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评价 2015/2016 年度季节性四价流感灭活疫苗效果的实验性病例对照研究和传统病例对照研究设计。

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.

机构信息

Department of Pediatrics, Tokyo Metropolitan Ohtsuka Hospital, 2-8-1 Minamiohtsuka, Toshima-ku, Tokyo, 170-8476, Japan.

Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, Japan.

出版信息

Eur J Pediatr. 2018 Jul;177(7):1009-1017. doi: 10.1007/s00431-018-3145-7. Epub 2018 Apr 21.

Abstract

UNLABELLED

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) × 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.

CONCLUSION

Both studies confirmed significant VE against influenza A, significant two-dose VE against influenza B, and better two-dose VE than one-dose VE. What is Known: • Influenza vaccine effectiveness (VE) varies from year to year. • Observational studies are conventionally used for VE assessment. However, they are inherently susceptible to bias and confounding. What is New: • This is the first report of influenza VE assessment using more than one observational study and performed in a specific area during the same season. • VE estimates obtained in our traditional case-control study were lower than those in our test-negative case-control study, but both studies found significant VE against influenza.

摘要

目的

本研究旨在评估甲型流感(H1N1)pdm 主导的 2015/2016 季节中同一地理区域内两种观察性研究方法(传统病例对照研究和检验阴性病例对照研究)联合评估流感疫苗有效性(VE)的效果。

方法

我们的检验阴性病例对照研究共纳入了 331 例因发热就诊于我院的 6 个月至 15 岁儿童,其中 182 例为流感患者;我们的传统病例对照研究纳入了 812 例 6 个月至 15 岁的儿科门诊患者,其中 214 例为流感患者。研究回顾了流感感染和疫苗接种史,并计算 VE 为(1-比值比)×100。在检验阴性病例对照研究中,针对甲型流感的总体 VE 为 68%(95%CI 47-81),两剂疫苗的 VE 为 70%(48-83);针对乙型流感的 VE 为 37%(-12-64),两剂疫苗的 VE 为 49%(2-74)。在传统病例对照研究中,针对甲型流感的总体 VE 为 44%(15-63),两剂疫苗的 VE 为 44%(13-64),针对乙型流感的 VE 为 24%(-19-52),两剂疫苗的 VE 为 41%(3-64)。

结论

两项研究均证实了甲型流感疫苗具有显著的 VE,乙型流感两剂疫苗具有显著的 VE,且两剂疫苗的 VE 优于一剂疫苗。本研究是首次报道在同一季节同一地区采用两种以上观察性研究评估流感 VE,并且研究结果显示,两种方法均发现流感疫苗具有显著的效果。

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