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Rationale:
- Susceptible travelers to high or intermediate endemic areas are at substantial risk for HAV infection.
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Evidence:
- A meta-analysis of retrospective, cohort, and seroepidemiologic studies identified from Index Medicus (1974-1983) and Medline
(1984-1993), as well as unpublished data from the CDC, suggests that hepatitis A is the most frequent infection in travelers
that may be prevented by immunization (30).
- A case-control study of travelers to developing countries compared with travelers to the Greek or Canary Islands determined
that hepatitis A is the most frequent vaccine-preventable disease in travelers to developing countries (31).
- A literature review of hepatitis A vaccine use in travelers to developing countries suggests that hepatitis A vaccine is a
safe and effective method for travelers to HAV-endemic areas to protect themselves against hepatitis A (32).
- A literature review of numerous studies conducted over the past four decades indicates that immunoglobulin is safe and effective
for short-term preexposure prevention against hepatitis A (33).
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Comments:
- Travel to endemic areas of the world is the most commonly reported risk factor for hepatitis A among reported cases in which
a risk factor is identified (34).
- The risk of travel-associated hepatitis A may be decreasing; however, the risk to nonimmune patients, including immigrants
returning to visit friends and relatives, remains considerable (35; 36).
- Hepatitis A vaccination is preferred for children aged 1 year or older, adolescents, and adults who plan frequent travel to
or who reside for long periods in high-risk areas.
- Immunoglobulin does not provide long-term protection and must be administered every 2 to 6 months, depending on the dose administered.
- Hepatitis A vaccine and immunoglobulin may be administered simultaneously.
- Manufacturers of hepatitis A vaccine (GlaxoSmithKline [HAVRIX®] and Merck & Co. [VAQTA®]) recommend that primary immunization
be completed at least 2 weeks before expected exposure.
- Although hepatitis A vaccine is recommended to be given 2 to 4 weeks before travel, vaccine may be beneficial in the last-minute
traveler (37).
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Brian J. McMahon, MD, MACP has no financial relationships with pharmaceutical companies, biomedical device manufacturers, or health-care related organizations.
Catherine M. Dentinger, FNP, MS has no financial relationships with pharmaceutical companies, biomedical device manufacturers, or health-care related organizations.
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The information included herein should never be used as a substitute
for clinical judgment and does not represent an official position of
ACP. Because all PIER modules are updated regularly, printed web pages
or PDFs may rapidly become obsolete. Therefore, PIER users should
compare the date of the last update on the website with any printout
to ensure that the information being referred to is the most current
available.
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PIER is copyrighted (c) 2008 by the American College of Physicians,
190 N. Independence Mall West, Philadelphia, PA 19106-1572, USA.
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