86190117 the Expanded Program on Immunization Lecture

The Expanded Program On

Immunization (EPI)

By

Prof. Drs

Asmaa ABelAziz Alaa Hassan

The Expanded Program On Immunization

(EPI)

The Objectives of the lecture:

State the objectives of EPI.

Outlines the schedule of compulsory immunization of KSA.

Recognize the scientific principles of immunization .

List the contraindications to vaccination.

Explain the four strategies for the vaccine delivery.

Define missed opportunity for immunization.

Mention the reasons for missed opportunity.

Define the cold chain.

Discuss the three components of the cold chain.

Interpret the tools for the cold chain monitoring.

The objectives of EPI: 1. To achieve 100% coverage with all EPI vaccines.

Example:

The coverage rate for measles vaccine by the year 2002 in a

city Y=

The No. of the infants received measles vaccine in the year 2002 in city Y X100 The total No. of the targeted infants during the same year & locality

2. Eradication of polio to maintain polio free status.

3. Elimination of measles.

4. Reduce

seroprevalence of

(HBsAg)to

5.Elimination of Neonatal Tetanus .

6. To maintain zero level of diphtheria.

7.Prevention of severe forms of TB ( TB meningitis

&military TB).

12 year old girl with TB meningitis

8. To reduce the incidence of whooping cough

.

9-Reduce the incidence of Bacteria Meningitis due to

haemophelus influenza

9. To maintain immunization safety.

10.To prepare for introduction of new vaccines

The Schedule of Compulsory Vaccination

in KSA

Diseases Type of vaccine Dose Rout of administration

1-BCG

2-HBV

TB

Hepatitis B

Live attenuated,

variant Recombinant, yeast

derived HBs antigen

0.01ml

0.5 ml

ID injection in left

deltoid IM thigh

At birth

Rout of

administration

Dose Type of vaccine Diseases

oral

2 drops

Live attenuated

Polio

1-OPV

IM thigh

0.5 ml

polysaccharide

conjugate

Hib disease

2-HiB

IM thigh

0.5 ml

Recombinant, yeast

derived HBs antigen

Hepatitis B

3-HBV

IM thigh

0.5 ml

Toxoid (D)

Toxoid (T)

Killed pertussis (P)

Diphtheria

Tetanus

Whooping

cough

4-DPT

2ndmonth

Rout of

administration


oral

2 drops

Live attenuated

Polio

1-OPV

IM thigh

0.5 ml

polysaccharide

conjugate

Hib disease

2-HiB

IM thigh

0.5 ml

Toxoid (D)

Toxoid (T)


Diphtheria

Tetanus

Whooping

cough

3-DPT

4th month

Rout of

administration


oral

2 drops

Live attenuated

Polio

1-OPV

IM thigh

0.5 ml

polysaccharide

conjugate

Hib disease

2-HiB

IM thigh

0.5 ml

Recombinant, yeast

derived HBs antigen

Hepatitis B

3-HBV

IM thigh

0.5 ml

Toxoid (D)

Toxoid (T)


Diphtheria

Tetanus

Whooping

cough

4-DPT

6 th month

Mode of

administration

Dose

Type of the

vaccine

The

disease

Subcutaneous

0.5 ml

All

Live attenuated

Measles, Mumps German Measles

1-MMR

12th month

Rout of

administration


oral

2 drops

Live attenuated

Polio

1-OPV

IM thigh

0.5 ml

polysaccharide

conjugate

Hib disease

2-HiB

IM thigh

0.5 ml

Toxoid (D)

Toxoid (T)


Diphtheria

Tetanus

Whooping

cough

3-DPT

18th month

Rout of

administration


oral

2 drops

Live attenuated

Polio

1-OPV

IM thigh

0.5 ml

All

Live attenuated

- Measles

- Mumps

- German

Measles

2-MMR

IM thigh

0.5 ml

Toxoid (D)

Toxoid (T)


Diphtheria

Tetanus

Whooping

cough

3-DPT

4- 6th years

BCG (At birth)

Live attenuated variant.

0.01ml .

ID injection in left deltoid (Why)

HB Vaccine: at birth,2nd,6th month

Recombinant, yeast derived HBs antigen

0.5 ml IM anterolateral of the thigh

OPV : (Sabin)

2nd , 4th, 6th, 18th& 4- 6th years

OPV live attenuated ,2drops

,Oral

Haemophilus influenzae type b

Severe bacterial infection,

particularly among infants

During late 19th century believed

to cause influenza

Immunology and microbiology

clarified in 1930s

Hib Vaccine


Pathogenesis

Organism colonizes nasopharynx

In some persons organism invades

bloodstream and cause infection at distant site

Antecedent upper respiratory tract infection

may be a contributing factor

Cellulitis

6%

Arthritis

8% Bacteremia

2%

Meningitis

50%

Epiglottitis

17%

Pneumonia

15%

Osteomyelitis

2%

Haemophilus influenzae type b Clinical Features*

*prevaccination era

The Type of Hib vaccine inactivated polysaccharide

conjugate vaccine,

It is made by joining a piece of the polysaccharide capsule

that surrounds the Hib bacterium to a protein carrier.

This joining process is called conjugation.


Meningitis Accounted for approximately

50%-65% of cases in the prevaccine era

Hearing impairment or neurologic sequelae in 15%-

30%

Case-fatality rate 2%-5% despite of effective

antimicrobial therapy

05

10

15

20

25

1990 1992 1994 1996 1998 2000 2002 2004

Inc

ide

nc

eIncidence*of Invasive Hib Disease,

1990-2004 *Rate per 100,000 in

children

After a Hib primary series of two or three doses,95% of

infants develop protective antibodies

Although Hib vaccines provide long lasting immunity the

duration of immunity is not known

The recommended dose for all is 0.5 mL.

Always administer by the IM injection in the thigh.

The preferred injection site in older children and adults is

the deltoid muscle in the upper arm.

Small child receiving Hib

vaccine into the muscles of

the thigh.

Adolescent receiving Hib

vaccine into the deltoid muscle

of the arm.

Storage of the vaccine

The vaccine should not kept frozen or exposed to

freezing

Store at 2 to 8C

Shake vial vigorously before withdrawal and use.

Do not use if resuspension does not occur with vigorous

shaking.

The vaccine should be administered shortly after

withdrawal from the vial.

Give all infants, including premature infants,

a primary series of Hib vaccine beginning at 2

months of age.

Do not administer Hib vaccine to infants

younger than 6 weeks of age because this

may induce immunologic tolerance to further

doses of Hib vaccine.

The most common adverse reactions after Hib

vaccination are

1-local reactions: swelling, redness, or pain

at the injection site.

2-Fever also can occur in as many as 5% of

recipients.

Fever usually starts within the 1st 24 hours of

vaccination and may last for 2 to 3 days.

These reactions can be treated with

a non-aspirin pain reliever, if needed.

local reactions: swelling, redness, or pain at the injection site.

The main contraindication to Hib vaccine :

Severe allergic reaction Do not give Hib-containing

vaccine to anyone who has had a prior severe allergic

reaction to a dose of Hib vaccine or to a component

in the vaccine.

Persons who are severely allergic to diphtheria

toxoid, meningococcal vaccine, or tetanus toxoid

also may be sensitive to a particular Hib vaccine

because of the protein carriers used to create the

conjugate vaccines.

DPT vaccine: 2nd, 4th ,6th, 18th months& 4-6 years

(D ,T) Toxoid & Diphtheria , (P) Killed pertussis

0.5 ml ,IM thigh

DPT:

2nd, 4th ,6th, 18th months& 4-6 years

DT: No pertussis component

It is given as subsequent doses to an infant who showed severe adverse effects

due to pertussis component.

dT: No pertussis component.

A small dose of diphtheria toxoid is given at school entry or after the age of six years.

MMR Vaccination:

12th month& 4-6 years

Live attenuated ( Three : measles, German

measles& Mumps)

0.5 ml

Subcutaneous arm

Basic Principles to be considered in immunization

schedule:

1-All EPI antigens are safe and effective if administered

simultaneously.

2-The recommended interval between two doses of

- Live attenuated vaccine .

- Inactivated vaccines.

3-The only live attenuated vaccine given to HIV child is

measles

4-Tetanus immunoglobulin (250 IU) must be given to

babies :

i) Born outside hospital in unsanitary home

conditions

ii) Seen within 10 days after birth.

ii) Whose mothers are not given two documented

doses of TT.

5- Introduction of HB vaccine in 1990.

6-MMR vaccine is given not before the 12months not to

be neutralized by maternal antibodies

Contraindications to vaccinations:

Absolute

Temporary

Contraindications to live attenuated vaccines: Absolute: 1- History of anaphylactic reactions.

2- Subsequent doses of pertussis vaccines are absolutely

contraindicated if the child gets (within 48 hours of vaccination )

Fever (40.5) ,

Collapse or shock .

Persistent crying for 3 hours without apparent cause.

Convulsion with or without fever within 3 hours after

vaccination.

3- HIV infection is an absolute contraindication to administration of

live attenuated vaccines ( OPV & BCG).

Temporary:

1- Pregnancy.

2- Severe illness that needs hospitalization.

3- Immunosuppression.

4- Recent receipt of blood.

The strategy for the vaccine delivery:

(I) The static immunization strategy.

(II) The National Immunization Days (NIDs).

(III) Mopping up Immunization.

(IV) Outreach immunization.

I) The static immunization strategy:

Advantages of integration of immunization services through (MCH):

1-Available resources.

2- Cold Chain maintenance.

3- Save ,time, effort and money.

(II) The National Immunization Days (NIDs):

It is periodic immunization of all the eligible targets in a defined

group over a large geographic areas within a short period of time. It

is one of the strategy for polio eradication and tetanus elimination.

For successful NIDs for polio:

Two doses of OPV are given to all children in the age group

0-59 months within 1-3 days.

It is conducted in two rounds (4-6weeks apart).

The doses of OPV given are extradoses and do not replace the

routine doses given during infancy.

The NIDs are conducted during low season of polio transmission

Most countries conduct NIDs annually for at least three years

and until polio is reduced from being an endemic disease to a

disease that occurs only in focal areas. Then the Mopping Up

Immunization is conducted.

(III) Mopping up Immunization:

It is house-to-house immunization with OPV in high risk districts.

It consists of two to three rounds 4-6 weeks apart .

Each round should be completed within a short period of time (3days).

High risk districts are those:

Where the wild polio virus is still circulating

( polio case in the last 36 months) .

With low immunization coverage.

Transient population, with overcrowding poor sanitary

environment and low access to health services.

(IV) Outreach immunization:

What is the difference between the NIDs and the out reach

Strategy?

The outreach is carried for routine immuniation that is compusory

for the targets in certain areas where:

- immunization services are not accessible.

- vaccination coverage is Low.

The outreach is carried during any time without specific duration.

Limitations:

(i) Expensive

(ii) Cold chain failure.

(iii) Difficulty to arrange the immunization schedule.

Missed opportunity :

It occurs when a child or a woman in child bearing period comes to

the health facility or outreach site and does not receive any of the

vaccine doses for which he or she is eligible.

The reasons for missed opportunity are:

Health workers` practices.

Logistical problems.

Failure to administer simultaneously all the vaccines for which the child is eligible.

False contraindications to immunization.

False contraindications to immunization:

Conditions that are wrongly considered as contraindications:

Minor illness( respiratory tract infections ,diarrhea, fever < 38.5C).

Prematurely or small for date infants.

Child being breast-fed.

Family history of convulsion.

History of jaundice at birth

Chronic health problems: Malnutrition ,allergy, asthma, other atopic

manifestations, hay fever ,chronic diseases of heart, lungs, kidney or

liver, cerebral palsy & Down syndrome ,dermatoses, local skin lesion.

Treatment with antibiotics, low dose corticosteroids( local or inhaled)

The cold chain:

It is the system of storage and transportation of the vaccine at

low temperature (cold condition) from the manufacture till it is

consumed.

Polio vaccine is the most sensitive vaccine to heat.

Live attenuated vaccines are allowed to be frozen

(OPV, Measles, MMR and BCG).

Inactivated vaccines must not be frozen ( DPT, DT, dT

, TT and HB) .

The levels of cold chain

The administrative

level

Storage

period

Temperature

The vaccines

Central & regional

stores

Maximum

three months

- 20 to- 30C

OPV, Measles,

MMR,BCG

+2 to +8C DPT, DT, dT,

TT& HB,Hib

Districts stores&

local immunization

centers

Maximum

one month

0C to+8C

OPV, Measles,

MMR, BCG

+2 to +8C

DPT, DT, dT,

TT& HB,Hib

The administrative levels of cold chain according to the

duration of the storage and the temperature required to keep

the vaccine potent

The equipment and tools

The procedures The health staff

The components of the cold chain :

Refrigeration equipment:

Refrigerator

Cold boxes

Vaccine carriers

The ice packs retained in the freezer

-To stabilize the temperature of the refrigerator at the

optimum level.

- Fully frozen ice-packs are used for lining the vaccines

carriers and the cold boxes during storing the vaccines

1-The refrigerator :

Placed in the coolest place of the health centers away from sunlight

Well ventilated and adequate air circulation around it .

Kept locked and open only when necessary.

Defrosted regularly .

Ice packs are kept in the freezer.

Its temperature is recorded twice daily.

Drugs, drinks or food must not be stored in the refrigerator.

Both the monitor and thermometer are placed in the refrigerator.

The temperature chart is stuck on the door outside the refrigerator.

The diluents should be kept on the lowest shelf.

Question:

What is the optimum Temperature of the

refrigerator in the health center?

+2 C to +8C

Cold box

ice Packs

Vaccine carrier

Tools for monitoring the cold chain:

1- Cold Chain Monitor Card.

2- Freeze Watch Indicator

3- Cold Chain Refrigerator Graph

4- Vaccine Vial Monitors

5- Shake Test

Cold Chain Refrigerator Graph The vaccines are stored in refrigerators, they are monitored twice a day

and readings are recorded on a chart to ensure a safe temperature is

maintained. Emergency provisions made. Vaccines moved to cold

storage for 48 hours.

+2C

+8C

2-Cold Chain Monitor

Card: is used to show

cumulative exposure to

Temp. above the safe

range during storage&

transportation . It has an

indicator that responds

to two different Temps:

the first part marked as

ABC, responds to Temp

above +10C; the 2nd

part marked as D

responds to Temps.

above +34C.

2-Cold Chain Monitor Card:

The front of the cold chain monitor has:

(1)A record form that health workers fill in to show when vaccines

are received.

(2) An indicator that is a heat-sensitive strip with four windows,

marked A, B, C and D.

(3) An interpretation guide explaining what to do with vaccines that

have been exposed to high temperatures.

(4) A space for filling in the following information: name of

supplier/manufacturer, type of vaccine.

The back of the cold chain monitor has:

Instructions on use.

A table giving information on the time and

temperature characteristics of the Monitor.

3-Vaccine vial monitors:

Every vial is also shipped with a

temperature-sensitive label, that health

workers monitor during vaccination

sessions.

SAFE

If the inner square is

lighter than the outer

ring and the expiration

date is valid, the

vaccine is

usable

SPOILED

If the inner square

matches or is darker

than the outer ring,

the vaccine must be

discarded.

4-The shake test

DPT, hepatitis B and

tetanus toxoid vaccines

can all be damaged by

freezing. By shaking two

vials, side-by-side, one

that might have been

frozen and one that has

never been frozen, health

workers can determine if a

vaccine has spoiled.

What damage the Vaccines?

1. Any defect in the cold chain.

2. Out date expiry.

3. Using skin antiseptic at the site of injection (e.g. BCG).

4. Using the reconstituted vaccine (MMR, measles, BCG)

after the recommended period ( 6 hours).

5. Exposure of the vaccine to unacceptable temperature

during the immunization session.

6. Exposure of the vaccine to direct sunlight (BCG)

86190117 the Expanded Program on Immunization Lecture

Documents

Transcript of 86190117 the Expanded Program on Immunization Lecture