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Effectiveness of inactivated quadrivalent influenza vaccine in the 2015/2016 season as assessed in both a test-negative case-control study design and a traditional case-control study design

机译:在测试负重案例控制研究设计和传统案例控制设计中评估2015/2016赛季灭活四价流感疫苗的有效性

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Both traditional case-control studies (TCCSs) and test-negative case-control studies (TNCCSs) are commonly used to assess influenza vaccine effectiveness (VE). To compensate for the fact that observational studies are susceptible to bias, we combined both methods to assess VE in one geographical area during the 2015/2016 season, when influenza A (H1N1)pdm was dominant. Our TNCCS covered 331 children aged 6 months to 15 years who visited our hospital with fever, including 182 with influenza, and our TCCS covered 812 pediatric outpatients aged 6 months to 15 years, including 214 with influenza. Influenza infection and vaccination history were reviewed, and VE was calculated as (1 - odds ratio) x 100. In the TNCCS, VE against influenza A was 68% (95% CI 47-81) overall, and 70% (48-83) for those given two doses; against influenza B, VE was 37% (- 12-64) overall and 49% (2-74) for two doses. In the TCCS, VE against influenza A was 44% (15-63) overall and 44% (13-64) for two doses, and VE against influenza B was 24% (- 19-52) overall and 41% (3-64) for two doses.
机译:传统病例对照研究(TCCSS)和测试阴性病例对照研究(TNCCS)通常用于评估流感疫苗效果(VE)。为了弥补观察性研究易受偏见的事实,我们将两种方法组合在2015/2016赛季中的一个地理区域中评估VE,当甲型流感A(H1N1)PDM占主导地位时。我们的TNCCS涵盖了331名6个月的儿童达到了15岁,患有过度发烧的医院,其中包括182名与流感,我们的TCCS涵盖了812名6个月的儿科门诊病,包括214名与流感214人。综述流感感染和疫苗接种历史,并计算为(1 - odds比率)x 100.在TNCCS中,对抗流感A A的VE总体为68%(95%CI 47-81),70%(48-83 )对于那些给予两剂的人;对抗流感B,ve总共为37%( - 12-64),两剂量为49%(2-74)。在TCCS中,对抗流感A的ve是44%(15-63),两剂量为44%(13-64),对抗流感B的ve总共24%( - 19-52),41%(3- 64)两剂量。

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