Published online March 30, 2009
PEDIATRICS Vol. 123 No. 5 May 2009, pp. 1412-1420 (doi:10.1542/peds.2009-0466)
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POLICY STATEMENT

Prevention of Rotavirus Disease: Updated Guidelines for Use of Rotavirus Vaccine

Committee on Infectious Diseases

This statement updates and replaces the 2007 American Academy of Pediatrics statement for prevention of rotavirus gastroenteritis. In February 2006, a live oral human-bovine reassortant rotavirus vaccine (RV5 [RotaTeq]) was licensed as a 3-dose series for use in infants in the United States. The American Academy of Pediatrics recommended routine use of RV5 in infants in the United States. In April 2008, a live, oral, human attenuated rotavirus vaccine (RV1 [Rotarix]) was licensed as a 2-dose series for use in infants in the United States. The American Academy of Pediatrics recommends routine immunization of infants in the United States with rotavirus vaccine. The American Academy of Pediatrics does not express a preference for either RV5 or RV1. RV5 is to be administered orally in a 3-dose series with doses administered at 2, 4, and 6 months of age; RV1 is to be administered orally in a 2-dose series with doses administered at 2 and 4 months of age. The first dose of rotavirus vaccine should be administered from 6 weeks through 14 weeks, 6 days of age. The minimum interval between doses of rotavirus vaccine is 4 weeks. All doses should be administered by 8 months, 0 days of age. Recommendations in this statement also address the maximum ages for doses, contraindications, precautions, and special situations for administration of rotavirus vaccine.

Key Words: rotavirus vaccine • rotavirus gastroenteritis

Abbreviations: RV1—live, oral human attenuated rotavirus vaccine • AAP—American Academy of Pediatrics • RV5—live, oral human-bovine reassortant rotavirus vaccine • RR—relative risk • CI—confidence interval • CDC—Centers for Disease Control and Prevention


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