IMMUNIZATION
IMMUNIZATION
• Immunisation is the process by which acquired
immunity is induced.
Acquired Immunity
• Protection from disease
• Provided by introduction antigens or premade
antibodies into the body
Acquired Immunity
Active immunity
• In response to stimulus by an
antigen characterized by the
production of antibodies by the
host.
Passive immunity
• Immunity transferred in ready
made form.ie,no role of
immunesystem of the recipient.
Active immunity
Naturally acquired
• Repeated clinical &
subclinical infection
in childhood give
immunity.
• Eg:chicken pox
Artificially acquired
• Immunity induced
by vaccination
Passive immunity
Naturally acquired
• Transfer of maternal
antibodies
• Eg:
– Through placenta=Ig G
– Through colostrum=Ig A
Artificially acquired
• Following
administration of
Immune globulin or
antiserum
• Eg:Anti tetanus
serum(ATS)
Immunizing agents
• vaccines
• immunuglobulins
• antisera
VACCINATION
• A vaccine is an immuno-biological
substance(Ag) designed to produce specific
protection against a given disease.
• A vaccine is “antigenic” but not “pathogenic”.
Types of vaccines
• Attenuated live vaccines
• Inactivated killed vaccines
• Toxoids
• Polysaccharide and polypeptide (cellular fraction) vaccines
• Surface antigen (recombinant) vaccines.
Live Vaccines
Advantages
• Single dose enough
• Produce local immunity
• lnduce cell mediated immunity
• More convenient for mass immunization
Disadvantages
• Reversion to virulence
• Difficulty in storage
Killed Vaccines
Advantages
• No danger of spread
• Stability and safety
Disadvantages
• Multiple injection may be required
• May be contaminated with
• dangerous infectious agent
Live
Attenuated
vaccines
Killed
Inactivated
vaccines
Toxoids Cellular fraction
vaccines
Recombinant
vaccines
•BCG
•Typhoid
oral
•Plague
•Oral polio
•Yellow
fever
•Measles
•Mumps
•Rubella
•Intranasal
Influenza
•Typhus
•Typhoid
•Cholera
•Pertussis
•Plague
•Rabies
•Salk polio
•Intra-
muscular
influenza
•Japanise
encephalitis
•Diphtheria
•Tetanus
•Meningococcal
polysaccharide
vaccine
•Pneumococcal
polysaccharide
vaccine
•Hepatitis B
polypeptide
vaccine
•Hepatitis B
vaccine
Route
Intradermal BCG
Subcutaneous Measles, MMR, Meningococcal, Varicella
Intramuscular
DTwP / DTaP, Hib, Hep A, Hep B, DTwP-Hep
B-Hib, DTwP-Hep B, DTwP-Hib, Hep A-Hep
B
VACCINE ADVERSE REACTIONS
• Local
– Pain, swelling, redness at site of injection
– Common with inactivated vaccines
– Usually mild and self-limited
• Systemic
– Fever, malaise, headache
– Nonspecific
– May be unrelated to vaccine
• Allergic
– Due to vaccine or vaccine component
– Rare
VACCINE COLD CHAIN
• The system of transporting, storing and distributing vaccines in
a potent state at the recommended temperature from the
point of manufacture to the point of use is the Cold Chain.
• Vaccine potency once lost cannot be restored.
VACCINE COLD CHAIN
Vaccine vial monitor
• Whole cell vaccine
–Contains suspension of whole bacterial cells
that have been killed. Eg: DTwP
–More effective but less safe
• Acellular vaccine
–Cell free vaccine prepared from purified
antigenic component of cell free
microorganism.
–ie,doesnot have complete cell but contains
fragments of cell best suited to stimulate
immune response. Eg: DTaP
–Less effective than DTwP but more safe
Vaccine Failure
• Primary = administration of recommended dose of vaccine
doesnot result in adequate protection against disease.
• Secondary = disease occur inspite of immunsiation.
INDIVIDUAL VACCINES
BCG VACCINE
• Live attenuated vaccine (Bacille Calmettee – Guerin strain)
• Dose: 0.05ml in neonates & 0.1ml in others
• Intradermal injection in to left hand on deltoid area.
• Controls hematogenous spread thus preventing Miliary TB,
Disseminated TB, TB Meningo encephalitis(80%)
• Reconstitute with 1 ml of Sodium Chloride Inj. IP.
• Complications:ulceration ,lymphadenitis...
• C.I ---immunocompromised
Oral Polio Vaccine
• OPV – Live attenuated Polio virus
– Type I - Type II - Type III
• Dose – 2 drops oral at birth,6,10, 14 weeks, 16-24 months
• Contraindication-in immunocompromised, diarrhea, infectious fever
• MgCl2 is the stablizing agent
• Pulse polio immunization -- giving 2 doses 1month apart
• Complications: Vaccine associated paralytic polio--VAPP (due to type
2)
Injectable Polio Vaccine
• Formaldehyde killed and purified poilio virus
– Type I-40
– Type II-8 D antigen units
– Type III-32
• Immunity – humoral, local pharyngeal,
intestinal
• Safe
• 6,10,14 weeks according to IAP
DTwP / DTaP vaccines
• DTaP has been licensed in India for private use
• Current recommendations for use of DTaP
– For infants who had severe reaction to 1st dose of DTwP
– For adolescents and adults
– For infant immunized abroad with DTaP
• DTaP adult formulation has now been recommended as booster by
WHO for adolescents and adults.
• Absolute contra indications for DTwP
– Anaphylaxis to previous dose
– Progressive neurological disorder
– Hypotensive hyporesponsive episodes
MEASLES VACCINE
• Live attenuated vaccine (Edmonston-Zagreb strain)
• Given IM or SC
• Given at 9 months (because at that time maternal antibody
wean off)
• Contraindications
– Malignancy
– Therapy with alkylating agent/ corticosteroid
– Immune deficiency
• Side effect -- TSS (toxic shock syndrome) due to bacterial
contamination.
MMR vaccine
• Measles---Edmonston-Zagreb strain
• Mumps-Jeryl Lynn strain
• Rubell--RA 27/3 strain
• Dose is 0.5 ml (2 dose one at 15 month and another 8 weeks later)
(S / C).
• Contraindication--pregnancy,immunosuppression
HEPATITIS B VACCINE
• Recombinant DNA vaccine (in yeast)
• 0.5 mL IM in <1 year and 1 mL > 1 year
• 3 doses at 0, 1, 6 months
• HBIG gives passive immunity
• HBIG should be given preferably within 48 hours of exposure.
TYPHOID VACCINE
• 2 doses
• 0.5 mL SC 1 month interval (killed vaccine)
• Typhoral-- oral live vaccine (stable mutant S. typhi strain type 2
Ia)
• Typhim-- give SC or IM single dose
Hib VACCINE
• Capsular polysaccharide used as antigen
• Given particularly prior to splenectomy
• 3 dose below six months
• 2 dose between 6-12 months
• 1 dose between 12-15 months
• And a booster dose should be in this children at 18
months
• >15 months--only one dose
HPV Vaccine
• 0.5 mL IM deltoid
• Recommended age for initiation of vaccine is
10-12 years
• 3 doses at 0,2,6 months
Chickenpox Vaccine
• Dose--0.5 mL S /C or IM 2 doses 4-8 weeks apart
>13 years
Pentavalent vaccine
• Trail in Kerala,Tamil Nadu
• Contains D , P , T , Hib , Hep B.
• Schedule-6,10, 14 week
National Immunization Schedule
Age Vaccines
Birth BCG, OPV0 (for institutional deliveries)
6 weeks DTwP1, OPV1, HepB1, Hib1$$ (BCG if not
given at birth)
10 weeks DTwP2, OPV2, HepB2, Hib2
14 weeks DTwP3, POV3, HepB3, Hib3
9-12 months Measles
16-24 months DTwP B1, OPV4, MMR
5-6 years DTwP
10 years TT
16 years TT
Pregnant women TT1 (early in pregnancy)
TT2 (1 month later)
TT booster (if vaccinated in past 3 years)
IAP recommended vaccines for
routine use
Vaccines under special
circumstances
BCG,
OPV
IPV
DTwP/DTaP
DT
Td
Tdap
Measles
Typhoid
Hib
Hep B
MMR
HPV
PCV
Hepatitis A
Chicken Pox
Rotavirus vaccine
Rabies
Influenza
PPSV23
Japanese Encephalitis
Meningococcal
Cholera
Yellow Fever
IAP Immunization Time Table
(recommended vaccines for routine use)
Age (completed weeks/ months/years) Vaccines
Birth BCG
OPV0
HepB 1
6 weeks DTwP1/DTaP1
OPV1*/ OPV1 + IPV1
Hib1
HepB2
Rotavirus 1 *#
PCV 1
10 weeks DTwP2/ DTaP2
OPV2*/ OPV2 + IPV2
Hib 2
Rotavirus 2
PCV 2
14 weeks DTwP3/ DTaP3
OPV3*/ OPV3 + IPV3
Hib3
Rotavirus 3
HepB3**
PCV 3
9 months Measles
12 months Hepatitis A 1
15 months MMR1
Varicella
PCV booster
16 to 18 months DTwP B1/ DTaP B1
OPV4*/ OPV4 + IPVB1
Hib B1
18 months Hepatitis A 2
2 years Typhoid 1
5 years DTwP B2 / DTaP B2
OPV5
MMR2
Typhoid 2
Varicella 2
10 to 12 years Tdap/Td
HPV^
vaccination schedule for an unimmunized child
Visit Suggested vaccines
First Measles (MMR if more than 12 months)
DTwP1/DTaP1 (Tdap if 7 years or more)
OPV1/IPV1 (only if less than 5 years)
Hib 1 (Only if less than 5 years)
Hep B 1
Second visit
(after 1 month of first visit)
BCG (only in less than 5 years)
DTwP2/ DTaP2 (Td if 7 years or more)
OPV 2 (if OPV given earlier)
Hep B 2
Hib 2 (if less than 15 mths
Third visit
(after 1 month of second visit)
OPV3/IPV2
MMR (if more than 12 months)
Typhoid (if more than 2 years)
Fourth visit
(6 months after first visit)
DTwP3/DTaP3 (Td if 7 years or more)
OPV4/IPVB1
HepB3
Do’s and Don'ts After Vaccine Administration
• Do not rub the site vigorously.
• Gentle pressure at the site for a few seconds will suffice.
• If blood oozes do not blot. Just apply gentle pressure
with cotton swab.
• No Heat, Ice or Cold Water fomentation is advocated.
• The wet cloth soaked in ordinary portable water can be
applied at the site of swelling or tenderness for about
5 – 10 minutes.
• Repeat the procedure, if necessary, 3-4 times a day.
THANK YOU

immunizationn-140429082910-phpapp02.pptx

  • 1.
  • 2.
    IMMUNIZATION • Immunisation isthe process by which acquired immunity is induced. Acquired Immunity • Protection from disease • Provided by introduction antigens or premade antibodies into the body
  • 3.
    Acquired Immunity Active immunity •In response to stimulus by an antigen characterized by the production of antibodies by the host. Passive immunity • Immunity transferred in ready made form.ie,no role of immunesystem of the recipient.
  • 4.
    Active immunity Naturally acquired •Repeated clinical & subclinical infection in childhood give immunity. • Eg:chicken pox Artificially acquired • Immunity induced by vaccination
  • 5.
    Passive immunity Naturally acquired •Transfer of maternal antibodies • Eg: – Through placenta=Ig G – Through colostrum=Ig A Artificially acquired • Following administration of Immune globulin or antiserum • Eg:Anti tetanus serum(ATS)
  • 6.
    Immunizing agents • vaccines •immunuglobulins • antisera
  • 7.
    VACCINATION • A vaccineis an immuno-biological substance(Ag) designed to produce specific protection against a given disease. • A vaccine is “antigenic” but not “pathogenic”.
  • 8.
    Types of vaccines •Attenuated live vaccines • Inactivated killed vaccines • Toxoids • Polysaccharide and polypeptide (cellular fraction) vaccines • Surface antigen (recombinant) vaccines.
  • 9.
    Live Vaccines Advantages • Singledose enough • Produce local immunity • lnduce cell mediated immunity • More convenient for mass immunization Disadvantages • Reversion to virulence • Difficulty in storage
  • 10.
    Killed Vaccines Advantages • Nodanger of spread • Stability and safety Disadvantages • Multiple injection may be required • May be contaminated with • dangerous infectious agent
  • 11.
    Live Attenuated vaccines Killed Inactivated vaccines Toxoids Cellular fraction vaccines Recombinant vaccines •BCG •Typhoid oral •Plague •Oralpolio •Yellow fever •Measles •Mumps •Rubella •Intranasal Influenza •Typhus •Typhoid •Cholera •Pertussis •Plague •Rabies •Salk polio •Intra- muscular influenza •Japanise encephalitis •Diphtheria •Tetanus •Meningococcal polysaccharide vaccine •Pneumococcal polysaccharide vaccine •Hepatitis B polypeptide vaccine •Hepatitis B vaccine
  • 12.
    Route Intradermal BCG Subcutaneous Measles,MMR, Meningococcal, Varicella Intramuscular DTwP / DTaP, Hib, Hep A, Hep B, DTwP-Hep B-Hib, DTwP-Hep B, DTwP-Hib, Hep A-Hep B
  • 13.
    VACCINE ADVERSE REACTIONS •Local – Pain, swelling, redness at site of injection – Common with inactivated vaccines – Usually mild and self-limited • Systemic – Fever, malaise, headache – Nonspecific – May be unrelated to vaccine • Allergic – Due to vaccine or vaccine component – Rare
  • 14.
    VACCINE COLD CHAIN •The system of transporting, storing and distributing vaccines in a potent state at the recommended temperature from the point of manufacture to the point of use is the Cold Chain. • Vaccine potency once lost cannot be restored.
  • 15.
  • 16.
  • 17.
    • Whole cellvaccine –Contains suspension of whole bacterial cells that have been killed. Eg: DTwP –More effective but less safe • Acellular vaccine –Cell free vaccine prepared from purified antigenic component of cell free microorganism. –ie,doesnot have complete cell but contains fragments of cell best suited to stimulate immune response. Eg: DTaP –Less effective than DTwP but more safe
  • 18.
    Vaccine Failure • Primary= administration of recommended dose of vaccine doesnot result in adequate protection against disease. • Secondary = disease occur inspite of immunsiation.
  • 19.
  • 20.
    BCG VACCINE • Liveattenuated vaccine (Bacille Calmettee – Guerin strain) • Dose: 0.05ml in neonates & 0.1ml in others • Intradermal injection in to left hand on deltoid area. • Controls hematogenous spread thus preventing Miliary TB, Disseminated TB, TB Meningo encephalitis(80%) • Reconstitute with 1 ml of Sodium Chloride Inj. IP. • Complications:ulceration ,lymphadenitis... • C.I ---immunocompromised
  • 21.
    Oral Polio Vaccine •OPV – Live attenuated Polio virus – Type I - Type II - Type III • Dose – 2 drops oral at birth,6,10, 14 weeks, 16-24 months • Contraindication-in immunocompromised, diarrhea, infectious fever • MgCl2 is the stablizing agent • Pulse polio immunization -- giving 2 doses 1month apart • Complications: Vaccine associated paralytic polio--VAPP (due to type 2)
  • 22.
    Injectable Polio Vaccine •Formaldehyde killed and purified poilio virus – Type I-40 – Type II-8 D antigen units – Type III-32 • Immunity – humoral, local pharyngeal, intestinal • Safe • 6,10,14 weeks according to IAP
  • 23.
    DTwP / DTaPvaccines • DTaP has been licensed in India for private use • Current recommendations for use of DTaP – For infants who had severe reaction to 1st dose of DTwP – For adolescents and adults – For infant immunized abroad with DTaP • DTaP adult formulation has now been recommended as booster by WHO for adolescents and adults. • Absolute contra indications for DTwP – Anaphylaxis to previous dose – Progressive neurological disorder – Hypotensive hyporesponsive episodes
  • 24.
    MEASLES VACCINE • Liveattenuated vaccine (Edmonston-Zagreb strain) • Given IM or SC • Given at 9 months (because at that time maternal antibody wean off) • Contraindications – Malignancy – Therapy with alkylating agent/ corticosteroid – Immune deficiency • Side effect -- TSS (toxic shock syndrome) due to bacterial contamination.
  • 25.
    MMR vaccine • Measles---Edmonston-Zagrebstrain • Mumps-Jeryl Lynn strain • Rubell--RA 27/3 strain • Dose is 0.5 ml (2 dose one at 15 month and another 8 weeks later) (S / C). • Contraindication--pregnancy,immunosuppression
  • 26.
    HEPATITIS B VACCINE •Recombinant DNA vaccine (in yeast) • 0.5 mL IM in <1 year and 1 mL > 1 year • 3 doses at 0, 1, 6 months • HBIG gives passive immunity • HBIG should be given preferably within 48 hours of exposure.
  • 27.
    TYPHOID VACCINE • 2doses • 0.5 mL SC 1 month interval (killed vaccine) • Typhoral-- oral live vaccine (stable mutant S. typhi strain type 2 Ia) • Typhim-- give SC or IM single dose
  • 28.
    Hib VACCINE • Capsularpolysaccharide used as antigen • Given particularly prior to splenectomy • 3 dose below six months • 2 dose between 6-12 months • 1 dose between 12-15 months • And a booster dose should be in this children at 18 months • >15 months--only one dose
  • 29.
    HPV Vaccine • 0.5mL IM deltoid • Recommended age for initiation of vaccine is 10-12 years • 3 doses at 0,2,6 months
  • 30.
    Chickenpox Vaccine • Dose--0.5mL S /C or IM 2 doses 4-8 weeks apart >13 years Pentavalent vaccine • Trail in Kerala,Tamil Nadu • Contains D , P , T , Hib , Hep B. • Schedule-6,10, 14 week
  • 31.
    National Immunization Schedule AgeVaccines Birth BCG, OPV0 (for institutional deliveries) 6 weeks DTwP1, OPV1, HepB1, Hib1$$ (BCG if not given at birth) 10 weeks DTwP2, OPV2, HepB2, Hib2 14 weeks DTwP3, POV3, HepB3, Hib3 9-12 months Measles 16-24 months DTwP B1, OPV4, MMR 5-6 years DTwP 10 years TT 16 years TT Pregnant women TT1 (early in pregnancy) TT2 (1 month later) TT booster (if vaccinated in past 3 years)
  • 32.
    IAP recommended vaccinesfor routine use Vaccines under special circumstances BCG, OPV IPV DTwP/DTaP DT Td Tdap Measles Typhoid Hib Hep B MMR HPV PCV Hepatitis A Chicken Pox Rotavirus vaccine Rabies Influenza PPSV23 Japanese Encephalitis Meningococcal Cholera Yellow Fever
  • 33.
    IAP Immunization TimeTable (recommended vaccines for routine use) Age (completed weeks/ months/years) Vaccines Birth BCG OPV0 HepB 1 6 weeks DTwP1/DTaP1 OPV1*/ OPV1 + IPV1 Hib1 HepB2 Rotavirus 1 *# PCV 1 10 weeks DTwP2/ DTaP2 OPV2*/ OPV2 + IPV2 Hib 2 Rotavirus 2 PCV 2
  • 34.
    14 weeks DTwP3/DTaP3 OPV3*/ OPV3 + IPV3 Hib3 Rotavirus 3 HepB3** PCV 3 9 months Measles 12 months Hepatitis A 1 15 months MMR1 Varicella PCV booster 16 to 18 months DTwP B1/ DTaP B1 OPV4*/ OPV4 + IPVB1 Hib B1
  • 35.
    18 months HepatitisA 2 2 years Typhoid 1 5 years DTwP B2 / DTaP B2 OPV5 MMR2 Typhoid 2 Varicella 2 10 to 12 years Tdap/Td HPV^
  • 36.
    vaccination schedule foran unimmunized child Visit Suggested vaccines First Measles (MMR if more than 12 months) DTwP1/DTaP1 (Tdap if 7 years or more) OPV1/IPV1 (only if less than 5 years) Hib 1 (Only if less than 5 years) Hep B 1 Second visit (after 1 month of first visit) BCG (only in less than 5 years) DTwP2/ DTaP2 (Td if 7 years or more) OPV 2 (if OPV given earlier) Hep B 2 Hib 2 (if less than 15 mths Third visit (after 1 month of second visit) OPV3/IPV2 MMR (if more than 12 months) Typhoid (if more than 2 years) Fourth visit (6 months after first visit) DTwP3/DTaP3 (Td if 7 years or more) OPV4/IPVB1 HepB3
  • 37.
    Do’s and Don'tsAfter Vaccine Administration • Do not rub the site vigorously. • Gentle pressure at the site for a few seconds will suffice. • If blood oozes do not blot. Just apply gentle pressure with cotton swab. • No Heat, Ice or Cold Water fomentation is advocated. • The wet cloth soaked in ordinary portable water can be applied at the site of swelling or tenderness for about 5 – 10 minutes. • Repeat the procedure, if necessary, 3-4 times a day.
  • 38.