SlideShare a Scribd company logo
Vaccination
Immunization
Madeeha Kamal
Sr. Consultant Pediatrics Hamad Medical Corporation
Sidra
Associate Professor at Weill-Cornell Qatar
Associate Professor at Qatar University
Clerkship Director Qatar University
Welcome to Pediatrics
Professionalism
We expect students to demonstrate:
-positive attitude towards learning
-Intellectual curiosity
Honesty, reliabiltiy and responsibility
 Flexibility when differences of opinion arise
Introduction
• Immunization is one of the most effective preventive
health measures
• Vaccination programs directly benefit the immunized
child.
– indirectly benefit unimmunized persons through
community ("herd") immunity
6. Child Immunization lecture about child immunization
6. Child Immunization lecture about child immunization
6. Child Immunization lecture about child immunization
6. Child Immunization lecture about child immunization
6. Child Immunization lecture about child immunization
6. Child Immunization lecture about child immunization
6. Child Immunization lecture about child immunization
6. Child Immunization lecture about child immunization
SLIDE 13
Types of
vaccines
•Live virus vaccines
must be given on the
same day or atleast 28
days apart from each
other.
•If immunoglobulins or
blood products have
been administered , live
vaccines should be
delayed 6-10 months to
avoid interference with
immune response.
•Live virus vaccines
should never be given
to
immunocompromised
persons or pregnant
women.
SLIDE 14
Live attenuated vaccines
• Virulent pathogenic organisms are
treated to become attenuated and
avirulent but antigenic.
• They have lost their capacity to induce
full-blown disease but retain their
immunogenicity.
SLIDE 15
Inactivated (killed) vaccines
• Organisms are killed or inactivated by
heat or chemicals but remain antigenic.
• They are usually safe but less effective
than live attenuated vaccines.
SLIDE 16
The only absolute contraindication to their administration
is a severe local or general reaction to a previous dose.
It is safe to administer many combinations of vaccines
simultaneously.
Inactivated vaccines can be given together or at any time
after different vaccines.
SLIDE 17
Toxoids
• They are prepared by detoxifying the
exotoxins of some bacteria rendering
them antigenic but not pathogenic.
Adjuvants are used to increase the
potency of vaccine.
• In general toxoids are highly
efficacious and safe immunizing
agents.
SLIDE 18
Routes of
administration
IM
SC
ID
Oral
6. Child Immunization lecture about child immunization
SLIDE 20
Scheme of immunization
• Primary vaccination
– One dose vaccines (BCG, measles,
mumps, rubella,varicella )
– Multiple dose vaccines (Polio, DTaP,
Hepatitis B,PCV 13)
• Booster vaccination
To maintain immunity level after it
declines after some time has elapsed
(DTaP, OPV ,PCV 13).
SLIDE 21
Periods of maintained immunity due to vaccines
• Short period (months): cholera
vaccine
• Two years: Typhoid vaccine
• Three to five years:Meningitis
• Five or more years: BCG vaccine,
DTaP
• Ten years: Yellow fever vaccine,
Hepatitis A ,Hepatitis B
• Solid immunity: MMR, varicella
vaccines.
How many doses of Hepatitis B ?
Interval between Hepatitis B doses ?
Do we need to check Hepatitis B
antibody titres ?
Why do some people have no antibodies
despite receiving complete series of
Hepatitis B vaccination ?
Hepatitis B
• 3-dose series can be started at any age.
• Routine checking of antibodies after vaccinations is
not recommended
• Do not restart series, no matter how long since
previous dose.
• Minimum intervals between doses:
– 4wks between #1 and #2,
– 8wks between #2 and #3,
– at least 16wks between #1 and #3.
• Vaccinate all newborns with prior
to hospital discharge. (Birth dose or
Zero dose)
• At birth dose of hepatitis B is given
within 24 hrs of birth
• If mother is HBsAg-positive or
HBsAg status is unknown: Give the
newborn HBIG and dose #1 within
12hrs of birth; complete series by
age 6m.
DTaP/D
T
Tdap/Td
Tetan
us
Toxoid
Wound
management?
Pregnancy ?
Adults ?
Defaulters ?
Animal bites ?
Booster doses ?
Travellers ?
• DTaP given at ages 2m, 4m,
6m, 15–18m, 4–6yrs.
• Do not give DTaP/DT to
children age 7yrs and older
–use Tdap or Td.
6. Child Immunization lecture about child immunization
6. Child Immunization lecture about child immunization
• Contraindications
• For DTaP/Tdap only: encephalopathy
not attributable to an identifiable
cause, within 7d after
DTP/DTaP/Tdap.
• Precautions
• Guillain-Barré syndrome (GBS)
within 6wks after previous dose of
tetanus-toxoid-containing vaccine.
 Temperature of 105°F (40.5°C) or
higher within 48hrs
 Continuous crying for 3hrs or more
within 48hrs
 Collapse or shock-like state within
48hrs
 Seizure within 3d
• For DTaP/Tdap only:
• Progressive or unstable neurologic
disorder
• Uncontrolled seizures, or progressive
encephalopathy until the condition has
stabilized.
High risk factors for influenza related
complications
People factors
• Children less than 5 years (especially under 2 years
of age).
• People less than 19 years on long term aspirin
therapy.
• Adults more than 65 years of age.
• Lower socio economic status
• Certain ethnic groups
• Residents of nursing homes or chronic care facilities
• Health care personnel
• Travelers- Hajj and Umra
High risk factors for influenza related
complications
Medical condition factors
• Asthma
• Neurological conditions like cerebral palsy , epilepsy, stroke.
• Chronic lung diseases like CF, COPD
• Heart disease
• Blood disease like sickle cell anemia
• Endocrine and metabolic disorders ( Diabetes, obesity)
• Kidney disease
• Liver disease
• Compromised immune system (Cancer , HIV, chronic steroid therapy,
organ transplant)
• Splenectomy
FIGURE 1. Influenza vaccine dosing algorithm for children
aged 6 months through 8 years — Advisory Committee on
Immunization Practices, United States, 2013–14 influenza
season
•Doses should be administered at least 4 weeks apart.
•Pregnant women especially in the 2nd and 3rd trimesters , their
unborn babies or their new infants are at greater risk from
complications associated with the flu.
•There are a range of changes that occur during pregnancy that put
expectant mothers at greater risk, including changes to lung capacity,
the immune system and heart rate response.
•Pregnant women with existing medical conditions are at even
greater risk of severe influenza-related illness.
•Because of the higher risk of influenza infection to both mother and
baby, the World Health Organization (WHO) recommends that
pregnant women should be the highest priority in seasonal influenza
vaccination programmes.
•The influenza vaccine does not actually cross the placenta to the
baby.
The vaccine simply stimulates immune system to make antibodies
that can fight
off the virus.
Act-Hib
• Give at ages 2m, 4m, 6m, 12–15m (booster
dose).
• Hib is not routinely given to healthy children
age 5yrs and older.
Rotavirus
• Rotarix (RV1): give at ages 2m, 4m.
• RotaTeq (RV5): give at ages 2m, 4m, 6m.
• May give dose #1 as early as age 6wks.
• Give final dose no later than age 6 months.
• Do not begin series in infants older than age 14wks 6 days.
• Minimum interval may be as short as 4wks
• Contraindications
• Allergy to latex, use RV5.
• History of intussusception.
• Diagnosis of severe combined
immunodeficiency (SCID).
• Precautions
• Moderate or severe acute illness.
• Immunosuppressed
• Chronic gastrointestinal disease.
• Spina bifida or bladder exstrophy.
How many doses of MMR ?
What if MMR was taken before 12 months of age ?
MMR and PPD test
What if a pregnant woman is not immune to
Measles , Mumps and Rubella ?
MMR
• 2 doses at age 12m and 18 m.
• Adult should receive MMR if no
record of vaccine
MMR
• For women of childbearing age who
lack rubella immunity , give 1 dose
of MMR .
• If pregnant, MMR should be given
postpartum
• Within 72hrs of measles exposure,
give 1 dose of MMR as
postexposure prophylaxis to
susceptible healthy children age
12m and older
• Contraindications
• Pregnancy or possibility of
pregnancy within 4wks.
• Severe immunodeficiency
• Precautions
• If blood, plasma, or immune
globulin given in past 11m
• History of thrombocytopenia or
thrombocytopenic purpura.
Varicella
• 2 doses at age 12m and 4–6yrs.
• All adults ,older children and adolescents who lack
evidence of vaccination or immunity to varicella should
receive two doses of varicella vaccine .
• If younger than age 13yrs, space dose #1 and #2 at least 3m
apart. If age 13yrs and older, space at least 4wks apart.
• May use as postexposure prophylaxis if given within 5d.
• Contraindications
• Pregnancy or possibility of
pregnancy within 4wks.
• Immunosuppression
PCV 13 or PCV
23 ?
Which age group?
Defaulters
High risk groups
Which one should be
taken first ?
Total number of doses
Time intervals
PCV 13
• Give at ages 2m, 4m, 6m, 12–15m
(booster dose).
• Dose #1 may be given as early as age
6wks.
• Healthy persons above 5 years are not
routinely given PCV 13.
– If there is no or incomplete or unclear
history of vaccination with PCV 13, a
single dose of PCV 13 may be given
• Contraindication
• Previous anaphylaxis to a PCV vaccine
or diptheria , tetanus and pertussis
vaccines
PPSV23 • High-risk children
age 2yrs and older.
• All adults aged 65
years and older
• Adults younger than
age 65 years with
high risk conditions
Dual Pneumococcal vaccination
recommendations for adults
• All adults aged 65 years should receive
PCV 13 followed by PPV 23. PCV 13
may also be given at 50 years of age .
• Travelers to Hajj and Umra with high
risk conditions
• Age 2- 64 years with
immunocomprimising and high risk
conditions
Chest x ray of miliary
TB
Decorticate posture in TB
meningitis
BCG vaccination
Contraindications for BCG
vaccine
• Immunosuppression
• Pregnancy.
• A past history of TB.
• A positive pre-immunization tuberculin test.
• A previous anaphylactic reaction to vaccine component.
• Generalized septic skin conditions.
• Acute illnesses with fever or systemic upset
• Previous BCG vaccination
Adverse events with BCG vaccination
1. Pain and scarring at the site of injection
2. Keloids—large, raised scars
3. If given subcutaneously, it may induce local infection and spread to the regional
lymph nodes, causing either suppurative and nonsuppurative lymphadenitis
4. Abscesses can occur due to haematogenous and lymphangiomatous spread.
5. Regional bone infection (BCG osteomyelitis or osteitis) and disseminated BCG
infection are rare complications of BCG vaccination, but potentially life
threatening.
6. If BCG is accidentally given to an immunocompromised patient (e.g., an infant
with SCID or HIV), it can cause disseminated or life-threatening infection
Meningitis
• Microbiologists routinely exposed to isolates of
Neisseria meningitidis
• Military recruits
• Travellers to countries in which meningococcal
disease is hyperendemic or epidemic. ( Subsaharan
Africa . Saudi Arabia for Hajj or Umra , India )
• College students if they have not received a dose
on or after their 16th birthday
• Close contacts of persons with meningcoccal
meningitis
• Persons with functional asplenia or persistent
complement component deficiencies.
• HIV-infected persons
Meningococcal • MCV4 Menactra,
Menveo Give IM
• Provides immunity
against serotypes A C Y
and W 135
Updated defaulters schedule
Infant and child immunization
defaulters
• Defination:
Infants or children from 3 months- 18 years of
age who :
1. Start vaccination late or have delayed
vaccination for more than 1 month according
to National Immunization Schedule
Infant and child immunization
defaulters
1. Have not completed vaccination series of
recommended vaccines in National
Immunization Schedule
2. Lack reliable evidence of immunity or
immunizations
Defaulters Schedule
summary
All children must complete
• MMR-2 doses
• Varicella-2doses
• Hepatitis B-3 doses
• DTaP
 3months – 1years: 5 doses
 1year -5 years : 4-5 doses
 5years-7 years: 3 doses
• Tdap
 1 dose above 7years followed by 2 doses of Td if no doses
or incomplete doses of DTaP were given before 7 years of
age.
 Booster dose at 13-16 years
• IPV/OPV
 1-2 doses of IPV and 3-4 doses of OPV
Rotavirus- 2 doses before 6 months
Hepatitis A-2 doses between 12-24 months and above 24
months for travelers to endemic areas
Vaccinating high risk groups
• Live vaccines are
contraindicated in
immunocompromised
and pregnant patients
• Persons with HIV
infection should
receive pneumococcal
vaccine as soon as
possible after their
diagnosis.
Adult
Immunizati
on Schedule
Why do we need adult
vaccinations?
• Some adults incorrectly assume that the vaccines they
received as children will protect them for the rest of their
lives. Generally this is true, except that:
• Some adults were never vaccinated or partially vaccinated as
children
• Newer vaccines were not available when some adults were
children Immunity wanes over time.
• As we age, we become more susceptible to serious diseases
caused by common infections, such as shingles, flu &
pneumonia. This results in otherwise preventable morbidity
& mortality.
• Considerable vaccine-preventable morbidity
– Excess hospitalization
– Diminished quality of life (post-herpetic neuralgia)
– Missed work
– Medical complications
Vaccine General Recommendation for Use in Pregnant Women
(CDC)
Hepatitis A Can be given if otherwise indicated
Hepatitis B Can be given if otherwise indicated ( Can be used for high
risk situations or accidental exposure )
HPV Not recommended
Influenza
inactivated
Recommended ( Infants born to women who receive
influenza vaccine in the 2nd and 3rd trimesters may have
protective antibodies lasting up to 6 months)
Influenza live intranasal Contraindicated
MMR, Varicella, Zoster, Yellow
fever
Contraindicated
MCV4,MPSV4 Can be given if otherwise indicated
PCV 13 , PPSV 23 No specific recommendation , inadequate data
Polio May be used if needed
Td May be used if needed
Tdap
Recommended in the last trimester of pregnancy . ( Most
effective way of preventing pertussis and tetanus in
newborns and children )
Rabies May be used if needed ( In case of bite with a rabid
animal rabies vaccination is life saving procedure )
HPV
• Human papillomavirus (HPV) is a sexually transmitted
pathogen that causes
• Anogenital and oropharyngeal disease in males and
females.
• High-risk HPV genotypes causes cancers of the
cervix.
The high-risk HPV genotypes
• 16 and 18 cause
– 70 % of all cervical cancers
– 90 %of anal cancers , oropharyngeal cancer,
vulvar, vaginal cancer, and penile cancer.
• Additional 20 % of cervical cancer caused by types
31, 33, 45, 52,58
• 6 and 11 cause 90 percent of anogenital warts.
• Three different vaccines:
– Quadrivalent HPV vaccine (Gardasil) targets HPV
types 6, 11, 16, and 18.
– 9-valent vaccine (Gardasil 9) targets the same HPV
types as the quadrivalent vaccine 6, 11, 16,18, 31,
33, 45, 52, and 58.
– Bivalent vaccine (Cervarix) targets HPV types 16
and 18.
HPV vaccines
• Prophylactic vaccines, designed to prevent initial HPV
infection and subsequent HPV-associated lesions.
• Therapeutic vaccines, designed to induce regression
of existing HPV-associated lesions, are in
development but are not clinically available
• HPV vaccine provides a direct benefit to female
recipients (protecting against cancers)
• Cervical cancer is common cancer among females
Recommended age
• <15 years
• 2 doses of HPV vaccine at
– 0
– 6 to 12 months.
– Minimum interval is 5 months between the 2
doses
• ≥15 years
• 3 doses at
– 0
– 1 to 2 ( min 4 weeks between 1st & 2nd)
– 6 months.( min 12 weeks between 2nd & 3rd)
• If a vaccine dose is administered at a shorter
interval, it should be re-administered
Many thanks to Dr Samina ( ministry of
health) for sharing her slides with
students at Qatar University 2018
• Thank you
• Questions
Addressing parents concerns
• Acknowledging parents’ concerns
– Listen respectfully
– Provide accurate information about both benefits and risks
of vaccines
Several factors contribute to parental vaccine concerns,
hesitancy, of vaccines, including:
Addressing parents concerns
• Lack of information about the vaccine and about
immunizations in general
• Lack of understanding of the severity diseases
Addressing parents concerns
• Opposing information and misinformation from
other sources (eg, alternative medicine practitioners,
anti-vaccination organizations and Web sites, and
some religious groups)
• Perceived risk of serious vaccine adverse effects
Addressing parents concerns
• Mistrust of the source of information regarding
vaccines (eg, vaccine manufacturer, the government)
• Concern regarding number of injections to be
administered simultaneously
Addressing parents concerns
• Delivery of information in a culturally insensitive
manner or that is not tailored to individual concern.
• Delivery of information at an inconvenient time or in
a hurried manner.
• Some people view the risk of immunization as
disproportionately greater than the risk of disease
Managing Injection Pain
• Talk to your child ( pinch you not hurt you)
• Physical techniques
– skin to skin contact between the mother and
infant, breastfeeding
– older children sit on parents lap
– position the limb allow relaxation of the muscle
– give multiple injections simultaneously at multiple
sites
• Psychological (breathing, distraction, blowing
bubbles)
• Pharmacological techniques
Syncope
• Syncope following immunization has been reported
among teens.
• Its advised to observe the teen for 15 minutes after
immunization.
Lapsed Immunization
• A lapse in the immunization schedule does not
require reinitiation of the entire series.
Vaccine Contraindications and
precautions
• Contraindication when increased risk of an adverse
reaction outweighs the benefit of the vaccine.
Vaccine Contraindications and
precautions
• A vaccine should not be administered when a
contraindication is present.
• The only contraindication applicable to all vaccines is
a history of anaphylaxis to a previous dose.
• Vaccinations may be deferred when a precaution is
present until the health condition resulting in the
precaution improves or resolves.
• Vaccination may be recommended in the presence of
a precaution if the benefit outweighs the risk.
• Most precautions are the result of temporary
conditions (eg, moderate or severe illness), and a
vaccine can be administered when the illness
subsides.
• Severely immunocompromised people generally
should not receive live vaccines.
• Pregnant women should not receive live-virus
vaccines because of a theoretical risk to the fetus.
• Personal or family history of seizures is a precaution,
rather than a contraindication, for MMRV vaccination
in a child.
Common conditions that should not delay vaccination but
often are considered mistakenly to be contraindications i
• Diarrhea
• Minor upper respiratory tract illnesses (including
otitis media) with or without fever
Common conditions that should not delay vaccination but
often are considered mistakenly to be contraindications i
• Mild to moderate local reactions to a previous
dose of vaccine
• Exposure to an infectious disease
• Current antimicrobial therapy
• Being in the convalescent phase of an acute
illness
Common conditions that should not delay vaccination but
often are considered mistakenly to be contraindications
• Allergy to an antibiotic (except anaphylactic
reaction to neomycin, gentamicin, or
streptomycin, if any of these are in the vaccine
to be administered)
• History of nonanaphylactic allergy to egg
Common conditions that should not delay vaccination but
often are considered mistakenly to be contraindications
• Personal or family history of seizures
• Family history of sudden unexpected death
• Family history of an adverse event following
immunization
• Breastfeeding or pregnancy in a household
contact
Summary
• The childhood and adolescents immunization
schedule is complex.
• Although serious adverse reactions to immunizations
are uncommon
– clinicians must be knowledgeable in these
reactions as well as the contraindications and
precautions to each vaccine.

More Related Content

PPTX
VACCINATION IN ELDERLY INDICATIONS AND CONTRAINDICATIONS.pptx
PPTX
D.G.F. Guidelines on Immunization for Indian Adolescents Girls
PPTX
Delhi gynaecologist forum Guidelines on Immunization for Indian Adolescent...
PPTX
Immunization for INDIAN Adolescents Dr. Jyoti Agarwal Dr. Sharda Jain Dr. J...
PDF
Catch up vaccine
PPTX
Immunization programme
PPTX
Vaccinations along all age groups in India
PPT
Preventive medicine
VACCINATION IN ELDERLY INDICATIONS AND CONTRAINDICATIONS.pptx
D.G.F. Guidelines on Immunization for Indian Adolescents Girls
Delhi gynaecologist forum Guidelines on Immunization for Indian Adolescent...
Immunization for INDIAN Adolescents Dr. Jyoti Agarwal Dr. Sharda Jain Dr. J...
Catch up vaccine
Immunization programme
Vaccinations along all age groups in India
Preventive medicine

Similar to 6. Child Immunization lecture about child immunization (20)

PPTX
Vaccination turkey
PPTX
Measles
PPTX
Dr Swati Rajagopal_ ADULT VACCINATION.pptx
PPTX
Vaccinology.pptx hgccgccyuhfyjugkyigukkjk
PPT
PDF
Final Immunization for all age in pedia.pptx
PPTX
Immunization in adults, geriatrics and paediatrics.
PPT
Immunisation -the recent advances in India
PPTX
IMMUNISATION- LAPSED, SPECIAL SITUATION AND AEFI.pptx
PPTX
Vaccination in Preterms by - Dr Padmesh - Neonatology
PPTX
2020 CDC ACIP Updates to the Child/Adolescent and Adult Immunization Recom...
PPTX
Adult immunisation in special population
PPTX
Standard immunizations for non pregnant a
PDF
2025-PIDSP-Immunization-Calendar.pdf …….
PPTX
Vaccination in women from adolescence to menopause
PPTX
DR JRK ADULT IMMUNIZATION programme.pptx
PPT
Childhood immunization
PPT
Adultvaccinationy 121010201616-phpapp02
Vaccination turkey
Measles
Dr Swati Rajagopal_ ADULT VACCINATION.pptx
Vaccinology.pptx hgccgccyuhfyjugkyigukkjk
Final Immunization for all age in pedia.pptx
Immunization in adults, geriatrics and paediatrics.
Immunisation -the recent advances in India
IMMUNISATION- LAPSED, SPECIAL SITUATION AND AEFI.pptx
Vaccination in Preterms by - Dr Padmesh - Neonatology
2020 CDC ACIP Updates to the Child/Adolescent and Adult Immunization Recom...
Adult immunisation in special population
Standard immunizations for non pregnant a
2025-PIDSP-Immunization-Calendar.pdf …….
Vaccination in women from adolescence to menopause
DR JRK ADULT IMMUNIZATION programme.pptx
Childhood immunization
Adultvaccinationy 121010201616-phpapp02
Ad

Recently uploaded (20)

PPT
OPIOID ANALGESICS AND THEIR IMPLICATIONS
PPTX
Cardiovascular - antihypertensive medical backgrounds
PPTX
Clinical approach and Radiotherapy principles.pptx
PDF
Copy of OB - Exam #2 Study Guide. pdf
PDF
Medical Evidence in the Criminal Justice Delivery System in.pdf
PPTX
History and examination of abdomen, & pelvis .pptx
PPTX
Spontaneous Subarachinoid Haemorrhage. Ppt
PPTX
MANAGEMENT SNAKE BITE IN THE TROPICALS.pptx
PDF
شيت_عطا_0000000000000000000000000000.pdf
PPTX
PRESENTACION DE TRAUMA CRANEAL, CAUSAS, CONSEC, ETC.
PPT
Management of Acute Kidney Injury at LAUTECH
PPTX
Electrolyte Disturbance in Paediatric - Nitthi.pptx
PPTX
NRPchitwan6ab2802f9.pptxnepalindiaindiaindiapakistan
PPTX
JUVENILE NASOPHARYNGEAL ANGIOFIBROMA.pptx
PPTX
2 neonat neotnatology dr hussein neonatologist
PPT
STD NOTES INTRODUCTION TO COMMUNITY HEALT STRATEGY.ppt
PPTX
Transforming Regulatory Affairs with ChatGPT-5.pptx
PPTX
anaemia in PGJKKKKKKKKKKKKKKKKHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH...
PDF
focused on the development and application of glycoHILIC, pepHILIC, and comm...
PPTX
Human Reproduction: Anatomy, Physiology & Clinical Insights.pptx
OPIOID ANALGESICS AND THEIR IMPLICATIONS
Cardiovascular - antihypertensive medical backgrounds
Clinical approach and Radiotherapy principles.pptx
Copy of OB - Exam #2 Study Guide. pdf
Medical Evidence in the Criminal Justice Delivery System in.pdf
History and examination of abdomen, & pelvis .pptx
Spontaneous Subarachinoid Haemorrhage. Ppt
MANAGEMENT SNAKE BITE IN THE TROPICALS.pptx
شيت_عطا_0000000000000000000000000000.pdf
PRESENTACION DE TRAUMA CRANEAL, CAUSAS, CONSEC, ETC.
Management of Acute Kidney Injury at LAUTECH
Electrolyte Disturbance in Paediatric - Nitthi.pptx
NRPchitwan6ab2802f9.pptxnepalindiaindiaindiapakistan
JUVENILE NASOPHARYNGEAL ANGIOFIBROMA.pptx
2 neonat neotnatology dr hussein neonatologist
STD NOTES INTRODUCTION TO COMMUNITY HEALT STRATEGY.ppt
Transforming Regulatory Affairs with ChatGPT-5.pptx
anaemia in PGJKKKKKKKKKKKKKKKKHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH...
focused on the development and application of glycoHILIC, pepHILIC, and comm...
Human Reproduction: Anatomy, Physiology & Clinical Insights.pptx
Ad

6. Child Immunization lecture about child immunization

  • 1. Vaccination Immunization Madeeha Kamal Sr. Consultant Pediatrics Hamad Medical Corporation Sidra Associate Professor at Weill-Cornell Qatar Associate Professor at Qatar University Clerkship Director Qatar University
  • 3. Professionalism We expect students to demonstrate: -positive attitude towards learning -Intellectual curiosity Honesty, reliabiltiy and responsibility  Flexibility when differences of opinion arise
  • 4. Introduction • Immunization is one of the most effective preventive health measures • Vaccination programs directly benefit the immunized child. – indirectly benefit unimmunized persons through community ("herd") immunity
  • 13. SLIDE 13 Types of vaccines •Live virus vaccines must be given on the same day or atleast 28 days apart from each other. •If immunoglobulins or blood products have been administered , live vaccines should be delayed 6-10 months to avoid interference with immune response. •Live virus vaccines should never be given to immunocompromised persons or pregnant women.
  • 14. SLIDE 14 Live attenuated vaccines • Virulent pathogenic organisms are treated to become attenuated and avirulent but antigenic. • They have lost their capacity to induce full-blown disease but retain their immunogenicity.
  • 15. SLIDE 15 Inactivated (killed) vaccines • Organisms are killed or inactivated by heat or chemicals but remain antigenic. • They are usually safe but less effective than live attenuated vaccines.
  • 16. SLIDE 16 The only absolute contraindication to their administration is a severe local or general reaction to a previous dose. It is safe to administer many combinations of vaccines simultaneously. Inactivated vaccines can be given together or at any time after different vaccines.
  • 17. SLIDE 17 Toxoids • They are prepared by detoxifying the exotoxins of some bacteria rendering them antigenic but not pathogenic. Adjuvants are used to increase the potency of vaccine. • In general toxoids are highly efficacious and safe immunizing agents.
  • 20. SLIDE 20 Scheme of immunization • Primary vaccination – One dose vaccines (BCG, measles, mumps, rubella,varicella ) – Multiple dose vaccines (Polio, DTaP, Hepatitis B,PCV 13) • Booster vaccination To maintain immunity level after it declines after some time has elapsed (DTaP, OPV ,PCV 13).
  • 21. SLIDE 21 Periods of maintained immunity due to vaccines • Short period (months): cholera vaccine • Two years: Typhoid vaccine • Three to five years:Meningitis • Five or more years: BCG vaccine, DTaP • Ten years: Yellow fever vaccine, Hepatitis A ,Hepatitis B • Solid immunity: MMR, varicella vaccines.
  • 22. How many doses of Hepatitis B ? Interval between Hepatitis B doses ? Do we need to check Hepatitis B antibody titres ? Why do some people have no antibodies despite receiving complete series of Hepatitis B vaccination ? Hepatitis B
  • 23. • 3-dose series can be started at any age. • Routine checking of antibodies after vaccinations is not recommended • Do not restart series, no matter how long since previous dose. • Minimum intervals between doses: – 4wks between #1 and #2, – 8wks between #2 and #3, – at least 16wks between #1 and #3.
  • 24. • Vaccinate all newborns with prior to hospital discharge. (Birth dose or Zero dose) • At birth dose of hepatitis B is given within 24 hrs of birth • If mother is HBsAg-positive or HBsAg status is unknown: Give the newborn HBIG and dose #1 within 12hrs of birth; complete series by age 6m.
  • 26. • DTaP given at ages 2m, 4m, 6m, 15–18m, 4–6yrs. • Do not give DTaP/DT to children age 7yrs and older –use Tdap or Td.
  • 29. • Contraindications • For DTaP/Tdap only: encephalopathy not attributable to an identifiable cause, within 7d after DTP/DTaP/Tdap. • Precautions • Guillain-Barré syndrome (GBS) within 6wks after previous dose of tetanus-toxoid-containing vaccine.
  • 30.  Temperature of 105°F (40.5°C) or higher within 48hrs  Continuous crying for 3hrs or more within 48hrs  Collapse or shock-like state within 48hrs  Seizure within 3d • For DTaP/Tdap only: • Progressive or unstable neurologic disorder • Uncontrolled seizures, or progressive encephalopathy until the condition has stabilized.
  • 31. High risk factors for influenza related complications People factors • Children less than 5 years (especially under 2 years of age). • People less than 19 years on long term aspirin therapy. • Adults more than 65 years of age. • Lower socio economic status • Certain ethnic groups • Residents of nursing homes or chronic care facilities • Health care personnel • Travelers- Hajj and Umra
  • 32. High risk factors for influenza related complications Medical condition factors • Asthma • Neurological conditions like cerebral palsy , epilepsy, stroke. • Chronic lung diseases like CF, COPD • Heart disease • Blood disease like sickle cell anemia • Endocrine and metabolic disorders ( Diabetes, obesity) • Kidney disease • Liver disease • Compromised immune system (Cancer , HIV, chronic steroid therapy, organ transplant) • Splenectomy
  • 33. FIGURE 1. Influenza vaccine dosing algorithm for children aged 6 months through 8 years — Advisory Committee on Immunization Practices, United States, 2013–14 influenza season •Doses should be administered at least 4 weeks apart.
  • 34. •Pregnant women especially in the 2nd and 3rd trimesters , their unborn babies or their new infants are at greater risk from complications associated with the flu. •There are a range of changes that occur during pregnancy that put expectant mothers at greater risk, including changes to lung capacity, the immune system and heart rate response. •Pregnant women with existing medical conditions are at even greater risk of severe influenza-related illness. •Because of the higher risk of influenza infection to both mother and baby, the World Health Organization (WHO) recommends that pregnant women should be the highest priority in seasonal influenza vaccination programmes. •The influenza vaccine does not actually cross the placenta to the baby. The vaccine simply stimulates immune system to make antibodies that can fight off the virus.
  • 35. Act-Hib • Give at ages 2m, 4m, 6m, 12–15m (booster dose). • Hib is not routinely given to healthy children age 5yrs and older.
  • 36. Rotavirus • Rotarix (RV1): give at ages 2m, 4m. • RotaTeq (RV5): give at ages 2m, 4m, 6m. • May give dose #1 as early as age 6wks. • Give final dose no later than age 6 months. • Do not begin series in infants older than age 14wks 6 days. • Minimum interval may be as short as 4wks
  • 37. • Contraindications • Allergy to latex, use RV5. • History of intussusception. • Diagnosis of severe combined immunodeficiency (SCID). • Precautions • Moderate or severe acute illness. • Immunosuppressed • Chronic gastrointestinal disease. • Spina bifida or bladder exstrophy.
  • 38. How many doses of MMR ? What if MMR was taken before 12 months of age ? MMR and PPD test What if a pregnant woman is not immune to Measles , Mumps and Rubella ?
  • 39. MMR • 2 doses at age 12m and 18 m. • Adult should receive MMR if no record of vaccine
  • 40. MMR • For women of childbearing age who lack rubella immunity , give 1 dose of MMR . • If pregnant, MMR should be given postpartum • Within 72hrs of measles exposure, give 1 dose of MMR as postexposure prophylaxis to susceptible healthy children age 12m and older
  • 41. • Contraindications • Pregnancy or possibility of pregnancy within 4wks. • Severe immunodeficiency • Precautions • If blood, plasma, or immune globulin given in past 11m • History of thrombocytopenia or thrombocytopenic purpura.
  • 42. Varicella • 2 doses at age 12m and 4–6yrs. • All adults ,older children and adolescents who lack evidence of vaccination or immunity to varicella should receive two doses of varicella vaccine . • If younger than age 13yrs, space dose #1 and #2 at least 3m apart. If age 13yrs and older, space at least 4wks apart. • May use as postexposure prophylaxis if given within 5d.
  • 43. • Contraindications • Pregnancy or possibility of pregnancy within 4wks. • Immunosuppression
  • 44. PCV 13 or PCV 23 ? Which age group? Defaulters High risk groups Which one should be taken first ? Total number of doses Time intervals
  • 45. PCV 13 • Give at ages 2m, 4m, 6m, 12–15m (booster dose). • Dose #1 may be given as early as age 6wks. • Healthy persons above 5 years are not routinely given PCV 13. – If there is no or incomplete or unclear history of vaccination with PCV 13, a single dose of PCV 13 may be given
  • 46. • Contraindication • Previous anaphylaxis to a PCV vaccine or diptheria , tetanus and pertussis vaccines
  • 47. PPSV23 • High-risk children age 2yrs and older. • All adults aged 65 years and older • Adults younger than age 65 years with high risk conditions
  • 48. Dual Pneumococcal vaccination recommendations for adults • All adults aged 65 years should receive PCV 13 followed by PPV 23. PCV 13 may also be given at 50 years of age . • Travelers to Hajj and Umra with high risk conditions • Age 2- 64 years with immunocomprimising and high risk conditions
  • 49. Chest x ray of miliary TB Decorticate posture in TB meningitis BCG vaccination
  • 50. Contraindications for BCG vaccine • Immunosuppression • Pregnancy. • A past history of TB. • A positive pre-immunization tuberculin test. • A previous anaphylactic reaction to vaccine component. • Generalized septic skin conditions. • Acute illnesses with fever or systemic upset • Previous BCG vaccination
  • 51. Adverse events with BCG vaccination 1. Pain and scarring at the site of injection 2. Keloids—large, raised scars 3. If given subcutaneously, it may induce local infection and spread to the regional lymph nodes, causing either suppurative and nonsuppurative lymphadenitis 4. Abscesses can occur due to haematogenous and lymphangiomatous spread. 5. Regional bone infection (BCG osteomyelitis or osteitis) and disseminated BCG infection are rare complications of BCG vaccination, but potentially life threatening. 6. If BCG is accidentally given to an immunocompromised patient (e.g., an infant with SCID or HIV), it can cause disseminated or life-threatening infection
  • 52. Meningitis • Microbiologists routinely exposed to isolates of Neisseria meningitidis • Military recruits • Travellers to countries in which meningococcal disease is hyperendemic or epidemic. ( Subsaharan Africa . Saudi Arabia for Hajj or Umra , India ) • College students if they have not received a dose on or after their 16th birthday • Close contacts of persons with meningcoccal meningitis • Persons with functional asplenia or persistent complement component deficiencies. • HIV-infected persons
  • 53. Meningococcal • MCV4 Menactra, Menveo Give IM • Provides immunity against serotypes A C Y and W 135
  • 55. Infant and child immunization defaulters • Defination: Infants or children from 3 months- 18 years of age who : 1. Start vaccination late or have delayed vaccination for more than 1 month according to National Immunization Schedule
  • 56. Infant and child immunization defaulters 1. Have not completed vaccination series of recommended vaccines in National Immunization Schedule 2. Lack reliable evidence of immunity or immunizations
  • 57. Defaulters Schedule summary All children must complete • MMR-2 doses • Varicella-2doses • Hepatitis B-3 doses • DTaP  3months – 1years: 5 doses  1year -5 years : 4-5 doses  5years-7 years: 3 doses • Tdap  1 dose above 7years followed by 2 doses of Td if no doses or incomplete doses of DTaP were given before 7 years of age.  Booster dose at 13-16 years • IPV/OPV  1-2 doses of IPV and 3-4 doses of OPV Rotavirus- 2 doses before 6 months Hepatitis A-2 doses between 12-24 months and above 24 months for travelers to endemic areas
  • 58. Vaccinating high risk groups • Live vaccines are contraindicated in immunocompromised and pregnant patients • Persons with HIV infection should receive pneumococcal vaccine as soon as possible after their diagnosis.
  • 60. Why do we need adult vaccinations? • Some adults incorrectly assume that the vaccines they received as children will protect them for the rest of their lives. Generally this is true, except that: • Some adults were never vaccinated or partially vaccinated as children • Newer vaccines were not available when some adults were children Immunity wanes over time. • As we age, we become more susceptible to serious diseases caused by common infections, such as shingles, flu & pneumonia. This results in otherwise preventable morbidity & mortality. • Considerable vaccine-preventable morbidity – Excess hospitalization – Diminished quality of life (post-herpetic neuralgia) – Missed work – Medical complications
  • 61. Vaccine General Recommendation for Use in Pregnant Women (CDC) Hepatitis A Can be given if otherwise indicated Hepatitis B Can be given if otherwise indicated ( Can be used for high risk situations or accidental exposure ) HPV Not recommended Influenza inactivated Recommended ( Infants born to women who receive influenza vaccine in the 2nd and 3rd trimesters may have protective antibodies lasting up to 6 months) Influenza live intranasal Contraindicated MMR, Varicella, Zoster, Yellow fever Contraindicated MCV4,MPSV4 Can be given if otherwise indicated PCV 13 , PPSV 23 No specific recommendation , inadequate data Polio May be used if needed Td May be used if needed Tdap Recommended in the last trimester of pregnancy . ( Most effective way of preventing pertussis and tetanus in newborns and children ) Rabies May be used if needed ( In case of bite with a rabid animal rabies vaccination is life saving procedure )
  • 62. HPV • Human papillomavirus (HPV) is a sexually transmitted pathogen that causes • Anogenital and oropharyngeal disease in males and females. • High-risk HPV genotypes causes cancers of the cervix.
  • 63. The high-risk HPV genotypes • 16 and 18 cause – 70 % of all cervical cancers – 90 %of anal cancers , oropharyngeal cancer, vulvar, vaginal cancer, and penile cancer. • Additional 20 % of cervical cancer caused by types 31, 33, 45, 52,58 • 6 and 11 cause 90 percent of anogenital warts.
  • 64. • Three different vaccines: – Quadrivalent HPV vaccine (Gardasil) targets HPV types 6, 11, 16, and 18. – 9-valent vaccine (Gardasil 9) targets the same HPV types as the quadrivalent vaccine 6, 11, 16,18, 31, 33, 45, 52, and 58. – Bivalent vaccine (Cervarix) targets HPV types 16 and 18.
  • 65. HPV vaccines • Prophylactic vaccines, designed to prevent initial HPV infection and subsequent HPV-associated lesions. • Therapeutic vaccines, designed to induce regression of existing HPV-associated lesions, are in development but are not clinically available
  • 66. • HPV vaccine provides a direct benefit to female recipients (protecting against cancers) • Cervical cancer is common cancer among females
  • 67. Recommended age • <15 years • 2 doses of HPV vaccine at – 0 – 6 to 12 months. – Minimum interval is 5 months between the 2 doses
  • 68. • ≥15 years • 3 doses at – 0 – 1 to 2 ( min 4 weeks between 1st & 2nd) – 6 months.( min 12 weeks between 2nd & 3rd) • If a vaccine dose is administered at a shorter interval, it should be re-administered
  • 69. Many thanks to Dr Samina ( ministry of health) for sharing her slides with students at Qatar University 2018
  • 70. • Thank you • Questions
  • 71. Addressing parents concerns • Acknowledging parents’ concerns – Listen respectfully – Provide accurate information about both benefits and risks of vaccines Several factors contribute to parental vaccine concerns, hesitancy, of vaccines, including:
  • 72. Addressing parents concerns • Lack of information about the vaccine and about immunizations in general • Lack of understanding of the severity diseases
  • 73. Addressing parents concerns • Opposing information and misinformation from other sources (eg, alternative medicine practitioners, anti-vaccination organizations and Web sites, and some religious groups) • Perceived risk of serious vaccine adverse effects
  • 74. Addressing parents concerns • Mistrust of the source of information regarding vaccines (eg, vaccine manufacturer, the government) • Concern regarding number of injections to be administered simultaneously
  • 75. Addressing parents concerns • Delivery of information in a culturally insensitive manner or that is not tailored to individual concern. • Delivery of information at an inconvenient time or in a hurried manner. • Some people view the risk of immunization as disproportionately greater than the risk of disease
  • 76. Managing Injection Pain • Talk to your child ( pinch you not hurt you) • Physical techniques – skin to skin contact between the mother and infant, breastfeeding – older children sit on parents lap – position the limb allow relaxation of the muscle – give multiple injections simultaneously at multiple sites • Psychological (breathing, distraction, blowing bubbles) • Pharmacological techniques
  • 77. Syncope • Syncope following immunization has been reported among teens. • Its advised to observe the teen for 15 minutes after immunization.
  • 78. Lapsed Immunization • A lapse in the immunization schedule does not require reinitiation of the entire series.
  • 79. Vaccine Contraindications and precautions • Contraindication when increased risk of an adverse reaction outweighs the benefit of the vaccine.
  • 80. Vaccine Contraindications and precautions • A vaccine should not be administered when a contraindication is present. • The only contraindication applicable to all vaccines is a history of anaphylaxis to a previous dose.
  • 81. • Vaccinations may be deferred when a precaution is present until the health condition resulting in the precaution improves or resolves.
  • 82. • Vaccination may be recommended in the presence of a precaution if the benefit outweighs the risk. • Most precautions are the result of temporary conditions (eg, moderate or severe illness), and a vaccine can be administered when the illness subsides.
  • 83. • Severely immunocompromised people generally should not receive live vaccines.
  • 84. • Pregnant women should not receive live-virus vaccines because of a theoretical risk to the fetus. • Personal or family history of seizures is a precaution, rather than a contraindication, for MMRV vaccination in a child.
  • 85. Common conditions that should not delay vaccination but often are considered mistakenly to be contraindications i • Diarrhea • Minor upper respiratory tract illnesses (including otitis media) with or without fever
  • 86. Common conditions that should not delay vaccination but often are considered mistakenly to be contraindications i • Mild to moderate local reactions to a previous dose of vaccine • Exposure to an infectious disease • Current antimicrobial therapy • Being in the convalescent phase of an acute illness
  • 87. Common conditions that should not delay vaccination but often are considered mistakenly to be contraindications • Allergy to an antibiotic (except anaphylactic reaction to neomycin, gentamicin, or streptomycin, if any of these are in the vaccine to be administered) • History of nonanaphylactic allergy to egg
  • 88. Common conditions that should not delay vaccination but often are considered mistakenly to be contraindications • Personal or family history of seizures • Family history of sudden unexpected death • Family history of an adverse event following immunization • Breastfeeding or pregnancy in a household contact
  • 89. Summary • The childhood and adolescents immunization schedule is complex. • Although serious adverse reactions to immunizations are uncommon – clinicians must be knowledgeable in these reactions as well as the contraindications and precautions to each vaccine.