Hepatitis A Vaccination: Indications, Contraindications, and Dosing
Hepatitis A vaccine should be administered as a 2-dose series starting at age 12 months or older, with the second dose given at least 6 months after the first dose, and is indicated for routine childhood immunization, international travelers, high-risk groups, and postexposure prophylaxis in persons ≥12 months of age. 1
Standard Dosing Schedule
The complete vaccination series requires 2 doses separated by at least 6 months for long-term immunity. 1
- Vaqta (Merck): Adults receive 1.0 mL (50 U) intramuscularly initially, followed by a booster at 6-12 months; children 2-17 years receive 0.5 mL (25 U) with booster at 6-18 months 2
- Havrix (SmithKline Beecham): Adults receive 1.0 mL (1440 ELISA units) intramuscularly initially, followed by 1.0 mL booster at 6-12 months; children 2-18 years receive 0.5 mL (720 ELISA units) 2
- The second dose should not be administered sooner than 6 months after the first dose, regardless of HAV exposure risk 1
- Seroconversion rates exceed 95% in healthy children and adults 2
Primary Indications
Routine Vaccination
- All children starting at age 12 months 1
- Travelers to regions with intermediate to high endemic hepatitis A rates 2, 3
High-Risk Groups
- Homosexual males 2
- Users of illicit intravenous drugs 2
- Persons working directly with nonhuman primates or hepatitis A virus 2
- Patients older than 30 years with chronic liver disease 2
- Persons who have received or are awaiting liver transplant 2
- Children living in high-prevalence areas or communities with periodic outbreaks 3
Postexposure Prophylaxis (PEP)
Hepatitis A vaccine is the preferred agent for PEP in persons ≥12 months, administered within 2 weeks of exposure. 1
Age-Specific PEP Recommendations
- Infants <12 months: Immune globulin (IG) only at 0.1 mL/kg; vaccine contraindicated 1
- Ages 12 months-40 years (healthy): 1 dose of vaccine alone; no IG needed 1
- Ages >40 years (healthy): 1 dose of vaccine; IG (0.1 mL/kg) may be added based on provider's risk assessment 1
- Ages ≥12 months (immunocompromised or chronic liver disease): 1 dose of vaccine PLUS IG (0.1 mL/kg) administered simultaneously at different anatomic sites 1
A second dose is not required for PEP efficacy, but should be completed at least 6 months later for long-term immunity. 1
Preexposure Protection for International Travelers
Infants and Young Children
- Infants <6 months: IG only at 0.1-0.2 mL/kg (0.1 mL/kg for travel up to 1 month; 0.2 mL/kg for travel up to 2 months) 1
- Infants 6-11 months: 1 dose of vaccine (this dose does NOT count toward the routine 2-dose series, which must begin at age 12 months) 1
- Ages 12 months-40 years: 1 dose of vaccine; no IG needed 1
Adults and Special Populations
- Ages >40 years: 1 dose of vaccine; IG (0.1-0.2 mL/kg) may be added based on provider's risk assessment 1
- All ages (immunocompromised): 1 dose of vaccine PLUS IG (0.1-0.2 mL/kg) based on provider's risk assessment 1
For persons not previously vaccinated, administer the first dose as soon as travel is considered and complete the series according to the routine schedule. 1
Contraindications
The only absolute contraindication is a life-threatening allergic reaction to a previous dose of hepatitis A vaccine or severe allergy to any vaccine component. 1
- Persons with vaccine contraindications should receive IG (0.1 mL/kg) for PEP instead 1
- Both vaccines are safe for use in pregnancy 2
Critical Timing Considerations
Postexposure prophylaxis must be administered within 2 weeks of exposure to be effective. 1
Important caveat: MMR and varicella vaccines should not be administered for at least 3 months after receipt of IG, as IG can interfere with live virus vaccine immunogenicity 1
For infants 6-11 months traveling internationally, simultaneous administration of MMR and hepatitis A vaccines is recommended, avoiding the need for IG which would delay MMR vaccination. 1
Long-Term Protection
Protective antibody levels persist for at least 25 years after completion of the 2-dose series, with 78.7-81.4% maintaining protective levels at 25 years. 4
Two-dose schedules provide more robust long-term protection than single-dose programs, with antibody persistence documented for at least 15 years (≥90%) versus 10 years (≥74%) for single-dose schedules. 5