Institute of Collective Health, Federal University of Bahia, Rua Basílio da Gama, s/n, Campus Universitário do Canela, CEP 40110-040, Salvador, Bahia, Brazil.
Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, Keppel Street, WC1H 7HT London, United Kingdom.
Vaccine. 2014 May 13;32(23):2740-7. doi: 10.1016/j.vaccine.2014.01.007. Epub 2014 Feb 5.
Rotavirus is one of the leading cause of hospitalization and outpatients visits among children under five years. This study evaluated overall and genotype-specific vaccine effectiveness of oral monovalent rotavirus vaccine (G1P[8] strain) in preventing hospital admission of Brazilian children with rotavirus acute diarrhea. A hospital based case-control study was conducted in five Regions of Brazil using the National Rotavirus Acute Diarrhea Surveillance System from July 2008 to August 2011. A total of 215 cases (aged 4-24 months) admitted with confirmed rotavirus diarrhea were recruited and 1961 controls hospitalized without diarrhea were frequency matched by sex and age group to cases. Two-dose adjusted vaccine effectiveness (adjusted by year of birth and the frequency matching variables) was 76% (95%CI: 58-86) lasting for two years. Effectiveness controlled by the available potential confounders was 72% (95%CI: 44-85), suggesting no appreciable confounding by those factors for which adjustment was made. In a half of the cases the rotavirus genotype was G2P[4] and in 15% G1P[8]. Genotype-specific VE (two doses) was 89% (95%CI: 78-95), for G1P[8] and 76% (95%CI: 64-84) for G2P[4]. For all G1, it was 74% (95%CI: 35-90), for all G2, 76% (95%CI: 63-84), and for all non G1/G2 genotypes, 63% (95%CI: -27-99). Effectiveness for one dose was 62% (95%CI: 39-97). Effectiveness of two-dose monovalent rotavirus vaccine in preventing hospital admission with rotavirus diarrhea was high, lasted for two years and it was similar against both G1P[8] and G2P[4]. Based on the findings of the study we recommend the continued use of rotavirus in the Brazilian National Immunization Program and the monitoring of the early emergence of unusual and novel rotavirus genotypes.
轮状病毒是导致 5 岁以下儿童住院和门诊就诊的主要原因之一。本研究评估了口服单价轮状病毒疫苗(G1P[8] 株)在预防巴西儿童轮状病毒急性腹泻住院方面的总体和基因型特异性疫苗有效性。使用国家轮状病毒急性腹泻监测系统,从 2008 年 7 月至 2011 年 8 月,在巴西五个地区开展了一项基于医院的病例对照研究。共招募了 215 例(4-24 月龄)确诊轮状病毒腹泻住院病例,并按照性别和年龄组与病例进行频数匹配,招募了 1961 例无腹泻住院的对照。两剂调整后的疫苗有效性(通过出生年份和频数匹配变量调整)为 76%(95%CI:58-86),持续 2 年。通过可用潜在混杂因素控制的有效性为 72%(95%CI:44-85),提示对于所调整的因素,没有明显的混杂。在一半的病例中,轮状病毒基因型为 G2P[4],15%为 G1P[8]。两剂 G 型特异性 VE(G1P[8])为 89%(95%CI:78-95),G2P[4]为 76%(95%CI:64-84)。所有 G1 为 74%(95%CI:35-90),所有 G2 为 76%(95%CI:63-84),所有非 G1/G2 基因型为 63%(95%CI:-27-99)。一剂的有效性为 62%(95%CI:39-97)。两剂单价轮状病毒疫苗预防轮状病毒腹泻住院的有效性较高,持续 2 年,对 G1P[8]和 G2P[4]的效果相似。基于研究结果,我们建议继续在巴西国家免疫规划中使用轮状病毒,并监测新型轮状病毒基因型的早期出现。