This document discusses Pakistan's Expanded Program of Immunization (EPI). It began in 1976 with the goal of preventing six major childhood diseases. However, Pakistan has yet to reach targets for polio eradication and measles. The document outlines the EPI vaccination schedule, types of vaccines including live attenuated, inactivated, subunit, and toxoid vaccines. It also discusses the importance of maintaining the cold chain for vaccine storage and transportation from manufacture to use.
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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
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Immunization is the process whereby a person is made immune or resistant to an infectious disease, typically by the administration of a vaccine. Immunization helps protect the child from life threatening diseases. It also helps reduce the spread of disease to others. Vaccines stimulate the body’s own immune system to protect the person against subsequent infection or
disease. Babies are born with some natural immunity which they get from their mother through breast-feeding. This immunity gradually diminishes as the baby's own immune system starts to develop. Immunization is one of the most cost-effective health investments and vaccination does not require any
major lifestyle change. There are two main types of immunization, active immunization and passive immunization.
Both types of immunization prepare the body to fight against certain diseases.
It includes the five most common immunization vaccines for the infant and these are the BCG, DPT, OPV, Hep B and Measles and also the Tetanus Toxoid for both infant and mother.
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Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
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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
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2. OBJECTIVES
To learn about EPI and current
situation of EPI in Pakistan
To understand mechanism of Cold
Chain and maintenance of vaccines
2
3. 3
Today’s Situation
10.5 million infant and childhood deaths
each year in the developing world
70% are due to five conditions:
pneumonia, diarrhea, measles, malaria,
and malnutrition.
Two thirds of neonatal mortality occur in
the first week of life, of these two thirds
die within the first 24 hours of life
4. Current situation in Pakistan
Despite significant efforts by the Government and its
partners, Pakistan’s immunization indicators have yet to
reach the expected benchmarks.
The key goals of polio eradication, and measles, have not
been achieved.
Punjab is the first province to achieve elimination of maternal
and neonatal tetanus in 2016
Pakistan is third among countries with the most unvaccinated
and under-vaccinated children
4
5. 5
Definition
Immunization: A process by which a person
becomes protected against a disease
through vaccination
Vaccination is the administration of antigenic
material (the Vaccine) to produce immunity to a
disease.
6. 6
Vaccination
Vaccination (Latin: vacca—cow) is so
named because the first vaccine was
derived from a virus affecting cows, which
provides a degree of immunity to
smallpox.
7. 7
Under Global Smallpox Eradication Program, it was experienced
that immunization is the most powerful and cost effective
weapon for the prevention and control and even eradication of a
disease.
So in May 1974, WHO officially launched a global immunization
program, known as Expanded Program of Immunization (EPI) for
the prevention and control of six major, killer diseases of
children, namely tuberculosis, diphtheria, pertussis, tetanus,
poliomyelitis and measles, all over the world.
Expanded Programme Of
Immunization (EPI)
8. Expanded Programme of Immunization
The EPI in Pakistan was initiated in 1976.
Was launched at federal level in 1978.
Was Established nation-wide by 1981.
The program currently targets seven vaccine preventable diseases i.e.
• Tuberculosis,
• Diphtheria ,
• Pertusis,
• Tetanus,
• Poliomyelitis
• Heapitis B
• Measles ,
• HIB
9. 9
EPI Vaccination Schedule
AGE Vaccines to be given Route of
administration
At Birth BCG, OPV Intra dermal, oral
At 6 Weeks OPV 1 ,DPT 1
HBV-1 ,Hib 1
Intra muscular
Oral
At 10 Weeks OPV 2, DPT 2 HBV-
2
, Hib 2
Intra muscular
Oral
At 14 Weeks OPV-3, DPT-3 , HBV-3
, Hib-3
Intra muscular
Oral
At 9 completed
months
Measles Sub Cutaneous
At 9 months with
measles vaccine
Vitamin – A (1st dose) Oral
Immunization Schedule for Infants:
Recommended by WHO - Expanded Program on Immunization
10. Passive vs active immunity
Passive Active
MEANS OF
ACQUISITION
Receiving preformed
antibodies
Exposure to exogenous
antigens
ONSET Rapid Slow
DURATION Short span of antibodies
(half-life = 3 weeks)
Long-lasting protection
(memory
EXAMPLES IgA in breast milk,
maternal IgG crossing
placenta, antitoxin,
humanized antibody
Natural infection, vaccines,
toxoid
10
11. VACCINATION Induces an active immune
response (humoral and/or cellular) to specific pathogens.
VACCINE
TYPE
DESCRIPTION PROS/CON S EXAMPLES
Live
attenuated
vaccine
Microorganism
loses its
pathogenicity but
retains capacity
for transient
growth within
inoculated host.
Pros: induces
strong, often
lifelong immunity.
Cons: may revert
to virulent form
Adenovirus
Typhoid (Ty21a, oral),
Polio (Sabin),
Varicella (chickenpox),
Smallpox, BCG, Yellow
fever, Influenza
(intranasal),
MMR,
Rotavirus
Attention Teachers!
Please Vaccinate
Small, Beautiful Young
Infants with MMR
Regularly!
11
12. Vaccination (continue)
12
VACCINE
TYPE
DESCRIPTION PROS/CON S EXAMPLES
Killed or
inactivated
vaccine
Pathogen is
inactivated by
heat or
chemicals.
Maintaining
epitope structure
on surface
antigens is
important for
immune
response.
Pros: safer than
live vaccines.
Cons: weaker
immune
response; booster
shots usually
required.
Hepatitis A, Typhoid
(Vi polysaccharide,
intramuscular),
Rabies, Influenza,
Polio (SalK)
A TRIP could Kill you
13. Vaccination (continue)
VACCINE
TYPE
DESCRIPTION PROS/CON S EXAMPLES
Subunit Includes only the
antigens that
best stimulate
the immune
system
Pros: lower
chance of adverse
reactions.
Cons: expensive
HBV,
Streptococcus
pneumoniae,
acellular
pertussis (aP),
Haemophilus
influenzae type
b.
13
14. Vaccination (continue)
14
VACCINE
TYPE
DESCRIPTION PROS/CON S EXAMPLES
Toxoid Denatured
bacterial toxin
with an intact
receptor binding
site. Stimulates
the immune
system to make
antibodies
Pros: protects
against the
bacterial toxins.
Cons: antitoxin
levels decrease
with time, may
require a booster
Clostridium tetani,
Corynebacterium
diphtheriae
15. 15
COMBINATIONS
When more than one kind of immunizing agent is included in
the vaccine it is called a mixed or combined vaccine.
Combined vaccines simplify administration, reduce cost.
Examples are DPT, DT, DP, DPT and Typhoid vaccine, MMR,
DPTP(DPT plus inactivated Polio).
17. ANTISERA OR ANTITOXIN
Materials prepared in the animals.
Passive immunization is achieved by
administration of Antisera.
Antitoxins prepared from non human sources
against Tetanus, Diphtheria, Botulism, Gas
gangrene and snake bite.
18. COLD-CHAIN
It is a system of storage and
transportation of the vaccines at
recommended, low temperature (+2 to
+8°C) all along from the time and place
of the manufacture to the time and
place of its use.
18