This document provides information about poliomyelitis (polio) including its history, epidemiology, clinical features, diagnosis, treatment, vaccination, and global eradication efforts. It notes that polio cases have declined globally from over 350,000 cases in more than 125 endemic countries in 1985 to just 22 cases in Afghanistan and Pakistan in 2019. India was declared polio-free in 2014 and key milestones in India's polio eradication program are highlighted. Oral polio vaccine and inactivated polio vaccine are discussed.
In this presentation you will find summary for poliomyelitis. what is polio ? what are the causes ? and what will be the prevention?
here you'll also find about the rehabilitation program for polio as well..
Poliovirus is a picornaviridae. it has 3 wildtypes, Wildtype 2 has been eradicated from the world. All countries have been declared polio free except Pakistan, Afghanistan and Nigeria. Global Polio Eradication Initiative has been discussed.
In this presentation you will find summary for poliomyelitis. what is polio ? what are the causes ? and what will be the prevention?
here you'll also find about the rehabilitation program for polio as well..
Poliovirus is a picornaviridae. it has 3 wildtypes, Wildtype 2 has been eradicated from the world. All countries have been declared polio free except Pakistan, Afghanistan and Nigeria. Global Polio Eradication Initiative has been discussed.
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In this study Professor Kathryn M. Edwards (Sarah H. Sell and Cornelius Vanderbilt Professor - Division of Pediatric Infectious Diseases - Vanderbilt University Medical Center) provides an update on measles and its prevention.
To learn more, please visit www.waidid.org!
Peste des-ruminants-is-a-rinderpest.doc pdfGudyne Wafubwa
Peste des petits ruminant virus (PPRV) is a disease mostly affecting goats and sheep. Since its first discovery, it has caused massive economic loss to most small pastoralists in Africa and other developing countries. It is the integral role of all stakeholders to join hands so as to eradicate the disease.
Millennium Development Goal progress report 2014, The
Millennium Development Goals (MDGs) were a pledge
to uphold the principles of human dignity, equality and
equity, and free the world from extreme poverty. The
MDGs, with eight goals and a set of measurable timebound
targets, established a blueprint for tackling the
most pressing development challenges of our time. This report examines the latest progress towards
achieving the MDGs. It reaffirms that the MDGs
have made a profound difference in people’s lives.
Global poverty has been halved five years ahead of
the 2015 timeframe. Ninety per cent of children in
developing regions now enjoy primary education, and
disparities between boys and girls in enrolment have
narrowed. Remarkable gains have also been made in
the fight against malaria and tuberculosis, along with
improvements in all health indicators. The likelihood of
a child dying before age five has been nearly cut in half
over the last two decades. That means that about 17,000
children are saved every day. We also met the target
of halving the proportion of people who lack access to
improved sources of water.
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Integrated management of Neonatal and Childhood illness among Infants of 0 to 2 months, Difference between IMCI and IMNCI, Objective, Elements, Management of Diarrhea, Bacterial Infections, Jaundice, Hypothermia, Feeding problem, counseling of mothers, followup
Integrated child development Scheme, ICDS Mission the broad framework for implementation, The challenges Evoluation and progress, ICDS strengthening, Restructuring, Mechanism of implementation, Strengthening human resources, Training and capacity building, Logistic management, AWCs Monitoring and review
Guidelines for Control of Iron deficiency Anemia, National Iron plus Initiative by Govt. of India, Causes of Iron deficiency anemia in Infants, Children, Adolescents, Non pregnant and Pregnant Women, Supplementary Nutrition for all under ICDS project
Millennium development Goals, MDGs Framework, Millennium development goals, Targets, Indicators, Targets for 2015, India achievement till 2013, National Health Programmes under 12th national Plan (2012- 2017)
Vitamin a presentation, Vitamin A Deficiency, Vitamin A toxicityDhruvendra Pandey
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this presentation will contains problem of old age, how can they affect the life of geriatric peoples, prevention and control of geriatric problems, national program for better health of old peoples, initiations done by private trusts to improve their health
This presentation contains Complete cold chain system, Importance and requirement of cold chain, detail of each equipment of cold chain system.
This presentation contain brief detail of THE SHAKE TEST, Reverse cold chain.
This is fully equipped with knowledge of Field facts of cold chain system.
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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
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
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The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
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Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
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
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.
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
2. From 125 Polio Endemic
countries
to 3 endemic countries
0
100
200
300
400
1985
1986
1987
1988
1989
1990
1991
1992
1993
1994
1995
1996
1997
1998
1999
2000
2001
2002
2003
2004
2005
2006
2007
2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
Polio
cases
(thousands)
Wild Poliovirus (WPV) Eradication, 1985–2019*
Last type 2 polio in
the world
Last Polio
Case in
India
Last type 3
polio
In the world
Eradication
of WPV 2
11/26/2022
5. Global WPV1 & cVDPV Cases1, Previous 6 Months
Endemic country (WPV1)
11/26/2022
WPV1 cases (latest onset)
Afghanistan: 10 (10 Nov 2019)
Pakistan: 61 (16 Nov 2019)
cVDPV1 cases (latest onset)
Myanmar: 4 (09 Aug 2019)
Philippines: 1 (28 Oct 2019)
Malaysia: 1 (30 Oct 2019)
cVDPV2 cases (latest onset)
Angola: 64 (21 Oct 2019)
Benin: 6 (15 Oct 2019)
CAR: 14 (06 Oct 2019)
Chad: 1 (09 Sep 2019)
DRC: 39 (21 Oct 2019)
Ethiopia: 4 (09 Sep 2019)
Ghana: 9 (23 Oct 2019)
Nigeria: 7 (09 Oct 2019)
Pakistan: 11 (03 Nov 2019)
Philippines: 9 (25 Oct 2019)
Togo: 3 (16 Oct 2019)
Zambia: 1 (16 Jul 2019)
1Excludes viruses detected from environmental surveillance ; 2Onset of paralysis: 11 Jun 2019 – 10 Dec 2019
6. WPV1 cases (latest onset)
Afghanistan: 22 (10 Nov
2019)
Pakistan: 98 (16 Nov 2019)
cVDPV1 cases (latest onset)
Philippines: 1 (28 Oct 2019)
Malaysia: 1 (30 Oct 2019)
Myanmar: 6 (09 Aug 2019)
cVDPV2 cases (latest onset)
Angola: 71 (21 Oct 2019)
Benin: 6 (15 Oct 2019)
CAR: 16 (06 Oct 2019)
Chad: 1 (09 Sep 2019)
China: 1 (25 Apr 2019)
DRC: 53 (21 Oct 2019)
Ethiopia: 5 (09 Sep 2019)
Ghana: 9 (23 Oct 2019)
Niger: 1 (03 Apr 2019)
Nigeria: 18 (09 Oct 2019)
Pakistan: 11 (03 Nov 2019)
Philippines: 9 (25 Oct 2019)
Somalia: 3 (08 May 2019)
Togo: 3 (16 Oct 2019)
Zambia: 1 (16 Jul 2019)
Global WPV1 & cVDPV Cases1, Previous 12 Months2
Endemic country (WPV1)
1Excludes viruses detected from environmental surveillance; 2Onset of paralysis 11 Dec 2018 – 10 Dec 2019
11/26/2022
Public Health Emergency
of International Concern
First declared under the International
Health Regulations in May 2014
Confirmed on 16 September 2019
8. Pakistan/Afghanistan: Main Risks
• Ongoing transmission in the Southern & Northern corridors
• Accessing all children in highly mobile populations
• Impact of elections and sustaining government commitment at all levels
• Systemic weaknesses in EPI throughout many parts of both countries
• Resistance to vaccination (both overt and covert)
• In Afghanistan
Bans on house to house campaigns in Southern Province
Increasing inaccessibility in Eastern region
Deteriorating security situation creating environment of fear
Challenges in getting female front line workers particularly in high risk areas
11. India - Major Milestones Achieved
2011 : Last polio case due to
WPV
(13 January, 2011)
2012 : Removed from list of
polio endemic countries
2014 : Received polio-free
certification on 27
March
2015: Introduction of IPV in RI
2016: tOPV - bOPV switch, 25
April 2016
Rukhsar, the last polio
case due to wild
poliovirus (WPV) in India
!
13. * data as on 7 December 2019
Year
a i a c i
2009 1 1 4 15
2010 1 3 1
2011 4 2
2012 1
2013 2 3
2014 3
2015 1 1
2016 1
2017
2018
2019
Total 1 1 15 18 9
1
1
type 1 type 2 type 3
i
Figure 7: Vaccine-derived Poliovirus inAFPcases,, India, 2009 - 2019
a-VDPV
c-VDPV
i-VDPV
Vaccine-derived Poliovirus in AFP Cases, India, 2009 – 19*
14. INTRODUCTION
• Polio – Grey, Muellos – marrow ( Greek )
• Acute viral infection, occurs mainly in children
• Caused by RNA virus
• Primarily infection of GIT
• It may infect CNS in < 1 %
– May cause varying degree of paralysis
• First described - Michael Underwood -1789
• First outbreak described in U.S. -1843
• 21,000 paralytic cases reported- U. S. - 1952
• Global eradication in near future
15. HISTORY
• Heine - described Polio in 1840
• Medin - in 1890
• Hence called as Heine-Medin disease
• Landsteiner & Popper – Identified the virus in 1909
• Enders, Robbibs, Waller– Cultivated the virus - Nobel
• Salk vaccine – Killed vaccine 1955
• Sabin vaccine – Live attenuated vaccine in 1959
16. EPIDEMIOLOGY - TREND
• It can occur sporadically, Endemically & Epidemically
• Earlier it was a sporadic disease
• Evolved as epidemic disease
• Earlier it was disease of infants, later started affecting
older age group
• Earlier seen in temperate climate now in tropical
climate also
17. AGENT
• Poliovirus – 3 serotypes 1, 2 & 3
– Type 1– Brunhilde, 2 – Lansing, 3 - Loen
• Most outbreaks - type 1 virus
• It can survive outside the human body for 4 months
in cold season, 6 months – faeces
• Rapidly destroyed by pasteurization, chemical,
physical agents, drying (not available in freeze dried
form )
18. RESERVOIR OF INFECTION
• Man is the only source of infection
• Most cases – Mild, sub clinical – Play an imp. role in
spread of the infection
• For every clinical case of Polio – 1000 sub clinical
cases in children & 75 in adults
• Period of communicability – 7–10 days before & after
the onset of symptoms
19. HOST
• Age – Infants & children
• Most vulnerable age – 6 months–3 years
• Sex – 3 males to 1 female
• Maternal antibody– Protect 6 months after birth
• Infection– Confers long lasting immunity, but no
protection against another strain
20. FACTORS– PROVOCATE LATENT
INFECTION
• Injection
– DPT (Vascularisation part spinal cord)
• Fatigue
– Trauma, Excercise
• Surgery
– Head & Neck region
21. ENVIRONMENT
• Likely to occur rainy season
• In India – 60 % cases – June – September
• Environmental sources – Contaminated water, food,
through flies
• Over crowding, poor sanitation – Opportunity for
infection
23. PATHOGENESIS
• Portal of entry- Oral route. Adheres to the epithelial
cells and replicates. Passes to the submucosa and
replicates in Peyer`s patches & tonsils
• Travels to regional L.N. and gives rise to initial
viraemia.
• Localization and replication occurs in R.E.Cells
• A second viraemia occurs with localization in
different organs
24. PATHOGENESIS
• CNS infection- most likely to occur during viraemia
either through muscle end plate or blood stream
• Virus detectable in oro-pharynx up to 3 weeks and in
stool up to 12 weeks and up to 1 year in immuno-
deficient patients
• In GIT, during replication, the oral polio virus can
undergo mutation and convert into more neuro
virulent phenotype
25. SUMMARY - PATHOGENESIS
• Entry into mouth
• Replication in pharynx, GI tract,
local lymphatics
• Hematologic spread to lymphatics and central
nervous system
• Viral spread along nerve fibers
• Destruction of motor neurons
27. ASEPTIC MENINGITIS
• 1% cases
• CSF findings - raised proteins, normal sugar,
pleocytosis (<1000 cells, Polymorphonuclear
predominance)
• Lasting for 2-10 days.
• Non paralytic polio
28. PARALYTIC POLIO
• < 1% of cases.
• Occurring one or more days after symptoms of
aseptic meningitis
• Sudden onset fever, vomiting, anorexia
• Back & neck muscle pain
• Followed by lower motor neuron paralysis (Flaccid)
29. CONTD…..
• Mild cases- Few muscles paralysed
• More proximal than distal
• Severe cases entire limb paralysed
• No sensory loss ( DD- GBS )
• Deep Tendon Reflexes (DTR) – Diminished
• 2-3 days full paralysis (Asymmetrical)
• Residual paralysis
32. BULBAR POLIOMYELITIS
• Fever, weakness swallowing, coughing
• Paralysis of pharynx
• Collection of secretion in the throat
• Inability to swallow threatens life
• Recovery good but slow ( If they survive )
33. POST POLIO SYNDROME
• New occurence of weakness, fatigue, fasciculations
and pain with atrophy of groups of muscles involved
in initial episode of paralysis
• May occur after 20-40 years
• May extend over 1-10 years
• Due to dysfunction and exhaustion of motor neurons
that compensated for the neurons lost and not due
to re-infection or reactivation.
34. DIAGNOSIS
• Isolation of the virus- Stool
• Virus cannot be grown in culture - from throat
swab, CSF or Blood
• Rise in antibody titer – Confirmatory
• Aseptic meningitis- 1%.
– With CSF revealing raised proteins, normal sugar,
pleocytosis (<1000 cells, PMN predominance)
Lasting for 2-10 days
35. MANAGEMENT
• General supportive care
– Isolation
– Concurrent disinfection – Stool – 10 % Cresol
– Bed rest – avoid stress on affected muscles
– Paracetamol – Fever, Pain
– Prophylactic oral antibiotics
– Splints – to prevent deformity
– Fluid & electrolyte balance ( Oral )
– Physiotherapy – After acute phase of illness – 6
weeks
36. DIFFERENTIAL DIAGNOSIS FOR POLIO
• Transverse myelitis
– No fever, symmetrical paralysis lower extremity,
marked sensory loss, in children > 4 yrs., CSF – N
• Traumatic neuritis
– H/O IM injection, paralysis of limb with pain, Limb
affected below knee, foot drop, slow recovery, any
age group
38. PREVENTION
• Immunization is the only way to protect children
against polio
• All children by the age of 6 months– Fully immunized
• Both Killed & Live vaccines are available
39. POLIO VACCINE
• 1955 Inactivated vaccine
• 1959 Live attenuated vaccine
• 1987 Enhanced-potency IPV (IPV)
– It can be given with DPT, sero-conversion is better
compared to OPV after 3 doses
– It can also prevent the multiplication of virus in
the pharynx
40. INACTIVATED KILLED VACCINE
• Also known as Salk Vaccine
• Contains all 3 types – Polio virus
• 4 doses required – 1st 3 when child 6 weeks old with
1-2 months interval
• 4th dose – 6- 12 months after the 3rd dose
• Additional doses every 5 years till the age of 18 years
41. CONTD…..
• Sabin 1957
• Contains live attenuated virus ( all 3 types )
• Ideal to give each type as monovalent vaccine
• Administrative purpose trivalent vaccine given
• Vaccine contains – 3 lakh TCID 50 of type 1, 1 lakh
TCID 50 of type 2 & 3 lakh TCID 50 of type 3 (TCID –
Tissue culture infective dose)
42. DIFF. BETWEEN IPV & OPV
• IPV ( Salk )
– Killed ,
– IM, strict Cold chain not
req
– Systemic immunity
– Doesn’t protect gut – Re-
inf. With wild virus
– Not useful – to control
epidemics / Eradication
– Trained person req.
– Imm. Shorter – 5 years
– No vaccine associated
paralysis
• OPV ( Sabin )
– Live attenuated
– Oral, strict Cold chain
req.
– Local & Systemic imm.
– Protects gut from re inf.
With wild virus
– Useful – Control
epidemics / Eradication
– Trained person not req
– Immunity – Lifelong
– Vaccine associated
paralysis can occur
43. NATIONAL IMMUNIZATION SCHEDULE
• Soon after birth – Zero dose polio
• 1st dose – 6 weeks
• 2nd dose 10 weeks
• 3rd dose 14 weeks
• 1st booster 18 months
• 2nd booster – 4 years 6 months - 5 years
• Dose – 2 drops
• Vaccine associated paralytic polio esp with type 3
virus due to mutation
44. REASON FOR VACCINE FAILURE
• Incomplete schedule
• Use of date expired vaccine
• Instability of vaccine
• Lack of cold chain maintenance
– Vaccine vial monitor -
• Vaccine associated paralytic polio
46. ERADICATION OF POLIOMYELITIS
• A country is said to be free from polio – Zero
incidence for continuous 3 years
• Why eradicate polio ?
– Humans – only reservoir
– No chronic carrier state
– Half life – excreted wild polio virus in sewage – 48
hours
– Potent vaccine is available
– Lifelong immunity if schedule is completed
correctly
47. CONTD…..
• Last case in United States in 1979
• Western Hemisphere certified polio free in 1994
• Last isolate of type 2 poliovirus in India in October
1999
• Global eradication goal
48. STRATEGIES OF POLIO ERADICATION
• High level routine immunization coverage
• Pulse polio immunization
• Acute flaccid paralysis surveillance
• Mop up immunization
49. PULSE POLIO IMMUNIZATION
• GOI – introduced 1995
• Supplementary programme – Routine imm.
• PPI started - in-spite of good routine immunization
coverage, because 10 % remained unimmunized
• For 100 % Immunization coverage < 3 yrs
• Later on it was extended to < 5 yrs children
• PPI on NID on 2 occasions with 4-6 weeks gap
50. HOW PPI HELPS TO ERADICATE POLIO
• Wild polio virus requires un immunized gut for its
multiplication within 1-2 days of its excretion
• Immunized children’s gut doesn’t allow
multiplication of wild polio virus
• Hence if all children < 5years get immunized against
polio, on PPI day, wild polio virus can’t survive
51. AFP SURVEILLANCE
• Introduced– 1997 in India
• To detect final reservoir of wild polio virus
• AFP– Sudden onset of paralysis of the limb <4 weeks
duration in child <15 years
• AFP surveillance– Detecting all cases of acute
paralysis not only polio cases, it ensures that polio
cases are not missed
• Hence AFP surveillance is tool to detect suspected
polio cases
52. OBJECTIVES OF AFP SURVEILLANCE
• To detect high risk areas – to plan immunization
• To monitor progress of AFP cases
• To certify country polio free
• It is an indicator of sensitivity of surveillance
system
53. EVENTS AFTER DETECTING AFP CASE
(60 days Follow Up)
AFPcase–
2 stool
samples
Wild Polio
virus
Confirmed
case
No wild
polio virus
Discard
Inadequate
sample
Residual
weakness
Died, Lost - FU
Confirm
No residual
weakness
Discard
54. REPORTING OF AFP CASES
• All AFP cases reported to District immunization
officer – DIO, as early as possible
• In case no AFP cases- Zero reporting is must
– Initial phase AFP required – detecting polio virus
– Later stages – to prove the absence of polio virus
• AFP – Public health emergency
55. LINE LISTING OF CASES
• Reporting of every case of AFP in a prescribed
proforma
• It includes
– Name, age, sex, address, imm. Status, date of
onset of paralysis, clinical findings etc
• Helps in avoiding duplication of case
• Follow up of the case
• Identify high risk areas
• Implement control measures
56. MOP UP IMMUNIZATION
• Last stage in polio eradication
• Door to door immunization of all children in high risk
area – circulation of wild polio virus is reported or
suspected
• All children within 5 km area immunized
• About 2000- 3000 children are immunized
• Started within 48 hrs of reporting a case of AFP and
to complete within 7 days
57. INTENSIVE PULSE POLIO IMMUNIZATION- IPPI
• In- spite of PPI, AFP cases do occur
• GOI – 1999 intensified PPI
• 3 days programme
• 1st day – Children immunized in Booth
• 2nd day – House to house survey
– X mark if child not immunized, non co-operation,
locked houses
– P mark if child is immunized ( GV mark on the
finger of the child indicate immunization )
58. CONTD…..
• 3rd day – Only X marked houses are visited
– Children are immunized with OPV
– X mark is wiped
– P mark is put on the door
• Purpose of IPPI – not to miss even single child
59. SUPPLEMENTARY IMMUNIZATION ACTIVITIES-
SNID
• In some states – UP , Bihar
• To supplement PPI, 2 more round of OPV from
October - January
• Better coverage of children
• Consistency in vaccine coverage
• To maintain high level of AFP surveillance
61. International
importation
Gaps in AFP
surveillance or
delays in detection
of WPV
Delayed and/or
inadequate
response to
importation
Areas with low
population
immunity
Risks to Polio Eradication in India
Emergence of
VDPVs
Complacency/
Lack of focus
Risks
62. Polio Eradication & Endgame Strategic Plan 2013-18
• Objective 1
–Polio virus detection and interruption
• Objective 2
–Immunization systems strengthening, IPV
introduction & OPV withdrawal
• Objective 3
–Containment and certification
• Objective 4
–Transition planning
“…ensure that the investments made to eradicate poliomyelitis contribute
to future health goals, through a programme of work to systematically
document and transition the knowledge, lessons learned and assets of
the Global Polio Eradication Initiative….”
63. GPEI Strategy 2019-2023: Why a Revised Strategy?
The Polio Eradication & Endgame Strategic Plan (PEESP) 2013-2018 was developed
to guide the program to the anticipated goal of polio eradication
Though progress continues, transmission still not interrupted in Pakistan and
Afghanistan
The polio program is being extended to achieve eradication
‒A new budget for the period 2019-2023 was approved by the Polio Oversight Board in September
2018 to support program’s work
65. Endgame strategy
• Eventual cessation of all OPV use globally at some point in the
future (e.g. 2017-2018 period).
• A tOPV-bOPV switch globally, potentially as early as April
2014
• Use of IPV in conjunction with OPV
• Support research activities to generate evidence to guide
decision making
- tOPV-bOPV switch and introduction of IPV in routine
immunization
- bOPV assessment study to understand the efficacy of
additional bOPV products from different manufacturers