BCG ,DPT ,POLIO
VACCINES
Dr M.Sanjeevappa
Designated Associate Professor
Dept of Paediatrics
GMC ,Anantapur
BCG VACCINE
Tuberculosis occurs most commonly in
children less than 5 years.
-PTB : 60 –70 %
-Extrapulmonary: 30–40%
In 2016, an estimated 253,000 children died
of TB and 52,000 of them are HIV-infected
children.
BCG VACCINE
Bacillus -Calmette-Guerin.
Live attenuated vaccine against Tuberculosis.
Protects against TB Meningitis, MiliaryTB
Common strains used-Copenhagen(Danish1331),
Pasteur , Glaxo
Danish 1331-Produced at Guindy, Tamil Nadu,
India
Available as lyophilised(freeze dried) powder
Reconstituted with sterile normal saline.
BCG VACCINE
BCG VACCINE
Dose –0.05ml (neonates) , 0.1ml (infants and
children)
Route of administration –intradermal(26G needle)
Site –left upper arm at insertion of deltoid.
BCG VACCINE
Papule at site of injection (2-3 weeks)
Breaks into shallow ulcer with crust
Permanent tiny round scar 4-8mm diameter.
Healing occurs (6-12 weeks)
Increases size with diameter of 4-8mm (5-6
weeks)
BCG VACCINE
SCHEDULE
National Immunization Program
At birth
Catch up till 1 yr
IAP 2016
At birth
Catch up till 5 yr
BCG VACCINE
CONTRAINDICATION
Immunodeficiency (HIV, leukemia, lymphoma)
Generalized eczema
Infective dermatosis
Hypogammaglobinemia
STORAGE
2-8°C
Sensitive to heat and light
Discard unused vaccine after 4hours of
reconstitution
DPT VACCINE
EPIDEMIOLOGY
Diphtheria : 2,599 cases and 176 deaths in 2016.
5,293 cases and 148 deaths in 2017.
Pertusis: 39,091 cases in 2011.
23,779 cases and 6 deaths in 2017.
Tetanus : 23,356 cases in 1990
4,702 cases in 2017.
Neonatal tetanus : 588 cases in 2012
295 cases with 9 deaths in 2017
DPT VACCINE
COMPONENTS :
Tetanus toxoid: from 20 Lf to 30 Lf units.
Diphtheria toxoid: from 5 Lf to 25 Lf units.
Killed whole-cell pertussis(wP) bacilli.
Adsorbed on insoluble aluminum salts which act as
adjuvants
DPT VACCINE
EFFICACY
The efficacy against diphtheria and
tetanus exceeds 95%.
The efficacy of wPvaccine against pertussis
in children is 78%
The efficacy of combination DTwPvaccines
ranged from 46% to 92%
DPT VACCINE
ADVERSE EFFECTS
Serious adverse effects :
fever more than 40.5°C –0.2 –4.4 /1000 doses
persistent crying -4–8.8 /1000 doses
hypotonic hyporesponsiveepisodes (HHEs)-0.06–
0.8/1000 doses
seizures 0.16–0.39 /1000 doses
Encephalopathy-0.007/ 1000 doses
Minor adverse effects :
pain, swelling, and redness at the local site,
fever,
fussiness,
anorexia, and vomiting are reported in almost half the
vaccineesafter any of the three primary doses.
DPT VACCINE
ABSOLUTE CONTRAINDICATIONS :
History of anaphylaxis or
Development of encephalopathy within 7 days
following previous DTwPvaccination.
RELATIVE CONTRAINDICATION :
Progressive or evolving neurological illnesses.
DPT VACCINE
RECOMMENDATIONS FOR USE :
Standard schedule :
primary doses at 6, 10, and 14 weeks
two boosters at 15–18 months and 4–5 years.
Catch-up vaccination :
three doses at 0, 1, and 6 months.
DTwPis not recommended in children beyond 7
years of age due to increased risk of side-effects.
DPT VACCINE
COLD CHAIN AND ADMINISTRATION :
Stored at 2–8°C.
Never be frozen,
if frozen accidentally, should be discarded.
The dose is 0.5 ml intramuscularly(IM).
the preferred site is the anterolateralaspect of
the thigh.
DPT VACCINE
DTaP:
These vaccines contain ≥1 of the separately
purified antigens :
pertussistoxin (PT).
filamentous hemagglutinin(FHA).
pertactin(PRN).
fimbrialhemagglutinins1, 2, and 3.
POLIO VACCINES
EPIDEMIOLOGY :
Poliomyelitis is an acute infection by three poliovirus
serotypes 1, 2, or 3, and was the leading cause of
permanent disability in children in the past.
In 1988, more than 125 countries had WPV transmission
with 350,000 of paralytic polio cases.
As of November 2019 only 2 countries—Afghanistan (20)
and Pakistan (82) remain endemic.
The last case of poliomyelitis caused by WPV type 2
(WPV2) was recorded in India in 1999.
Global eradication of WPV2 was certified in 2015.
POLIO VACCINE
IPV first developed and licensed in 1955.
mOPVvaccine was licensed in 1961.
tOPVwas licensed in 1963.
bOPVlicensed and used in some settings
since December 2009.
Following the global switch from tOPVto bOPV
in April 2016, tOPVwill no longer be available
and will be replaced by bOPV.
ORAL POLIO VACCINE
Included in
Pulse Polio Immunization
Supplementary immunization activities.
National Polio Surveillance Project.
National Immunization program
ORAL POLIO VACCINE
DEVELOPMENT OF IMMUNITY
Administration of vaccine
Infect intestinal mucosa
Multiplication in mucosal cells (take)
Provides local as well as systemic immunity
ORAL POLIO VACCINE
Dose –2 drops.
Route of administration –Oral’
Method of administration :
Tilt the child’s back and gently squeeze the
cheeks or pinch the nose to make the mouth
open. Let the drops fall from the dropper onto
the child’s tongue. Repeat the process if child
spits out the vaccine.
ORAL POLIO VACCINE
ORAL POLIO VACCINE
SCHEDULE
National Immunization Program
OPV0 at birth.
OPV1 at 6th week
OPV2 at 10th week
OPV3 at 14th week
OPV booster at 15-18 months and 5yr.
IAP 2016
OPV at birth, 6mo, 9mo and 5yr (In case of
sequential IPV-OPV Schedule)
ORAL POLIO VACCINE
VAPP :
clinically resembles paralytic polio by WPV.
one case per 1.4 million children vaccinated.
type 3 poliovirus (42%).
type 2 (26%).
type 1 (20%).
mixtures of more than one virus (15%).
ORAL POLIO VACCINE
VDPV
The attenuated viruses in live OPV vaccines
may reacquire neurovirulenceand
transmission capacity through replication and
genetic divergence effect.
Three categories:
(1) cVDPVs.
(2) iVDPVs.
(3)aVDPVs.
ORALPOLIO VACCINE
Immunogenicity and Effectiveness :
In developed countries :
100% for all three poliovirus types.
In developing countries :
73%, 90%, and 70% to poliovirus type 1, 2,
and 3, respectively.
ORAL POLIO VACCINE
CONTRAINDICATIONS :
Immunocompromisedindividuals (symptomatic
HIV, leukemia, malignancy, those under
corticosteroids)
Active viral infections
ORAL POLIO VACCINE
STORAGE :
Stable at 4-8°C for 3-4 months.
-20degree C for a year.
Potency drops rapidly with temperature
fluctuations , Potency monitored using Vaccine
Vial Monitor (VVM).
Vaccine discarded if color of inner square in
vvmis as dark as or darker than color of outer
circle
ORAL POLIO VACCINE
INACTIVATED POLIO VACCINE
Developed by Salk
Suspension of formaldehyde killed poliovirus
grown in monkey kidney, human diploid or vero
cell culture
Induces humoralimmune response and gives
protection from paralysis
Does not induce local immunity
Vaccine potency measured by ‘D’ antigen
Currently used Enhanced potency IPV (eIPV)
contain 40D, 8D, 32D units of types 1, 2, 3
polioviruses.
INACTIVATED POLIO VACCINE
Highly immunogenic.
Seroconversion–90-95% in infants beyond
8 weeks age administered of two doses of
IPV 2months apart.
99% of those given 3 doses 4 weeks apart.
INACTIVATED POLIO VACCINE
Dose –0.5ml
Route of administration –intramuscular or
subcutaneous
INACTIVATED POLIO VACCINE
SCHEDULE
National Immunization Program
At 14 weeks
IAP 2016
Sequential IPV-OPV schedule
3 doses IPV at 6, 10 and 14 weeks , or
2 doses IPV at 8 and 16 weeks (primary) and 1
dose IPV at 15-18 months (booster)
Also give OPV at birth , 6mo, 9mo, and 5yr and
on NIDs and SIAs
Catchupup to 5yr; 3 doses at 0, 2 and 6months
INACTIVATED POLIO VACCINE
ADVANTAGES :
Efficacy of IPV in preventing poliomyelitis is
excellent.
Does not cause Vaccine associated paralytic
poliomyelitis.
Vaccine of choice in patients with
immunodeficiency.
Can be administered to pregnant women.
INACTIVATED POLIO VACCINE
DISADVANTAGE :
Immunity not rapidly achieved.
Injections during epidemic can precipitate
paralysis.
Does not produce local immunity , virus can
multiply in gut and can be a source of infection
to others.
INACTIVATED POLIO VACCINE
ADVERSE REACTIONS :
No serious adverse reactions.
Minor local erythema, induration, swelling and
tenderness.
CONTRAINDICATIONS
Any known allergy
STORAGE
2-8°C
Sensitive to light