What is the recommended Engerix-B (hepatitis B vaccine) vaccination schedule for different patient populations?

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Engerix-B Vaccination Schedules

Standard Adult Schedule (≥20 years)

For healthy adults aged 20 years and older, administer Engerix-B 20 μg (1.0 mL) intramuscularly at 0,1, and 6 months. 1, 2

  • This 3-dose series achieves seroprotection (anti-HBs ≥10 mIU/mL) in 79% by month 6 and 96% by month 7, with a geometric mean titer (GMT) of 2,204 mIU/mL among seroconverters 2
  • Seroprotection rates exceed 93-100% one month after completing the series in healthy adults 3, 4
  • Note that vaccine response declines with age: adults over 40 years achieve only 88% seroprotection with lower GMTs (610 mIU/mL) compared to younger adults 2

Adolescent Schedule (11-19 years)

For adolescents aged 11-19 years, administer Engerix-B 10 μg (0.5 mL) at 0,1, and 6 months. 1, 2

  • This achieves 97% seroprotection at month 8 with a GMT of 1,989 mIU/mL 2
  • An alternative 20 μg dose produces 99% seroprotection with higher GMT (7,672 mIU/mL), though the clinical significance is unclear 2

Alternative Extended Schedule for Low-Risk Adolescents

For children and adolescents aged 5-16 years at low risk of immediate HBV exposure, you can use an extended schedule of 0,12, and 24 months with 10 μg doses. 5

  • This achieves 88.8% seroprotection before the third dose and 98.1% one month after completion 5
  • GMTs are slightly lower (3,159 mIU/mL) compared to the standard 0-1-6 month schedule (5,687 mIU/mL), though the clinical relevance is unknown 2, 5

Pediatric Schedule (6 months to 10 years)

For children aged 6 months to 10 years, administer Engerix-B 10 μg at 0,1, and 6 months. 2

  • This achieves 98% seroprotection 1-2 months after the third dose with a GMT of 4,023 mIU/mL 2

Infant Schedule

For infants, administer Engerix-B 10 μg at 0,1, and 2 months, followed by a fourth dose at 12 months. 2

  • The 0-1-2 month series produces 96% seroprotection by month 4 with a GMT of 210 mIU/mL 2
  • The additional dose at 12 months dramatically increases GMT to 2,941 mIU/mL at month 13 2
  • Critical pitfall: Do not administer the final dose before 24 weeks of age 6

Accelerated Schedule for Rapid Protection

For adults requiring rapid protection (recent exposure, travelers, neonates of HBV-positive mothers), use the accelerated 4-dose schedule: 0,1,2, and 12 months with 20 μg doses. 1, 2

  • This achieves 99% seroprotection by month 3 and maintains protection through month 12 2
  • The fourth dose at 12 months is essential for long-term protection, producing a GMT of 9,163 mIU/mL at month 13 2
  • Alternative intervals of 0,1,4 months or 0,2,4 months produce similar seroprotection to the standard schedule 1

Immunocompromised and Hemodialysis Patients

For hemodialysis patients and immunocompromised adults aged ≥20 years, administer Engerix-B 40 μg (2.0 mL) at 0,1,2, and 6 months. 7, 1

  • This 4-dose regimen achieves 67% seroprotection with a GMT of 93 mIU/mL among seroconverters 2
  • This is substantially lower than healthy adults, reflecting the impaired immune response in this population 3
  • The 4-dose schedule is superior to the standard 3-dose regimen in hemodialysis patients 2

HIV-Infected Patients

For HIV-infected adults without evidence of past or present HBV infection, administer either 40 μg Recombivax HB on a 3-dose schedule OR 40 μg Engerix-B (administered as 2 doses of 20 μg simultaneously) on a 4-dose schedule at 0,1,2, and 6 months. 7

  • Test for anti-HBs response 1-2 months after the third dose or at the next scheduled clinic visit 7

Pregnancy Considerations

Pregnant women requiring hepatitis B vaccination should receive only Engerix-B, Recombivax HB, or Twinrix, as Heplisav-B and PreHevbrio lack sufficient safety data in pregnancy. 1, 6

Managing Interrupted Schedules

If the vaccination schedule is interrupted, never restart the series—simply continue where you left off. 1, 6

  • The second and third doses must be separated by ≥8 weeks 1, 6
  • The final dose must be administered at least 16 weeks after the first dose 6
  • Minimum intervals: 4 weeks between doses 1 and 2; 8 weeks between doses 2 and 3; 16 weeks between doses 1 and 3 1, 6
  • Doses administered ≤4 days before the minimum interval are considered valid 1
  • There is no maximum interval between doses—delayed doses do not require restarting 6

Post-Vaccination Testing

Routine serologic testing is not necessary for most adults, but test for anti-HBs 1-2 months after series completion for healthcare workers, public safety workers, and other high-risk groups. 1

  • Protective level is anti-HBs ≥10 mIU/mL 1
  • Pre-vaccination testing is not required and should not be a barrier to vaccination 1

Common Pitfalls to Avoid

  • Do not restart the series if doses are delayed—there is no maximum interval between doses 6
  • Do not use Heplisav-B or PreHevbrio in pregnant women, hemodialysis patients, or children 1, 6
  • Do not assume lower response in older adults means failure—88% still achieve protection, but consider higher doses or additional doses if initial response is inadequate 2
  • Do not forget the fourth dose at 12 months when using accelerated schedules—it is essential for long-term protection 2

References

Guideline

Hepatitis B Vaccine Dosing and Schedule Recommendations

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Recombinant hepatitis B vaccine: a review of its immunogenicity and protective efficacy against hepatitis B.

BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 1998

Guideline

Hepatitis B Vaccination Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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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