What is the recommended hepatitis A and B vaccination schedule?

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Hepatitis B Vaccination Schedule

For most populations, administer hepatitis B vaccine at 0,1, and 6 months, which achieves >90% seroprotection after the third dose. 1, 2

Infants and Children

Newborns

  • All infants should receive the first dose within 12 hours of birth, before hospital discharge 2
  • For infants born to HBsAg-negative mothers: administer doses at birth, 1-2 months, and 6 months 2
  • For infants born to HBsAg-positive mothers: give the first dose within 12 hours of birth PLUS hepatitis B immune globulin (HBIG), then at 1-2 months and 6 months 2, 3
  • Delaying the birth dose beyond 12 hours in HBsAg-positive mothers significantly increases infection risk 2, 3
  • The final dose must not be given before 24 weeks of age, regardless of when earlier doses were administered 3, 4

Children and Adolescents (Previously Unvaccinated)

  • Standard schedule: 3 doses at 0,1, and 6 months 2, 4
  • Alternative 2-dose schedule for adolescents aged 11-15 years: adult formulation of Recombivax HB (10 μg) at 0 and 4-6 months 1, 2, 4

Adults

Standard Adult Schedule

  • Three doses at 0,1, and 6 months for adults ≥18 years 2, 3, 4
  • After dose 1: 30-55% achieve protective antibody levels 1, 3
  • After dose 2: 75% achieve protection 1, 3
  • After dose 3: >90% achieve protection 1, 3

Alternative Adult Schedules

  • Accelerated schedule: 0,1,2, and 12 months (Engerix-B) for rapid protection 3, 4
  • Alternative schedules at 0,2, and 4 months produce similar seroprotection rates 3
  • Longer intervals between the last two doses (≥4 months) result in higher final antibody titers 3, 5

Heplisav-B (2-Dose Schedule)

  • Adults ≥18 years: two doses (20 μg each) separated by 1 month 1
  • Achieves approximately 90% seroprotection compared to 70.5-90.2% with Engerix-B 1, 3
  • Do not use in infants, children, adolescents, pregnant women, or hemodialysis patients 1, 3

Special Populations

Hemodialysis and Immunocompromised Patients

  • Administer higher doses: 40 μg of Recombivax HB or 40 μg of Engerix-B (two 1.0-mL doses at one site) 1, 3, 4
  • Schedule: 0,1, and 6 months (Recombivax HB) or 0,1,2, and 6 months (Engerix-B) 1, 4
  • Perform annual anti-HBs testing with booster doses when levels fall below 10 mIU/mL 2, 3, 4
  • Post-vaccination testing recommended 1-2 months after completing the series 2, 4

Pregnant Women

  • Use only Engerix-B, Recombivax HB, or Twinrix 3
  • Do not use Heplisav-B or PreHevbrio due to insufficient safety data in pregnancy 3

Minimum Dosing Intervals

Critical timing requirements to ensure adequate immune response:

  • Minimum interval between doses 1 and 2: 4 weeks 2, 3, 4
  • Minimum interval between doses 2 and 3: 8 weeks 2, 3, 4
  • Minimum interval between doses 1 and 3: 16 weeks 2, 3, 4
  • Doses given ≤4 days before the minimum interval are considered valid 3, 4

Interrupted Schedules

If the vaccination series is interrupted, do not restart—simply continue where you left off 3, 4

  • If interrupted after dose 1: give dose 2 as soon as possible, then dose 3 at least 8 weeks after dose 2 3
  • Increasing intervals between doses has little effect on final immunogenicity 3
  • Vaccine-induced immunity persists for >30 years 1, 3

Combined Hepatitis A and B Vaccine (Twinrix)

Indications

  • Use Twinrix only for patients requiring protection against both hepatitis A and B 3
  • Appropriate for international travelers to endemic regions, men who have sex with men at risk for both infections, and persons with chronic liver disease 3

Twinrix Schedules

  • Standard schedule: 3 doses at 0,1, and 6 months 3, 6
  • Accelerated schedule for rapid protection: 4 doses at days 0,7, and 21-30, followed by a booster at 12 months 3
  • At month 2, >99% are seropositive for anti-HAV and 84% are protected against hepatitis B 6
  • After completion, nearly all vaccinees have protective titers against both viruses 6

Post-Vaccination Testing

Routine testing after vaccination is unnecessary for immunocompetent persons 1

Testing Recommended For:

  • Infants born to HBsAg-positive mothers (test at 9-15 months for HBsAg and anti-HBs) 2, 3
  • Healthcare personnel 2
  • Hemodialysis patients 2
  • HIV-infected persons 2
  • Other immunocompromised persons 2
  • Perform testing 1-2 months after completing the vaccination series 2
  • Anti-HBs level ≥10 mIU/mL indicates adequate protection 2

Common Pitfalls to Avoid

  • Never restart the series if interrupted—this wastes doses and delays protection 3, 4
  • Do not give the third dose before 16 weeks from the first dose, even if 8 weeks have passed since the second dose 3, 4
  • Do not give the final infant dose before 24 weeks of age, as this may compromise long-term immunity 3, 4
  • Do not use standard adult doses in hemodialysis patients—they require 40 μg doses 1, 3, 4
  • Do not use Twinrix simply for hepatitis B vaccination when the patient has no indication for hepatitis A protection 3
  • Do not administer doses at shorter-than-recommended intervals, as this results in suboptimal immune response 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Hepatitis B Vaccination Schedule Recommendations

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Hepatitis B Vaccination Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Hepatitis B Vaccine Schedule Recommendations

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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