What is the recommended Haemophilus influenzae type b (Hib) vaccination schedule?

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Haemophilus influenzae type b (Hib) Vaccination Schedule

The Advisory Committee on Immunization Practices (ACIP) recommends routine administration of Hib conjugate vaccine beginning at age 2 months, with either a 2-dose primary series (PRP-OMP vaccines) or 3-dose primary series (PRP-T vaccines), followed by a booster dose at 12-15 months of age. 1

Routine Vaccination Schedule

Primary Series Options:

  • PRP-OMP vaccines (PedvaxHIB or Comvax):

    • 2 doses at 2 and 4 months
    • Preferred for American Indian/Alaska Native infants due to substantial protection after first dose 2
  • PRP-T vaccines (ActHib, Pentacel, MenHibRix):

    • 3 doses at 2,4, and 6 months

Booster Dose:

  • All children should receive a booster dose at 12-15 months
  • Any licensed Hib conjugate vaccine can be used for the booster, regardless of what was used for the primary series
  • Booster should be given at least 8 weeks after the most recent Hib vaccination 1, 3

Important Administration Guidelines

  • Doses in the primary series should ideally be administered 8 weeks apart
  • If necessary, a minimum interval of 4 weeks between doses is acceptable
  • First dose can be administered as early as 6 weeks of age 1, 3
  • If PRP-OMP vaccine is not used for both primary doses or there's uncertainty about previous products used, a third primary dose is needed 1
  • Hiberix should only be used for the booster dose in children 12 months through 4 years who have received at least 1 previous Hib dose 1

Catch-up Vaccination Schedule

For children with delayed vaccination:

  • First dose at <7 months:

    • 2 doses of PRP-OMP or 3 doses of PRP-T with minimum 4-week intervals
    • Booster at 12-15 months (only if primary doses given before 12 months)
  • First dose at 7-11 months:

    • Second dose at least 4 weeks later
    • Final dose at 12-15 months or 8 weeks after second dose (whichever is later)
  • First dose at 12-14 months:

    • Second dose 8 weeks after first dose
    • No third dose needed
  • First dose at 15-59 months:

    • Single dose only, no additional doses needed 1, 3

Special Populations

For children at increased risk for invasive Hib disease (asplenia, HIV, immunodeficiency, etc.):

  • <12 months: Follow routine recommendations

  • 12-59 months:

    • If unimmunized or received 0-1 dose before 12 months: 2 doses, 8 weeks apart
    • If received ≥2 doses before 12 months: 1 dose 8 weeks after last dose
    • If completed primary series and received booster ≥12 months: no additional doses
  • Chemotherapy/radiation therapy patients <60 months:

    • If routine doses given ≥14 days before therapy: no revaccination needed
    • If dose given <14 days before or during therapy: repeat doses ≥3 months after therapy completion
  • Hematopoietic stem cell transplant recipients (all ages):

    • 3 doses (≥4 weeks apart) beginning 6-12 months after transplant 1

Common Pitfalls and Caveats

  1. Vaccine type confusion: Don't confuse PRP-OMP with PRP-T vaccines, as they have different primary series requirements (2 vs. 3 doses) 3

  2. Combination vaccines: Be aware that Hib is available in several combination vaccines:

    • Comvax (Hib-HepB)
    • Pentacel (DTaP-IPV-Hib)
    • MenHibRix (Hib-MenCY)
    • Vaxelis (DTaP-IPV-Hib-HepB) - preferred for AI/AN infants due to PRP-OMP component 2
  3. Vaccine shortages: During shortages, prioritize the primary series for all children and defer booster doses for children not at high risk for disease 4

  4. Special populations: Pay special attention to high-risk groups who may need additional doses or modified schedules 1

  5. Documentation: Clearly document which Hib vaccine product is used to ensure proper completion of the primary series 1, 3

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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