the identification and training status of the RRT members. lProcure sufficient buffer stocks of bOPV, tOPV and mOPVs to manage the mop-ups. lDevelop a media response plan by end of April 2011 that includes mechanisms of harmonizing messages from union and state governments to the detection of any polio cases. The following states have been identified at a high or medium risk of importation based on past epidemiology of polio: Haryana, Delhi, Uttarakhand, Maharashtra, Punjab, Rajasthan, West Bengal, Gujarat, Jharkhand, Madhya Pradesh, Assam, Orissa, Andhra Pradesh, Himachal Pradesh, Jammu & Kashmir and 2.2 State level 2.2.1 States at risk of importation Karnataka. Endemic states States at high & medium risk of importation States at low risk of importation lHigh Risk of Importation: 8 or more importations and 5 years or more with importations lMedium Risk of Importation: 5 or more importations and 3 to 4 years with importations Risk Categorization of States based on history of polio importations during last fiveyears
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    ................................ 7 7 AN N E X U R E S 2.2.2 State Level Actions Each state at high or medium risk should undertake the following actions to prepare for the emergency response: lConstitute a State Emergency Preparedness and Response Group chaired by the Secretary (Health & Family Welfare) and comprised of senior officials from the State Government such as the Director Health Services, State EPI Officer and other nominated senior government officials. State representatives of WHO- NPSP, UNICEF and Rotary International should also be a part of the group. This group should monitor the preparedness and implementation of the mop-up. lUndertake a risk analysis, in coordination with WHO- NPSP officials, to identify districts, blocks or urban areas at high risk of importation and spread of poliovirus. This analysis should identify areas that have had repeated importations of polio viruses during previous years or a recent clustering of polio compatible cases in time and space, or are hard-to-reach areas or have demographic/ environmental factors that would facilitate the spread of wild polio virus following an introduction (such as high population density, poor sanitation). Special focus should be on the identification of areas with low routine immunization coverage and areas with migratory or mobile populations in each state as per guidelines issued by GOI in 2010. This risk analysis should be completed at the earliest by each state and the lists of all high-risk areas and populations shared with GOI. lUndertake a communication risk analysis in coordination with UNICEF/ WHO- NPSP and based on the analysis develop a communication plan for issues related to n o n - c o m p l i a n c e / r e s i s t a n c e t o administration of polio vaccines. lDevelop a media response plan to be used in case a virus is detected. lDevelop and implement a plan to increase polio SIA coverage and RI coverage in these high-risk areas/ populations to achieve high immunity against polioviruses in these areas, which in turn will prevent spread and establishment of circulation of any imported wild polioviruses. These areas should be targeted for better planning, training, social mobilization and monitoring efforts during the SIAs in 2011–12. The states should also begin the process of harmonizing the polio microplans with Routine Immunization plans in the high-risk areas. lIdentify and nominate two to four experienced medical officers to be a part of the Rapid Response Teams (RRTs). lReview the surveillance quality in these areas with the district and block officials in coordination with NPSP officials to identify actions to strengthen surveillance sensitivity in these areas, which in turn will assist with early detection and response following any importation. lAssign senior state government officials to visit high risk districts and blocks to review progress in updating and implementing microplans for improving immunization coverage and surveillance sensitivity. Summary of the state actions with the proposed time frame: lConstitute a State Emergency Preparedness and Response group by end of April 2011. lIdentify RRT members by end of April 2011. lIdentify high-risk districts and high-risk are as within districts by mid-May 2011. lIdentify and assign senior officials to high-risk districts by third week of May 2011. lThe above items should be reported back to the Central Emergency Preparedness and Response Group by the end of May 2011.
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    7 8M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 3. Response and actions following the detection of wild poliovirus 3.1 Key steps in the planning phase of the mopping up vaccination campaign 3.1.1 National-Level Actions: lThe Ministry of Health and Family Welfare will be informed about the detection of the virus without delay. lThe Ministry of Health and Family Welfare will inform the Chief Secretary of the affected state of the detection of the polio case in the state. lThe Central Emergency Preparedness and Response Group will meet within 24 hours of receiving the information. The Group will review and analyze, in detail, the field epidemiological investigation findings pertaining to the polio case. Based on the above findings, the areas and populations at risk of poliovirus circulation will be identified and a SIA response within the broad strategic framework recommended by the IEAG will be decided. The group will make specific recommendations on: §Timing of the response §Areas to be covered during the response §Type of vaccine to be used during the response §Number of proposed rounds §Additional investigations and analyses to be conducted lMembers from the Central Emergency Preparedness and Response Group will visit the concerned state to meet the state health secretary and other state officials. The members of the National and State Emergency Preparedness and Response groups will subsequently visit the concerned districts accompanied by the state RRT members to review planning for an emergency response. lThe Central Emergency Preparedness and Response Group will meet on a weekly basis to review the planning and implementation o f t h e r e s p o n s e a n d p r o v i d e recommendations to the immunization division and state authorities to make improvements. lVaccine will be mobilized to reach the state or districts undertaking the mop-up at least three days before the start of the campaign. lMoHFW shall seek support from other government departments such as Social Welfare, Railways, Panchayati Raj, Urban Development, Education, for the emergency mop-up operation. lThe State Emergency Preparedness and Response Group should be activated within 24 hours of receipt of information to initiative the following actions: §Inform the Divisional Commissioners and the District Magistrates of the areas undertaking the mop-up within 24 hours of receipt of information. §Allocate geographical areas and operational responsibilities to all RRT members ensuring an appropriate distribution of human resource within 72 hours of receipt of information. §Assign senior state officials to the districts and members of the State Emergency Preparedness and Response Group to visit and mobilize the districts within 72 hours of confirmation of case. lThe currently existing State-level Steering/Coordination Committee for polio eradication should be requested to organize a meeting within five days of case confirmation to seek support and coordinate activities with other government departments and NGOs. lDistrict-level officials from health and administration should begin mobilizing block officials to start preparations within 48 hours of identify the importation. 3.1.2 State level Actions: 3.1.3 District-level Actions:
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    ................................ 7 9 AN N E X U R E S lDistrict Task Force (DTF) meetings should be organized in the district with RRT members, NPSP, UNICEF staff and key government officials to allocate specific responsibilities within the district and ensure participation of all sectors for a successful implementation of the mop-up. The first DTF to be conducted within five days of confirmation of the case. Subsequently there should be a weekly DTF to take stock of the situation and address requirements of the response activities. lDivisional Commissioners should review the preparedness through participation in DTFs and field visits. lTehsil or Block Task force meetings should be organized at sub-district level in all urban and rural areas within sevendays of the confirmation of the case. lAll existing micro plans should be reviewed as per operational guide for mop-up with special emphasis to ensure no areas are missed and there is high coverage of high risk areas and migratory populations. All micro plans should be reviewed and modified within 10 days of confirmation of the case. lAll vaccinators should be retrained on operational and IPC skills in the week before the start of the mop-up. lThe district and block in consultation with UNICEF and other social mobilization partners should plan and initiate IEC and social mobilization measures based on solid data collected through standardized data tools. lDevelop a media response plan to be used in case a virus is detected. lIn consultation with the government, NPSP should develop a monitoring plan for intensive monitoring and mid course corrections during the activity. Additional independent monitors should be deployed by NPSP in addition to the existing NPSP and UNICEF staff present in the district. 3.2 Key actions during the mopping up vaccination campaign 3.2.1 National-level Actions 3.2.2 State-level Actions 3.2.3 District/ Sub District-level Actions: lMembers from the Central Emergency Preparedness and Response Group will monitor the activity in the highest risk blocks. lThe Central Emergency Preparedness and Response Group will meet to review the feedback from its members, states, RRTs and provide directions for corrective actions. lMembers of the State Emergency Preparedness and Response Group and the State monitors should visit high risk blocks to monitor the activity and provide feedback to the State Principal Secretary (H & FW) lThe State Emergency Preparedness and Response Group should meet daily to review feedback from the districts and plan corrections. lThe district should implement the SIA activity under the direction of the District Magistrate (DM) and supervision of the Chief Medical Officer/Civil Surgeon. The DMs should report on the quality of the activity to the State Principal Secretary (H & FW). lDaily monitoring and review of activity to plan for corrective actions over subsequent days §Senior district-level officials from health and administration (Divisional Commissioner/ D M / A D M / C M O / D P O / D y CMO/BDOs) should monitor the implementation of the activity and attend evening meetings at the high risk blocks. §A daily evening review meeting should be organized at the district under the chairmanship of the District Magistrate.
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    8 0M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 4. Key actions at the end of the activity 5. Role of partners 6. States at low risk of importation of poliovirus lThe District Magistrate should send a report of the completed activity to the State Emergency Preparedness and Response Group for review and corrective actions. lThe State Emergency Preparedness and Response Group should meet to review this and forward the report to the Central Emergency Preparedness and Response Group. lThe Central Emergency Preparedness and Response Group will review the activity and inform the Union Minister who, at his discretion, will inform the Chief Minister of the concerned state about the quality of response activities and ongoing risk assessment. Partners should participate in the Central and State Emergency Preparedness and Response Groups. The key role of the partners will be as follows: lNPSP: Provide surveillance data, epidemiologic analysis and strategic planning and other technical support to the group as well as support monitoring of the preparedness and response at the district, state and national levels. lUNICEF: Provide support to the communication/ social mobilization and media strategies and their implementation and monitor their impact lRotary International:Provide support to the advocacy at the state and district levels and to the communication strategy and social mobilization activities lUndertake a risk analysis, in coordination with WHO-NPSP officials, to identify districts, blocks, and urban areas at higher risk of importation and spread of poliovirus. This analysis should include identification of areas that have had importations of polio viruses during previous years or a recent clustering of compatibles in time and space, or are hard-to-reach areas or have demographic or environmental factors that would facilitate the spread of wild poliovirus following an introduction (such as low routine immunization coverage, high population density, migrant sites, poor sanitation). Special focus should be on the identification of areas with migratory or mobile populations in each state as per guidelines issued by GOI in 2010. This risk analysis should be completed at the earliest and the lists of all high risk areas and populations shared by each state with GOI. lThe state should assign Senior State Government officials to visit high risk districts and blocks to review progress in updating and implementing micro plans prior to the 2011 NIDs for improving immunization coverage and surveillance sensitivity. The basic aim of the mop-up would be to vaccinate all under-5 children in the mop-up area. Each household in the mop-up area will be visited by vaccination teams to vaccinate all under-5 children. The duration of the house-to-house (h-t-h) search and vaccination would be decided by the number of available vaccination teams in the area. In principle, there would be a minimum of 2 to 5-day h-t-h activity in all areas to ensure a rational workload for each vaccination team. Additional 1 to 2 days of h-t-h activity will be undertaken in special areas with lesser number of available teams e.g. in large urban areas. B team activity will continue in UP and Bihar. Transit teams and mobile teams will be deployed to cover migrant and mobile populations. In areas that have used booths during the SNID/NID, booths will also be setup on day 1 of the mop-up campaign because of their IEC/SM value. 7. Strategy for mop-ups
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    ................................ 8 1 AN N E X U R E S The mop-ups shall be implemented as per the Operational Guide for SIAs published by Government of India in 2006. The following guidelines as recommended by the WHA andIEAG should be followed: lSpeed of response: As early as possible but no later than two weeks from confirmation of the case. lExtent of mop-ups: The response should consist of at least three large scale, house-to-house rounds of immunization. The World Health Assembly Resolution (59.1) calls for coverage of 2 to 5 million children in each round. Mop-ups should cover at a minimum the infected district and all districts contiguous with it, across state boundaries if necessary. Where there is a clear genetic link of the virus to the strains in another area, the area of origin should also be included. In the demographic context of India and considering that this is the final 7.1 General principles for mopping-up operations stage of polio eradication, the 18th IEAG has recommended the appropriate target population for mop-ups around 5 million children per round. o In high risk areas: SNID rounds may constitute one or more of the three rounds, but in principle at least one additional round should be carried out in an appropriate area using a short interval approach – all rounds must be of the highest possible quality! o In non-high risk areas: Mop-ups should consist of a minimum of three high quality rounds, using a short interval approach (minimum interval of two weeks but within four weeks) – all rounds must be of the highest possiblequality! lVaccine of choice for mop-ups is mOPV appropriate to the local epidemiology or bOPV; a rolling stockpile of 30 million doses of bOPV and 10 million doses of mOPV1 should be maintained to allow for rapid implementation of mopping up vaccination with the appropriate vaccine.
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    ................................ 8 3 Costingand Financial Sustainability of the Universal Immunization Program 7
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    ................................ 8 5 1. Introduction Indiais at an important time in the development of its Universal Immunization Program (UIP). It is planning several improvements such as the addition of many new and underutilized vaccines as well as adding new staff at different administrative levels. India will need to secure other sources of financing as it will probably be graduating from GAVI support since its high Gross National 1 Income (GNI) per capita will make it ineligible for support. As a result, information on the costs and sources of financing for the UIP will be particularly important for policy-makers to make informed decisions on phasing-in strategies and timing of these Program improvements. The report on costing and financial sustainability of the India Immunization Program was developed during the period June to December 2013, under the auspices of the Immunization Technical Support Unit (ITSU) in India and assisted by the immunization partners, WHO and UNICEF. The team that collected and analyzed the data was led by a research scientist from the Public Health Foundation of India and consisted of Government of India officials, and experts from the Immunization Technical Support Unit (ITSU-MoHFW) and the immunization partners. Data was collected from June to September 2013. Then meetings were held with ministry officials to go over the preliminary findings and assumptions to be made in the analysis. Finally, from September to December 2013 the data was analyzed and put into a report. The main findings of the cost analysis are the following: lTotal baseline expenditure was INR 3,446 2 crore ($718 million), including shared 3 personnel costs, and INR 2,131 crore ($444 million) without shared costs. o Expenditure on the routine Program was INR 1,253 crore ($261 million) and, on the supplemental immunization activities (SIAs), was INR 878 crore ($182 million). l 2. Summary of Findings on Baseline Expenditures Table 1 shows total baseline expenditures with shared costs and selected indicators on cost per output and Program financing. 1 Countries' GAVI eligibility for the year 2014 is GNI per capita lower or equal to $1,570. 2 1 crore= ten million (10,000,000) 3 Shared costs include the value of inputs that are not specific to immunization and which are used by different Programs or activities in the health sector — i.e. their utilization for immunization is less than 100%. Table 1. Baseline Expenditures and Selected Indicators, 2012. Total Expenditures (USD) 261,089,884 182,995,523 444,085,407 273,942,919 718,028,326 0.2 14 90 1 2 0.03 Total Expenditures (INR) 12,532,314,431 8,783,785,120 21,316,099,550 13,149,260,100 34,465,359,650 9.6 672 90 1 2 0.03 Baseline Indicators Routine Immunization only Campaigns Total immunization specific expenditure (A) Total shared cost (B) Grand Total (A + B) Per capita Per DTP3 child Percentage national funding Percentage total health expenditures Percentage govt. health expenditures Percentage GDP C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
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    8 6M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 3. Details of Baseline Program Cost and Financing The year 2012 is the baseline for the cost and financing projections since it has the most recent complete information. The actual expenses of the government and the immunization partners were taken into account for the baseline cost calculation. Table 2 shows the baseline cost profile. In 2012, the total estimated cost of the UIP was INR 3,446 crore ($718 million), including shared cost. Shared personnel cost (those who spent less than 100 percent of their time for immunization) contributed the maximum in total expenditure (38 percent) while all routine recurrent cost contributed 36 percent. The contribution of SIAs was 25 percent in total cost. The detailed expenditure on shared personnel cost is provided in Table 3. Vaccines and injection supplies under routine recurrent cost are those used for Routine Immunization only. The amount spent on vaccines and injection supplies for supplementary immunization has been provided under SIAs. Personnel cost includes salaries and benefits for all who spent 100 percent of their time for immunization starting from the national level. Transport cost included the operational cost of Teeka Express, vaccine handling cost at GMSD and the petrol, oil, lubricant for vaccine transport. It was assumed that there were a total of 700 vaccine vans (250 4WD and 450 2WD) and 120 Teeka Express in 2012. Training cost included the actual expenditure of the government on training as well as the training expenses by immunization partners. The components and detailed expenditures under social mobilization, Program management and other routine recurrent cost are shown in Tables 4, 5 and 6 respectively.
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    ................................ 8 7 Table 2.Baseline Universal Immunization Program Costs, 2012 Routine Recurrent Costs Vaccines Injection Supplies Personnel Transport Cold chain maintenance Training Social mobilization, advocacy, communication activities Disease surveillance Program management Other routine recurrent costs Subtotal Capital Costs Cold chain equipment Subtotal Total Routine Costs (without shared costs) Supplemental Immunization Activities (SIAs) Polio Vaccines and Injection supplies Operational costs Total Measles Vaccines and Injection supplies Operational costs Total JE Vaccines and injection supplies Operational costs Total Subtotal SIAs Shared personnel costs GRAND TOTAL 2012 (USD million) 59.92 16.46 11.40 27.09 9.24 5.94 50.23 18.97 9.67 37.91 246.81 14.28 14.28 261.09 95.22 53.00 148.21 15.14 13.11 28.25 4.85 1.68 6.54 183.00 273.94 718.03 2012 (INR crore) 287.60 79.00 54.72 130.02 44.34 28.53 241.10 91.04 46.40 181.96 1,184.71 68.52 68.52 1,253.23 457.04 254.37 711.41 72.69 62.91 135.59 23.30 8.08 31.38 878.38 1,314.93 3,446.54 Percent 8.3 2.3 1.6 3.8 1.3 0.8 7.0 2.6 1.3 5.3 34.4 2.0 2.0 36.4 13.2 7.4 20.6 2.1 1.8 3.9 0.7 0.2 0.9 25.5 38.1 100.0 C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
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    8 8M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Numbers in 2012* 4,833 4,833 24,049 207,578 14,648 16,109 24,049 296,099 Percentage of time spent on immunization 10 5 10 33 33 33 5 Shared personnel MO (in charge) at block level Data entry operators at block level MO (in charge) at PHC level ANM MPW LHV Data entry operators at PHC level Total Table 3: Details of shared personnel cost in 2012 Salary per month (INR) 35,000 8,000 35,000 12,500 12,500 12,500 8,000 INR (crore) 20.30 2.32 101.01 1027.51 72.51 79.74 11.54 1,314.93 USD (million) 4.23 0.48 21.04 214.06 15.11 16.61 2.40 273.94 Table 4: Details of expenditure on social mobilization, advocacy and communication activities in 2012 Cost components ASHA incentives for social mobilizations Printed materials (banners, posters, IEC materials) BCC tool Advocacy and communication (UNICEF) SMNet (UNICEF) Total INR Crore 194.62 24.98 5.73 15.77 241.10 USD million 40.55 5.20 1.19 3.29 50.23 Table 5: Details of Program management expenditure in 2012 Cost components Evaluations, program reviews and assessment meetings Office supplies and consumables Micro planning Immunization Technical Support Unit (ITSU) Operational cost of polio and other VPDs (UNICEF) Operational cost of polio and other VPDs (WHO) Total INR Crore 10.97 0.31 2.17 4.77 9.36 18.83 46.40 USD million 2.29 0.06 0.45 0.99 1.95 3.92 9.67 * Source: Rural Health Statistics in India, 2012.
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    ................................ 8 9 Table 6:Details of expenditure for other activities under routine immunization in 2012 Cost components Cost components Service provision in underserved and hard to reach areas (including slums) ASHA Incentives Planning, supportive supervision and monitoring Intensification of Routine Immunization (WHO) Research studies (Govt. + WHO) Measles, JE control Program (UNICEF) Other state-specific activities Total INR Crore INR Crore 18.39 132.29 6.56 0.41 4.05 1.92 18.35 181.96 USD million USD million 3.83 27.56 1.37 0.09 0.84 0.40 3.82 37.91 Figure 1. Baseline Cost Profile (without shared costs), 2012 6% 15% 23% 4% 6% 4% 4% 7% 10% 19% Vaccines (routine vaccines only) Injection supplies Personnel Transporation Cold chain maintenance Training Social mobilization, advocacy and communication activites Disease surveillance Program management Other routine recurrent costs Cold chain equipment (capital cost) C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
  • 105.
    90% 4% 3% 3% Govt. WHO UNICEF GAVI 9 0MU L T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Figure 2. Baseline Financing, Indian Immunization Program, 2012 Figure 2 shows the sources of financing in the baseline year for the UIP. The Government of India paid for most of the Program expenditures (90 percent). Other sources of financing were WHO (4 percent), UNICEF (3 4 percent), and GAVI (3 percent). 4. Recurrent Costs - Structure and Analysis 4.1 Demographic projections The calculation of the birth cohort and other target groups is based on Indian government estimates and on the latest census of India (Table 7). The population growth rate is 1 percent and the infant mortality rate is assumed to decrease from 44 per 1000 in 2012 to 25 per 1000 in 2017. Demographic Variable Birth Cohort Population Growth Rate Infant Mortality Rate Childbearing age women 2012 24,676,883 1% 44 15% 2017 26,323,130 1% 25 15% Table 7. Key Demographic Variables for India, 2012 and 2017 4 WHO and UNICEF are implementing partners and their activities are funded by BMGF, GAVI and other external partners.
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    ................................ 9 1 4.2 Vaccineand injection supplies The vaccine prices used for the baseline and projections are shown in Table 8. The costs are a mixture of GAVI prices as well as prices obtainable by the government of India. India is unique since it has many local manufacturers from which it can purchase vaccines for the national Program. Vaccines BCG Hep B (birth dose) OPV Measles DTP TT JE DTP-Hib-HepB (penta) IPV MR Rotavirus Pneumococcal Implementation strategy Routine Routine Routine Routine Routine Routine Campaign Roll out to all states 2014 - 11 states 2015 - 16 states Pan India Pending NTAGI endorsement. Start with campaign (1-15 yr olds) in 2014. 2015 onwards under routine at 9 months or 1.5 years old. Pending NTAGI Pending NTAGI Sources of financing Govt. Govt. Govt. Govt. Govt. Govt. Govt. GAVI up to 2015 Govt. Govt. Govt. Govt. Table 8. Prices per Dose and Expected start year, and Implementation Strategy for Vaccines Expected start year NA NA NA NA NA NA NA 2014-15 2015-16 2014-15 2016-17 2017 Price per dose USD 0.05 USD 0.05 USD 0.06 USD 0.16 USD 0.04 USD 0.02 USD 0.18 USD 2.11 USD 1.00 USD 0.50* USD 1.00 (Bharat) USD 3.30** Sources: *MR: http://www.gavialliance.org/library/news/press-releases/2013/over-700- million-children-in-49-countries-to-be-protected-against-measles-and-rubella/ **Pneumococcal: http://www.pfizer.com/news/press-release/press-release-detail/pfizer signs new agreement with unicef to supply a total of up to 740 million doses of prevenar 13 for the world's poorest countries through 2025 C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
  • 107.
    9 2M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Figure 3 and Table 9 show projected resource requirements for vaccines from 2013 until 2017. The vaccine wastage rates are given in Annex Table A.1. During the first four years, the resource requirements are highest for pentavalent vaccine as it is scaled up in the country. However, by 2017, the larger share of resource requirements will shift to PCV vaccine if the vaccine is introduced nationwide in 2017. Introduction of IPV and MR in 2015 will increase vaccine resource requirements from INR 633 crore in 2014 to INR 1,455 crore in 2015 (Table 9). Adding rotavirus vaccine in 2016 will increase resource requirements for vaccines by INR 315 crore while introducing PCV vaccine in 2017 will double the requirements for vaccines. It should be noted, though, that the estimate of resource requirements in 2017 is probably an over- estimate since it assumes that PCV will be introduced nationwide although the vaccine will probably be phased-in over time. Another factor that will affect the impact of the total resource requirements for India is that it will likely be graduating from GAVI support during the period of the cMYP. Thus, it will have to secure a larger proportion of funding for new vaccines as well as for pentavalent. Figure 3. Resource requirements for Vaccines, Routine Immunization, 2013–2017 INRCrore 4000 3500 3000 2500 2000 1500 1000 500 0 2013 2014 2015 2016 2017 PCV Rotavirus MR IPV TT JE Measles Pentavalent Help B (primary schedule) DTP3 OPV3 Hep B (Birth dose) BCG
  • 108.
    ................................ 9 3 Table 9also shows pentavalent vaccine will be gradually scaled-up until it is provided nationwide in 2015. As pentavalent vaccine is scaled-up, DTP and Hepatitis B (primary schedule) vaccines will be phased out while the birth dose of Hepatitis B vaccine will continue. Resource requirements for pentavalent vaccine are projected to decrease in 2016 as the price per dose is assumed to decline from $2.11 to $1.54. Annex Table A.2 provides the resource requirements for vaccines in USD. Table 10 shows the resource requirements for vaccines for SIAs by antigen and year in INR crore (see Annex Table A.3 for US$). Polio SIAs are assumed to take place every year while measles (monovalent) SIAs end in 2013. Starting in 2015, as part of the commitments to reach the target of measles elimination in the region by 2020, UIP will introduce the measles- rubella vaccine through SIAs phased between 2015 and 2016. As JE campaign will depend on the epidemiological situation, we couldn't project any cost for the same. 2015 15.9 7.1 35.6 858.1 8.0 59.6 6.7 31.1 7.5 230.3 195.1 NA NA 1,455.1 2016 16.1 8.2 37.7 807.4 NA 64.2 7.1 31.7 NA 203.1 184.0 410.4 NA 1,769.9 2014 15.9 6.1 33.8 459.9 12.7 54.2 6.6 30.5 13.2 NA NA NA NA 632.8 2013 14.9 6.5 37.4 312.7 21.0 53.4 7.6 37.4 19.7 NA NA NA NA 510.6 Table 9. Vaccine Resource Requirements for Routine Immunization by Type and Year, INR Crore, 2013–2017 2017 16.3 9.3 40.7 773.8 NA 68.8 7.1 32.2 NA 203.4 223.0 474.0 1738.8 3,587.1 Vaccines BCG Hep B (Birth dose) OPV DTP-HepB-Hib (pentavalent) DTP Measles TT JE Hep B (primary schedule) IPV MR Rotavirus PCV Total 2015 279.2 NA 704.1 983.2 2016 242.4 NA 704.1 946.5 2014 279.2 NA NA 279.2 2013 315.4 39.7 NA 355.2 2017 242.4 NA NA 242.4 Vaccines OPV Measles MR Total Table 10. Vaccine Resource Requirements for Supplementary Immunization Activities by Type and Year, INR crore, 2013-2017 C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
  • 109.
    9 4M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 4.3 Personnel Costs Resource requirements for health care staff are projected based on assumptions about salary ranges, the percentage of time spent on immunization, increase in number of staff per year and annual increases in salary levels. The assumptions on staffing are shown in annex Tables A.4 to A.6. The assumptions about the need for new staffing are based on the findings and recommendations of the 2011 HR Needs Assessment Study (GoI 2011). The study found inadequacies in staffing for the UIP at the national and state levels. Thus, the estimates include recommended additional staff at MOH level (three deputy commissioners and 12 assistant commissioners) and at state level (two Program officers; one MIS officer; one administrative and finance officers; one data analyst; two cold chain / vaccine handler and vaccine store technicians in each state). At the state level, the estimates also include some new immunization staff such as cold chain/vaccine handler and vaccine store technicians. Apart from full-time staff, there are shared personnel who work for immunization. Figure 4 shows that resource requirements on shared personnel are much higher than those of full- time staff and are increasing due to annual salary increments and additions to the number of total staff. The amount spent on full-time personnel will increase from INR 55 crore in 2012 to INR 101 crore in 2017 if all new staff are hired as per assumptions given in annex tables. On the other hand, the shared personnel cost will increase from INR 1,315 crore in 2012 to INR 2,509 crore in 2017 (Tables 2 and 11). Figure 4. Personnel Costs, 2012-2017, INR Crore INRCrore 2012 2013 2014 2015 2016 2017 3000 2000 1000 0 Baseline Full time personnel Shared personnel 4.4 Training, Program Management, Disease Surveillance, Social Mobilization, Advocacy and Communication Training: The government is the main source of funding for trainings (Figure 5). However, the immunization partners such as WHO and UNICEF also implement some training programs on immunization. The amount spent by the government on training will increase from INR 21 crore in 2012 to INR 42 crore in 2017. The resource requirements are projected to double by 2017 because of the increased need for trainings due to recruitment of health workers, new vaccine introduction and planned SIAs.
  • 110.
    ................................ 9 5 Program management:Expenditure under this category includes evaluations and meeting related expenses, micro planning, office supplies and consumables, operational cost of immunization technical support unit (ITSU) and operational cost of different vaccine preventable diseases. Much of the Program management is supported through the ITSU. The Ministry of Health and Family Welfare (MoHFW) and the Public Health Foundation of India (PHFI) established ITSU in April 2012 with support from the Bill & Melinda Gates Foundation (BMGF). The primary mandate of ITSU has been to strengthen human resource capacity for the UIP and to provide technical and managerial support to MoHFW for revitalizing, and successfully implementing India's UIP. ITSU is currently focusing its efforts towards improving immunization coverage in four states of India: Bihar, Madhya Pradesh, Rajasthan and Uttar Pradesh, which have been identified as high priority states with low immunization coverage. Figure 6 shows the baseline costs for Program management in 2012 as well as the projected resource requirements for 2013-2017. The projected resource requirements for Program management increase rapidly from 2013-2016 due to increased funding under GAVI HSS. The GAVI HSS grant which has been channeled to UNDP from 2013-14 is projected to be taken over by the government in 2017. This will result an increase in government spending on Program management from INR 12 crore in 2012 to INR 183 crore in 2017. Figure 5. Training Costs, 2012-2017, INR Crore 60 50 40 30 20 10 0 Baseline 2012 2013 2014 2015 2016 2017 Govt. WHO UNICEF INRCrore Figure 6. Program Management Costs, 2012–2017, INR Crore Baseline INRCrore 3000 250 200 150 100 50 0 2012 2013 2014 2015 2016 2017 GAVI HSS BMGF UNICEF WHO Govt. C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
  • 111.
    9 6M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Disease Surveillance: WHO is the implementer of the disease surveillance activities. Resource requirements for disease surveillance activities are expected to more than double by 2017, due to introduction of new vaccines. The requirements for surveillance will increase from INR 132 crore in 2013 to INR 259 crore in 2017 and will be fully financed by WHO (2013-2016 as "secure" funding; whereas 2017 is set as "probable" funding). Donor funding in this area will be phasing out and the government will need to increase its investment in disease surveillance. Social Mobilization, Advocacy and Communication Activities: Under this category, we considered ASHA incentives for social mobilization, government expenditure for printing materials such as banners, and posters, and advocacy, communication activities and SMNet cost for UNICEF. The government is the main source of financing for social mobilization activities and is projected to double its spending by 2017 (Figure 7). In 2012, the actual expenditure of the government under this head was INR 220 crore which is projected to be INR 451 crore in 2017. Figure 7. Social Mobilization, Advocacy and Communication Activities Costs, 2012-2017, INR Crore Baseline INRCrore 600 500 400 300 200 100 0 2012 2013 2014 2015 2016 2017 Govt. UNICEF Other Routine Recurrent Cost: We considered service provision in underserved / hard-to- reach areas (including slums), ASHA incentives for complete immunization, planning, supportive supervision and monitoring activities, intensification of routine immunization, research related expenses and different state specific activities under this category. The government is the main source of funding for these activities while WHO and UNICEF also support some of these (Figure 8). Government expenditure under this category will increase from INR 173 crore in 2012 to INR 270 crore in 2017.
  • 112.
    ................................ 9 7 4.5 ColdChain The cold chain related projections are based on the current assessment of cold chain situation in India and future needs. The assumptions are shown in Annex Table A.7. It should be noted that the number of existing cold chain equipment includes both the government purchases as well as those purchased through partner support (UNICEF). It should also be noted that KFW is providing 180 crore for cold chain equipment in 2014-15. We present the cold chain maintenance related expenditure in Figure 9. Government finances the most for cold chain maintenance and the requirement increases from INR 39 crore in 2012 to INR 218 crore if all assumptions related to cold chain requirement in India are fulfilled. Figure 8: Other Routine Recurrent Costs, 2012-2017, INR Crore Baseline INRCrore 350 300 250 200 150 100 50 0 2012 2013 2014 2015 2016 2017 Govt. WHO UNICEF Figure 9: Cold Chain Maintenance Costs, 2012-2017, INR Crore Baseline INRCrore 250 200 150 100 50 0 2012 2013 2014 2015 2016 2017 Govt. UNICEF C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m
  • 113.
    9 8M UL T I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 5.0. Future Resource Requirements Table 11 and Figure 10 show the future resource requirements for the routine immunization Program by Program components. Total requirement for the five-year period is INR 34,336 crore ($5,282 million). Resource requirements for vaccines increase rapidly from INR 510 crore in 2013 to INR 3,587 crore in 2017 as new vaccines are assumed to be introduced in the Program. The amount in USD is presented in Annex Table A.8. Cost Category Vaccines (routine vaccines only) Injection supplies Personnel Transportation Cold chain and other capital equipment maintenance Training Social mobilization / advocacy / communication activities Disease surveillance Program management Other routine recurrent costs Cold chain equipment Supplemental Immunization Activities Shared personnel costs Total 2013 510.6 71.8 78.7 203.4 116.3 30.8 284.1 132.9 94.1 219.3 131.4 789.6 1,907.1 4,570.0 Table 11. Resource Requirements for India National Immunization Program, INR crore, 2013-2017 2014 632.8 72.3 84.7 234.9 149.4 36.5 373.8 161.4 225.5 248.4 198.2 740.6 2,042.5 5,201.0 2015 1,455.1 89.7 89.9 271.3 175.9 41.5 421.3 186.4 215.4 266.3 269.2 1,520.7 2,187.5 7,190.2 2016 1,769.9 84.7 95.5 313.3 207.0 47.4 467.9 215.3 231.7 282.0 343.6 1,522.6 2,342.8 7,923.9 2017 3,587.1 102.9 101.4 361.9 220.9 54.1 483.1 248.7 248.5 300.2 419.7 813.5 2,509.1 9,451.0 Total 7,955.5 421.4 450.2 1,384.8 869.4 210.3 2,030.3 944.7 1,015.2 1,316.3 1,362.1 5,386.9 10,989.0 34,336.1
  • 114.
    ................................ 9 9 6.0. FutureFinancing and funding gap analysis Figure 11 shows the future secure financing and gaps in financing for 2013-2017. This figure does not include other financing that is 5 probable. The largest source of financing for UIP is the government. The financing gap increases from INR 56 crore in 2013 to 815 crore in 2015 and further to INR 3,537 crore in 2017 and reflects the fact that funding has not yet been secured for the new vaccines to be introduced during those years. Figure 10. Total Resource Requirements for UIP, 2013-2017, INR CroreINRCrore 10000 9000 8000 7000 6000 5000 4000 3000 2000 1000 0 2013 2014 2015 2016 2017 Shared personnel costs Supplemental Immunization Activities Cold chain equipment Other routine recurrent costs Program managememt Disease surveillance Social mobilization / advocacy / communication activities Training Cold chain and other capital equipment maintenance Personnel Injection supplies Vaccines (routine vaccines only) Transportation 5 cMYP costing & financing tool has two categories of funding: 1.Secure funding refers to projected future financing available in the short term, that is considered assured; 2.Probable funding refers to all other funding that is not assured but is likely to be made available in the short and medium term. C o s t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m Figure 11. Future Secure Financing and Funding Gaps, 2013-2017, INR Crore INRCrore 10000 8000 6000 4000 2000 0 2013 2014 2015 2016 2017 Funding Gap GAVI HSS BMGF (ITSU) GAVI UNICEF WHO Govt.
  • 115.
    100M U LT I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Figure 12 shows the Program financing with probable as well as secure funding. In this scenario, the government and GAVI will provide financing for the new vaccines. As can be seen, if probable funding is included, funding gap is insignificant. Figure 12. Future Secure and Probable Financing and Funding Gaps, 2013-2017, INR Crore INRCrore 10000 9000 8000 7000 6000 5000 4000 3000 2000 1000 0 2013 2014 2015 2016 2017 Funding gap GAVI HSS BMGF (ITSU) GAVI UNICEF WHO Govt. Conclusion Total UIP cost in 2012 was: • INR 3,446 crore ($718 million), including shared health systems costs • INR 2,131 crore ($444 million) without shared costs. Expenditure on the routine program was INR 1,253 crore ($261 million) and, on the supplemental immunization activities, was INR 878 crore ($182 million). The cost per capita for the Program was INR 9.6 ($0.2) and cost per DTP3 child was INR 672 ($14). The total projected resource requirement for 2013-2017 is INR 34,336 crore ($5,282 million). The resource requirement will increase from INR 4,570 crore in 2013 to INR 9,451 crore in 2017 due to the new vaccine i n t r o d u c t i o n a n d o t h e r P r o g r a m improvements. Supplementary immunization activities are projected to cost INR 5,387 crore ($829 million) during the five-year period. However, it should be noted that the vaccine requirement in 2017 is overestimated as we assumed PCV will be introduced throughout the country in 2017 while probably it will be introduced in a phased manner. Secondly, the total resource requirement is under estimated as we couldn't project anything for JE campaign in coming years as the campaign will depend on the epidemiological situation. The majority of the UIP resource requirement is financed by the Government of India. External partners do, however, provide critical funding support to technical partners such as WHO and UNICEF for training, disease surveillance, IEC/social mobilization. As the total resource requirement increases steadily, the funding gap also increases and in order to fill this gap, the government health budget needs to increase in the coming years. The projected increase of government health expenditure for immunization is from 2.5% in 2013 to 3.3% in 2017. The UIP could improve its financial sustainability by improving Program efficiency through the following: • reviewing immunization expenditure annually; • monitoring Program performance and input productivity; • reducing wastage, and • introducing less resource-intensive means of service delivery. The Program should investigate some potential strategies to improve Program efficiency, particularly since India will be taking over more of the costs of the Program after the funding from GAVI and other donors ends.
  • 116.
    ................................ 101 C os t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m Annexures A.1 Wastage rates Proposed wastage rates for single and ten dose vials are in line with WHO/UNICEF recommendations and others are as per government wastage rate calculations. Vaccine BCG Hep B (birth dose) OPV DTP-Hep B- Hib (Penta) DTP3 Measles MR Hepatitis B IPV JE TT Table A.1. Assumptions on Wastage Rates by Antigen 2013 (percentage) 50 15 25 25 25 25 25 25 30 25 25 2017 (percentage) 10 10 25 10 30 10 Table A.2. Vaccine Resource Requirements for Routine Immunization by Type and Year, US$ millions, 2013-2017 Vaccines BCG Hep B (Birth dose) OPV3 DTP-Hep B-Hib (Pentavalent) DTP Measles TT JE Hep B (primary schedule) IPV MR Rotavirus PCV Total 2013 2.3 1.0 5.8 48.1 3.2 8.2 1.2 5.8 3.0 NA NA NA NA 78.5 2014 2.4 0.9 5.2 70.8 1.9 8.3 1.0 4.7 2.0 NA NA NA NA 97.4 2015 2.4 1.1 5.5 132.0 1.2 9.2 1.0 4.8 1.2 35.4 30.0 N N 223.9 2016 2.5 1.3 5.8 124.2 0.0 9.9 1.1 4.9 NA 31.3 28.3 63.1 NA 272.3 2017 2.5 1.4 6.3 119.0 0.0 10.6 1.1 4.9 NA 31.3 34.3 72.9 267.5 551.9
  • 118.
    ................................ 103 C os t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m Vaccine OPV Measles MR Total Table A.3. Vaccine resource requirements for supplementary immunization activities by type and year, USD (million), 2013-2017 2013 48.5 6.1 NA 54.6 2014 42.9 NA NA 42.9 2015 42.9 NA 108.3 151.2 2016 37.3 NA 108.3 145.6 2017 37.3 NA NA 37.3 Table A.4. Assumptions on health staff on salaries, annual increases in number and salary, and time spent on immunization Salary range Rs. 1,0000 to Rs. 15,000 per month Rs. 35,000 to Rs. 45,000 per month Rs. 40,000 to Rs. 50,000 per month Rs. 30,000 to Rs. 40,000 per month Rs. 8,000 to Rs. 15,000 per month Rs. 12,500 per month 991,200 per annum (Total) Rs. 637,700 per annum (Total) Rs. 50,130 per month Rs. 22,355 per month Rs. 12,496 per month Rs. 75,000 per month Percentage time spent on immunization 33 10 100 100 Based on sessions 5 100 15 staff (100%) (including contract staff) 8 staff (100%) 100 100 100 100 Increase in number per year 2% 2% NA NA 2% increase in sessions per year Salary increase per year 5% 5% 5% 5% 5% 5% 5% 5% 5% 5% 5% 5% Staff category ANM, MPW, LHV Mos SIO / DIO State cold chain officer ASHAs Data entry operators from PHC to block level Cold chain technician At Ministry At Ministry (Partner support) Research consultant Data analyst Admin staff NRHM consultants AEFI related staff (from 2013-14)
  • 120.
    ................................ 105 C os t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m Staff category District vaccine logistics manager Cold chain / vaccine handler Divisional Vaccine logistics manager State HEMR unit with engineers supported by state vaccine store technician WIC/WIF handler in govt. medical store depot (in shift) Refrigerator technician at Govt. medical store depot State vaccine logistics manager Vaccine logistics manager at GMSD Salary range Rs. 15,000 to Rs. 22,000 per month Rs. 15,000 to Rs. 22,000 per month Rs. 35,000 per month Rs. 30,000 per month Rs. 8,000 per month Rs. 12,500 per month Rs. 35,000 per month Rs. 45,000 per month Table A.5. Assumptions on new immunization staff Where posted One in each district Two in each state vaccine store One handles four districts Two in large states - population 40 million and above;one in small states Four in each depot (semi- skilled helper) One in each depot One in each state One each at GMSD Year of recruitment 2014-15 2014-15 2014-15 2014-15 2014-15 2014-15 2014-15 2014-15 Staff category Deputy commissioners at ministry (3) Assistant commissioners at ministry (12) State Program officer (immunization) (2 in each state) State logistics manager (immunization) (1 in each state) State MIS manager (immunization) (1 in each state) Administration and Finance officer (immunization) (1 in each state) State immunization technology and research officer (1 in each state) Quality control and AEFI officer (immunization) (1 in each state) IEC officer (immunization) (1 in each state) Assistant cold chain officer (1 in each state) Store officer (immunization) (1 in each state) Data analyst (1 in each state) Gross salary per month Rs. 200,000 Rs. 150,000 Rs. 35,000 - Rs. 45,000 Rs. 35,000 - Rs. 45,000 Rs. 35,000 - Rs. 45,000 Rs. 35,000 - Rs. 45,000 Rs. 35,000 - Rs. 45,000 Rs. 35,000 - Rs. 45,000 Rs. 35,000 - Rs. 45,000 Rs. 30,000 - Rs. 35,000 Rs. 30,000 - Rs. 35,000 Rs. 15,000 - Rs. 18,000 Table A.6. New proposed staff in Mavalankar report (these positions will be started filling up from 2014 onwards in a phased manner)
  • 121.
    106M U LT I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Number of cold chain points (existing) Cold chain points required Total cold chain points required New cold chain points required Present number of ILR in cold chain points Present number of DF in cold chain points Existing ILR/DF needs replacement New ILR / DF required at cold chain points Cold chain points need solar or hybrid . Existing solar or hybrid Solar or hybrid At GMSD level Present number of WIC at GMSD Present number of WIF at GMSD Required WICs/WIFs 27,000 One cold chain point per 30,000 population (2011 census) 40,340 28,238 27,000 (assuming one in each cold chain point) 27,000 (assuming one in each cold chain point) 50% (27,000) needs immediate replacement - should be replaced within 2-3 years The required number (56,476) will be procured within 3 years 30% of all PHCs will have less than 8 hours electricity; hence need solar or hybrid 50% of these will be hybrid where there is supply for 4-6 hours Solar - 270; Hybrid - 300. The required number (Solar - 5,781; hybrid - 5,751) will be procured in 2-3 years At each GMSD, 8 WIC of 40 cub. Mt; 4 WIF to accommodate rotavirus / IPV vaccine 8 6 Required number at GMSD level (22 WICs / 10 WIFs) will be available in 2 years State report NCCMIS CCO meeting minutes CCO meeting minutes CCO meeting minutes CCO meeting minutes + standard assumptions CCO meeting minutes + standard assumptions Based on NCCMIS of ageing and useful life of 10 years Based on NCCMIS of ageing and useful life of 10 years NCCMIS . State CCO Report NCCMIS National EVM, 2013 National EVM, 2013 National EVM, 2013 National EVM, 2013 Table A.7 Cold chain related assumptions Assumptions Sources
  • 122.
    ................................ 107 C os t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m At state vaccine store level WIC/WIF needs replacement at state vaccine store level At divisional vaccine store level WIC/WIF required replacement at divisional store level At district vaccines stores . WIC/WIF/ILR/DF required replacement at district store level Cold boxes (large and small) at cold chain points Cold boxes need replacement Cold boxes at state / divisional vaccine stores Cold boxes need replacement Cold boxes at district vaccine stores Cold boxes need replacement At each vaccine store, at least 4 WIC and 2 WIF of 40 cu. Mt 50% of the total needs replacement (117 nos.) - should be replaced within 2-3 years At each store, at least 4 WIC of 40 cu. mt and 2 WIF of 20 cu. mt 50% of the total needs replacement (62 nos. each) - to be replaced within 2-3 years District with population more than 20 lakh, one WIC and 6 DFs are required Districts with population less than 20 lakh, 8 large ILR and 4 large DF 231 WICs; 1,386 DFs; 3,272 ILRs and 1,636 large DFs need replacement within 2-3 years Every cold chain points (30,000 population) should have two 20 lit cold boxes; and four 5 lit cold boxes 30% (40,340 large; 80,680 small) needs immediate replacement - should be replaced within 2-3 years for 30000 population, 2 large cold boxes 30% (1,034) needs immediate replacement - should be replaced within 2-3 years Per store, 20 large cold boxes are required 30% (6,400) need immediate replacement - should be replaced within 2-3 years National EVM, 2013 NCCMIS Personal discussion with UNICEF and ministry Personal discussion with UNICEF and ministry Personal discussion with UNICEF and ministry . NCCMIS CCO Meeting minutes NCCMIS Personal discussion with UNICEF and ministry NCCMIS Personal discussion with UNICEF and ministry Personal discussion with UNICEF and ministry Assumptions Sources
  • 123.
    108M U LT I - Y E A R S T R A T E G I C P L A N 2 0 1 3 - 1 7 Cold boxes at GMSD level Cold boxes need replacement Vaccine carrier Carriers replacement Ice packs Ice packs replacement Voltage stabilizer Stabilizer needs replacement Tool kit Total number of technicians / toolkit Toolkit supplied by UNICEF Toolkit to be procured Temperature monitoring device Total number required Spare parts Wireless data logger required UNICEF supply Wireless data logger Assumptions 50 large cold boxes are required at the GMSD level 30% (100) need immediate replacement - should be replaced within 2-3 years Each ANM should have 2 vaccine carriers 20% every 3 years (presently 103,789 need replacement). Should be replaced within 2-3 years Each vaccine carrier should have four ice packs Every 2 years, 50% ice packs should be replaced. (830,312 needs immediate replacement - should be replaced within 2 years) Every ILR/DF will have its own stabilizer 50% (31,385) needs immediate replacement - will be replaced within 2-3 years Each technician will have one toolkit - should be replaced within 3-5 years 427 .200 227 (To be procured within 2 years) Every ILR/DF should have one temperature monitoring device - should be replaced in 5 years 75,615; should be procured within 2-3 years Every year 2 million dollar - presently supplied by UNICEF One each in each WIC / WIF - total required - 743. 54 The required number 689 will be procured in 3 years Sources Personal discussion with UNICEF and ministry Personal discussion with UNICEF and ministry Personal discussion with UNICEF and ministry Personal discussion with UNICEF and ministry Personal discussion with UNICEF and ministry Personal discussion with UNICEF and ministry NCCMIS NCCMIS NCCMIS NCCMIS NCCMIS NCCMIS Personal discussion with UNICEF and ministry Personal discussion with UNICEF and ministry Personal discussion with UNICEF and ministry NCCMIS / NEVM UNICEF Personal discussion with UNICEF and ministry
  • 124.
    ................................ 109 C os t i n g a n d F i n a n c i a l S u s t a i n a b i l i t y o f t h e U n i v e r s a l I m m u n i z a t i o n P r o g r a m Table A.8. Resource requirements for India Universal Immunization Program, USD (millions), 2013–2017 Cost Category Vaccines (routine vaccines only) Injection supplies Personnel Transportation Cold chain and other capital equipment maintenance Training Social mobilization / advocacy / communication activities Disease surveillance Program management Other routine recurrent costs Cold chain equipment Supplemental Immunization Activities Shared personnel costs Total 2013 78.5 11.0 12.1 31.3 17.9 4.7 43.7 20.4 14.5 33.7 20.2 121.5 293.4 703.1 2014 97.4 11.1 13.0 36.1 23.0 5.6 57.5 24.8 34.7 38.2 30.5 113.9 314.2 800.2 2015 223.9 13.8 13.8 41.7 27.1 6.4 64.8 28.7 33.1 41.0 41.4 234.0 336.5 1,106.2 2016 272.3 13.0 14.7 48.2 31.8 7.3 72.0 33.1 35.7 43.4 52.9 234.2 360.4 1,219.1 2017 551.9 15.8 15.6 55.7 34.0 8.3 74.3 38.3 38.2 46.2 64.6 125.1 386.0 1,454.0 Total 1,223.9 64.8 69.3 213.0 133.8 32.3 312.3 145.3 156.2 202.5 209.6 828.8 1,690.6 5,282.5 Other cold chain related assumptions • Price of ILR or DF (large): Rs. 50,000 • Price of ILR or DF (small): Rs. 40,000 • Price of solar: Rs. 200,000 • Price of hybrid: Rs. 13, 00,000 (this is an alternative source of power – supports entire PHC with a load of 2.5 KVA including cold chain equipment) • Price of WIC / WIF of 40 cu. Mt: Rs. 18, 00,000 (including procurement, installation and 5 years CMC) • Price of WIF of 20 cu. Mt: Rs. 15, 00,000 (including procurement, installation and 5 years CMC) • Price of large cold box (20 lit.): Rs. 7,350 • Price of small cold box (5 lit): Rs. 5,000 • Price of vaccine carrier: Rs. 1,000 • Price of ice packs: Rs. 35 • Price of voltage stabilizer: Rs. 5,000 • Price of toolkit: Rs. 115,500 • Price of temperature monitoring device: Rs. 10,100 (including installation) (30 percent reduction of price for bulk purchase) • WIC/WIF wireless data logger: 1 lakh including equipment, installation, internet, AMC, and CMC for 5 years • ILR, DF, WIC and WIF: 10 years • Cold boxes and tool kit: 5 years • Voltage stabilizer and vaccine carrier: 3 years • Ice packs: 2 years The following numbers of buildings need to be built over the cMYP period: • At the district level, 64 percent of the buildings (410 buildings) (Source: National EVM Assessment Report 2013) • At the state level, 75 percent of the buildings (29 buildings) • At the divisional level, 75 percent of the buildings (92 buildings) Building construction costs: • In districts with 20 lakh population: 22–25 lakh • At state and divisional level: 50 lakh Price increase over the years: 10 percent Useful life Building