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Authordc.contributor.authorLinhares, Alexandre C. 
Authordc.contributor.authorVelázquez, F. Raúl es_CL
Authordc.contributor.authorPérez Schael, Irene es_CL
Authordc.contributor.authorSáez Llorens, Xavier es_CL
Authordc.contributor.authorAbate, Héctor es_CL
Authordc.contributor.authorEspinoza, Félix es_CL
Authordc.contributor.authorLópez, Pío es_CL
Authordc.contributor.authorMacías Parra, Mercedes es_CL
Authordc.contributor.authorOrtega Barría, Eduardo es_CL
Authordc.contributor.authorRivera Medina, Doris Maribel es_CL
Authordc.contributor.authorRivera, Luis es_CL
Authordc.contributor.authorPavia Ruz, Noris es_CL
Authordc.contributor.authorNúñez, Ernesto es_CL
Authordc.contributor.authorDamaso, Silvia es_CL
Authordc.contributor.authorRuiz Palacios, Guillermo M. es_CL
Authordc.contributor.authorDe Vos, Béatrice es_CL
Authordc.contributor.authorO'Ryan Gallardo, Miguel es_CL
Authordc.contributor.authorGillard, Paul es_CL
Authordc.contributor.authorBouckenooghe, Alain es_CL
Admission datedc.date.accessioned2010-01-28T13:18:47Z
Available datedc.date.available2010-01-28T13:18:47Z
Publication datedc.date.issued2008-04-05
Cita de ítemdc.identifier.citationLANCET Volume: 371 Issue: 9619 Pages: 1181-1189 Published: APR 5 2008en_US
Identifierdc.identifier.issn0140-6736
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/128395
Abstractdc.description.abstractBackground Peak incidence of rotavirus gastroenteritis is seen in infants between 6 and 24 months of age. We therefore aimed to assess the 2-year efficacy and safety of an oral live attenuated human rotavirus vaccine for prevention of severe gastroenteritis in infants. Methods 15183 healthy infants aged 6-13 weeks from ten Latin American countries randomly assigned in a 1 to 1 ratio to receive two oral doses of RIX4414 or placebo at about 2 and 4 months of age in a double-blind, placebo-controlled phase III study were followed up until about 2 years of age. Primary endpoint was vaccine efficacy from 2 weeks after dose two until 1 year of age. Treatment allocation was concealed from investigators and parents of participating infants. Efficacy follow-up for gastroenteritis episodes was undertaken from 2 weeks after dose two until about 2 years of age. Analysis was according to protocol. This study is registered with ClinicalTrials.gov, number NCT00140673 (eTrack444563-023). Findings 897 infants were excluded from the according-to-protocol analysis. Fewer cases (p<0.0001) of severe rotavirus gastroenteritis were recorded for the combined 2-year period in the RIX4414 group (32 [0.4%] of 7205; 95% CI 0 . 3-0.6) than in the placebo group (161 [2.3%] of 7081; 1 . 9-2.6), resulting in a vaccine efficacy of 80.5% (71.3-87. 1) to 82.1% (64.6-91.9) against wild-type G1, 77.5% (64.7-86.2) against pooled non-G1 strains, and 80.5% (67.9-88 . 8) against pooled non-G1 P[81 strains. Vaccine efficacy for hospital admission for rotavirus gastroenteritis was 83. 0% (73.1-89.7) and for admission for diarrhoea of any cause was 39.3% (29.1-48 . 1). No cases of intussusception were reported during the second year of follow-up. Interpretation Two doses of RIX4414 were effective against severe rotavirus gastroenteritis during the first 2 years of life in a Latin American setting. Inclusion of RIX4414 in routine paediatric immunisations should reduce the burden of rotavirus gastroenteritis worldwide.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherELSEVIERen_US
Keywordsdc.subjectINFECTIONen_US
Títulodc.titleEfficacy and safety of an oral live attenuated human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in Latin American infants: a randomised, double-blind, placebo-controlled phase III studyen_US
Document typedc.typeArtículo de revista


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