EDWARDEDWARD
JENNERJENNER
May 14May 14
17961796
Opisthotonos: body is bent backwardOpisthotonos: body is bent backward
LGF, toxic, pseudomembrane, bull neckLGF, toxic, pseudomembrane, bull neck
v. severe cough,v. severe cough,
vomiting, ribbon likevomiting, ribbon like
tenacious sputumtenacious sputum
Immunisefirsttohugme!Immunisefirsttohugme!
Immunisefirsttohugme!Immunisefirsttohugme!
WELCOME ALLWELCOME ALL
““Few things give more benefitsFew things give more benefits
for child survival thanfor child survival than
immunization”immunization”
At the end …. you will learnAt the end …. you will learn
• Immunization is an essential part of child-careImmunization is an essential part of child-care
• .. has a.. has a greatgreat role in reducing IDs, NMR, IMRrole in reducing IDs, NMR, IMR
• .. is.. is cost effectivecost effective
• Vax.Vax. varyvary in efficacy, dosing, safety, stabilityin efficacy, dosing, safety, stability
• It addresses allIt addresses all susceptiblesusceptible personspersons
• SchedulesSchedules varyvary among countriesamong countries
The best Vax. for a newbornThe best Vax. for a newborn
is BMis BM
Vaccines: the BasicsVaccines: the Basics
• Vax. contain the same germs that cause d. ButVax. contain the same germs that cause d. But
they are either killed/weakenedthey are either killed/weakened: no sickness: no sickness
• Some vax. contain only aSome vax. contain only a partpart of germof germ
• Vax. stimulates immune sys. to make AB, exactlyVax. stimulates immune sys. to make AB, exactly
like it would do to the d.like it would do to the d.
Vax. are powerful medicines. But unlike mostVax. are powerful medicines. But unlike most
medicines, vax.medicines, vax. preventprevent the d.the d.
Why vaccinate ?Why vaccinate ?
 Immunization prevents vax.-preventable d.:Immunization prevents vax.-preventable d.:
110 million110 million illnessesillnesses areare preventedprevented
 3.5 million lives3.5 million lives areare saved every yearsaved every year
 Uptake of new and underused vax. is increasingUptake of new and underused vax. is increasing
 But 18.7 million infants worldwide are still missing outBut 18.7 million infants worldwide are still missing out
on basic vaccineson basic vaccines
ImmunisationImmunisation ReducesReduces
MortalityMortality
MorbidityMorbidity
MalnutritionMalnutrition
VADXVADX
Drop out from schoolDrop out from school
Childhood strokeChildhood stroke
Successes Story of ImmunisationSuccesses Story of Immunisation
Small pox eradicatedSmall pox eradicated
Polio… soonPolio… soon
Measles… nextMeasles… next
Dramatic fall in IDDramatic fall in ID
Dramatic rise in child survivalDramatic rise in child survival
Significant fall in malnutritionSignificant fall in malnutrition
Economic upliftEconomic uplift
10 myths and facts about vax.10 myths and facts about vax.
1.1. Better hygiene-sanitation will make ds. disappearBetter hygiene-sanitation will make ds. disappear
–– No need of vax.No need of vax. FALSEFALSE
2. Vax. have damaging SE; can even be fatal2. Vax. have damaging SE; can even be fatal. FALSE. FALSE
3. DTP and polio vax. cause3. DTP and polio vax. cause SIDS.SIDS. FALSEFALSE
4. Vax. Target Ds. are almost eradicated in my country4. Vax. Target Ds. are almost eradicated in my country
-- No need of vax.-- No need of vax. FALSEFALSE
5. Vax.-preventable ds. are just a fact of life.5. Vax.-preventable ds. are just a fact of life. FALSEFALSE
6.6. >1 vax. at a time can increase risk and overload the>1 vax. at a time can increase risk and overload the
child’s immune systemchild’s immune system. FALSE. FALSE
7.7. Flu is just a nuisance, the vax. isn’t v. effective.Flu is just a nuisance, the vax. isn’t v. effective. FALSEFALSE
8.8. Better to be immune by disease than by vax.Better to be immune by disease than by vax. FALSEFALSE
9.9. Vax. containVax. contain mercurymercury which is dangerous.which is dangerous. FALSEFALSE
10.10. Vaccines cause autismVaccines cause autism FALSEFALSE
10 myths and facts about vax. …10 myths and facts about vax. …
Thiomersal: organic, mercury added to some vax. As preservative; most widely-used
preservative in multi-dose vials; no evidence to suggest it poses a health risk
ImmunityImmunity
…… body'sbody's ability toability to self-protectself-protect
ActiveActive
PassivePassive
Sensitizing with anSensitizing with an germ/antigen togerm/antigen to
make Abmake Ab
naturalnatural :: infectioninfection
artificialartificial :: vax.vax.
Memory remains in immune sys.Memory remains in immune sys.
Active immunityActive immunity
Passive ImmunityPassive Immunity
A.A. From mother:From mother:
B.B. External sources:External sources:
TIGTIG
VZIGVZIG
HBIGHBIG
ADSADS
RIGRIG
AGSAGS
AntivenomsAntivenoms
Antibotulin, etc.Antibotulin, etc.
Mainly forMainly for RxRx
BBy givingy giving Antibody:Antibody: ((TemporaryTemporary effecteffect))
Transplacental AntibodiesTransplacental Antibodies
• DPT, Polio, MMR, Influenza, HBVDPT, Polio, MMR, Influenza, HBV
• Transferred from 2Transferred from 2ndnd
TMTM. Only IgG. Only IgG
• These can inhibit vax. response in 1These can inhibit vax. response in 1stst
y of life: usuallyy of life: usually
overcome by booster dosesovercome by booster doses
Transfer of IgA in BM for gut of the babyTransfer of IgA in BM for gut of the baby
Fetus starts IgM at 20wFetus starts IgM at 20w
What isWhat is immunisationimmunisation??
Giving a vax.Giving a vax. for immunityfor immunity
Target DiseasesTarget Diseases
1010 EPI diseasesEPI diseases
OthersOthers
AnthraxAnthrax
Chicken poxChicken pox
CholeraCholera
HAVHAV
HPVHPV
JB encephalitisJB encephalitis
InfluenzaInfluenza
MeningoccusMeningoccus
Mumps, rubellaMumps, rubella
PneumococcusPneumococcus
RabiesRabies
Rota virusRota virus
TyphoidTyphoid
Yellow fever, etc.Yellow fever, etc.
Vax. in BangladeshVax. in Bangladesh
• BCGBCG
• DPTDPT
• PolioPolio
• HBVHBV
• HIBHIB
• HAVHAV
• HPVHPV
• MMRMMR
• MeningococcusMeningococcus
• RabiesRabies
• Rota virusRota virus
• TyphoidTyphoid
• VaricellaVaricella
• CholeraCholera
• PneumococcusPneumococcus
• InfluenzaInfluenza
Future vax. sFuture vax. s
MalariaMalaria
LeprosyLeprosy
Dengue, ChikungunyaDengue, Chikungunya
Improved BCGImproved BCG
HCVHCV
HEVHEV
AIDSAIDS
EbolaEbola
MERSMERS
3 types of vaccine3 types of vaccine
Characteristics of Live Vax.Characteristics of Live Vax.
SingleSingle shot.shot. DurableDurable immunityimmunity
…… of Killed Vax.of Killed Vax.
Multiple shotsMultiple shots ((1y1y series)series) followed byfollowed by booster(s)booster(s)
…… of Extract/toxoidof Extract/toxoid
• 1y1y series followed byseries followed by booster(sbooster(s))
∀ ⇑⇑ immunogenic withimmunogenic with adjuvantadjuvant
Live vax. : BCGLive vax. : BCG
ImmediatelyImmediately after birthafter birth
One i.d. doseOne i.d. dose
ConflictingConflicting reports of efficacyreports of efficacy
Protects fromProtects from lethal TBlethal TB
Advantages DisadvantagesAdvantages Disadvantages
 One shot.One shot. Very safeVery safe
 Expertise for i.d. inj.Expertise for i.d. inj.
 Does not prevent TBDoes not prevent TB
 Light sensitiveLight sensitive
 Generalized vacciniaGeneralized vaccinia
 not stable at room temp.not stable at room temp.
 UlcerUlcer nn scarscar
‘‘Bull neck’Bull neck’
Diphtheria Pertussis TetanusDiphtheria Pertussis Tetanus
DPTDPT
3x3x 0.5ml i.m. at 6-10-14w0.5ml i.m. at 6-10-14w
Booster 6-12mo laterBooster 6-12mo later
Protects forProtects for 1010 yy
Advantages DisadvantagesAdvantages Disadvantages
• DTDT very effectivevery effective
• Whole cell pertussis:Whole cell pertussis: 60%60% effectiveeffective
• Acellular pertussis (aP/Pa) is superiorAcellular pertussis (aP/Pa) is superior
F, restlessF, restless,, inconsolable cryinconsolable cry
Redness swelling at prick siteRedness swelling at prick site
• Anaphylaxis febrile fit may occurAnaphylaxis febrile fit may occur
Pertussis Deaths, USA: 2000-2009Pertussis Deaths, USA: 2000-2009
A young girl with bulbar polio with tripod sign attempts to sitA young girl with bulbar polio with tripod sign attempts to sit
Poliomyelitis:Poliomyelitis: 3 strains3 strains
• OPV (live)/IPV (killed)OPV (live)/IPV (killed)
• 3 doses: 6-10-14w (with DPT)3 doses: 6-10-14w (with DPT)
• 44thth
with measles vax.with measles vax.
• PulsePulse dosing for developing countriesdosing for developing countries
Advantages DisadvantagesAdvantages Disadvantages
• OPV is easy, cheap, rapid;OPV is easy, cheap, rapid; herdherd immunityimmunity
• Permanent protectionPermanent protection
• No OPV in immunocompromised (Give IPV)No OPV in immunocompromised (Give IPV)
• Breast milk may killBreast milk may kill
• Change to wild virus (VAPP:Change to wild virus (VAPP: 1/2.5million doses)1/2.5million doses)
VAPP: vax. Assoc. polio paralysisVAPP: vax. Assoc. polio paralysis
Measles vax.Measles vax.
AttenuatedAttenuated live viruslive virus
• 0.5ml s.c. at 9mo; better as MMR0.5ml s.c. at 9mo; better as MMR
• 2 doses: 22 doses: 2ndnd
at 15at 15thth
momo
– no primary vax. failureno primary vax. failure
– permanent immunitypermanent immunity
• LastingLasting protectionprotection
Advantages DisadvantagesAdvantages Disadvantages
Measles vax. isMeasles vax. is veryvery effective, safeeffective, safe
Sensitive to heatSensitive to heat
NotNot effective <effective <6 mo6 mo age (maternal antibody)age (maternal antibody)
schedule varies among countriesschedule varies among countries
MUMPS vax.MUMPS vax.
• Live-attenuatedLive-attenuated
• MMR preferredMMR preferred
• 0.5 ml s.c. +/- other vax.0.5 ml s.c. +/- other vax.
• >95% with>95% with singlesingle dosedose
• 2 doses: 100%2 doses: 100%
Must immunize before pubertyMust immunize before puberty
Measles
German measles
"blueberry muffin (ecchymoses)"
Newborn with CRS
Rubella vax.Rubella vax.
• 2 doses2 doses
• MMR preferredMMR preferred
• Can protect within 3d of exposureCan protect within 3d of exposure
• 2nd dose before 11y2nd dose before 11y
• No conception within 28dNo conception within 28d
Adverse Reactions: MMRAdverse Reactions: MMR
• Common:Common: F, rash, lowF, rash, low
plateletsplatelets
• LAP, arthralgia,LAP, arthralgia, arthritis inarthritis in
adult femalesadult females after 1-3wafter 1-3w
(reactive)(reactive)
• Rare:Rare: orchitis, LGF,orchitis, LGF,
parotitis, limb painparotitis, limb pain
• Very rare:Very rare: febrile fit,febrile fit,
deafness, meningitis,deafness, meningitis,
encephalitis, pruritusencephalitis, pruritus
MMR contraindicationsMMR contraindications
• Administration of IG, blood transfusion:Administration of IG, blood transfusion:
• Altered immunity (live vax):Altered immunity (live vax):
• Corticosteroids (live vax):Corticosteroids (live vax):
• Pregnancy (live vax):Pregnancy (live vax):
• Ig in high doses (Kawasaki, GBS) can inhibitIg in high doses (Kawasaki, GBS) can inhibit
responseresponse
– push 2w before or 3mo after Ig/BTpush 2w before or 3mo after Ig/BT
Ig and BTIg and BT
• NoNo live vax.live vax. inin
– malignancy, chemotherapymalignancy, chemotherapy
– pregnancypregnancy
– HD steroid, radiation,HD steroid, radiation, AIDSAIDS
• Vax. mumps virusVax. mumps virus do notdo not transmittransmit
• Risk of mumps/rubella in immunodeficient can beRisk of mumps/rubella in immunodeficient can be ⇓⇓ byby
vax. for close contactsvax. for close contacts
ImmunodeficienciesImmunodeficiencies
GlucocorticosteroidsGlucocorticosteroids
• At 2mg/kg/d or >20mg/d x2w:At 2mg/kg/d or >20mg/d x2w: wait for 1 mowait for 1 mo
• Postpone steroids if vax. is essentialPostpone steroids if vax. is essential
PregnancyPregnancy
• No conception for 4w after live vax.No conception for 4w after live vax.
• Vax. virus infects placenta (2%), not the fetusVax. virus infects placenta (2%), not the fetus
• Accidental vax. in preg.: no cong. defects:Accidental vax. in preg.: no cong. defects:
– not an indication for terminationnot an indication for termination
Vax. before pregnancy?Vax. before pregnancy? Any vax.Any vax.
• It's the best to have a medical CU before preg.It's the best to have a medical CU before preg.
Vax. in pregnancy: principlesVax. in pregnancy: principles
• Generally: no live vax.Generally: no live vax.
• Toxoids, inactivated vax., Ig are safeToxoids, inactivated vax., Ig are safe
• Start in 2Start in 2ndnd
TM (except flu): miscarriage, fetal anomalyTM (except flu): miscarriage, fetal anomaly
• Post-exposure Ig anytime:Post-exposure Ig anytime: HA&B, measles, rabies,HA&B, measles, rabies,
tetanus, varicellatetanus, varicella
• TT, HBV, DTP, flu, pneumococcusTT, HBV, DTP, flu, pneumococcus
• Vax. can protect both mom and fetusVax. can protect both mom and fetus
TM: trimester. HA&B: hepatitis A and BTM: trimester. HA&B: hepatitis A and B
• If no prior Tdap, get it before preg. Td is better (safety ofIf no prior Tdap, get it before preg. Td is better (safety of
pertussis part Is not fully known)pertussis part Is not fully known)
• Hib: prior splenectomy, menigococcal anytimeHib: prior splenectomy, menigococcal anytime
• Inactive Typhoid, HBV. Rabies: if exposedInactive Typhoid, HBV. Rabies: if exposed
• Cholera, plague, J. encephalitis: if high riskCholera, plague, J. encephalitis: if high risk
• Anthrax: post-exposure prophylaxis and vax.Anthrax: post-exposure prophylaxis and vax.
None of these are live vax.None of these are live vax.
Vax. in pregnancy …Vax. in pregnancy …
Recommendations for TdapRecommendations for Tdap
• Age: 11y or older sAge: 11y or older specially forpecially for
• adults in contact with young children, padults in contact with young children, pregnant womenregnant women
• healthcare professionalshealthcare professionals
• grandparents (including those >65ygrandparents (including those >65y
• 10 yearly Td booster for those who got 1 Tdap10 yearly Td booster for those who got 1 Tdap
– 5 years for wound management5 years for wound management
Vax avoided in pregnancyVax avoided in pregnancy
• Nasal spray flu vax. (flu shot is killed virus)Nasal spray flu vax. (flu shot is killed virus)
• MMR, Varicella, BCG: postpone pregnancy for 4wMMR, Varicella, BCG: postpone pregnancy for 4w
• Little info. about other vax.: Polio, HA, Anthrax, J.Little info. about other vax.: Polio, HA, Anthrax, J.
encephalitis, Typhoid, smallpox, Yellow Fencephalitis, Typhoid, smallpox, Yellow F
• Some of these vax. contain live viruses. Carefully weighSome of these vax. contain live viruses. Carefully weigh
the risks and benefits and decidethe risks and benefits and decide
No HPV in preg.: under studyNo HPV in preg.: under study
Postpartum vaccination:Postpartum vaccination: ACIPACIP
• All EXCEPT smallpox are safe during lactationAll EXCEPT smallpox are safe during lactation
• MMR for rubella nonimmuneMMR for rubella nonimmune
• Varicella dose 1 in hospital and 2Varicella dose 1 in hospital and 2ndnd
in 4-8win 4-8w
• Tdap: if not given (Tdap: if not given (prevents pertussis to NB)prevents pertussis to NB)
• Anti-D if baby is Rh+veAnti-D if baby is Rh+ve
• If <26y: HPVIf <26y: HPV
HPVHPV>130 strains>130 strains
• Double stranded DNA virusDouble stranded DNA virus
– Non-oncogenic/oncogenicNon-oncogenic/oncogenic
• ~ everyone will be infected at least once in life~ everyone will be infected at least once in life
– Most unaware when infectedMost unaware when infected
– Most common STD in M and FMost common STD in M and F
STD: sexually transmitted diseaseSTD: sexually transmitted disease
HPVHPV
• Ca cervix kills 275,000 women, mostly in 3WCCa cervix kills 275,000 women, mostly in 3WC
• Prevents also vulval, vaginal, penile, colorectal,Prevents also vulval, vaginal, penile, colorectal,
head-neck and some skin cancershead-neck and some skin cancers
• 2 types. Premarital vax. are 100% effective in2 types. Premarital vax. are 100% effective in
preventing precancerpreventing precancer
• Age: 9y and aboveAge: 9y and above
• Very safeVery safe
HPVHPV
• Females: Routine: 9-26yFemales: Routine: 9-26y
– Either HPV4 or HPV2Either HPV4 or HPV2
• Males: Routine: at 11yMales: Routine: at 11y
– HPV4 is recommendedHPV4 is recommended
• 22ndnd
dose 1-2 mo of 1dose 1-2 mo of 1stst
and 3and 3rdrd
6 mo after 16 mo after 1stst
HIV and Adult VaccinationHIV and Adult Vaccination
Vaccines are esp. critical for people with chr. d. like HIVVaccines are esp. critical for people with chr. d. like HIV
If CD4 count is ≥200:If CD4 count is ≥200:
• fluflu,, TdapTdap ,, Pneumo-Pneumo-, HB, HPV (man/woman up to 26y), HB, HPV (man/woman up to 26y)
• MMR (born in 1957/later or not have immunity)MMR (born in 1957/later or not have immunity)
• Varicella (born in 1980/later and have not gotten 2Varicella (born in 1980/later and have not gotten 2
doses or have no immunity)doses or have no immunity)
CD4 count is <200:CD4 count is <200: flu, Tdap, Pneumococcal, HB, HPVflu, Tdap, Pneumococcal, HB, HPV
Asplenia and Adult VaccinationAsplenia and Adult Vaccination
Vax. are esp. critical for chr. d. like aspleniaVax. are esp. critical for chr. d. like asplenia
• Flu, Tdap, Hib (if not vaccinated)Flu, Tdap, Hib (if not vaccinated)
• Pneumo- , Meningococcal, Zoster (if 60y or older), HPVPneumo- , Meningococcal, Zoster (if 60y or older), HPV
• MMR (not vaccinated or no immunity)MMR (not vaccinated or no immunity)
Title
•
Flu vax: inactivated virusFlu vax: inactivated virus
• UniversalUniversal
• High risk:High risk: children, elderly, immunodeficient, preg.,children, elderly, immunodeficient, preg.,
chr. Illnesschr. Illness
• Dose: initial 2 shots; i.m.; then single dose annuallyDose: initial 2 shots; i.m.; then single dose annually
for new strainfor new strain
• Age 6-36 mo: half the adult doseAge 6-36 mo: half the adult dose
Yellow fever
• Ac. viral hemorrhagic F (mosquitoes)Ac. viral hemorrhagic F (mosquitoes)
• 2013: in routine imm. in 35/44 countries/territories at risk2013: in routine imm. in 35/44 countries/territories at risk
in Africa and Americas (cov.41%)in Africa and Americas (cov.41%)
• Single dose is sufficient‡. At 9-12mo (measles), s.c.Single dose is sufficient‡. At 9-12mo (measles), s.c.
• CI: in <6 mo and immunodeficientCI: in <6 mo and immunodeficient
• Mass vaccination for inhabitants at riskMass vaccination for inhabitants at risk
Bangladesh EPIBangladesh EPI
1979: launched1979: launched
1995: Polio eradication; elimination of1995: Polio eradication; elimination of
maternal and NTmaternal and NT
2003: Introduced HBV2003: Introduced HBV
2009: HIB2009: HIB
2012: rubella2012: rubella
Next: pneumococcus, HPVNext: pneumococcus, HPV
Objectives of EPI:
• Disease reduction
• vax. coverage
Targets
 Eliminate NT (<1 /1000) 2005√
 Measles ⇓ 95% 2005√
Vax. coverage 90% 2005√
 Polio eradication 2007√
 ⇓ HBV 80% in U5 2010
ImmunisationImmunisation ScheduleSchedule
• At birthAt birth BCGBCG
HBV 1HBV 1
• 6-10-14 weeks6-10-14 weeks DPT 1,2,3DPT 1,2,3
OPV1,2,3OPV1,2,3
HIB 1,2,3HIB 1,2,3
HBV 2,0,0HBV 2,0,0
• 6 months6 months HBV 3HBV 3
• 9 mo:9 mo: (270d)(270d) MR.MR. OPV 4OPV 4
Pulse dosing of OPVPulse dosing of OPV
• 22 doses ondoses on 22 occasions (6mo) foroccasions (6mo) for U-5U-5 (up to(up to 1010
doses)doses)
• Repeat OPV replacesRepeat OPV replaces wild viruswild virus in thein the
environmentenvironment
YesYes!!
 Benefits far outweigh risksBenefits far outweigh risks
 Exception: if severe reaction to DPT (fits) theException: if severe reaction to DPT (fits) the
pertussispertussis isis omittedomitted
Our body can handleOur body can handle 15000 Ag15000 Ag at a timeat a time!!
A child who does not need hospitalization canA child who does not need hospitalization can
get the shotget the shot
Can aCan a sicksick child be immunized?child be immunized?
Missed DatesMissed Dates
Give as soon as possibleGive as soon as possible
Longer gap? Still theLonger gap? Still the nextnext dosedose
Only complete doses requiredOnly complete doses required
For remote areas altered schedules, NIDsFor remote areas altered schedules, NIDs
are usedare used
EPI gives no boosterEPI gives no booster
After 7y: pertussis is omittedAfter 7y: pertussis is omitted
In Mid- East measles vax. is given at 6 moIn Mid- East measles vax. is given at 6 mo
Schedule varies among countriesSchedule varies among countries
MoreMore InfoInfo
Every nonimmune is targetedEvery nonimmune is targeted
Consider susceptibilityConsider susceptibility
Age or weight not importantAge or weight not important
A child should be fully immunized by 9moA child should be fully immunized by 9mo
EPI targets children and CB womenEPI targets children and CB women
WhoWho be immunized?be immunized? AgeAge??
WomenWomen
 2 TTs for NT2 TTs for NT
 5 TTs5 TTs ⇒⇒ protectprotect all futureall future babiesbabies
 Woman with 3 DPTs need 2Woman with 3 DPTs need 2
 MRMR
Hygienic cord Rx is less effective than immunizingHygienic cord Rx is less effective than immunizing
the motherthe mother
Principles of ImmunisationPrinciples of Immunisation
 Follow a schedule; but not strict!Follow a schedule; but not strict!
 Schedule variesSchedule varies
 Date flexibleDate flexible
 4w = 1mo4w = 1mo
 No Vax in 3mo ofNo Vax in 3mo of IgIg
11stst
polio as IPVpolio as IPV
After DTP diseases,After DTP diseases,
Vax is still requiredVax is still required
2 TT in 12 TT in 1stst
preg. (4-7preg. (4-7
mo) 1 shot for latermo) 1 shot for later
Not a ContraindicationNot a Contraindication
 A child needingA child needing
no admissionno admission
 Mild RTIMild RTI
 DVDV
 AsthmaAsthma
 EczemaEczema
 AB TherapyAB Therapy
 Chr. Lung DsChr. Lung Ds
 Heart diseaseHeart disease
 Febrile fitFebrile fit
ContraindicationsContraindications
 Ac. IllnessAc. Illness
 Severe reactionsSevere reactions
 Hypersensitivity to a component of VaxHypersensitivity to a component of Vax
(neomycin, polymyxin B, egg protein)(neomycin, polymyxin B, egg protein)
 Progressive neuropathy for pertussis VaxProgressive neuropathy for pertussis Vax
All not equal;All not equal; depends ondepends on
immune systemimmune system
immunogenecityimmunogenecity
• All not equally stableAll not equally stable
Most stable is TTMost stable is TT
• Best herd immunity with OPV; none with toxoidBest herd immunity with OPV; none with toxoid
or inactivated vax.or inactivated vax.
• The most effective is the TTThe most effective is the TT
Effectiveness of vax. sEffectiveness of vax. s
Essential Cold ChainEssential Cold Chain
• Once opened dispensed within coupleOnce opened dispensed within couple
of hours e.g. BCGof hours e.g. BCG
5 Adverse Reactions5 Adverse Reactions
• vax. reactionsvax. reactions
• Program errorProgram error
• Injection reactionInjection reaction
• CoincidentalCoincidental
• UnknownUnknown
vax.vax. ReactionsReactions
Most vax. are safeMost vax. are safe
 MMRMMR ⇒⇒mildmild disease.disease. None with extractNone with extract
 Serious:Serious:⇐⇐ pertussis Vx.:pertussis Vx.: inconsolable cry, fever,inconsolable cry, fever,
irritability a few hours later, febrile fitirritability a few hours later, febrile fit
 Rare anaphylaxis, GBSRare anaphylaxis, GBS with some vax. swith some vax. s
To minimize reactions:To minimize reactions: do not rub prick site, givedo not rub prick site, give
paracetamolparacetamol
SafeSafe InjectionInjection
No harm to recipientNo harm to recipient
No harm to you! me!No harm to you! me!
Correct pushCorrect push ⇒⇒ no abscessno abscess
No dangerous wasteNo dangerous waste
Dispo-syringe and needle: rDispo-syringe and needle: rememberemember
1 child: 1 syringe 1 needle!1 child: 1 syringe 1 needle!
Not in buttocksNot in buttocks
IM at right angle into AL thighIM at right angle into AL thigh
No IM in bleeding disordersNo IM in bleeding disorders
S.c. Vax is given in thigh, forearmS.c. Vax is given in thigh, forearm
Jet gunsJet guns not used for vaccinationnot used for vaccination
‘‘ZZ track’track’ inj.inj. ⇒⇒less leakage, infiltrationless leakage, infiltration
SitesSites of Administrationof Administration
ID push needs expertiseID push needs expertise
Deltoid area for BCG, not very up or low.Deltoid area for BCG, not very up or low.
Avoid thighAvoid thigh
SC routeSC route
MMR, Varicella, MeningitisMMR, Varicella, Meningitis
IM routeIM route
DTP, Typhoid, HBV, HAV, RabiesDTP, Typhoid, HBV, HAV, Rabies
ImmuneImmune ResponseResponse
• Primary responsePrimary response
Traceable AB:Traceable AB: 1-2 weeks: IgM1-2 weeks: IgM
• Secondary responseSecondary response
High titre:High titre: 4-5d mainly IgG4-5d mainly IgG
MCQMCQ
• EPI targets only childrenEPI targets only children
• BCG is highly effectiveBCG is highly effective
• Pertussis vax. has more SEPertussis vax. has more SE
• TT is very stableTT is very stable
• Herd immunity can be achieved by IPVHerd immunity can be achieved by IPV
MCQMCQ
• Vaccinating NB with TT can prevent NTVaccinating NB with TT can prevent NT
• Cold or cough is a CI for vaccinationCold or cough is a CI for vaccination
• TT in pregnancy is started during 3TT in pregnancy is started during 3rdrd
TMTM
• DTP vax. can cause febrile fitDTP vax. can cause febrile fit
• Having pertussis excludes immunizationHaving pertussis excludes immunization
MCQMCQ
• TT gives herd immunityTT gives herd immunity
• Strict immunization schedule is essentialStrict immunization schedule is essential
• Having tetanus gives natural immunityHaving tetanus gives natural immunity
• Having diphtheria gives natural immunityHaving diphtheria gives natural immunity
• Parenteral typhoid vax is CI in AIDSParenteral typhoid vax is CI in AIDS
• Typhoid vax. is protective against all EFsTyphoid vax. is protective against all EFs
MCQMCQ
• MMR OPV are recommended in HIVMMR OPV are recommended in HIV
• BCG is CI in HIVBCG is CI in HIV
• In bleeding disorder an IM vax is given SCIn bleeding disorder an IM vax is given SC
• GBS may follow after some vaccinationGBS may follow after some vaccination
• Hygienic cord Rx is as equally effective to preventHygienic cord Rx is as equally effective to prevent
tetanus as immunizing the mothertetanus as immunizing the mother
NEXT LECTURENEXT LECTURE::
AGN and NSAGN and NS
THANK YOU

Immunisation

  • 5.
  • 6.
    Opisthotonos: body isbent backwardOpisthotonos: body is bent backward
  • 7.
    LGF, toxic, pseudomembrane,bull neckLGF, toxic, pseudomembrane, bull neck
  • 8.
    v. severe cough,v.severe cough, vomiting, ribbon likevomiting, ribbon like tenacious sputumtenacious sputum
  • 11.
  • 12.
  • 13.
    ““Few things givemore benefitsFew things give more benefits for child survival thanfor child survival than immunization”immunization”
  • 14.
    At the end…. you will learnAt the end …. you will learn • Immunization is an essential part of child-careImmunization is an essential part of child-care • .. has a.. has a greatgreat role in reducing IDs, NMR, IMRrole in reducing IDs, NMR, IMR • .. is.. is cost effectivecost effective • Vax.Vax. varyvary in efficacy, dosing, safety, stabilityin efficacy, dosing, safety, stability • It addresses allIt addresses all susceptiblesusceptible personspersons • SchedulesSchedules varyvary among countriesamong countries The best Vax. for a newbornThe best Vax. for a newborn is BMis BM
  • 15.
    Vaccines: the BasicsVaccines:the Basics • Vax. contain the same germs that cause d. ButVax. contain the same germs that cause d. But they are either killed/weakenedthey are either killed/weakened: no sickness: no sickness • Some vax. contain only aSome vax. contain only a partpart of germof germ • Vax. stimulates immune sys. to make AB, exactlyVax. stimulates immune sys. to make AB, exactly like it would do to the d.like it would do to the d. Vax. are powerful medicines. But unlike mostVax. are powerful medicines. But unlike most medicines, vax.medicines, vax. preventprevent the d.the d.
  • 16.
    Why vaccinate ?Whyvaccinate ?  Immunization prevents vax.-preventable d.:Immunization prevents vax.-preventable d.: 110 million110 million illnessesillnesses areare preventedprevented  3.5 million lives3.5 million lives areare saved every yearsaved every year  Uptake of new and underused vax. is increasingUptake of new and underused vax. is increasing  But 18.7 million infants worldwide are still missing outBut 18.7 million infants worldwide are still missing out on basic vaccineson basic vaccines
  • 17.
  • 18.
    Successes Story ofImmunisationSuccesses Story of Immunisation Small pox eradicatedSmall pox eradicated Polio… soonPolio… soon Measles… nextMeasles… next Dramatic fall in IDDramatic fall in ID Dramatic rise in child survivalDramatic rise in child survival Significant fall in malnutritionSignificant fall in malnutrition Economic upliftEconomic uplift
  • 19.
    10 myths andfacts about vax.10 myths and facts about vax. 1.1. Better hygiene-sanitation will make ds. disappearBetter hygiene-sanitation will make ds. disappear –– No need of vax.No need of vax. FALSEFALSE 2. Vax. have damaging SE; can even be fatal2. Vax. have damaging SE; can even be fatal. FALSE. FALSE 3. DTP and polio vax. cause3. DTP and polio vax. cause SIDS.SIDS. FALSEFALSE 4. Vax. Target Ds. are almost eradicated in my country4. Vax. Target Ds. are almost eradicated in my country -- No need of vax.-- No need of vax. FALSEFALSE 5. Vax.-preventable ds. are just a fact of life.5. Vax.-preventable ds. are just a fact of life. FALSEFALSE
  • 20.
    6.6. >1 vax.at a time can increase risk and overload the>1 vax. at a time can increase risk and overload the child’s immune systemchild’s immune system. FALSE. FALSE 7.7. Flu is just a nuisance, the vax. isn’t v. effective.Flu is just a nuisance, the vax. isn’t v. effective. FALSEFALSE 8.8. Better to be immune by disease than by vax.Better to be immune by disease than by vax. FALSEFALSE 9.9. Vax. containVax. contain mercurymercury which is dangerous.which is dangerous. FALSEFALSE 10.10. Vaccines cause autismVaccines cause autism FALSEFALSE 10 myths and facts about vax. …10 myths and facts about vax. … Thiomersal: organic, mercury added to some vax. As preservative; most widely-used preservative in multi-dose vials; no evidence to suggest it poses a health risk
  • 21.
    ImmunityImmunity …… body'sbody's abilitytoability to self-protectself-protect ActiveActive PassivePassive
  • 22.
    Sensitizing with anSensitizingwith an germ/antigen togerm/antigen to make Abmake Ab naturalnatural :: infectioninfection artificialartificial :: vax.vax. Memory remains in immune sys.Memory remains in immune sys. Active immunityActive immunity
  • 23.
    Passive ImmunityPassive Immunity A.A.From mother:From mother: B.B. External sources:External sources: TIGTIG VZIGVZIG HBIGHBIG ADSADS RIGRIG AGSAGS AntivenomsAntivenoms Antibotulin, etc.Antibotulin, etc. Mainly forMainly for RxRx BBy givingy giving Antibody:Antibody: ((TemporaryTemporary effecteffect))
  • 24.
    Transplacental AntibodiesTransplacental Antibodies •DPT, Polio, MMR, Influenza, HBVDPT, Polio, MMR, Influenza, HBV • Transferred from 2Transferred from 2ndnd TMTM. Only IgG. Only IgG • These can inhibit vax. response in 1These can inhibit vax. response in 1stst y of life: usuallyy of life: usually overcome by booster dosesovercome by booster doses Transfer of IgA in BM for gut of the babyTransfer of IgA in BM for gut of the baby Fetus starts IgM at 20wFetus starts IgM at 20w
  • 25.
    What isWhat isimmunisationimmunisation?? Giving a vax.Giving a vax. for immunityfor immunity
  • 26.
    Target DiseasesTarget Diseases 1010EPI diseasesEPI diseases OthersOthers AnthraxAnthrax Chicken poxChicken pox CholeraCholera HAVHAV HPVHPV JB encephalitisJB encephalitis InfluenzaInfluenza MeningoccusMeningoccus Mumps, rubellaMumps, rubella PneumococcusPneumococcus RabiesRabies Rota virusRota virus TyphoidTyphoid Yellow fever, etc.Yellow fever, etc.
  • 27.
    Vax. in BangladeshVax.in Bangladesh • BCGBCG • DPTDPT • PolioPolio • HBVHBV • HIBHIB • HAVHAV • HPVHPV • MMRMMR • MeningococcusMeningococcus • RabiesRabies • Rota virusRota virus • TyphoidTyphoid • VaricellaVaricella • CholeraCholera • PneumococcusPneumococcus • InfluenzaInfluenza
  • 28.
    Future vax. sFuturevax. s MalariaMalaria LeprosyLeprosy Dengue, ChikungunyaDengue, Chikungunya Improved BCGImproved BCG HCVHCV HEVHEV AIDSAIDS EbolaEbola MERSMERS
  • 29.
    3 types ofvaccine3 types of vaccine
  • 30.
    Characteristics of LiveVax.Characteristics of Live Vax. SingleSingle shot.shot. DurableDurable immunityimmunity …… of Killed Vax.of Killed Vax. Multiple shotsMultiple shots ((1y1y series)series) followed byfollowed by booster(s)booster(s) …… of Extract/toxoidof Extract/toxoid • 1y1y series followed byseries followed by booster(sbooster(s)) ∀ ⇑⇑ immunogenic withimmunogenic with adjuvantadjuvant
  • 31.
    Live vax. :BCGLive vax. : BCG ImmediatelyImmediately after birthafter birth One i.d. doseOne i.d. dose ConflictingConflicting reports of efficacyreports of efficacy Protects fromProtects from lethal TBlethal TB
  • 32.
    Advantages DisadvantagesAdvantages Disadvantages One shot.One shot. Very safeVery safe  Expertise for i.d. inj.Expertise for i.d. inj.  Does not prevent TBDoes not prevent TB  Light sensitiveLight sensitive  Generalized vacciniaGeneralized vaccinia  not stable at room temp.not stable at room temp.  UlcerUlcer nn scarscar
  • 33.
  • 36.
    Diphtheria Pertussis TetanusDiphtheriaPertussis Tetanus DPTDPT 3x3x 0.5ml i.m. at 6-10-14w0.5ml i.m. at 6-10-14w Booster 6-12mo laterBooster 6-12mo later Protects forProtects for 1010 yy
  • 37.
    Advantages DisadvantagesAdvantages Disadvantages •DTDT very effectivevery effective • Whole cell pertussis:Whole cell pertussis: 60%60% effectiveeffective • Acellular pertussis (aP/Pa) is superiorAcellular pertussis (aP/Pa) is superior F, restlessF, restless,, inconsolable cryinconsolable cry Redness swelling at prick siteRedness swelling at prick site • Anaphylaxis febrile fit may occurAnaphylaxis febrile fit may occur
  • 38.
    Pertussis Deaths, USA:2000-2009Pertussis Deaths, USA: 2000-2009
  • 39.
    A young girlwith bulbar polio with tripod sign attempts to sitA young girl with bulbar polio with tripod sign attempts to sit
  • 42.
    Poliomyelitis:Poliomyelitis: 3 strains3strains • OPV (live)/IPV (killed)OPV (live)/IPV (killed) • 3 doses: 6-10-14w (with DPT)3 doses: 6-10-14w (with DPT) • 44thth with measles vax.with measles vax. • PulsePulse dosing for developing countriesdosing for developing countries
  • 43.
    Advantages DisadvantagesAdvantages Disadvantages •OPV is easy, cheap, rapid;OPV is easy, cheap, rapid; herdherd immunityimmunity • Permanent protectionPermanent protection • No OPV in immunocompromised (Give IPV)No OPV in immunocompromised (Give IPV) • Breast milk may killBreast milk may kill • Change to wild virus (VAPP:Change to wild virus (VAPP: 1/2.5million doses)1/2.5million doses) VAPP: vax. Assoc. polio paralysisVAPP: vax. Assoc. polio paralysis
  • 48.
    Measles vax.Measles vax. AttenuatedAttenuatedlive viruslive virus • 0.5ml s.c. at 9mo; better as MMR0.5ml s.c. at 9mo; better as MMR • 2 doses: 22 doses: 2ndnd at 15at 15thth momo – no primary vax. failureno primary vax. failure – permanent immunitypermanent immunity • LastingLasting protectionprotection
  • 49.
    Advantages DisadvantagesAdvantages Disadvantages Measlesvax. isMeasles vax. is veryvery effective, safeeffective, safe Sensitive to heatSensitive to heat NotNot effective <effective <6 mo6 mo age (maternal antibody)age (maternal antibody) schedule varies among countriesschedule varies among countries
  • 52.
    MUMPS vax.MUMPS vax. •Live-attenuatedLive-attenuated • MMR preferredMMR preferred • 0.5 ml s.c. +/- other vax.0.5 ml s.c. +/- other vax. • >95% with>95% with singlesingle dosedose • 2 doses: 100%2 doses: 100% Must immunize before pubertyMust immunize before puberty
  • 53.
  • 54.
  • 56.
  • 57.
    Rubella vax.Rubella vax. •2 doses2 doses • MMR preferredMMR preferred • Can protect within 3d of exposureCan protect within 3d of exposure • 2nd dose before 11y2nd dose before 11y • No conception within 28dNo conception within 28d
  • 58.
    Adverse Reactions: MMRAdverseReactions: MMR • Common:Common: F, rash, lowF, rash, low plateletsplatelets • LAP, arthralgia,LAP, arthralgia, arthritis inarthritis in adult femalesadult females after 1-3wafter 1-3w (reactive)(reactive) • Rare:Rare: orchitis, LGF,orchitis, LGF, parotitis, limb painparotitis, limb pain • Very rare:Very rare: febrile fit,febrile fit, deafness, meningitis,deafness, meningitis, encephalitis, pruritusencephalitis, pruritus
  • 59.
    MMR contraindicationsMMR contraindications •Administration of IG, blood transfusion:Administration of IG, blood transfusion: • Altered immunity (live vax):Altered immunity (live vax): • Corticosteroids (live vax):Corticosteroids (live vax): • Pregnancy (live vax):Pregnancy (live vax):
  • 60.
    • Ig inhigh doses (Kawasaki, GBS) can inhibitIg in high doses (Kawasaki, GBS) can inhibit responseresponse – push 2w before or 3mo after Ig/BTpush 2w before or 3mo after Ig/BT Ig and BTIg and BT
  • 61.
    • NoNo livevax.live vax. inin – malignancy, chemotherapymalignancy, chemotherapy – pregnancypregnancy – HD steroid, radiation,HD steroid, radiation, AIDSAIDS • Vax. mumps virusVax. mumps virus do notdo not transmittransmit • Risk of mumps/rubella in immunodeficient can beRisk of mumps/rubella in immunodeficient can be ⇓⇓ byby vax. for close contactsvax. for close contacts ImmunodeficienciesImmunodeficiencies
  • 62.
    GlucocorticosteroidsGlucocorticosteroids • At 2mg/kg/dor >20mg/d x2w:At 2mg/kg/d or >20mg/d x2w: wait for 1 mowait for 1 mo • Postpone steroids if vax. is essentialPostpone steroids if vax. is essential
  • 63.
    PregnancyPregnancy • No conceptionfor 4w after live vax.No conception for 4w after live vax. • Vax. virus infects placenta (2%), not the fetusVax. virus infects placenta (2%), not the fetus • Accidental vax. in preg.: no cong. defects:Accidental vax. in preg.: no cong. defects: – not an indication for terminationnot an indication for termination Vax. before pregnancy?Vax. before pregnancy? Any vax.Any vax. • It's the best to have a medical CU before preg.It's the best to have a medical CU before preg.
  • 64.
    Vax. in pregnancy:principlesVax. in pregnancy: principles • Generally: no live vax.Generally: no live vax. • Toxoids, inactivated vax., Ig are safeToxoids, inactivated vax., Ig are safe • Start in 2Start in 2ndnd TM (except flu): miscarriage, fetal anomalyTM (except flu): miscarriage, fetal anomaly • Post-exposure Ig anytime:Post-exposure Ig anytime: HA&B, measles, rabies,HA&B, measles, rabies, tetanus, varicellatetanus, varicella • TT, HBV, DTP, flu, pneumococcusTT, HBV, DTP, flu, pneumococcus • Vax. can protect both mom and fetusVax. can protect both mom and fetus TM: trimester. HA&B: hepatitis A and BTM: trimester. HA&B: hepatitis A and B
  • 65.
    • If noprior Tdap, get it before preg. Td is better (safety ofIf no prior Tdap, get it before preg. Td is better (safety of pertussis part Is not fully known)pertussis part Is not fully known) • Hib: prior splenectomy, menigococcal anytimeHib: prior splenectomy, menigococcal anytime • Inactive Typhoid, HBV. Rabies: if exposedInactive Typhoid, HBV. Rabies: if exposed • Cholera, plague, J. encephalitis: if high riskCholera, plague, J. encephalitis: if high risk • Anthrax: post-exposure prophylaxis and vax.Anthrax: post-exposure prophylaxis and vax. None of these are live vax.None of these are live vax. Vax. in pregnancy …Vax. in pregnancy …
  • 66.
    Recommendations for TdapRecommendationsfor Tdap • Age: 11y or older sAge: 11y or older specially forpecially for • adults in contact with young children, padults in contact with young children, pregnant womenregnant women • healthcare professionalshealthcare professionals • grandparents (including those >65ygrandparents (including those >65y • 10 yearly Td booster for those who got 1 Tdap10 yearly Td booster for those who got 1 Tdap – 5 years for wound management5 years for wound management
  • 67.
    Vax avoided inpregnancyVax avoided in pregnancy • Nasal spray flu vax. (flu shot is killed virus)Nasal spray flu vax. (flu shot is killed virus) • MMR, Varicella, BCG: postpone pregnancy for 4wMMR, Varicella, BCG: postpone pregnancy for 4w • Little info. about other vax.: Polio, HA, Anthrax, J.Little info. about other vax.: Polio, HA, Anthrax, J. encephalitis, Typhoid, smallpox, Yellow Fencephalitis, Typhoid, smallpox, Yellow F • Some of these vax. contain live viruses. Carefully weighSome of these vax. contain live viruses. Carefully weigh the risks and benefits and decidethe risks and benefits and decide No HPV in preg.: under studyNo HPV in preg.: under study
  • 68.
    Postpartum vaccination:Postpartum vaccination:ACIPACIP • All EXCEPT smallpox are safe during lactationAll EXCEPT smallpox are safe during lactation • MMR for rubella nonimmuneMMR for rubella nonimmune • Varicella dose 1 in hospital and 2Varicella dose 1 in hospital and 2ndnd in 4-8win 4-8w • Tdap: if not given (Tdap: if not given (prevents pertussis to NB)prevents pertussis to NB) • Anti-D if baby is Rh+veAnti-D if baby is Rh+ve • If <26y: HPVIf <26y: HPV
  • 69.
    HPVHPV>130 strains>130 strains •Double stranded DNA virusDouble stranded DNA virus – Non-oncogenic/oncogenicNon-oncogenic/oncogenic • ~ everyone will be infected at least once in life~ everyone will be infected at least once in life – Most unaware when infectedMost unaware when infected – Most common STD in M and FMost common STD in M and F STD: sexually transmitted diseaseSTD: sexually transmitted disease
  • 70.
    HPVHPV • Ca cervixkills 275,000 women, mostly in 3WCCa cervix kills 275,000 women, mostly in 3WC • Prevents also vulval, vaginal, penile, colorectal,Prevents also vulval, vaginal, penile, colorectal, head-neck and some skin cancershead-neck and some skin cancers • 2 types. Premarital vax. are 100% effective in2 types. Premarital vax. are 100% effective in preventing precancerpreventing precancer • Age: 9y and aboveAge: 9y and above • Very safeVery safe
  • 71.
    HPVHPV • Females: Routine:9-26yFemales: Routine: 9-26y – Either HPV4 or HPV2Either HPV4 or HPV2 • Males: Routine: at 11yMales: Routine: at 11y – HPV4 is recommendedHPV4 is recommended • 22ndnd dose 1-2 mo of 1dose 1-2 mo of 1stst and 3and 3rdrd 6 mo after 16 mo after 1stst
  • 72.
    HIV and AdultVaccinationHIV and Adult Vaccination Vaccines are esp. critical for people with chr. d. like HIVVaccines are esp. critical for people with chr. d. like HIV If CD4 count is ≥200:If CD4 count is ≥200: • fluflu,, TdapTdap ,, Pneumo-Pneumo-, HB, HPV (man/woman up to 26y), HB, HPV (man/woman up to 26y) • MMR (born in 1957/later or not have immunity)MMR (born in 1957/later or not have immunity) • Varicella (born in 1980/later and have not gotten 2Varicella (born in 1980/later and have not gotten 2 doses or have no immunity)doses or have no immunity) CD4 count is <200:CD4 count is <200: flu, Tdap, Pneumococcal, HB, HPVflu, Tdap, Pneumococcal, HB, HPV
  • 73.
    Asplenia and AdultVaccinationAsplenia and Adult Vaccination Vax. are esp. critical for chr. d. like aspleniaVax. are esp. critical for chr. d. like asplenia • Flu, Tdap, Hib (if not vaccinated)Flu, Tdap, Hib (if not vaccinated) • Pneumo- , Meningococcal, Zoster (if 60y or older), HPVPneumo- , Meningococcal, Zoster (if 60y or older), HPV • MMR (not vaccinated or no immunity)MMR (not vaccinated or no immunity)
  • 75.
  • 76.
    Flu vax: inactivatedvirusFlu vax: inactivated virus • UniversalUniversal • High risk:High risk: children, elderly, immunodeficient, preg.,children, elderly, immunodeficient, preg., chr. Illnesschr. Illness • Dose: initial 2 shots; i.m.; then single dose annuallyDose: initial 2 shots; i.m.; then single dose annually for new strainfor new strain • Age 6-36 mo: half the adult doseAge 6-36 mo: half the adult dose
  • 77.
    Yellow fever • Ac.viral hemorrhagic F (mosquitoes)Ac. viral hemorrhagic F (mosquitoes) • 2013: in routine imm. in 35/44 countries/territories at risk2013: in routine imm. in 35/44 countries/territories at risk in Africa and Americas (cov.41%)in Africa and Americas (cov.41%) • Single dose is sufficient‡. At 9-12mo (measles), s.c.Single dose is sufficient‡. At 9-12mo (measles), s.c. • CI: in <6 mo and immunodeficientCI: in <6 mo and immunodeficient • Mass vaccination for inhabitants at riskMass vaccination for inhabitants at risk
  • 78.
    Bangladesh EPIBangladesh EPI 1979:launched1979: launched 1995: Polio eradication; elimination of1995: Polio eradication; elimination of maternal and NTmaternal and NT 2003: Introduced HBV2003: Introduced HBV 2009: HIB2009: HIB 2012: rubella2012: rubella Next: pneumococcus, HPVNext: pneumococcus, HPV
  • 79.
    Objectives of EPI: •Disease reduction • vax. coverage
  • 80.
    Targets  Eliminate NT(<1 /1000) 2005√  Measles ⇓ 95% 2005√ Vax. coverage 90% 2005√  Polio eradication 2007√  ⇓ HBV 80% in U5 2010
  • 81.
    ImmunisationImmunisation ScheduleSchedule • AtbirthAt birth BCGBCG HBV 1HBV 1 • 6-10-14 weeks6-10-14 weeks DPT 1,2,3DPT 1,2,3 OPV1,2,3OPV1,2,3 HIB 1,2,3HIB 1,2,3 HBV 2,0,0HBV 2,0,0 • 6 months6 months HBV 3HBV 3 • 9 mo:9 mo: (270d)(270d) MR.MR. OPV 4OPV 4
  • 82.
    Pulse dosing ofOPVPulse dosing of OPV • 22 doses ondoses on 22 occasions (6mo) foroccasions (6mo) for U-5U-5 (up to(up to 1010 doses)doses) • Repeat OPV replacesRepeat OPV replaces wild viruswild virus in thein the environmentenvironment
  • 83.
    YesYes!!  Benefits faroutweigh risksBenefits far outweigh risks  Exception: if severe reaction to DPT (fits) theException: if severe reaction to DPT (fits) the pertussispertussis isis omittedomitted Our body can handleOur body can handle 15000 Ag15000 Ag at a timeat a time!! A child who does not need hospitalization canA child who does not need hospitalization can get the shotget the shot Can aCan a sicksick child be immunized?child be immunized?
  • 84.
    Missed DatesMissed Dates Giveas soon as possibleGive as soon as possible Longer gap? Still theLonger gap? Still the nextnext dosedose Only complete doses requiredOnly complete doses required For remote areas altered schedules, NIDsFor remote areas altered schedules, NIDs are usedare used
  • 86.
    EPI gives noboosterEPI gives no booster After 7y: pertussis is omittedAfter 7y: pertussis is omitted In Mid- East measles vax. is given at 6 moIn Mid- East measles vax. is given at 6 mo Schedule varies among countriesSchedule varies among countries MoreMore InfoInfo
  • 87.
    Every nonimmune istargetedEvery nonimmune is targeted Consider susceptibilityConsider susceptibility Age or weight not importantAge or weight not important A child should be fully immunized by 9moA child should be fully immunized by 9mo EPI targets children and CB womenEPI targets children and CB women WhoWho be immunized?be immunized? AgeAge??
  • 88.
    WomenWomen  2 TTsfor NT2 TTs for NT  5 TTs5 TTs ⇒⇒ protectprotect all futureall future babiesbabies  Woman with 3 DPTs need 2Woman with 3 DPTs need 2  MRMR Hygienic cord Rx is less effective than immunizingHygienic cord Rx is less effective than immunizing the motherthe mother
  • 89.
    Principles of ImmunisationPrinciplesof Immunisation  Follow a schedule; but not strict!Follow a schedule; but not strict!  Schedule variesSchedule varies  Date flexibleDate flexible  4w = 1mo4w = 1mo  No Vax in 3mo ofNo Vax in 3mo of IgIg 11stst polio as IPVpolio as IPV After DTP diseases,After DTP diseases, Vax is still requiredVax is still required 2 TT in 12 TT in 1stst preg. (4-7preg. (4-7 mo) 1 shot for latermo) 1 shot for later
  • 90.
    Not a ContraindicationNota Contraindication  A child needingA child needing no admissionno admission  Mild RTIMild RTI  DVDV  AsthmaAsthma  EczemaEczema  AB TherapyAB Therapy  Chr. Lung DsChr. Lung Ds  Heart diseaseHeart disease  Febrile fitFebrile fit
  • 91.
    ContraindicationsContraindications  Ac. IllnessAc.Illness  Severe reactionsSevere reactions  Hypersensitivity to a component of VaxHypersensitivity to a component of Vax (neomycin, polymyxin B, egg protein)(neomycin, polymyxin B, egg protein)  Progressive neuropathy for pertussis VaxProgressive neuropathy for pertussis Vax
  • 92.
    All not equal;Allnot equal; depends ondepends on immune systemimmune system immunogenecityimmunogenecity • All not equally stableAll not equally stable Most stable is TTMost stable is TT • Best herd immunity with OPV; none with toxoidBest herd immunity with OPV; none with toxoid or inactivated vax.or inactivated vax. • The most effective is the TTThe most effective is the TT Effectiveness of vax. sEffectiveness of vax. s
  • 93.
    Essential Cold ChainEssentialCold Chain • Once opened dispensed within coupleOnce opened dispensed within couple of hours e.g. BCGof hours e.g. BCG
  • 95.
    5 Adverse Reactions5Adverse Reactions • vax. reactionsvax. reactions • Program errorProgram error • Injection reactionInjection reaction • CoincidentalCoincidental • UnknownUnknown
  • 96.
    vax.vax. ReactionsReactions Most vax.are safeMost vax. are safe  MMRMMR ⇒⇒mildmild disease.disease. None with extractNone with extract  Serious:Serious:⇐⇐ pertussis Vx.:pertussis Vx.: inconsolable cry, fever,inconsolable cry, fever, irritability a few hours later, febrile fitirritability a few hours later, febrile fit  Rare anaphylaxis, GBSRare anaphylaxis, GBS with some vax. swith some vax. s To minimize reactions:To minimize reactions: do not rub prick site, givedo not rub prick site, give paracetamolparacetamol
  • 97.
    SafeSafe InjectionInjection No harmto recipientNo harm to recipient No harm to you! me!No harm to you! me! Correct pushCorrect push ⇒⇒ no abscessno abscess No dangerous wasteNo dangerous waste Dispo-syringe and needle: rDispo-syringe and needle: rememberemember 1 child: 1 syringe 1 needle!1 child: 1 syringe 1 needle!
  • 99.
    Not in buttocksNotin buttocks IM at right angle into AL thighIM at right angle into AL thigh No IM in bleeding disordersNo IM in bleeding disorders S.c. Vax is given in thigh, forearmS.c. Vax is given in thigh, forearm Jet gunsJet guns not used for vaccinationnot used for vaccination ‘‘ZZ track’track’ inj.inj. ⇒⇒less leakage, infiltrationless leakage, infiltration SitesSites of Administrationof Administration
  • 100.
    ID push needsexpertiseID push needs expertise Deltoid area for BCG, not very up or low.Deltoid area for BCG, not very up or low. Avoid thighAvoid thigh SC routeSC route MMR, Varicella, MeningitisMMR, Varicella, Meningitis IM routeIM route DTP, Typhoid, HBV, HAV, RabiesDTP, Typhoid, HBV, HAV, Rabies
  • 102.
    ImmuneImmune ResponseResponse • PrimaryresponsePrimary response Traceable AB:Traceable AB: 1-2 weeks: IgM1-2 weeks: IgM • Secondary responseSecondary response High titre:High titre: 4-5d mainly IgG4-5d mainly IgG
  • 103.
    MCQMCQ • EPI targetsonly childrenEPI targets only children • BCG is highly effectiveBCG is highly effective • Pertussis vax. has more SEPertussis vax. has more SE • TT is very stableTT is very stable • Herd immunity can be achieved by IPVHerd immunity can be achieved by IPV
  • 104.
    MCQMCQ • Vaccinating NBwith TT can prevent NTVaccinating NB with TT can prevent NT • Cold or cough is a CI for vaccinationCold or cough is a CI for vaccination • TT in pregnancy is started during 3TT in pregnancy is started during 3rdrd TMTM • DTP vax. can cause febrile fitDTP vax. can cause febrile fit • Having pertussis excludes immunizationHaving pertussis excludes immunization
  • 105.
    MCQMCQ • TT givesherd immunityTT gives herd immunity • Strict immunization schedule is essentialStrict immunization schedule is essential • Having tetanus gives natural immunityHaving tetanus gives natural immunity • Having diphtheria gives natural immunityHaving diphtheria gives natural immunity • Parenteral typhoid vax is CI in AIDSParenteral typhoid vax is CI in AIDS • Typhoid vax. is protective against all EFsTyphoid vax. is protective against all EFs
  • 106.
    MCQMCQ • MMR OPVare recommended in HIVMMR OPV are recommended in HIV • BCG is CI in HIVBCG is CI in HIV • In bleeding disorder an IM vax is given SCIn bleeding disorder an IM vax is given SC • GBS may follow after some vaccinationGBS may follow after some vaccination • Hygienic cord Rx is as equally effective to preventHygienic cord Rx is as equally effective to prevent tetanus as immunizing the mothertetanus as immunizing the mother
  • 109.
  • 110.

Editor's Notes

  • #6 DR EDWARD JENNER 1749-1823
  • #8 Diphtheria: membranes covering tonsils and uvula in a 15y girl. DD: strep. throat, IM, V. angina, ac. toxoplasmosis, thrush, post-tonsillectomy m., leukemia, agranulocytosis, or less commonly tularemia and ac. CMV Agranulocytosis: A marked fall in granulocytes (wbc filled with granules with enzymes to digest microbe: neutrophils, eosinophils and basophils); they are part of immune sys. but do not respond exclusively to specific Ag, as do B and T cells. Causes frequent chr. bacterial inf. of skin, RT, etc. It literally means no granulocytes, but, in fact, too few (granulocytopenia). It can be inherited or acquired: an aspect of leukemia
  • #10 Hydrophobia
  • #20 Myth 1: Better hygiene and sanitation will make diseases disappear – vaccines are not necessary. FALSE Fact 1: The diseases we can vaccinate against will return if we stop vaccination programmes. While better hygiene, hand washing and clean water help protect people from infectious diseases, many infections can spread regardless of how clean we are. If people are not vaccinated, diseases that have become uncommon, such as polio and measles, will quickly reappear. Myth 2: Vaccines have several damaging and long-term side-effects that are yet unknown. Vaccination can even be fatal. FALSE Fact 2: Vaccines are very safe. Most vaccine reactions are usually minor and temporary, such as a sore arm or mild fever. Very serious health events are extremely rare and are carefully monitored and investigated. You are far more likely to be seriously injured by a vaccine-preventable disease than by a vaccine. For example, in the case of polio, the disease can cause paralysis, measles can cause encephalitis and blindness, and some vaccine-preventable diseases can even result in death. While any serious injury or death caused by vaccines is one too many, the benefits of vaccination greatly outweigh the risk, and many, many more injuries and deaths would occur without vaccines. Myth 3: The combined vaccine against diphtheria, tetanus and pertussis (whooping cough) and the vaccine against poliomyelitis cause sudden infant death syndrome. FALSE Fact 3: There is no causal link between the administering of the vaccines and sudden infant death, however, these vaccines are administered at a time when babies can suffer sudden infant death syndrome (SIDS).,. In other words, the SIDS deaths are co-incidental to vaccination and would have occurred even if no vaccinations had been given. It is important to remember that these four diseases are life-threatening and babies who are not vaccinated against them are at serious risk of death or serious disability. Myth 4: Vaccine-preventable diseases are almost eradicated in my country, so there is no reason to be vaccinated. FALSE Fact 4: Although vaccine preventable diseases have become uncommon in many countries, the infectious agents that cause them continue to circulate in some parts of the world. In a highly inter-connected world, these agents can cross geographical borders and infect anyone who is not protected. In western Europe, for example, measles outbreaks have occurred in unvaccinated populations in Austria, Belgium, Denmark, France, Germany, Italy, Spain, Switzerland and the United Kingdom since 2005. So two key reasons to get vaccinated are to protect ourselves and to protect those around us. Successful vaccination programmes, like successful societies, depend on the cooperation of every individual to ensure the good of all. We should not rely on people around us to stop the spread of disease; we, too, must do what we can. Myth 5: Vaccine-preventable childhood illnesses are just an unfortunate fact of life. FALSE Fact 5: Vaccine preventable diseases do not have to be ‘facts of life’. Illnesses such as measles, mumps and rubella are serious and can lead to severe complications in both children and adults, including pneumonia, encephalitis, blindness, diarrhoea, ear infections, congenital rubella syndrome (if a woman becomes infected with rubella in early pregnancy), and death. All these diseases and suffering can be prevented with vaccines. Failure to vaccinate against these diseases leaves children unnecessarily vulnerable. Myth 6: Giving a child more than one vaccine at a time can increase the risk of harmful side-effects, which can overload the child’s immune system. FALSE Fact 6: Scientific evidence shows that giving several vaccines at the same time has no adverse effect on a child’s immune system. Children are exposed to several hundred foreign substances that trigger an immune response every day. The simple act of eating food introduces new antigens into the body, and numerous bacteria live in the mouth and nose. A child is exposed to far more antigens from a common cold or sore throat than they are from vaccines. Key advantages of having several vaccines at once is fewer clinic visits, which saves time and money, and children are more likely to complete the recommended vaccinations on schedule. Also, when it is possible to have a combined vaccination, e.g. for measles, mumps and rubella, that means fewer injections. Myth 7: Influenza is just a nuisance, and the vaccine isn’t very effective. FALSE Fact 7: Influenza is much more than a nuisance. It is a serious disease that kills 300 000-500 000 people worldwide every year. Pregnant women, small children, elderly people with poor health and anyone with a chronic condition, like asthma or heart disease, are at higher risk for severe infection and death. Vaccinating pregnant women has the added benefit of protecting their newborns (there is currently no vaccine for babies under six months). Vaccination offers immunity to the three most prevalent strains circulating in any given season. It is the best way to reduce your chances of severe flu and of spreading it to others. Avoiding the flu means avoiding extra medical care costs and lost income from missing days of work or school. Myth 8: It is better to be immunized through disease than through vaccines. FALSE Fact 8: Vaccines interact with the immune system to produce an immune response similar to that produced by the natural infection, but they do not cause the disease or put the immunized person at risk of its potential complications. In contrast, the price paid for getting immunity through natural infection might be mental retardation from Haemophilus influenzae type b (Hib), birth defects from rubella, liver cancer from hepatitis B virus, or death from measles. Myth 9: Vaccines contain mercury which is dangerous. FALSE Fact 9: Thiomersal is an organic, mercury-containing compound added to some vaccines as a preservative. It is the most widely-used preservative for vaccines that are provided in multi-dose vials. There is no evidence to suggest that the amount of thiomersal used in vaccines poses a health risk. Myth 10: Vaccines cause autism FALSE Fact 10: The 1998 study which raised concerns about a possible link between measles-mumps-rubella (MMR) vaccine and autism was later found to be seriously flawed, and the paper has been retracted by the journal that published it. Unfortunately, its publication set off a panic that led to dropping immunization rates, and subsequent outbreaks of these diseases. There is no evidence of a link between MMR vaccine and autism or autistic disorders
  • #31 Live vax: single shot is enough. Produce durable immunity but not parallel to natural infection Human body can handle 15000 antigens at one exposure! OPV should not be given within 1 hr of breast feed
  • #33 Vaccinia: cutaneous and sometimes systemic reactions associated with smallpox vaccine See also COWPOX and PARAVACCINIA Vaccinia gangrenosa:  generalized vaccinia with failure to develop antibodies against the virus (due to AGAMMAGLOBULINEMIA), with spreading necrosis at the site and metastasis of lesions throughout the body. Generalized vaccinia:  widespread vaccinial lesions resulting from sensitivity response to smallpox vaccination and delayed production of neutralizing Ab.
  • #41 children&amp;apos;s legs damaged by paralytic poliomyelitis
  • #48 Stages of keratomalacia
  • #52 Mumps orchitis in a 6-y. Unusual in prepubertal boys. The highest risk is in 15-29 y
  • #54 Rubella rash on a child&amp;apos;s back. Distribution is similar to that of measles but the lesions are less intensely red
  • #55 Young adult with post-rubella thrombocytopenic purpura with large &amp;quot;blueberry muffin&amp;quot; skin lesions
  • #60 Antibody-Containing Blood Products These from US, like IG products, do not interfere with the immune response to yellow F vax. and are not believed to do such to live typhoid, live influenza, rota, or zoster vax. But MMR and varicella vax. response can be diminished. The duration of inhibition of these 2 is related to the dose of IG in the product. MMR and varicella vax. either should be pushed ≥2w before or 3–11mo after blood product, depending on the vax. IG may become necessary for another indication after MMR or varicella vax. have been given. Then, IG may interfere with the immune response to the MMR or varicella vax.. Vaccine virus replication and stimulation of immunity usually occur 2–3w after vax. If the interval between vax. and the subsequent IG is ≥2w, the vaccine need not be repeated. If less, it should be repeated after the interval as shown in Table, unless serologic testing indicates that antibodies have been produced. Such testing should be performed, to avoid detecting antibodies from the IG prepn. If IG becomes necessary, MMR or varicella vaccines can be administered simultaneously with IG, with the recognition that vaccine-induced immunity can be compromised. The vaccine should be administered at a body site different from that chosen for the IG injection. Vaccination should be repeated after the interval noted in Table, unless serologic testing indicates antibodies have been produced. When IG is given with the first dose of HA vaccine, the proportion of recipients who develop a protective level of antibody is not affected, but antibody conc. are lower. Because the final conc. of antibody are many times higher than those considered protective, this reduced immunogenicity is not expected to be clinically relevant. IG prepn. interact minimally with other inactivated vaccines and toxoids. Other inactivated vaccines may be given simultaneously, or at any time interval before or after an antibody-containing blood product is used. However, such vaccines should be administered at different sites from the IG
  • #79 1979: Launched EPI 1985-90: All areas as universal child immunisation (UCI) 1990: All target groups 1995: Polio eradication and elimination of maternal n NT 1997: AFP and NT Surveillance 2002: Introduced HBVx
  • #85 Give on date, it must be given as soon as possible If the gap is longer, still the next dose is given no need to start from below Only completed doses of Vx adequately protects a child In remote areas it is not possible to do this altered schedules, and NIDs have been used
  • #86 In Pakistan
  • #90 Follow a schedule Dates flexible, better late than never 4 weekly or monthly Schedule varies in countries: as median age of an ID varies Two live Vx given at 3 weeks apart If given same time, use different sites. Exception- MMR No Vx within 3 mo of Ig injection First dose polio is better as IPV Acquiring disease, specific Vx DTP will still be required 2 TT given in 1st preg. between 4th to 7th