What is the recommended Hepatitis B (HBV) vaccine schedule?

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Hepatitis B Vaccine Scheduling

All infants should receive the first dose of hepatitis B vaccine within 12 hours of birth before hospital discharge, followed by doses at 1-2 months and 6 months of age. 1

Standard Infant Schedule

The CDC-recommended schedule for all newborns consists of three doses administered at specific intervals: 1, 2, 3

  • First dose: Within 12 hours of birth (before hospital discharge)
  • Second dose: 1-2 months of age
  • Third dose: 6 months of age

The final dose must not be administered before 24 weeks of age, regardless of when earlier doses were given. 2 This timing is critical for optimal long-term immunity.

Infants Born to HBsAg-Positive Mothers

These high-risk infants require immediate intervention: 1, 2

  • First dose plus HBIG: Within 12 hours of birth (both administered simultaneously at different sites)
  • Second dose: 1-2 months of age
  • Third dose: 6 months of age
  • Post-vaccination testing: At 9-15 months of age for HBsAg and anti-HBs 4, 1

Delaying the birth dose beyond 12 hours in these infants significantly increases infection risk. 1 Only monovalent hepatitis B vaccine can be used for the birth dose; combination vaccines are acceptable for subsequent doses. 4

Children and Adolescents (Catch-Up Vaccination)

For unvaccinated children and adolescents, the CDC recommends: 1, 3

  • Standard 3-dose schedule: 0,1, and 6 months
  • Alternative 2-dose schedule (ages 11-15 years only): Adult formulation of Recombivax HB at 0 and 4-6 months 3

Adult Schedule

Adults aged ≥18 years follow a standard 3-dose schedule at 0,1, and 6 months. 1, 2, 3 Alternative schedules producing similar seroprotection include 0,2, and 4 months or 0,1, and 4 months. 2

Accelerated Schedules for Rapid Protection

When rapid protection is needed: 2

  • Engerix-B: 0,1,2, and 12 months (4 doses)
  • Twinrix (for combined hepatitis A and B protection): 0,7, and 21-30 days, followed by a dose at 12 months 2

Critical Minimum Intervals

These intervals must be strictly observed to ensure adequate immune response: 1, 2, 3

  • Between doses 1 and 2: Minimum 4 weeks
  • Between doses 2 and 3: Minimum 8 weeks
  • Between doses 1 and 3: Minimum 16 weeks

Doses administered ≤4 days before the minimum interval are considered valid ("grace period"). 2, 3 Do not administer the third dose before 16 weeks from the first dose, even if 8 weeks have passed since the second dose. 2

Interrupted Schedules

If the vaccination series is interrupted, do not restart the series—simply continue where you left off. 2, 3 This is a critical point that prevents wasting doses and delaying protection. If interrupted after dose 1, give dose 2 as soon as possible, then dose 3 at least 8 weeks after dose 2. 2

Increasing intervals between doses has little effect on final immunogenicity, and longer intervals between the last 2 doses actually result in higher final antibody levels. 2

Special Populations

Hemodialysis Patients and Immunocompromised Adults

These patients require higher doses and more intensive monitoring: 1, 2, 3

  • Dose: 40 μg (double the standard adult dose) using Recombivax HB
  • Schedule: 0,1, and 6 months (or 4-dose schedule at 0,1,2, and 6 months with Engerix-B)
  • Monitoring: Annual anti-HBs testing with booster doses when levels fall below 10 mIU/mL

Do not use standard adult doses in hemodialysis patients, as they require the higher 40 μg doses. 2

Pregnant Women

Pregnant women should use Engerix-B, Recombivax HB, or Twinrix only. 2 Do not use Heplisav-B or PreHevbrio in pregnant women due to insufficient safety data. 2

Preterm Infants

For infants born to HBsAg-negative mothers weighing ≥2,000 g (4.4 lbs), administer the first dose before hospital discharge. 5 For infants <2,000 g, many guidelines recommend delaying the birth dose until the infant reaches 2,000 g or one month of age, though this varies by jurisdiction. 6

Post-Vaccination Testing

Post-vaccination serologic testing (1-2 months after completing the series) is recommended for: 1

  • Infants born to HBsAg-positive mothers
  • Healthcare personnel
  • Hemodialysis patients
  • HIV-infected persons
  • Other immunocompromised persons

An anti-HBs level ≥10 mIU/mL indicates adequate protection. 1 After the standard 3-dose series, >90% of healthy adults under 40 years achieve protective antibody response, though response rates decline with age. 2

Immunogenicity Timeline

Understanding the progressive immune response helps explain the schedule rationale: 2

  • After dose 1: 30-55% achieve protective antibody levels
  • After dose 2: 75% achieve protection
  • After dose 3: >90% achieve protection with traditional vaccines

Vaccine-induced immunity persists for >30 years without need for routine boosters in immunocompetent individuals. 2, 7

Common Pitfalls to Avoid

  • Never restart the series if interrupted—this wastes doses and delays protection 2, 3
  • Do not give the third dose before 16 weeks from the first dose, even if 8 weeks have passed since the second dose 2
  • Do not give the final infant dose before 24 weeks of age, as this may compromise long-term immunity 2
  • Do not use Twinrix simply for hepatitis B vaccination when the patient has no indication for hepatitis A protection 2
  • Do not use Heplisav-B or PreHevbrio in pregnant women, children, or hemodialysis patients 2

References

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

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 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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