Assignment on Universal immunization schedule

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UNIVERSAL IMMUNIZATION PROGRAMME (UIP) - INDIA

A Comprehensive Assignment


1. Introduction

Immunization is one of the most cost-effective public health interventions available. By stimulating the immune system to produce protective antibodies without causing disease, vaccines prevent millions of deaths annually from infections that once caused widespread childhood mortality.
The concept of a structured, government-driven immunization schedule evolved from the WHO's Expanded Programme on Immunization (EPI), officially launched in May 1974 to protect all children worldwide against six vaccine-preventable diseases: diphtheria, whooping cough, tetanus, polio, tuberculosis, and measles.
India adopted this programme as the Universal Immunization Programme (UIP), launched on November 19, 1985, dedicated to the memory of Smt. Indira Gandhi. Its goal was to achieve universal immunization coverage of all eligible children and pregnant women by 1990.

2. Historical Background and Milestones

India's immunization journey began in 1962 with BCG vaccination as part of the National Tuberculosis Programme. The programme has expanded steadily over decades:
YearMilestone
1962BCG introduced under National TB Programme
1978EPI launched - BCG, DPT, OPV, Typhoid (urban areas)
1983TT vaccine added for pregnant women
1985UIP launched - Measles added, Typhoid removed; focus on children <1 year
1990Vitamin A supplementation added
1995Pulse Polio Immunization Programme launched (National Immunization Days)
1997Vaccine Vial Monitors (VVM) introduced
2002Hepatitis B introduced as pilot in 33 districts
2005National Rural Health Mission launched; Auto-disable syringes introduced
2006JE vaccine introduced in endemic districts
2010Pentavalent vaccine introduced (replacing separate DPT, Hep B, Hib)
2014India certified polio-free (WHO, March 27, 2014)
2014IPV (Inactivated Polio Vaccine) introduced
2016Rotavirus Vaccine (RVV) introduced
2017Pneumococcal Conjugate Vaccine (PCV) introduced
2017Measles-Rubella (MR) vaccine replaced standalone Measles vaccine
2022HPV vaccine (CERVAVAC - indigenous) introduced
2026Full immunization coverage reaches 98.4%
Source: Park's Textbook of Preventive and Social Medicine; PIB India, 2026

3. Objectives of UIP

  1. To reduce morbidity, mortality, and disability from vaccine-preventable diseases (VPDs)
  2. To achieve and sustain universal immunization coverage across all children under 2 years and pregnant women
  3. To interrupt disease transmission in the community (herd immunity)
  4. To eliminate/eradicate specific diseases (e.g., polio - achieved 2014; neonatal tetanus - near elimination)
  5. To ensure equitable access to vaccines across rural, urban, and tribal populations
  6. To introduce new vaccines as evidence and funding allows

4. Diseases Covered Under UIP (12 VPDs)

India's UIP currently vaccinates against 12 diseases:
  1. Tuberculosis (BCG)
  2. Diphtheria
  3. Pertussis (Whooping Cough)
  4. Tetanus
  5. Poliomyelitis
  6. Measles
  7. Rubella
  8. Hepatitis B
  9. Haemophilus influenzae type B (Hib) - meningitis/pneumonia
  10. Rotavirus diarrhoea
  11. Pneumococcal disease (pneumonia/meningitis)
  12. Japanese Encephalitis (in endemic districts only)

5. National Immunization Schedule (NIS) / UIP 2025

For Infants and Children

AgeVaccineRouteSiteDiseases Prevented
BirthBCGIntradermalLeft upper armTuberculosis
BirthOPV-0 (Birth dose)OralMouthPoliomyelitis
BirthHepatitis B (Birth dose)IMAntero-lateral thigh (right)Hepatitis B
6 WeeksOPV-1OralMouthPolio
6 WeeksPentavalent-1 (DPT+HepB+Hib)IMAntero-lateral thigh (left)Diphtheria, Pertussis, Tetanus, Hep B, Hib
6 WeeksRotavirus Vaccine (RVV)-1OralMouthRotavirus diarrhoea
6 WeeksfIPV-1 (Fractional IPV)IntradermalRight upper armPolio
6 WeeksPCV-1IMAntero-lateral thigh (right)Pneumococcal disease
10 WeeksOPV-2OralMouthPolio
10 WeeksPentavalent-2IMAntero-lateral thigh (left)As above
10 WeeksRVV-2OralMouthRotavirus
14 WeeksOPV-3OralMouthPolio
14 WeeksPentavalent-3IMAntero-lateral thigh (left)As above
14 WeeksRVV-3OralMouthRotavirus
14 WeeksfIPV-2IntradermalRight upper armPolio
14 WeeksPCV-2IMAntero-lateral thigh (right)Pneumococcal
9-12 MonthsMR-1 (Measles-Rubella)SCRight upper armMeasles, Rubella
9-12 MonthsJE-1*SCLeft upper armJapanese Encephalitis
9-12 MonthsPCV-BoosterIMAntero-lateral thigh (right)Pneumococcal
16-24 MonthsMR-2SCRight upper armMeasles, Rubella
16-24 MonthsJE-2*SCLeft upper armJapanese Encephalitis
16-24 MonthsDPT Booster-1IMAntero-lateral thigh (left)Diphtheria, Pertussis, Tetanus
16-24 MonthsOPV BoosterOralMouthPolio
5-6 YearsDPT Booster-2IMUpper arm (left)Diphtheria, Pertussis, Tetanus
10 YearsTd (Tetanus-Diphtheria)IMUpper armTetanus, Diphtheria
16 YearsTdIMUpper armTetanus, Diphtheria
*JE vaccines: Only in endemic districts
Source: PIB India 2025-26; IAP ACVIP 2025; Park's Textbook of Preventive and Social Medicine

For Pregnant Women

TimingVaccineDoseRoute
Early pregnancy (as early as possible)Td-11st doseIM
4 weeks after Td-1Td-22nd doseIM
If previously vaccinated (within 3 years)Td-BoosterSingle boosterIM
Purpose: Prevention of neonatal tetanus (NNT) and maternal tetanus. TT/Td is now replaced by Td (Tetanus-Diphtheria) containing reduced diphtheria toxoid (adult formulation).

6. IAP (Indian Academy of Pediatrics) Schedule - Additional Vaccines

The IAP ACVIP 2025 recommends additional vaccines beyond the UIP (available mainly in private sector):
AgeVaccineDisease
BirthBCG, OPV-0, Hep B-1TB, Polio, Hep B
6 weeksDTwP/DTaP, IPV, Hib, Hep B-2, Rotavirus, PCVMultiple
9-12 monthsMMR-1, Typhoid Conjugate (TCV)Measles, Mumps, Rubella, Typhoid
12 monthsHepatitis A-1Hepatitis A
15 monthsMMR-2, Varicella-1, PCV BoosterMeasles, Mumps, Rubella, Chickenpox
18 monthsDTwP/DTaP Booster, Hib BoosterDiphtheria, Tetanus, Pertussis, Hib
2 yearsHepatitis A-2Hepatitis A
4-6 yearsDTwP/DTaP Booster-2, OPV Booster, Varicella-2Multiple
9-14 years (girls)HPV (2 doses, 6 months apart)Cervical cancer
AnnualInfluenzaSeasonal flu

7. Key Vaccines - Individual Details

BCG (Bacillus Calmette-Guerin)

  • Type: Live attenuated (Mycobacterium bovis)
  • Dose: 0.1 mL (0.05 mL for neonates <1 month)
  • Route/Site: Intradermal, left upper arm
  • Age: At birth (up to 1 year if missed)
  • Contraindication: Immunodeficiency, symptomatic HIV
  • Storage: 2-8°C, sensitive to light and heat
  • Expected response: Koch's phenomenon (induration >5 mm at 4-6 weeks) confirms "take"

OPV (Oral Polio Vaccine)

  • Type: Live attenuated (Sabin), trivalent
  • Dose: 2 drops oral
  • Schedule: Birth, 6, 10, 14 weeks; booster at 16-24 months
  • Advantage: Produces intestinal immunity (IgA), induces herd protection
  • Contraindication: Immunodeficiency (use IPV instead)
  • Key note: Not given to symptomatic HIV-positive children

IPV/fIPV (Inactivated/Fractional IPV)

  • Type: Killed (Salk), fractional dose (1/5th of full dose) intradermal
  • Advantage: Safe in immunocompromised; produces systemic immunity
  • Given at: 6 and 14 weeks under UIP (fractional intradermal dose)

Pentavalent Vaccine (DPT + HepB + Hib)

  • Combines 5 antigens in a single injection
  • Reduces the number of injections from 5 to 1
  • Given at 6, 10, 14 weeks
  • Antero-lateral aspect of the thigh (left side)

Measles-Rubella (MR) Vaccine

  • Type: Live attenuated
  • Route: Subcutaneous, right upper arm
  • Schedule: 9-12 months (MR-1) and 16-24 months (MR-2)
  • Note: Replaced standalone measles vaccine; part of global measles-rubella elimination drive

Rotavirus Vaccine (RVV)

  • Type: Live attenuated oral (ROTAVAC - indigenous Indian vaccine by Bharat Biotech)
  • Schedule: 6, 10, 14 weeks (3-dose series)
  • Maximum age for first dose: 15 weeks
  • Maximum age for last dose: 8 months

PCV (Pneumococcal Conjugate Vaccine)

  • Type: Conjugate vaccine (PCV-13 or PCV-10)
  • Schedule: 6 weeks, 14 weeks, booster at 9-12 months
  • Prevents: Streptococcus pneumoniae invasive disease, pneumonia, meningitis

HPV Vaccine

  • Indigenous vaccine: CERVAVAC (quadrivalent, by Serum Institute of India)
  • Target: Girls 9-14 years (2-dose schedule, 6 months apart)
  • Prevents: Cervical cancer, genital warts (HPV types 6, 11, 16, 18)
  • Introduced into UIP (phased rollout from 2023 onwards)

8. Cold Chain and Vaccine Storage

Maintaining the cold chain is essential for vaccine potency. Key principles:
LevelEquipmentTemperature
National/State StoreCold rooms / Walk-in coolers+2°C to +8°C (or -15°C to -25°C for freeze-sensitive)
DistrictIce-lined refrigerators (ILR)+2°C to +8°C
PHC LevelILR / Domestic refrigerator+2°C to +8°C
FieldVaccine carrier with ice packs+2°C to +8°C
Key points:
  • Freeze-sensitive vaccines (DPT, TT, Hep B, Pentavalent, PCV, fIPV): Must NOT be frozen - stored at +2 to +8°C
  • Freeze-tolerant vaccines (OPV): Can be stored frozen (-15 to -25°C) at higher levels to extend shelf life
  • BCG and MR: Sensitive to heat and light; store at 2-8°C, protect from light
  • VVM (Vaccine Vial Monitor): Heat-sensitive label on each vial; inner square turning as dark or darker than outer ring indicates the vaccine should NOT be used
  • Open Vial Policy: Multi-dose vials of OPV, liquid pentavalent, liquid DPT, TT, Hep B, and MR can be used in subsequent sessions if VVM is intact and stored appropriately

9. Immunization Delivery Strategies

Fixed Sites

  • Sub-centre, PHC, CHC, district hospitals
  • AWC (Anganwadi Centres) - monthly immunization days

Outreach Sessions

  • ANM visits villages/habitations on fixed days
  • Village Health Sanitation and Nutrition Days (VHSND)
  • Outreach sessions reach underserved populations

Special Campaigns

  • Pulse Polio Immunization (National Immunization Days/NIDs): Annual OPV campaigns for all children <5 years (Dec-Jan); resulted in India being declared polio-free in 2014
  • Mission Indradhanush: Launched in 2014 to reach unvaccinated/partially vaccinated children; intensified version (IIM) since 2017
  • Intensified Mission Indradhanush (IMI): Targets districts with low coverage, pregnant women and children aged 0-2 years

10. Herd Immunity and Community Protection

Herd immunity is indirect protection conferred to unvaccinated individuals when a sufficient proportion of the population is immune (through vaccination or natural infection). This breaks the chain of transmission.
DiseaseHerd Immunity Threshold (% population immune)
Measles92-95%
Polio80-85%
Diphtheria83-85%
Rubella83-85%
Pertussis92-94%

11. Contraindications to Vaccination

Absolute Contraindications

  • Anaphylaxis to a previous dose or to a vaccine component
  • Severe immunodeficiency for live vaccines (BCG, OPV, MR)

Precautions (Not Contraindications)

  • Mild illness with low-grade fever: vaccinate (DO NOT postpone)
  • Diarrhoea in progress: OPV can be given but dose may not count; give IPV instead if available
  • Malnourished children: Vaccinate - they need protection most
  • Prematurity: Full doses as per chronological age
  • Breastfeeding: All vaccines can be given

False Contraindications (Common Myths - Must be Corrected)

  • Mild cold/URTI - NOT a contraindication
  • Low-grade fever - NOT a contraindication
  • Antibiotic use - NOT a contraindication
  • Malnutrition - NOT a contraindication
  • Previous febrile reaction to DPT (minor) - NOT a contraindication (give antifebrile, vaccinate)

12. Adverse Events Following Immunization (AEFI)

An Adverse Event Following Immunization (AEFI) is any untoward medical occurrence that follows immunization and does not necessarily have a causal relationship with the vaccine.

Classification (WHO 2013)

  1. Vaccine product-related reaction - caused by intrinsic properties of the vaccine
  2. Vaccine quality defect-related reaction - due to manufacturing defect
  3. Immunization error-related reaction - due to improper preparation/administration
  4. Immunization anxiety-related reaction - stress response, not vaccine-specific
  5. Coincidental event - temporal association only, not causal

Common AEFIs

VaccineCommon ReactionSerious/Rare Reaction
BCGLocal induration, scarBCG-itis, disseminated BCG (immunocompromised)
DPT/PentavalentLocal pain/swelling, feverFebrile seizures, HHE (hypotonic-hyporesponsive episode)
OPVNone usuallyVAPP (vaccine-associated paralytic polio) - 1:750,000
MMR/MRMild rash, fever (7-12 days)Thrombocytopenia, aseptic meningitis (very rare)
RotavirusMild vomiting/diarrhoeaIntussusception (very rare)
PCVLocal reactions, feverRare serious reactions
AEFI Reporting: All serious AEFIs must be reported to the Medical Officer (MO) and District Immunization Officer (DIO). India has a national AEFI surveillance system coordinated through MoHFW.

13. WHO EPI - Global Perspective

The WHO's EPI (renamed as now the Immunization Agenda 2030 / IA2030) sets global targets:
  • IA2030 goal: Reduce deaths from VPDs; achieve 90% national coverage with 3 primary doses of DTP-containing vaccine; reduce zero-dose children by 50% by 2030
  • GAVI (Global Alliance for Vaccines and Immunization): Finances vaccine procurement for lower-income countries
  • WHO EPI core vaccines: BCG, OPV/IPV, DTP, Hepatitis B, Hib, MCV (measles), Rubella

14. Achievements and Challenges

Achievements

  • Full immunization coverage: rose from 62% (2015) to 98.4% (January 2026)
  • India declared polio-free in 2014 (WHO certified)
  • Neonatal tetanus near-elimination
  • Dramatic decline in VPDs:
    • Polio cases: 28,257 (1987) → 0 (2018 onwards)
    • Neonatal tetanus: 11,849 (1987) → 181 (2018)
    • Pertussis: 163,786 (1987) → 18,006 (2018)
    • Measles: 247,519 (1987) → 20,815 (2018)

Remaining Challenges

  1. Zero-dose children: Still 0.06% of total population (2024), concentrated in urban slums, conflict-affected zones, tribal areas
  2. Cold chain gaps in remote/hilly regions
  3. Vaccine hesitancy - misinformation spread through social media
  4. Urban migration disrupts immunization schedules
  5. AEFI surveillance needs strengthening
  6. Gender gap in vaccination access in some regions
  7. Reaching scheduled castes/tribes and hard-to-reach populations

15. Mission Indradhanush

Launched in December 2014, Mission Indradhanush (MI) was designed to immunize all unvaccinated and partially vaccinated children up to 2 years and pregnant women who were not covered under routine immunization.
  • Named after the 7 colours of the rainbow representing the 7 vaccines initially targeted
  • Intensified Mission Indradhanush (IMI) launched in 2017 with 4 rounds of immunization activities
  • Focus on 190 high-priority districts with low immunization coverage
  • Result: Significant improvement in full immunization coverage in targeted districts

16. Summary

The Universal Immunization Programme is India's flagship public health initiative, protecting children and mothers from 12 vaccine-preventable diseases. Starting from barely 30% coverage in 1985-86, the UIP now achieves near-universal coverage (98.4%). The programme's success - including poliovirus eradication - stands as a global public health landmark. The future agenda includes sustaining high coverage, eliminating measles-rubella, strengthening AEFI surveillance, and introducing new vaccines (e.g., HPV, rotavirus across all states) to further reduce the burden of childhood diseases.

References

  1. Park, K. Park's Textbook of Preventive and Social Medicine, 27th ed. Jabalpur: Banarsidas Bhanot Publishers. (Immunization chapters, pp. 3497-3600)
  2. Ministry of Health and Family Welfare, Government of India. National Immunization Schedule 2025. New Delhi: MoHFW.
  3. Press Information Bureau, Government of India. UIP achievements and schedule 2025-26.
  4. Indian Academy of Pediatrics (IAP) Advisory Committee on Vaccines and Immunization Practices (ACVIP). IAP Immunization Schedule 2025.
  5. World Health Organization. Immunization Agenda 2030 (IA2030). Geneva: WHO.
  6. Wikipedia. Universal Immunisation Programme - India.

Note: This assignment covers the UIP/NIS 2025 schedule. The schedule is periodically updated by the National Technical Advisory Group on Immunization (NTAGI). Always verify with the latest MoHFW circular for the most current recommendations.

Assignment on Universal immunization schedule for community Health Nursing

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Here is a comprehensive, nursing-focused assignment on the Universal Immunization Programme:

UNIVERSAL IMMUNIZATION PROGRAMME (UIP)

Assignment for Community Health Nursing


1. INTRODUCTION

Immunization is one of the most powerful and cost-effective public health tools. By stimulating the immune system to develop protective antibodies without causing the actual disease, vaccines prevent millions of childhood deaths every year from infections that were once leading causes of under-5 mortality.
The community health nurse (CHN) plays a central and irreplaceable role in India's immunization programme - from planning and conducting sessions, maintaining cold chain, educating mothers, to identifying and reporting adverse events. Understanding the Universal Immunization Programme (UIP) in its entirety is therefore a core competency for every community health nurse.

2. DEFINITION AND BACKGROUND

Immunization is the process of making a person immune to an infectious disease, typically by the administration of a vaccine. Vaccines stimulate the body's own immune system to protect the individual against subsequent infection or disease.
Expanded Programme on Immunization (EPI): In May 1974, the WHO officially launched a global immunization programme - the EPI - to protect all children of the world against six vaccine-preventable diseases: diphtheria, whooping cough, tetanus, polio, tuberculosis, and measles. EPI was launched in India in January 1978.
Universal Immunization Programme (UIP): India launched the UIP on November 19, 1985, dedicated to the memory of Smt. Indira Gandhi. UNICEF in 1985 also renamed EPI as "Universal Child Immunization" (UCI) to achieve universal immunization by 1990. The UIP became part of:
  • Child Survival and Safe Motherhood Programme (1992)
  • National Reproductive and Child Health (RCH) Programme (1997)
  • National Rural Health Mission (NRHM) / National Health Mission (NHM) - 2005 onwards
The UIP is one of the largest public health programmes in the world, targeting approximately 2.67 crore newborns and 2.9 crore pregnant women annually across India.
Source: Park's Textbook of Preventive and Social Medicine

3. OBJECTIVES OF UIP

  1. To reduce morbidity, disability, and mortality from vaccine-preventable diseases (VPDs)
  2. To achieve and sustain universal immunization coverage for all eligible children and pregnant women
  3. To interrupt the chain of disease transmission in the community through herd immunity
  4. To eliminate/eradicate specific VPDs (polio - achieved 2014; neonatal tetanus - near elimination)
  5. To ensure free, equitable vaccine access across rural, urban, tribal, and slum populations
  6. To introduce new, evidence-based vaccines progressively into the national schedule

4. DISEASES COVERED UNDER UIP

India's UIP currently vaccinates against 12 vaccine-preventable diseases:
S.NoDiseaseVaccine Used
1TuberculosisBCG
2DiphtheriaPentavalent / DPT / Td
3Pertussis (Whooping Cough)Pentavalent / DPT
4TetanusPentavalent / DPT / Td
5PoliomyelitisOPV + fIPV
6MeaslesMR Vaccine
7RubellaMR Vaccine
8Hepatitis BPentavalent (HepB component)
9Haemophilus influenzae type B (Meningitis/Pneumonia)Pentavalent (Hib component)
10Rotavirus DiarrhoeaRVV (ROTAVAC)
11Pneumococcal Disease (Pneumonia/Meningitis)PCV
12Japanese EncephalitisJE Vaccine (endemic districts only)

5. NATIONAL IMMUNIZATION SCHEDULE (NIS) 2025

5a. For Pregnant Women

VaccineWhen to GiveDoseRouteSite
Td-1 (Tetanus-Diphtheria)Early in pregnancy0.5 mLIntramuscularUpper arm
Td-24 weeks after Td-10.5 mLIntramuscularUpper arm
Td-BoosterIf received 2 Td doses in a pregnancy within last 3 years0.5 mLIntramuscularUpper arm
Purpose: Prevents maternal and neonatal tetanus (NNT). NNT occurs when the newborn's umbilical stump is contaminated during delivery in unhygienic settings.

5b. For Infants and Children

AgeVaccineDoseRouteSiteDisease Prevented
At BirthBCG0.1 mL (0.05 mL if <1 month)IntradermalLeft upper armTuberculosis (especially TB meningitis, miliary TB)
BirthHepatitis B-Birth dose0.5 mLIntramuscularAntero-lateral mid-thighHepatitis B (prevents perinatal transmission)
BirthOPV-02 dropsOralMouthPoliomyelitis
6 WeeksOPV-12 dropsOralMouthPolio
6 WeeksPentavalent-1 (DPT+HepB+Hib)0.5 mLIntramuscularAntero-lateral mid-thighDiphtheria, Pertussis, Tetanus, Hep B, Hib
6 WeeksRotavirus Vaccine (RVV)-13 dropsOralMouthRotavirus diarrhoea
6 WeeksfIPV-1 (Fractional IPV)0.1 mLIntradermalRight upper armPolio (systemic immunity)
6 WeeksPCV-10.5 mLIntramuscularAntero-lateral mid-thighPneumococcal pneumonia/meningitis
10 WeeksOPV-22 dropsOralMouthPolio
10 WeeksPentavalent-20.5 mLIntramuscularAntero-lateral mid-thighAs above
10 WeeksRVV-23 dropsOralMouthRotavirus
14 WeeksOPV-32 dropsOralMouthPolio
14 WeeksPentavalent-30.5 mLIntramuscularAntero-lateral mid-thighAs above
14 WeeksRVV-33 dropsOralMouthRotavirus
14 WeeksfIPV-20.1 mLIntradermalRight upper armPolio
14 WeeksPCV-20.5 mLIntramuscularAntero-lateral mid-thighPneumococcal
9-12 MonthsMR-1 (Measles-Rubella)0.5 mLSubcutaneousRight upper armMeasles, Rubella
9-12 MonthsJE-1*0.5 mLSubcutaneousLeft upper armJapanese Encephalitis
9-12 MonthsPCV-Booster0.5 mLIntramuscularAntero-lateral mid-thighPneumococcal
16-24 MonthsMR-20.5 mLSubcutaneousRight upper armMeasles, Rubella
16-24 MonthsJE-2*0.5 mLSubcutaneousLeft upper armJapanese Encephalitis
16-24 MonthsDPT-Booster 10.5 mLIntramuscularAntero-lateral mid-thighDiphtheria, Pertussis, Tetanus
16-24 MonthsOPV-Booster2 dropsOralMouthPolio
5-6 YearsDPT-Booster 20.5 mLIntramuscularUpper arm (left)Diphtheria, Pertussis, Tetanus
10 YearsTd0.5 mLIntramuscularUpper armTetanus, Diphtheria
16 YearsTd0.5 mLIntramuscularUpper armTetanus, Diphtheria
*JE vaccine: Given only in JE-endemic districts
Source: National Immunization Schedule (NIS) India 2025; Park's Textbook of Preventive and Social Medicine, Table 43

6. NURSING RESPONSIBILITIES IN UIP

The community health nurse/ANM is the backbone of immunization delivery in India. Her responsibilities span the entire immunization cycle:

6a. Pre-Session Responsibilities (Preparation)

  1. Planning the session:
    • Prepare a list of beneficiaries (pregnant women, infants 0-2 years) from the sub-centre register
    • Fix a convenient day, time, and place for immunization sessions
    • Coordinate with AWW (Anganwadi Worker) and ASHA for mobilization
    • Plan session to minimize waiting time for mothers
  2. Vaccine and logistics indent:
    • Calculate vaccine requirements based on beneficiary count
    • Collect vaccines from PHC/CHC cold chain point
    • Verify expiry dates and VVM status before collecting vaccines
  3. Cold chain maintenance before session:
    • Place 4 conditioned ice packs in the vaccine carrier
    • Place vaccines in a plastic/zipper bag in the centre of the carrier - NOT directly on the ice
    • Freeze-sensitive vaccines (DPT, TT, Hep B, Pentavalent, PCV, fIPV) must NOT be placed directly on the ice pack
    • Reconstituted BCG and Measles/MR vaccines should be kept only on top of the ice pack during session
    • Diluents should be chilled at +2 to +8°C before reconstitution

6b. During the Session - Technical Nursing Skills

Before administering each vaccine:
  • Welcome beneficiaries warmly
  • Wash hands thoroughly before the session
  • Verify the immunization card and the age of the child
  • Screen for contraindications
  • Check the vaccine label and expiry date
  • Check the VVM (Vaccine Vial Monitor): DO NOT use the vaccine if the inner square is as dark as or darker than the outer circle
  • Lightly shake the T-series vaccine vial before drawing the dose
  • Use a new Auto-Disable (AD) syringe for each injection
Key technique points:
  • Do NOT clean the injection site with a spirit swab before vaccination - spirit can kill live vaccine components
  • Use the correct site for each vaccine (antero-lateral mid-thigh for IM injections, NOT the gluteal region - to prevent sciatic nerve injury and ensure adequate immune response)
  • For BCG: intradermal in the left upper arm - a pale, raised bleb of 5-7 mm indicates correct placement
  • For MR/Measles: subcutaneous, right upper arm only
  • Give all due vaccines on the same visit - do NOT miss an opportunity
After administering:
  • Fill in the immunization card and sub-centre register
  • Advise the mother to wait 30 minutes at the session site for observation for immediate reactions
  • Counsel on common expected reactions and what to do

6c. Post-Session Responsibilities

  1. Cold chain:
    • Return leftover vaccines to the cold chain immediately after the session
    • Multi-dose vials that were opened may be used in subsequent sessions within the same day (Open Vial Policy applies to OPV, liquid pentavalent, liquid DPT, TT, HepB, and MR)
    • Reconstituted BCG and MR vaccines must be discarded within 4 hours or at end of session (whichever is earlier)
  2. Record keeping:
    • Update the immunization register
    • Mark defaulters (children who did not turn up)
    • Plan for follow-up of defaulters
  3. AEFI surveillance:
    • Monitor for and record any adverse events
    • Report serious AEFIs to the MO and District Immunization Officer (DIO) using the prescribed AEFI reporting form

7. KEY VACCINES - NURSING NOTES

BCG Vaccine

  • Type: Live attenuated (Mycobacterium bovis)
  • Age: At birth, up to 1 year (never give above 1 year of age)
  • Dose: 0.1 mL (0.05 mL for neonates under 1 month)
  • Route/Site: Intradermal, left upper arm
  • Expected reaction: A small papule appears at 2 weeks, ulcerates, and heals to form the characteristic BCG scar by 6-12 weeks. This confirms a successful "take"
  • Koch's phenomenon: Induration >5 mm at 4-6 weeks post-vaccination (positive reaction in tuberculin-sensitive individuals)
  • Storage: 2-8°C, protected from light and heat
  • Contraindication: Immunodeficiency, symptomatic HIV infection

OPV (Oral Polio Vaccine)

  • Type: Live attenuated (Sabin vaccine), bivalent (types 1 and 3)
  • Dose: 2 drops oral
  • Advantage: Produces intestinal IgA (mucosal immunity), induces herd protection by eliminating virus from gut
  • Schedule in UIP: Birth dose (OPV-0), then 6, 10, 14 weeks; booster at 16-24 months
  • Nursing note: Do NOT give OPV to immunocompromised children - use IPV instead
  • VAPP risk: Vaccine-associated paralytic polio - extremely rare (1 in 2.7 million doses)

fIPV (Fractional Inactivated Polio Vaccine)

  • Given at 6 and 14 weeks under UIP (0.1 mL intradermal, right upper arm)
  • Fractional dose = 1/5th of the full IPV dose; given ID rather than IM
  • Safe for immunocompromised children
  • Produces strong systemic (blood) immunity

Pentavalent Vaccine (DPT + Hepatitis B + Hib)

  • Combines 5 antigens in one injection - reduces pain and visit burden
  • Given at 6, 10, and 14 weeks
  • Site: Antero-lateral aspect of mid-thigh (left)
  • Why NOT gluteal? Risk of sciatic nerve injury; fat in gluteal region reduces immune response
  • Minimum gap: 4 weeks between doses; decreasing the interval reduces optimal antibody production

Measles-Rubella (MR) Vaccine

  • Type: Live attenuated
  • Route: Subcutaneous, right upper arm only
  • Why right arm? Standardized so BCG scar on left arm can be distinguished from MR reaction
  • Schedule: MR-1 at 9-12 months; MR-2 at 16-24 months
  • Must be reconstituted with the supplied diluent; used within 4 hours of reconstitution
  • Key: If a child received only measles vaccine earlier, still give MR vaccine as per schedule

Rotavirus Vaccine (RVV - ROTAVAC)

  • Indigenous vaccine developed in India (Bharat Biotech) using neonatal strain 116E
  • 3-dose oral series: 6, 10, 14 weeks
  • First dose must be given before 15 weeks of age; last dose before 8 months
  • Reduces severe rotavirus diarrhoea hospitalizations by ~55-60%

Hepatitis B Birth Dose

  • Must be given within 24 hours of birth - this is critical for preventing perinatal (mother-to-child) transmission
  • If given after 24 hours, protective efficacy against perinatal transmission is significantly reduced
  • Given intramuscularly in the antero-lateral mid-thigh

DPT Catch-up Guidance

  • DPT can be given up to 7 years of age; OPV up to 5 years
  • If a child is brought late: do NOT restart the schedule - pick up from where it was left off
    • Example: Child had BCG, HepB-1, DPT-1, OPV-1 at 5 months and comes at 11 months → give DPT-2, HepB-2, OPV-2, and Measles; do NOT restart from DPT-1

8. COLD CHAIN MANAGEMENT - NURSING RESPONSIBILITIES

The cold chain is the system of transporting and storing vaccines at the correct temperature (2-8°C) from manufacturer to beneficiary.

Temperature Requirements

Vaccine TypeStorage RequirementWhat Happens if Rule Broken
Freeze-sensitive (DPT, TT, Td, Hep B, Pentavalent, PCV, fIPV)+2°C to +8°C - must NOT be frozenFreezing causes aggregation; reduced potency; flocculation test used to detect freeze damage
OPVCan be stored frozen at -15°C to -25°C at higher levelsHeat-sensitive; loses potency if warm
BCG, MR/Measles+2°C to +8°C; protect from lightBoth heat-sensitive AND light-sensitive

Cold Chain Equipment

LevelEquipment
National/StateCold rooms (+2 to +8°C) and freezer rooms (-15 to -25°C)
DistrictIce-Lined Refrigerators (ILR), deep freezers
PHC/Sub-centreILR, domestic front-load refrigerator
Field/OutreachVaccine carrier with 4 conditioned ice packs

Vaccine Vial Monitor (VVM)

  • A heat-sensitive sticker on each vaccine vial
  • The inner square changes from light to dark when the vaccine has been exposed to excessive heat
  • Rule: If inner square is as dark as or darker than the outer ring → DO NOT USE the vaccine
  • VVM helps identify heat-damaged vaccines even if expiry date has not passed

DO's and DON'Ts in Cold Chain (Park's Preventive Medicine)

DO'sDON'Ts
Check expiry date and VVM before each vaccinationLeave vaccine carrier in sunlight
Keep vaccines in plastic bag in centre of carrier with 4 ice packsLeave the lid of carrier open
Keep diluents chilled before reconstitutionDrop or sit on the vaccine carrier
Keep reconstituted BCG and MR only on top of the ice packKeep DPT, DT, TT, and Hep B directly on the ice pack
Return unused vaccines to cold chain after sessionCarry vaccines in a handbag

9. CONTRAINDICATIONS TO VACCINATION

True (Absolute) Contraindications

  • Anaphylaxis to a prior dose or known vaccine component
  • Symptomatic HIV / severe immunodeficiency: do NOT give live vaccines (BCG, OPV, MR)

False Contraindications - Conditions that are NOT Contraindications

The nurse must educate mothers about these common myths:
ConditionAction
Mild cold, cough, or URTIVaccinate
Low-grade feverVaccinate
DiarrhoeaVaccinate (give OPV, but may not count; give IPV if available)
MalnutritionVaccinate - these children need immunization most
PrematurityVaccinate at chronological age (not corrected age)
BreastfeedingAll vaccines can be given
Antibiotic therapyVaccinate
Previous mild febrile reaction to DPTVaccinate (give antipyretic before and after)
Park's Textbook states: "Immunization is frequently postponed if children are ill or malnourished. This is not acceptable in the light of present knowledge. In fact, it is particularly important to immunize children with malnutrition. Low grade fever, mild respiratory infections or diarrhoea and other minor illnesses should NOT be considered as contraindications to immunization. These are the very children who are most in need of immunization."

10. ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI)

An AEFI is any untoward medical occurrence that follows immunization and does not necessarily have a causal relationship with the vaccine.

WHO 2013 Classification of AEFI

TypeDescriptionExample
Vaccine product-relatedDue to intrinsic properties of the vaccineBCG osteitis, febrile seizure after DPT
Vaccine quality defect-relatedManufacturing defectContaminated vial
Immunization error-relatedImproper preparation, wrong siteAbscess from subcutaneous DPT
Immunization anxiety-relatedStress/anxiety, not from vaccineVasovagal syncope after injection
CoincidentalTemporal association onlyFever from concurrent URTI

Common AEFIs - Nursing Management

VaccineCommon ReactionNursing Management
BCGLocal induration, BCG scarReassure; it is normal
DPT / PentavalentPain, swelling at site; feverParacetamol; cold compress; reassure
OPVNone typicallyMonitor for rare VAPP
MRMild rash, fever at 7-12 daysReassure; antipyretics if needed
RotavirusMild vomiting/loose stoolsReassure; maintain hydration
DPT (rare)Hypotonic Hyporesponsive Episode (HHE)Lay flat; observe; report to MO

AEFI Reporting (Nursing Duty)

  • All serious AEFIs must be reported within 24 hours to the Medical Officer and District Immunization Officer
  • Use the prescribed AEFI reporting form (MoHFW format)
  • India has a national AEFI surveillance system under MoHFW/NHM
  • Child with DPT allergy/encephalopathy: give DTaP instead for remaining doses (P = whole-cell pertussis component is usually responsible)

11. IMMUNIZATION DELIVERY STRATEGIES

11a. Fixed Strategy

  • Sub-centres, PHCs, CHCs, district hospitals, AWCs (Anganwadi Centres)
  • Monthly immunization days (Village Health, Sanitation and Nutrition Day - VHSND)
  • Convenient for urban and peri-urban populations

11b. Outreach Strategy

  • ANM/CHN travels to villages, hamlets, and remote habitations
  • Fixed days and times announced in advance
  • Reaches populations without easy access to fixed facilities

11c. Mobile Strategy

  • Mobile immunization vans/teams for very remote/hilly areas
  • Used in tribal districts, islands, border areas

11d. Special Campaigns

  • Pulse Polio Immunization / National Immunization Days (NIDs): Annual OPV campaigns for all children under 5 years, irrespective of prior vaccination status. Conducted every December-January. Led to India being declared polio-free on March 27, 2014
  • Mission Indradhanush (MI): Launched December 2014 to immunize all unvaccinated/partially vaccinated children up to 2 years and pregnant women. Named for 7 colours of the rainbow = 7 vaccines
  • Intensified Mission Indradhanush (IMI): From 2017; 4 rounds per year in 190 high-priority low-coverage districts

12. HEALTH EDUCATION - NURSING ROLE

The community health nurse is the primary health educator for immunization. Key health education messages to be given to mothers:

What to Tell Mothers/Caregivers

  1. Why vaccinate? Vaccines prevent serious diseases that can kill or permanently disable your child
  2. When to vaccinate? Bring the child as per the schedule on the immunization card; do not miss any dose
  3. If a dose is missed: Come as soon as possible - you do NOT have to restart from the beginning
  4. What to expect after vaccination:
    • Mild fever, pain, swelling at injection site = normal, last 1-3 days
    • Give paracetamol if fever is high
    • BCG scar formation in 6-12 weeks is normal and expected
  5. When to come back urgently: High fever, convulsions, child becomes very unwell, excessive crying, difficulty breathing
  6. Dispelling myths:
    • Vaccines do NOT cause autism (scientifically disproven)
    • Mild illness or fever is NOT a reason to delay vaccination
    • Breastfeeding does NOT reduce vaccine effectiveness
    • Multiple vaccines on the same day are safe
  7. Keep the immunization card safe - bring it every time

13. HERD IMMUNITY

Herd (community) immunity occurs when a sufficiently high proportion of a population is immune, so that even unvaccinated individuals are protected because transmission is interrupted.
DiseaseHerd Immunity Threshold
Measles92-95%
Pertussis92-94%
Diphtheria83-85%
Polio80-85%
Rubella83-85%
This is why reaching the last unvaccinated child matters - even a small pocket of unvaccinated individuals can sustain a disease outbreak.

14. PROGRAMME ACHIEVEMENTS AND CHALLENGES

Achievements

  • Full immunization coverage: 62% (2015) → 98.4% (January 2026) (PIB, MoHFW 2026)
  • India declared polio-free on March 27, 2014 (WHO certified)
  • Zero-dose children declined from 0.11% (2023) to 0.06% (2024)
  • Dramatic decline in VPDs:
DiseaseCases in 1987Cases in 2018
Poliomyelitis28,2570
Neonatal tetanus11,849181
Pertussis1,63,78618,006
Measles2,47,51920,815
Diphtheria12,95211,720
Source: Park's Textbook of Preventive and Social Medicine, Table 9

Challenges

  1. Zero-dose children - concentrated in urban slums, conflict zones, tribal areas
  2. Cold chain gaps in remote/hilly/island regions
  3. Vaccine hesitancy - driven by misinformation and social media
  4. Urban migration disrupts immunization schedules
  5. Gender inequality - girls vaccinated less in some regions
  6. Weak AEFI surveillance at peripheral levels
  7. High dropout rates - children who receive first dose but not complete the series

15. NURSING PROCESS IN IMMUNIZATION (Applying the Nursing Process)

StepApplication
AssessmentIdentify all eligible beneficiaries (children 0-2 years, pregnant women) in the sub-centre area; assess immunization status from cards/registers; identify defaulters and zero-dose children
DiagnosisRisk for vaccine-preventable disease related to incomplete immunization; Knowledge deficit about immunization among caregivers
PlanningPlan immunization sessions (fixed + outreach); coordinate with ASHA/AWW for mobilization; arrange vaccine logistics and cold chain
ImplementationConduct immunization sessions; administer vaccines correctly; maintain cold chain; record keeping; health education to mothers
EvaluationMonitor immunization coverage rates; track defaulters; follow up missed children; report AEFIs; submit monthly reports to PHC/MO

16. SUMMARY

The Universal Immunization Programme is India's flagship public health initiative that has transformed child survival in the country. As a community health nurse, you are the most visible face of this programme. Your skills in vaccine administration, cold chain maintenance, beneficiary mobilization, health education, AEFI surveillance, and record keeping directly determine whether India's children are protected from vaccine-preventable diseases.
The programme has achieved remarkable success - rising from barely 30% coverage in 1985 to near-universal coverage of 98.4% in 2026, and eliminating polio entirely. The remaining challenge - reaching the last 1-2% of zero-dose children - requires the same commitment, community trust, and technical competence that community health nurses bring to every immunization session.

REFERENCES

  1. Park, K. Park's Textbook of Preventive and Social Medicine, 27th ed. Jabalpur: Banarsidas Bhanot Publishers - Chapter on Immunization, Tables 43, 8, and 9
  2. Ministry of Health and Family Welfare, Government of India. National Immunization Schedule 2025. New Delhi: MoHFW
  3. Press Information Bureau, Government of India. UIP achievements 2025-26 - Full immunization coverage 98.4% as of Jan 2026
  4. National Health Mission. Immunization - NHM India
  5. Indian Academy of Pediatrics (IAP). IAP Immunization Schedule 2025 - ACVIP Recommendations
  6. World Health Organization. Immunization Agenda 2030 (IA2030). Geneva: WHO

Examiner's Note: For community health nursing examinations, pay special attention to: (1) the complete NIS table with routes and sites, (2) nursing responsibilities at each phase of the immunization session, (3) cold chain do's and don'ts, (4) false contraindications, and (5) AEFI classification and reporting. These are the most frequently tested areas.

Universal immunization schedule for Pediatrics Nursing

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Universal Immunization Programme India pediatric nursing NIS 2025 vaccine schedule children

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I now have all the detailed content needed - full NIS table, AEFI classification, vaccine-specific Q&As, cold chain, and nursing specifics from Park's Preventive Medicine. Let me now compose the pediatric nursing-focused assignment.

UNIVERSAL IMMUNIZATION PROGRAMME (UIP)

Assignment for Pediatric Nursing


1. INTRODUCTION

Immunization is the single most important preventive strategy available to the pediatric nurse. Vaccine-preventable diseases remain among the leading causes of under-5 mortality globally, and the pediatric nurse - whether working in the hospital, community clinic, or outreach setting - is at the frontline of delivering, monitoring, and educating families about immunization.
The Universal Immunization Programme (UIP) of India is one of the largest public health programmes in the world, targeting approximately 2.67 crore newborns and 2.9 crore pregnant women annually. Understanding the complete immunization schedule, the pathophysiology of each vaccine-preventable disease, the correct technique of vaccine administration, and the recognition and management of adverse events is a core clinical competency for every pediatric nurse.

2. DEFINITION OF KEY TERMS

TermDefinition
ImmunizationThe process of making a person immune to an infectious disease, typically through vaccine administration, which stimulates the body's own immune system
VaccinationThe act of administering a vaccine; often used interchangeably with immunization
VaccineA biological preparation that provides active acquired immunity to a particular disease
Active immunityImmunity produced by the body's own immune response following vaccination or natural infection; long-lasting
Passive immunityTemporary immunity transferred from another source (e.g., maternal antibodies via placenta/breast milk, or immune globulin injections)
Herd immunityIndirect protection of unvaccinated individuals when sufficient population proportion is immune, interrupting disease transmission
VPDVaccine-preventable disease
AEFIAdverse Event Following Immunization
Cold chainSystem of storing and transporting vaccines at the correct temperature from manufacturer to beneficiary

3. TYPES OF VACCINES

3a. By Composition

TypeDescriptionExamples
Live attenuatedLive but weakened organisms; potent, long immunity, single/few dosesBCG, OPV, MR, Varicella
Killed/InactivatedDead organisms; safer in immunocompromised, needs multiple dosesIPV, Hepatitis A
ToxoidInactivated bacterial toxinDiphtheria toxoid, Tetanus toxoid (in DPT, Td)
Subunit/ConjugateSpecific antigenic components only; highly purifiedHepatitis B, Hib, PCV, HPV
RecombinantAntigen produced by recombinant DNA technologyHepatitis B vaccine

3b. By Route of Administration

RouteVaccinesTechnique
OralOPV, RVV2 drops / 3-5 drops directly into mouth
Intradermal (ID)BCG, fIPV0.1 mL using 26G needle at 10-15° angle; pale bleb confirms correct placement
Intramuscular (IM)Pentavalent, DPT, Hep B, PCV, Td0.5 mL; anterolateral mid-thigh in infants (<12 months); deltoid in older children
Subcutaneous (SC)MR, JE0.5 mL; pinch skin; 45° angle; right upper arm

4. NATIONAL IMMUNIZATION SCHEDULE (NIS) 2025 - INDIA

4a. Complete NIS - Age-wise Schedule

FOR PREGNANT WOMEN

VaccineWhen to GiveDoseRouteSitePurpose
Td-1Early pregnancy (as early as possible)0.5 mLIMUpper armPrevent maternal & neonatal tetanus
Td-24 weeks after Td-10.5 mLIMUpper armComplete primary protection
Td-BoosterIf received 2 Td doses within last 3 years0.5 mLIMUpper armBoost existing immunity

FOR INFANTS - BIRTH

VaccineDoseRouteSiteKey Nursing Point
BCG0.1 mL (0.05 mL if <1 month)IntradermalLeft upper armMust form a pale raised bleb (5-7 mm); confirms correct ID placement
Hepatitis B (Birth dose)0.5 mLIMAntero-lateral mid-thighMUST be given within 24 hours of birth to prevent perinatal transmission
OPV-02 dropsOralMouthGive as early as possible within first 15 days of birth

6 WEEKS

VaccineDoseRouteSite
OPV-12 dropsOralMouth
Pentavalent-1 (DPT + HepB + Hib)0.5 mLIMAntero-lateral mid-thigh
RVV-1 (Rotavirus)3 dropsOralMouth
fIPV-1 (Fractional IPV)0.1 mLIntradermalRight upper arm
PCV-1 (Pneumococcal Conjugate)0.5 mLIMAntero-lateral mid-thigh

10 WEEKS

VaccineDoseRouteSite
OPV-22 dropsOralMouth
Pentavalent-20.5 mLIMAntero-lateral mid-thigh
RVV-23 dropsOralMouth

14 WEEKS

VaccineDoseRouteSite
OPV-32 dropsOralMouth
Pentavalent-30.5 mLIMAntero-lateral mid-thigh
RVV-33 dropsOralMouth
fIPV-20.1 mLIntradermalRight upper arm
PCV-20.5 mLIMAntero-lateral mid-thigh

9-12 MONTHS

VaccineDoseRouteSiteNotes
MR-1 (Measles-Rubella)0.5 mLSubcutaneousRight upper armCan give up to 5 years if missed at 9-12 months
JE-1*0.5 mLSubcutaneousLeft upper armEndemic districts only
PCV-Booster0.5 mLIMAntero-lateral mid-thigh
Vitamin A - 1st dose1 mL (1 lakh IU)OralMouthGiven with MR-1

16-24 MONTHS

VaccineDoseRouteSite
MR-20.5 mLSubcutaneousRight upper arm
JE-2*0.5 mLSubcutaneousLeft upper arm
DPT Booster-10.5 mLIMAntero-lateral mid-thigh
OPV Booster2 dropsOralMouth
Vitamin A - 2nd dose2 mL (2 lakh IU)OralMouth

5-6 YEARS

VaccineDoseRouteSite
DPT Booster-20.5 mLIMLeft upper arm
Vitamin A (up to 9th dose, every 6 months until 5 years)2 mL (2 lakh IU)OralMouth

10 YEARS AND 16 YEARS

VaccineDoseRouteSite
Td0.5 mLIMUpper arm
*JE vaccine: Administered only in Japanese Encephalitis endemic districts
Source: National Immunization Schedule (NIS) India 2025; Park's Textbook of Preventive and Social Medicine, Table 43

5. DISEASES COVERED AND VACCINE-SPECIFIC NURSING NOTES

5a. BCG Vaccine - Tuberculosis Prevention

Disease prevented: Tuberculosis, especially life-threatening forms in children - TB meningitis, miliary TB, and disseminated TB
Vaccine details:
  • Type: Live attenuated (Mycobacterium bovis - Calmette-Guerin strain)
  • Age: At birth; can be given up to 1 year of age. NEVER give BCG above 1 year of age
  • Dose: 0.1 mL (0.05 mL in neonates under 1 month)
  • Route/site: Intradermal, left upper arm
Nursing technique (BCG):
  • Use a 26G, 3/8 inch needle; 1 mL syringe
  • Stretch the skin taut over the outer aspect of the left upper arm
  • Insert needle at 10-15° angle (almost horizontal, bevel upward)
  • Inject to raise a pale, discrete bleb of 5-7 mm = confirms correct intradermal placement
  • If no bleb or bleb disappears immediately = subcutaneous injection (incorrect) → repeat at different site
Expected response:
  • 2-3 weeks: small red papule at injection site
  • 4-6 weeks: papule ulcerates
  • 6-12 weeks: heals with a characteristic round scar (4-8 mm) = "BCG scar" = sign of successful vaccination
  • Absence of scar does NOT always mean vaccine failed - check tuberculin test (Mantoux) if in doubt
Contraindications: Immunodeficiency states, symptomatic HIV infection, generalized skin disease, premature <1 kg (delay until weight >2 kg)
Complications:
  • Local - abscess, keloid scar, regional lymphadenitis (BCG-itis)
  • Serious/rare - disseminated BCG disease (only in severe immunodeficiency)

5b. OPV - Oral Polio Vaccine

Disease prevented: Poliomyelitis - acute flaccid paralysis due to poliovirus types 1, 2, 3
Type: Live attenuated (Sabin vaccine; now bivalent - types 1 and 3 after type 2 eradication)
Key advantage: Produces gut immunity (secretory IgA) → prevents viral shedding → interrupts community transmission. This is why OPV is superior to IPV for eradication strategy.
Schedule: OPV-0 (birth), OPV 1,2,3 (6,10,14 weeks), Booster (16-24 months)
  • OPV can be given up to 5 years of age
Nursing notes:
  • 2 drops directly into the mouth; hold child horizontally, tilt head slightly back
  • If child vomits within 10 minutes - repeat the dose
  • Do NOT give OPV to immunocompromised children (use IPV instead) - risk of VAPP
  • Can be given concurrently with pentavalent vaccine (different sites)
VAPP: Vaccine-Associated Paralytic Polio - extremely rare (1 in 2.7 million doses); primarily in immunocompromised children

5c. fIPV - Fractional Inactivated Polio Vaccine

Type: Killed (Salk) vaccine, given as 1/5th dose (0.1 mL) intradermally
Advantages over full-dose IPV:
  • Lower cost (less antigen per dose)
  • Produces strong serum immunity (IgG)
  • Safe for immunocompromised children
  • Combined with OPV (complementary immunity - gut + systemic)
Given at: 6 weeks and 14 weeks - intradermal, right upper arm
Nursing note: Do not confuse the ID site of fIPV (right upper arm) with BCG (left upper arm)

5d. Pentavalent Vaccine (DPT + Hepatitis B + Hib)

Contains 5 antigens in one injection:
  1. Diphtheria toxoid - prevents diphtheria (pseudomembranous pharyngitis, "bull neck," airway obstruction)
  2. Pertussis (whole cell) - prevents whooping cough (paroxysmal cough + inspiratory "whoop" + post-tussive vomiting)
  3. Tetanus toxoid - prevents tetanus (lockjaw, risus sardonicus, opisthotonus)
  4. Hepatitis B antigen - prevents HBV infection (cirrhosis, hepatocellular carcinoma)
  5. Hib conjugate - prevents Haemophilus influenzae type B meningitis and pneumonia
Schedule: 6, 10, 14 weeks (primary series); can give up to 1 year of age
Nursing points:
  • Site: Antero-lateral mid-thigh (left); NEVER the gluteal region
    • Why not gluteal? Risk of sciatic nerve injury; fat tissue in gluteal area reduces immune response
  • Minimum interval: 4 weeks between doses (shorter intervals reduce antibody response)
  • Catch-up: DPT can be given up to 7 years of age; do NOT restart - pick up where left off
  • If child develops encephalopathy or severe allergy after DPT → switch to DTaP (acellular pertussis) for remaining doses (whole-cell pertussis component is usually responsible)
  • Shake vial before drawing up (T-series vaccines)
  • Do NOT freeze pentavalent vaccine - freeze damage reduces potency (perform "shake test" to detect freeze damage)

5e. PCV - Pneumococcal Conjugate Vaccine

Disease prevented: Streptococcus pneumoniae - leading cause of bacterial meningitis and lobar pneumonia in children under 5
Schedule: PCV-1 at 6 weeks, PCV-2 at 14 weeks, PCV-Booster at 9-12 months (2+1 schedule) Site: Antero-lateral mid-thigh (right side, separate from pentavalent given on left)

5f. RVV - Rotavirus Vaccine (ROTAVAC)

Disease prevented: Rotavirus diarrhoea - the commonest cause of severe dehydrating diarrhoea requiring hospitalization in children under 5 in India
Vaccine: ROTAVAC - India's first indigenous vaccine, neonatal strain 116E (Bharat Biotech)
Schedule: 3 oral doses at 6, 10, 14 weeks Critical age limits:
  • First dose: must be given before 15 weeks
  • Last dose: must be given before 8 months (risk of intussusception if given later)
Nursing notes:
  • 3 drops oral; hold upright position during and after administration
  • May cause mild loose stools/vomiting for 1-2 days - reassure parents
  • Store in refrigerator at +2 to +8°C; do NOT freeze

5g. MR Vaccine - Measles-Rubella

Diseases prevented:
  • Measles (Rubeola): High fever, cough, coryza, conjunctivitis, Koplik's spots, morbilliform rash; complications - pneumonia, encephalitis, SSPE
  • Rubella (German Measles): Mild febrile illness in children; devastating in pregnancy - Congenital Rubella Syndrome (CRS) causing heart defects, cataracts, deafness in newborns
Type: Live attenuated, combined Schedule: MR-1 at 9-12 months; MR-2 at 16-24 months
  • If missed: can give MR up to 5 years of age
  • If measles vaccine received before 9 months (e.g., during outbreak) → still give MR at 9 months and 16-24 months
Site: Subcutaneous, right upper arm (standardized for surveyors to verify receipt)
Nursing notes:
  • Reconstitute with supplied diluent only; use within 4 hours of reconstitution or end of session (whichever is earlier)
  • Given with Vitamin A 1st dose at 9 months
  • Expected reaction: mild rash and fever at 7-12 days post-vaccination (not immediately) - reassure parents

5h. Hepatitis B - Birth Dose

Critical rule: Give within 24 hours of birth
  • Hepatitis B vaccine given within 24 hours prevents 90% of perinatal (vertical) transmission
  • Efficacy drops significantly if given after 24 hours
  • Part of pentavalent at 6, 10, 14 weeks (combined with DPT + Hib)
  • Hepatitis B vaccine can be given up to 1 year of age

5i. Vitamin A Supplementation

Though not a vaccine, Vitamin A is co-administered with immunization under UIP:
DoseAgeAmountWhen
1st9 months1 lakh IU (1 mL)With MR-1
2nd16 months2 lakh IU (2 mL)With DPT Booster-1
3rd to 9thEvery 6 months up to 5 years2 lakh IU (2 mL)Routine
Vitamin A deficiency increases severity of measles, diarrhoea, and respiratory infections and is a leading preventable cause of childhood blindness.

6. IAP (Indian Academy of Pediatrics) RECOMMENDED SCHEDULE 2025

Additional vaccines recommended by IAP beyond UIP (mostly in private sector):
AgeVaccineDisease Prevented
BirthBCG, OPV-0, Hep B-1TB, Polio, Hep B
6 weeksDTwP or DTaP, IPV, Hib, Hep B-2, RVV-1, PCV-1Multiple
10 weeksDTwP/DTaP, IPV, Hib, RVV-2, PCV-2Multiple
14 weeksDTwP/DTaP, IPV, Hib, RVV-3, PCV-3Multiple
6 monthsHep B-3, Influenza-1Hep B, Flu
9-12 monthsMMR-1, Typhoid Conjugate (TCV)Measles, Mumps, Rubella, Typhoid
12 monthsHepatitis A-1, Influenza (annual)Hep A, Flu
15 monthsMMR-2, Varicella-1, PCV-BoosterMeasles, Mumps, Rubella, Chickenpox
18 monthsDTwP/DTaP Booster, Hib BoosterMultiple
2 yearsHepatitis A-2Hep A
4-6 yearsDTwP/DTaP Booster-2, OPV Booster, Varicella-2Multiple
9-14 years (girls)HPV (2 doses, 6 months apart)Cervical cancer
Annual (all ages)InfluenzaSeasonal flu
Key differences from UIP:
  • IAP includes MMR (Mumps component) vs. UIP's MR (no mumps)
  • IAP includes Varicella, Typhoid conjugate, Hepatitis A, Influenza, HPV
  • IAP uses IPV full dose; UIP uses fractional fIPV
  • IAP uses DTaP (acellular pertussis); UIP uses whole-cell pertussis

7. COLD CHAIN MANAGEMENT

7a. Why Cold Chain Matters in Pediatric Nursing

Vaccines are biological products. Exposure to temperatures outside the correct range - either too warm or (for some vaccines) too cold - permanently destroys vaccine potency. A visually normal vial can contain destroyed vaccine. A child who receives a cold-chain-broken vaccine gets no protection, yet neither the nurse nor the parent is aware.

7b. Temperature Requirements

Vaccine CategoryRequired TemperatureCritical Rule
Freeze-sensitive (DPT, TT, Td, Hep B, Pentavalent, PCV, fIPV)+2°C to +8°CNEVER freeze - freezing causes flocculation and loss of potency
Freeze-tolerant/OPVCan be frozen at -15°C to -25°C at higher levelsHeat-sensitive; loses potency rapidly if warm
BCG and MR+2°C to +8°CBoth heat-sensitive AND light-sensitive

7c. Vaccine Vial Monitor (VVM)

A heat-sensitive sticker affixed to each vaccine vial:
  • Inner square starts lighter than the outer circle
  • Progressive heat exposure darkens the inner square
  • Rule: If inner square = same shade as outer circle or darker → DISCARD, do NOT use
  • VVM detects cumulative heat exposure; vial may be within expiry date but still unusable if VVM is triggered

7d. Cold Chain Equipment at Each Level

LevelEquipment
National/State storesCold rooms (+2 to +8°C), Freezer rooms (-15 to -25°C)
DistrictIce-Lined Refrigerators (ILR), Deep freezers
PHC/Sub-centreILR, Front-load domestic refrigerator
Field (outreach)Vaccine carrier + 4 conditioned ice packs

7e. Critical Cold Chain DO's and DON'Ts

(Source: Park's Textbook of Preventive and Social Medicine)
DO'sDON'Ts
Check VVM and expiry date before each vaccinationLeave vaccine carrier in sunlight
Keep vaccines in a plastic/zipper bag in the CENTRE of the carrier - between the ice packsLeave the lid of the vaccine carrier open
Keep diluents chilled (+2 to +8°C) before reconstitutionPlace DPT, TT, Hep B, or Pentavalent directly on the ice pack (they will freeze)
Keep reconstituted BCG and MR only ON TOP of one ice packCarry vaccines in a handbag
Return unused vaccines to cold chain promptly after sessionDrop or sit on the vaccine carrier
Discard reconstituted BCG/MR within 4 hoursUse a vaccine with expired VVM, even if within expiry date

7f. Open Vial Policy

Multi-dose vials of the following can be used in subsequent sessions if properly stored: OPV, liquid Pentavalent, liquid DPT, TT/Td, Hepatitis B, MR
Reconstituted vials of BCG and MR must be discarded within 4 hours or at end of session.

8. NURSING PROCEDURE - VACCINE ADMINISTRATION (Step-by-Step)

Pre-Administration Assessment

  1. Verify child's age and immunization card
  2. Identify which vaccines are due at this visit
  3. Screen for contraindications (not false contraindications)
  4. Check VVM and expiry date on each vial
  5. Explain the procedure and expected reactions to the parent/caregiver
  6. Obtain informed consent (verbal)

Preparation

  1. Wash hands thoroughly
  2. Gather correct vaccines, syringes, diluents
  3. Reconstitute lyophilized vaccines (BCG, MR) with supplied diluent only - NOT normal saline from another source
  4. Draw up the correct dose in a new AD (Auto-Disable) syringe for each injection
  5. Never mix two vaccines in one syringe unless they are a fixed combination (e.g., pentavalent)

Administration Technique

Intradermal (BCG, fIPV):
  • 26G needle, 1 mL syringe, bevel up
  • Insert almost parallel to skin (10-15°)
  • Inject 0.1 mL - a pale bleb must form
  • Do NOT massage after injection
  • Never clean site with spirit before injection (kills live vaccine components)
Intramuscular (Pentavalent, DPT, Hep B, PCV, Td):
  • 23-25G needle; 1 mL syringe
  • Site: anterolateral mid-thigh in infants <1 year; deltoid in older children
  • 90° insertion; aspirate not required for pediatric IM (CDC/WHO)
  • Apply gentle pressure after injection; do NOT massage
Subcutaneous (MR, JE):
  • 23-25G needle
  • Pinch skin; insert at 45°
  • Site: right upper arm
Oral (OPV, RVV):
  • 2 or 3 drops directly into mouth
  • Ensure child does not spit out or vomit within 10 minutes

Post-Administration Care

  1. Observe child for 30 minutes at the immunization site
  2. Counsel parents: expected reactions, warning signs, when to return urgently
  3. Record in immunization card and register
  4. Dispose of all used syringes in puncture-proof sharps container (do NOT recap needles)
  5. Wash hands

9. CONTRAINDICATIONS TO VACCINATION

True Contraindications

ContraindicationVaccines Affected
Anaphylaxis to previous dose or vaccine componentAll
Severe immunodeficiency (congenital, HIV-AIDS, on immunosuppressants)All live vaccines (BCG, OPV, MR) - use killed alternatives
Encephalopathy within 7 days of previous DPTDPT whole-cell pertussis component - switch to DTaP

False Contraindications (Must be Corrected by the Pediatric Nurse)

The pediatric nurse must actively educate families and junior staff that the following are NOT contraindications:
ConditionCorrect Action
Mild cold, URTI, runny noseVaccinate
Low-grade fever (<38.5°C)Vaccinate
DiarrhoeaVaccinate (give OPV, but note dose may not count; give IPV if available)
MalnutritionVaccinate - these children have the highest VPD risk
PrematurityVaccinate at chronological age (not corrected age); full dose
BreastfeedingAll vaccines can and should be given
Antibiotic therapyVaccinate
Minor local reaction to prior doseVaccinate (use antipyretic pre/post)
Stable neurological conditionVaccinate
Park's Textbook states: "Low grade fever, mild respiratory infections or diarrhoea and other minor illnesses should not be considered as contraindications to immunization. These are the very children who are most in need of immunization."

10. ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI)

Definition

An AEFI is any untoward medical occurrence that follows immunization and does not necessarily have a causal relationship with the vaccine. (Source: WHO/CIOMS 2012; Park's Textbook)

CIOMS/WHO Classification of AEFIs (2012)

TypeDefinitionExample
Vaccine product-related reactionCaused by inherent properties of the vaccineBCG-itis, febrile convulsion post-DPT
Vaccine quality defect-related reactionDue to manufacturing defect in vaccineContaminated vial
Immunization error-related reactionDue to incorrect handling, preparation, or administrationAbscess from subcutaneous DPT, wrong dose
Immunization anxiety-related reactionStress response, NOT the vaccineVasovagal syncope after injection, hyperventilation
Coincidental eventTemporal association only - unrelated to vaccineFever from concurrent URTI

Common AEFIs and Pediatric Nursing Management

VaccineCommon/Expected ReactionSerious/Rare ReactionNursing Management
BCGLocal papule → ulcer → scar at 6-12 weeksBCG-itis, regional lymphadenitis, disseminated BCG (immunocompromised)Reassure parents about scar; report BCG-itis to MO; DO NOT give BCG to immunocompromised
DPT / PentavalentLocal pain, redness, swelling; fever 1-3 daysFebrile seizure; HHE (Hypotonic-Hyporesponsive Episode); persistent inconsolable crying >3 hoursParacetamol for fever; cold compress; lay child flat for HHE; report HHE to MO; switch to DTaP for subsequent doses
OPVNone typicallyVAPP (Vaccine-Associated Paralytic Polio) - 1 per 2.7 million doses; mainly in immunocompromisedBaseline neurological assessment; report any acute flaccid paralysis
MR / MeaslesMild rash, fever at 7-12 daysFebrile seizure; rare thrombocytopeniaReassure parents it is delayed (not immediate); antipyretics as needed
Rotavirus (RVV)Mild loose stools, vomiting 1-2 daysRare intussusception (watch for colicky abdominal pain, bloody stool)Reassure; maintain hydration; report intussusception immediately
PCVLocal redness, feverRare anaphylaxisMonitor 30 minutes; adrenaline available
Hepatitis BMild local sorenessAnaphylaxis (very rare)30-minute observation
fIPVSmall local reaction at ID siteRareReassure

Recognition of Anaphylaxis Post-Vaccination (MEDICAL EMERGENCY)

Signs: Urticaria, angioedema, bronchospasm, stridor, hypotension, collapse - onset within 15-30 minutes of vaccination
Nursing Action:
  1. Call for medical help IMMEDIATELY
  2. Lay child flat; elevate legs
  3. Administer adrenaline (epinephrine) 0.01 mg/kg IM (anterolateral thigh) - ANMs now authorized to give adrenaline IM under NHM protocol (2017)
  4. ABC (Airway, Breathing, Circulation)
  5. Transfer to emergency facility
  6. Report as AEFI

AEFI Reporting

  • All serious AEFIs must be reported within 24 hours to Medical Officer and District Immunization Officer (DIO)
  • Use MoHFW AEFI reporting form
  • National AEFI surveillance system: MoHFW → NHM → WHO

11. SPECIAL SITUATIONS IN PEDIATRIC IMMUNIZATION

11a. Preterm / Low Birth Weight Infants

  • Give all vaccines at chronological age (from date of birth), NOT corrected gestational age
  • BCG: Delay if weight <2 kg until baby gains adequate weight (>2 kg)
  • Hepatitis B birth dose: Give within 24 hours regardless of prematurity

11b. HIV-Positive Children

  • Asymptomatic HIV: Can receive BCG, OPV, MR
  • Symptomatic HIV / severe immunodeficiency: Do NOT give any live vaccines (BCG, OPV, MR)
    • Use IPV instead of OPV
    • Refer for DTaP, pneumococcal vaccine

11c. Child with Fever at Immunization Visit

  • Low-grade fever (<38.5°C): Vaccinate - do NOT postpone
  • High fever (>38.5°C): Postpone until fever resolves; schedule return visit

11d. Missed / Delayed Doses

  • NEVER restart the schedule - continue from where it was left off
  • Example: Child received BCG, Hep B-1, DPT-1, OPV-1 at 5 months, comes at 11 months → give DPT-2, Hep B-2, OPV-2, and MR-1
  • "Do not penalize the child or restart for late presentation"

11e. Catch-up Age Limits

VaccineMaximum Age for Administration
BCG1 year
OPV5 years
DPT7 years
Pentavalent1 year
Hepatitis B1 year (as part of pentavalent)
MR5 years
JE15 years
Td16 years (part of schedule)

12. NURSING PROCESS IN PEDIATRIC IMMUNIZATION

PhaseNursing Activity
AssessmentReview immunization card; identify vaccines due; assess for contraindications; check cold chain; assess parent's knowledge and anxiety level
Nursing Diagnosis- Risk for VPD related to incomplete immunization schedule; Knowledge deficit in parents regarding vaccine schedule and importance; Risk for AEFI related to vaccine administration
PlanningPrepare correct vaccines, diluents, syringes; plan order of vaccine administration (oral vaccines before injections); plan parent counseling; plan 30-minute post-vaccination observation
ImplementationAdminister vaccines using correct technique, route, site, and dose; counsel parents on expected reactions; record in immunization card and register
EvaluationVerify all due vaccines were administered; child observed for 30 minutes without adverse events; parent counseled and questions answered; records updated; follow-up date given

13. HEALTH EDUCATION FOR PARENTS - PEDIATRIC NURSE'S ROLE

Key Messages

  1. Why vaccinate? Vaccines protect your child from serious diseases that can kill, paralyze, or permanently disable
  2. Stick to the schedule - vaccines work best when given at the right age; immunity may be incomplete if delayed
  3. Bring the immunization card every visit - it is the baby's health passport
  4. What to expect after vaccination:
    • Mild fever, fussiness, pain/swelling at injection site - normal, resolves in 1-3 days
    • Give paracetamol syrup (15 mg/kg) for fever and discomfort
    • BCG scar develops over 6-12 weeks - this is expected and normal
    • MR rash/fever may appear 7-12 days later - reassure this is the vaccine working
  5. Return urgently if:
    • High-grade fever (>39°C)
    • Convulsions/fits
    • Collapse or unresponsiveness
    • Difficulty breathing
    • Persistent inconsolable crying >3 hours
  6. Dispelling myths:
    • Vaccines do NOT cause autism
    • Multiple vaccines in one visit are safe - the immune system can handle them
    • A sick child with mild illness should STILL be vaccinated
    • Breastfeeding should continue before and after vaccination (reduces crying)

Non-Pharmacological Comfort Measures During Vaccination

  • Breastfeed during injection (reduces pain and crying duration)
  • Skin-to-skin contact (kangaroo care) for neonates
  • Oral sucrose (2 mL of 24% sucrose 2 minutes before injection) for neonates and infants
  • Distraction techniques for toddlers
  • Give oral vaccines (OPV, RVV) before injections
  • Use the smallest gauge needle appropriate for the site

14. PROGRAMME OVERVIEW AND ACHIEVEMENTS

IndicatorValue
Annual target (newborns)2.67 crore
Annual target (pregnant women)2.9 crore
Full immunization coverage (2015)62%
Full immunization coverage (Jan 2026)98.4%
Zero-dose children (2024)0.06% of total population
Polio statusPolio-free since March 27, 2014 (WHO certified)
Decline in VPDs since UIP launch:
DiseaseCases in 1987Cases in 2018Change
Poliomyelitis28,2570Eradicated
Neonatal Tetanus11,849181-98.5%
Pertussis1,63,78618,006-89%
Measles2,47,51920,815-92%
Source: Park's Textbook of Preventive and Social Medicine, Table 9

15. SUMMARY

The Universal Immunization Programme is India's most successful public health initiative, and the pediatric nurse is its most important implementer at the bedside and in the community. Your role extends far beyond giving an injection - it encompasses thorough pre-vaccination assessment, selection of the right vaccine for the right child at the right age, technically correct administration, vigilant post-vaccination observation, recognition and management of AEFIs, accurate record-keeping, and empathetic parent education.
The NIS covers 12 diseases across 16+ different doses from birth to 16 years. Mastery of this schedule - with the correct vaccine, dose, route, site, and age - combined with confident cold chain knowledge and AEFI management skills, defines competent pediatric nursing practice in immunization.

REFERENCES

  1. Park, K. Park's Textbook of Preventive and Social Medicine, 27th ed. Jabalpur: Banarsidas Bhanot Publishers - Tables 8, 9, 35, 43; pp. 3497-3620
  2. Ministry of Health and Family Welfare, Government of India. National Immunization Schedule (NIS) 2025. New Delhi: MoHFW
  3. National Health Mission, Himachal Pradesh. NIS Schedule - UIP. NHM India
  4. Press Information Bureau, Government of India. India's UIP: 98.4% full immunization coverage, January 2026
  5. UNICEF India. Know Your Child's Immunization Schedule
  6. Indian Academy of Pediatrics (IAP). IAP ACVIP Immunization Schedule 2025
  7. WHO/CIOMS 2012. Causality Assessment of an Adverse Event Following Immunization (AEFI). Geneva: WHO

Exam Tips for Pediatric Nursing Students:
  • Memorize the complete NIS table (vaccine, age, dose, route, exact site)
  • Know the 5 CIOMS/WHO AEFI categories with examples
  • Know true vs. false contraindications (commonly tested)
  • Know the "why" behind each rule: Why antero-lateral thigh? Why NOT spirit before injection? Why BCG before 1 year only? Why Hep B within 24 hours?
  • Know catch-up age limits for each vaccine
  • Know VVM reading and cold chain do's/don'ts - these are high-yield for practical and theory exams
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