Effect of rotavirus vaccine on severe diarrhea in African infants

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dc.contributor.author Madhi, Shabir A.
dc.contributor.author Cunliffe, Nigel A.
dc.contributor.author Steele, Andrew Duncan
dc.contributor.author Witte, Desree
dc.contributor.author Kirsten, Mari
dc.contributor.author Louw, Cheryl
dc.contributor.author Ngwira, Bagrey
dc.contributor.author Victor, John C.
dc.contributor.author Gillard, Paul H.
dc.contributor.author Cheuvart, Brigitte B.
dc.contributor.author Han, Htay Htay
dc.contributor.author Neuzil, Kathleen M.
dc.date.accessioned 2011-06-13T13:01:39Z
dc.date.available 2011-06-13T13:01:39Z
dc.date.issued 2010-01
dc.description.abstract BACKGROUND: Rotavirus is the most common cause of severe gastroenteritis among young children worldwide. Data are needed to assess the efficacy of the rotavirus vaccine in African children. METHODS: We conducted a randomized, placebo-controlled, multicenter trial in South Africa (3166 infants; 64.1% of the total) and Malawi (1773 infants; 35.9% of the total) to evaluate the efficacy of a live, oral rotavirus vaccine in preventing severe rotavirus gastroenteritis. Healthy infants were randomly assigned in a 1:1:1 ratio to receive two doses of vaccine (in addition to one dose of placebo) or three doses of vaccine — the pooled vaccine group — or three doses of placebo at 6, 10, and 14 weeks of age. Episodes of gastroenteritis caused by wild-type rotavirus during the first year of life were assessed through active follow-up surveillance and were graded with the use of the Vesikari scale. RESULTS: A total of 4939 infants were enrolled and randomly assigned to one of the three groups; 1647 infants received two doses of the vaccine, 1651 infants received three doses of the vaccine, and 1641 received placebo. Of the 4417 infants included in the per-protocol efficacy analysis, severe rotavirus gastroenteritis occurred in 4.9% of the infants in the placebo group and in 1.9% of those in the pooled vaccine group (vaccine efficacy, 61.2%; 95% confidence interval, 44.0 to 73.2). Vaccine efficacy was lower in Malawi than in South Africa (49.4% vs. 76.9%); however, the number of episodes of severe rotavirus gastroenteritis that were prevented was greater in Malawi than in South Africa (6.7 vs. 4.2 cases prevented per 100 infants vaccinated per year). Efficacy against all-cause severe gastroenteritis was 30.2%. At least one serious adverse event was reported in 9.7% of the infants in the pooled vaccine group and in 11.5% of the infants in the placebo group. CONCLUSIONS: Human rotavirus vaccine significantly reduced the incidence of severe rotavirus gastroenteritis among African infants during the first year of life. (ClinicalTrials.gov number, NCT00241644.) en_US
dc.identifier.citation Madhi, SA, Cunliffe, NA, Steele, D, Witte, D, Kirsten, M, Louw, C Ngwira, B, Victor, JC, Gillard, PH, Cheuvart, BB, Han, HH & Neuzil, KM 2010, 'Effect of rotavirus vaccine on severe diarrhea in African infants', New England Journal of Medicine, vol. 362, no. 4, pp. 289-298. [http://www.nejm.org/] en_US
dc.identifier.issn 0028-4793 (print)
dc.identifier.issn 1533-4406 (online)
dc.identifier.uri http://hdl.handle.net/2263/16825
dc.language.iso en en_US
dc.publisher Massachusetts Medical Society en_US
dc.rights © 2010 Massachusetts Medical Society. All rights reserved. en_US
dc.subject Rotavirus vaccine en_US
dc.subject Diarrhea en_US
dc.subject African infants en_US
dc.subject.lcsh Rotaviruses -- Research -- South Africa en
dc.subject.lcsh Rotavirus infections -- South Africa en
dc.subject.lcsh Gastroenteritis -- South Africa en
dc.subject.lcsh Rotaviruses -- Research -- Malawi en
dc.title Effect of rotavirus vaccine on severe diarrhea in African infants en_US
dc.type Article en_US


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