Diaz Janepsy, Terrazas Solana, Bierrenbach Ana L, Toscano Cristiana M, Alencar Gizelton P, Alvarez Andrés, Valenzuela Maria T, Andrus Jon, del Aguila Roberto, Hormazábal Juan C, Araya Pamela, Pidal Paola, Matus Cuauhtemoc R, de Oliveira Lucia H
National Institute of Health, Santiago, Chile.
Sanas - epidemiologia e pesquisa, São Paulo, Brazil.
PLoS One. 2016 Apr 8;11(4):e0153141. doi: 10.1371/journal.pone.0153141. eCollection 2016.
The ten-valent pneumococcal conjugate vaccine (PCV10) was introduced into the Chilean National Immunization Program (NIP) in January 2011 with a 3+1 schedule (2, 4, 6 and 12 months) without catch-up vaccination. We evaluated the effectiveness of PCV10 on pneumonia morbidity and mortality among infants during the first two years after vaccine introduction.
This is a population-based nested case-control study using four merged nationwide case-based electronic health data registries: live birth, vaccination, hospitalization and mortality. Children born in 2010 and 2011 were followed from two moths of age for a period of two years. Using four different case definitions of pneumonia hospitalization and/or mortality (all-cause and pneumonia related deaths), all cases and four randomly selected matched controls per case were selected. Controls were matched to cases on analysis time. Vaccination status was then assessed. Vaccine effectiveness (VE) was estimated using conditional logistic regression.
There were a total of 497,996 children in the 2010 and 2011 Chilean live-birth cohorts. PCV10 VE was 11.2% (95%CI 8.5-13.6) when all pneumonia hospitalizations and deaths were used to define cases. VE increased to 20.7 (95%CI 17.3-23.8) when ICD10 codes used to denote viral pneumonia were excluded from the case definition. VE estimates on pneumonia deaths and all-cause deaths were 71.5 (95%CI 9.0-91.8) and 34.8 (95% CI 23.7-44.4), respectively.
PCV10 vaccination substantially reduced the number of hospitalizations due to pneumonia and deaths due to pneumonia and to all-causes over this study period. Our findings also reinforce the importance of having quality health information systems for measuring VE.
十价肺炎球菌结合疫苗(PCV10)于2011年1月被纳入智利国家免疫规划(NIP),接种程序为3+1(2、4、6和12月龄),不进行补种。我们评估了PCV10在引入疫苗后的头两年对婴儿肺炎发病率和死亡率的有效性。
这是一项基于人群的巢式病例对照研究,使用了四个全国性基于病例的电子健康数据登记库合并数据:活产、疫苗接种、住院和死亡。对2010年和2011年出生的儿童从两个月龄开始随访两年。使用四种不同的肺炎住院和/或死亡病例定义(全因死亡和肺炎相关死亡),选取所有病例以及每个病例随机选择的四个匹配对照。对照在分析时与病例进行匹配。然后评估疫苗接种状况。使用条件逻辑回归估计疫苗有效性(VE)。
2010年和2011年智利活产队列中共有497,996名儿童。当使用所有肺炎住院和死亡病例来定义病例时,PCV10的VE为11.2%(95%CI 8.5-13.6)。当病例定义中排除用于表示病毒性肺炎的ICD10编码时,VE增至20.7(95%CI 17.3-23.8)。肺炎死亡和全因死亡的VE估计值分别为71.5(95%CI 9.0-91.8)和34.8(95%CI 23.7-44.4)。
在本研究期间,PCV10疫苗接种显著减少了因肺炎住院的人数以及因肺炎和全因导致的死亡人数。我们的研究结果还强化了拥有高质量健康信息系统以测量VE的重要性。