This document provides an overview of India's Universal Immunization Programme (UIP). It discusses the history and development of immunization programs in India from their inception in 1978 with the Expanded Programme of Immunization up to the current UIP. Key details covered include the vaccines included in national and WHO schedules, program objectives, milestones such as polio elimination, and components of UIP implementation including the cold chain system, monitoring, and strategic communication.
Universal Immunization Programme (UIP), started in India in 1985.
Ministry of Health & Family Welfare provides several vaccines to infants, children & pregnant women through UIP.
Immunization is a process through which a person is made immune to an infectious disease.
On 19 November 1985, GOI renamed EPI program, modifying the schedule as ‘Universal Immunization Program’ dedicated to the memory of Late Prime Minister Mrs Indira Gandhi.
UIP has two vital components: immunization of pregnant women against tetanus, and immunization of children
Polio is a viral disease that destroys the nerve cells present in the spinal cord causing paralysis or muscle weakness to some part of the body.
Pulse Polio Programme was launched in 1995 after a resolution for a global initiative of polio eradication was adopted by World Health Assembly (WHA) in 1988.
Universal Immunization Programme (UIP), started in India in 1985.
Ministry of Health & Family Welfare provides several vaccines to infants, children & pregnant women through UIP.
Immunization is a process through which a person is made immune to an infectious disease.
On 19 November 1985, GOI renamed EPI program, modifying the schedule as ‘Universal Immunization Program’ dedicated to the memory of Late Prime Minister Mrs Indira Gandhi.
UIP has two vital components: immunization of pregnant women against tetanus, and immunization of children
Polio is a viral disease that destroys the nerve cells present in the spinal cord causing paralysis or muscle weakness to some part of the body.
Pulse Polio Programme was launched in 1995 after a resolution for a global initiative of polio eradication was adopted by World Health Assembly (WHA) in 1988.
A decentralized system of disease surveillance for timely and effective public health action with a focus on functional integration of surveillance components of various vertical programmes.
Universal Immunization Program is a vaccination program launched by the Government of India in 1985.
It became a part of Child Survival and Safe Motherhood Program in 1992 and is currently one of the key areas under National Rural Health Mission(NRHM) since 2005.
Program consists of vaccination for 12 diseases -
Tuberculosis
Diphtheria
Pertussis
Tetanus,
Poliomyelitis,
Measles,
Hepatitis B,
Diarrhea,
Japanese-Encephalitis,
Rubella,
Pneumonia
Pneumococcal diseases
Pulse Polio is an immunisation campaign established by the government of India to eliminate poliomyelitis (polio) in India by vaccinating all children under the age of five years against the polio virus.
This ppt contains all the information about Revised NationalTuberculosis Control programme (RNTCP) It is useful for students of the medical field learning Preventive and social medicine, Swasthavritta (Ayurved) and everyone who is interested in in knowing about it.
Pulse Polio is an immunization campaign established by the government of India to eliminate poliomyelitis (polio) in India by vaccinating all children under the age of five years against the polio virus.
The project fights polio through a large-scale , pulse vaccination programme and monitoring for poliomyelitis cases.
Vellore(Tamil Nadu) was the first Indian state to become 100% polio-free through the pulse strategy, and rest of India adopted the strategy in 1995.
this ppt contain history, causes, symptoms, who ,india , pulse polio programme, vaccination,future benefits of vaccination
Primary health centers are the corner stone of rural health services .
It act as a referral unit for 6 sub centers and refer out cases to CHCs.
It covers a population of 30,000 in plain area and 20,000 in hilly and tribal area.
There are 4-6 beds for patients and some diagnostic facilities are also available.
A decentralized system of disease surveillance for timely and effective public health action with a focus on functional integration of surveillance components of various vertical programmes.
Universal Immunization Program is a vaccination program launched by the Government of India in 1985.
It became a part of Child Survival and Safe Motherhood Program in 1992 and is currently one of the key areas under National Rural Health Mission(NRHM) since 2005.
Program consists of vaccination for 12 diseases -
Tuberculosis
Diphtheria
Pertussis
Tetanus,
Poliomyelitis,
Measles,
Hepatitis B,
Diarrhea,
Japanese-Encephalitis,
Rubella,
Pneumonia
Pneumococcal diseases
Pulse Polio is an immunisation campaign established by the government of India to eliminate poliomyelitis (polio) in India by vaccinating all children under the age of five years against the polio virus.
This ppt contains all the information about Revised NationalTuberculosis Control programme (RNTCP) It is useful for students of the medical field learning Preventive and social medicine, Swasthavritta (Ayurved) and everyone who is interested in in knowing about it.
Pulse Polio is an immunization campaign established by the government of India to eliminate poliomyelitis (polio) in India by vaccinating all children under the age of five years against the polio virus.
The project fights polio through a large-scale , pulse vaccination programme and monitoring for poliomyelitis cases.
Vellore(Tamil Nadu) was the first Indian state to become 100% polio-free through the pulse strategy, and rest of India adopted the strategy in 1995.
this ppt contain history, causes, symptoms, who ,india , pulse polio programme, vaccination,future benefits of vaccination
Primary health centers are the corner stone of rural health services .
It act as a referral unit for 6 sub centers and refer out cases to CHCs.
It covers a population of 30,000 in plain area and 20,000 in hilly and tribal area.
There are 4-6 beds for patients and some diagnostic facilities are also available.
National health programs are one of the measures taken by the government of India to improve the health status of the people.National health Programs useful to controlling or eradicating diseases which cause considerable morbidity and mortality in India
which are either centrally sponsored
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
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Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
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These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
2. Introduction
History
Aims
Objectives
Immunization schedules
1. National Immunization
Schedule
2. WHO EPI Schedule
New Vaccines
Implementation of Routine
Immunization
Components
1. Strategy and policy
2. Cold Chain System,
Vaccines and logistics
3. Injection Safety and
Waste disposal
4. AEFI Surveillance System
in India
5. Strategic communication
6. Immunization Things
7. Monitoring and
Evaluation
2
Pioneer Pharmacy Degree College
3. 3
Universal Immunization Programme (UIP) is one of the largest
public health programmes targeting close of 2.67 crore newborns
and 2.9 crore pregnant women annually.
It is one of the most cost-effective public health interventions and
largely responsible for reduction of vaccine preventable under-5
mortality rate.
Under UIP, immunization is providing free of cost against 12 vaccine
preventable diseases:
Nationally against 9 diseases - Diphtheria, Pertussis, Tetanus,
Polio, Measles, Rubella, severe form of Childhood Tuberculosis,
Hepatitis B and Meningitis & Pneumonia caused by Hemophilus
Influenza type B
Pioneer Pharmacy Degree College
4. Sub-nationally against 3 diseases - Rotavirus diarrhoea,
Pneumococcal Pneumonia and Japanese Encephalitis; of which
Rotavirus vaccine and Pneumococcal Conjugate vaccine are in
process of expansion while JE vaccine is provided only in endemic
districts.
A child is said to be fully immunized if child receives all due vaccine
as per national immunization schedule within 1st year age of child.
The two major milestones of UIP have been the elimination of polio
in 2014 and maternal and neonatal tetanus elimination in 2015.
4
Pioneer Pharmacy Degree College
5. Under Global Smallpox Eradication Programme, it was
experienced that immunization is the most powerful and cost
effective weapon for the prevention and control and even
eradication of a disease.
May 1974, WHO officially launched a global immunization
programme, known as Expanded Programme of Immunization for
the prevention and control of six major, killer disease of children,
namely tuberculosis, diphtheria, pertussis, tetanus, poliomyelitis,
and measles, all over the world by the year 2000. EPI was launched
in India in January 1978.
5
Pioneer Pharmacy Degree College
6. It was called Expanded because:
-Number of disease covered are more.
-Services are extended to all corners of the world, irrespective of
cast, creed, community and ability to pay for it.
-The child is immunized much before it is born.
Beneficiaries were all expectant mothers and children up to 16
years of age.
Immunization was recommended from 3rd month of infancy and for
pregnant mothers, 3 doses of TT, respectively during 16-24 weeks,
24-32 weeks and during 36 weeks.
6
Pioneer Pharmacy Degree College
7. Government of India launched same program with same schedule
on 1st January 1978 with the same objectives of reducing child
morbidity and mortality rates and to achieve self sufficiency in the
production of vaccines.
WHO launched a social target of achieving Health for all by 2000
AD.
In 1983, the schedule was revised and recommended only 2 doses
of TT during pregnancy, respectively during 16-24 weeks and 24-
36 weeks and commencing routine immunization as early as 6
weeks during infancy and services were concentrated to under 5.
7
Pioneer Pharmacy Degree College
8. The Programme is now called Universal Child Immunization, 1990-
that’s the name given to a declaration sponsored by UNICEF as
part of the ‘United Nations’ 40th anniversary in October 1985. It is
aimed at adding impetus to the global programme of EPI.
The Indian version, the ‘Universal Immunization Programme’, was
launched on November 19, 1985 and was dedicated to the memory
of Smt. Indira Gandhi. The National Health Policy was aimed at
achieving universal immunization coverage of the eligible
population by 1990.
Impetus was added to the existing program by shifting from under 5
to under 1 year of age and the quality of services was also
improved.
8
Pioneer Pharmacy Degree College
9. It was recommended to give 1st dose of TT to the pregnant mother
in the first contact and 2nd dose after 1 month and BCG and OPV to
the new born as early as at birth.
During 1992, immunization program become a component of Child
Survival and Safe Motherhood (CSSM) program. It was
recommended to cover 100% among infant also.
In 1995, Pulse Polio Immunization Programme was launched as a
strategy to eradicate poliomyelitis.
In 1997, immunization activities have been important component of
National Reproductive and Child Health Programme.
9
Pioneer Pharmacy Degree College
10. In 2005, immunization schedule was revised incorporating Hepatitis
vaccine, 2 doses of JE vaccine in selected endemic district, 1st
during 9-12 months and 2nd during 16-24 months and 2 doses of
Measles vaccine, 1st dose during 9-12 months and 2nd dose during
16-24 months, under National Rural Health Mission (NRHM).
In 2012, GOI declared 2012 as the “Year of Intensification of
Routine Immunization”.
In 2013, GOI along with other S-E Asia regions, declared
commitment towards measles elimination and congenital Rubella
syndrome control by 2020.
10
Pioneer Pharmacy Degree College
11. In 2014, India was certified as “Polio free country”.
To strengthen routine immunization, Government of India has
planned the State Programme Implementation Plan (PIP) part C.
11
Pioneer Pharmacy Degree College
12. 100% coverage of expectant mothers with 2 doses of Tetanus
toxoid(TT).
At least 85% coverage of infants with 3 doses DPT and OPV 1
dose each of BCG and Measles vaccine before child’s 1st birthday.
12
Pioneer Pharmacy Degree College
13. Rapidly increase immunization coverage.
Improve the quality of services.
Establish a reliable cold chain system to the health facility level.
Introduce a district-wise system for monitoring of performance.
Achieve self-sufficiency in vaccine production.
Elimination of neonatal tetanus.
Eradication of paralytic poliomyelitis.
13
Pioneer Pharmacy Degree College
14. Under UIP, following vaccines are provided:
1. BCG (Bacillus Calmette Guerin
2. DPT (Diphtheria, Pertussis and Tetanus Toxoid)
3. OPV (Oral Polio Vaccine)
4. Measles
5. Hepatitis B
6. TT (Tetanus Toxoid)
7. JE vaccination (Japanese Encephalitis) - (in selected high
disease burden district)
8. Hib containing Pentavalent vaccine
(DPT+Hep B+Hib) - (in selected states)
14
Pioneer Pharmacy Degree College
15. 1. National Immunization Schedule
The Indian Academy of Paediatrics(IAP) recommends inclusion of
more vaccines in the immunization schedule.
These vaccines are not included in the UIP because of financial
constraints.
15
Pioneer Pharmacy Degree College
16. The immunization schedule approved by the IAP is:
BCG - Birth - 2 weeks
OPV - Birth; 6 weeks, 10 weeks and 14 weeks;
16-18 months, 5 years
DPT - 6 weeks, 10 weeks and 14 weeks;
16-18 months, 5 years
Hepatitis B - Birth, 6 weeks and 14 weeks or
6 weeks, 10 weeks and 14 weeks
Hib Conjugate - 6 weeks,10 weeks and 14 weeks
Measles - 9 months, 16-24 months
MMR - 15 months
Typhoid - 2 years, 5 years, 8 years, 12 years
TT/Td - 10 years, 16 years
TT - 2 doses one month apart for pregnant women,
or booster dose if previously immunized. 16
Pioneer Pharmacy Degree College
17. Vaccines that can be given after discussion with parents:
Varicella - 15 months (or after 1 year)
Hepatitis A - High-risk selected infants,
18 months, and 6 months later
Pneumococcal - 6 weeks
conjugate vaccine
Influenza vaccine - 6 months of age to high risk selected
infants anually
17
Pioneer Pharmacy Degree College
18. contd…
Vaccine When to
give
Max.
Age
Dose Diluent Route Site
For Pregnant Women
TT- 1 Early in
pregnancy
0.5 ml NO Intra-
muscular
Upper
arm
TT- 2 4 weeks after
TT-1
0.5 ml NO Intra-
muscular
Upper
arm
TT-
Booster
If received
TT dose in
pregnancy
within the
last 3 years
0.5 ml NO Intra-
muscular
Upper
arm
18
Pioneer Pharmacy Degree College
19. Vaccine When
to give
Max. Age Dose Diluent Route Site
For Infants
BCG At birth Till 1 year
of age
0.1 ml (0.05
ml until 1
month of age)
Sodium
chloride
Intra-
dermal
Left upper
arm
Hepatitis
B
At birth Within 24
hrs
0.5 ml NO Intra-
muscular
Antero-
lateral
side of
mid thigh
OPV-0 At birth Within the
first 15
days
2 drops NO Oral
OPV- 1,2
& 3
At 6,10
and 14
wks
Till 5 years
of age
2 drops NO Oral
19
Pioneer Pharmacy Degree College
20. Rota Virus
vaccine
At 6,10 and
14 wks
Till 1 year
of age
5 drops NO Oral
IPV At 14 wks Up to 1
year of
age
0.5 ml NO Intra-
muscular
Antero-
lateral side
of mid thigh
Pentavalent
1,2 & 3
At 6,10 and
14 wks
Till 1 year
of age
0.5 ml NO Intra-
muscular
Antero-
lateral side
of mid thigh
Measles 1st
dose
9-12
completed
months
Till 5
years of
age
0.5 ml Sterile
water
Sub-
cutaneous
Right upper
arm
JE 1st dose 9-12
completed
months
Till 15
years of
age
0.5 ml Phosphate
buffer
Sub-
cutaneous
Left upper
arm
20
Contd…
Pioneer Pharmacy Degree College
21. Vitamin A
(1st dose)
At 9
completed
months with
measles
Till 5 years
of age
1 ml (1
lakh IU)
NO Oral
For Children
DPT
Booster-1
16-24
months
7 years 0.5 ml NO Intra-
muscular
Antero-
lateral side
of mid
thigh
Measles
2nd dose
16-24
months
Till 5 years
of age
0.5 ml Sterile
water
Sub-
cutaneous
Right
upper arm
OPV
Booster
16-24
months
Till 5 years
of age
2 drops NO Oral
21
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22. JE 2nd
dose
16-24
months
0.5 ml Phosphat
e buffer
Sub-
cutaneou
s
Left
upper
arm
Vitamin
A (2nd to
9th dose )
16 month
then 1
dose
every 6
months
Till 5
years of
age
2 ml (2
lakh IU)
NO Oral
DPT
Booster
2nd dose
5-6 years 7 years 0.5 ml NO Intra-
muscular
Upper
arm
TT 10 years
and 16
years
0.5 ml NO Intra-
muscular
Upper
arm
22
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23. 2. WHO EPI Schedule
The purpose is to assist health planners to develop an appropriate
country specific immunization schedule based on local conditions.
The health care workers should refer to their national immunization
schedules.
The WHO EPI Global Advisory Committee has strongly
recommended BCG and Polio vaccine to be given at birth or at first
contact, in countries where Tuberculosis and Polio have not be
controlled.
In all countries routine immunization with DPT and oral Polio
vaccine can be safely and effectively initiated at 6 weeks of age.
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24. New vaccines can be safely being added for the vaccination
schedule e.g., Hepatitis B, Rubella and Japanese
Encephalitis(JE) vaccines are now included in several country’s
programmes.
The immunization schedule may be altered to suit the local needs
of individuals and groups.
Interruption of the schedule with a delay between doses does not
interfere with the final immunity achieved.
There is no basis for the mistaken belief that if a second (or third)
dose in an immunization is delayed, the immunization schedule
must be started all over again.
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25. The WHO Scientific Advisory Group of Experts to EPI has indicated
the need to expand immunization activities beyond infancy, either
as part of routine immunization services or as part of disease
elimination or eradication measure.
The vaccines of interest are MR and MMR as part of Measles
outbreak prevention or elimination campaign, Td as booster dose
for neonatal Tetanus elimination, Hepatitis B, Influenza, Varicella
and HPV vaccines etc.
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26. In April 2016, India introduced the use of Fractional dose IPV
(FIPV) into the routine immunization programme in 8 states
(Odisha, Andhra Pradesh, Telangana, Karnataka, Tamil Nadu,
Pondicherry and Maharashtra).
Since March 2017 has been scaled up nationwide in all 36 states. 2
fractional doses of IPV 0.1 ml, are being given intradermally at 6
and 14 weeks.
On 5th Feb 2017, The Ministry of Health and Family Welfare
launched Measles Rubella (MR) vaccination campaign in the
country, following immunization, replacing the currently given 2
doses of measles vaccine, at 9-12 months and 16-24 months of age
in 5 states (karnataka, Tamil Nadu, Pondicherry, Goa and
Lakshadweep)
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27. In March 2016, the Rotavirus vaccine was first introduced in 4
states (Haryana, Himachal Pradesh, Andhra Pradesh and Odisha).
On 18 Feb 2017, Union Minister for Health and Family Welfare
announced the expansion of the Rotavirus vaccine under its UIP in
five additional states of Assam, Tripura, Madhya Pradesh,
Rajasthan and Tamil Nadu.
On 13 May 2017, Union Minister for Health and Family Welfare,
announced the introduction of pneumococcal conjugate
vaccine(PCV) in the UIP. Currently, the vaccine is being rolled out
to approximately 21 lakh children in Himachal Pradesh and parts of
Bihar and Uttar Pradesh in the first phase. This will be followed by
eventually be expanded to the country in a phased manner.
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28. RI targets vaccinate 26 million new born each year with all primary
doses and ~100 million children of 1-5 year age with booster doses
of UIP vaccines. In addition, 30 million pregnant mothers are
targeted for TT vaccination each year.
To vaccinate this cohort of 156 million beneficiaries, ~9 million
immunization sessions are conducted, majority of these are at
village level.
As per Coverage Evaluation Survey (2009), 89.8% of vaccination in
India is provided through Public sector [(53%) from outreach
session held at Anganwadi centre (25.6%), sub centre (18.9%) etc.]
while private sector contributed to only 8.7%.
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29. ASHA and AWW support ANM by mobilizing eligible children to
session site thus try to ensure that no child is missed. ASHA is also
provided an incentive of Rs.150/- per session for this activity.
To ensure potent and safe vaccines are delivered to children, a
network of ~27,000 cold chain points have been created across the
country where vaccines are stored at recommended temperatures.
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30. 1. Strategy and Policy:
Directed towards achieving an acceptable, affordable and
sustainable standard of health through an appropriate health
system.
Provision of universal immunization of children against vaccine
preventable disease is one of the major goals under this policy.
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31. Country developed a comprehensive Multi Year Strategic Plan for
Immunization in 2005 with an addendum in 2010 to achieve these
targets of improving access and utilization of immunization in the
country.
Ministry of Health and Family Welfare also revised the National
Vaccine Policy in 2011.
Goal - develop a long term plan to strengthen the UIP.
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32. 2. Cold Chain System,Vaccines and Logistics:
Cold Chain is a system of storing and transporting vaccine at the
recommended temperature range from the point of manufacture to
point of use.
The vaccines are supplied by manufactures directly to 4
Government Medical Store Depots (at Karnal, Mumbai,Chennai and
Kolkata) and state and regional vaccine stores.
Transportation of vaccines from states/regional stores to divisions
and districts is done in cold boxes using insulated vaccine vans.
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33. Vaccine carriers with ice packs are used to transport vaccines from
PHCs to the outreach sessions in the village.
At the PHCs and CHCs, cold chain handlers, who are health
personnel (pharmacists, male and female multi-purpose health
workers, etc) have been tasked with proper storage and handling of
vaccines and daily upkeep of Ice Lined Refrigerators (ILRs) and
Deep Freezers (DFs) including temperature charting.
The performance and efficiency of the cold chain system at different
levels is monitored continuously, through supervisory visits, review
meetings.
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34. 3. Injection safety and Waste Disposal:
To ensure safe injection practices, Government of India endeavors
to ensure continuous supply of injection safety equipments (AD
syringes, reconstitution syringes, hub cutters and waste disposal
bags).
Disposal of immunization waste is strictly as per Central Pollution
control Board (CPCB) guidelines for biomedical waste disposal.
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35. 4. AEFI Surveillance System in India:
The WHO defines AEFI as “A medical incident that takes place after
an immunization, causes concern, and believed to be caused by
immunization”.
AEFI surveillance in country monitors immunization safety, detects
and responds to adverse events following immunization; corrects
unsafe immunization practices, reduces the negative impact of the
event on health and contributes to the quality of immunization
activities.
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36. 5. Strategic Communication:
Strategic Communication refers to policy-making and guidance for
consistent information activity through coherent messaging.
The issue of media advocacy, proactive planning and effective
media response is emerging as one of the key elements of strategic
communication support to achieving full Routine Immunization
coverage in the country.
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37. 6.ImmunizationTrainings:
The Immunization Programme runs due to the coordinated efforts of
different cadres of health staff working in the States at different
levels(States, districts, PHCs and CHCs).
In the year of intensification of routine immunization (2012-2013),
the government of India has supported the training of approximately
12,50,000 frontline workers (ANMs, LHVs, anganwadi workers and
ASHAs) in 9 high priority States-UP, MP, Rajasthan, Bihar,
Chhattisgarh, Jharkhand, Haryana, Gujarat and West Bengal.
The objective is to motive and strengthen the capacity of frontline
workers to reduce dropouts and left outs and improve the quality of
services. The process followed is a cascade model.
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38. 7.Monitoring and evaluation
UIP performs monitoring and evaluation at three levels.
1. There is a regular reporting system from the health sub-centre to
PHC, districts, state and national level.
2. To evaluate immunization coverage, country conducts population
based surveys. These include National Family Health
Surveys(NFHS), District Level Health Surveys(DLHS), Annual Health
Survey(AHS) and UNICEF coverage evaluation survey(CES).
3. In between periodic surveys and administrative reporting, country also
plans targeted studies and surveys to evaluate the performance of
various components under UIP.
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39. Park’s Textbook of Preventive and Social Medicine;Bhanot;23rd
edition,page no.122-123.
Patnaik L. Universal Immunization Programme;slideshare;2018.
Dixit S. Universal Immunization Programme;slideshare;2017
Universal Immunization Programme,Government of India,Ministry of
Health and Family Welfare;2017.
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