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2015-2016 流感季英格兰因实验室确诊流感而住院的儿童流感疫苗有效性:一项病例对照试验。

Influenza vaccine effectiveness against hospitalisation due to laboratory-confirmed influenza in children in England in the 2015-2016 influenza season - a test-negative case-control study.

机构信息

Public Health England,London,UK.

Public Health England National Infection Service South West and Severn Infection Sciences, University Hospital Bristol,Bristol,UK.

出版信息

Epidemiol Infect. 2019 Jan;147:e201. doi: 10.1017/S0950268819000876.

Abstract

England has recently started a new paediatric influenza vaccine programme using a live-attenuated influenza vaccine (LAIV). There is uncertainty over how well the vaccine protects against more severe end-points. A test-negative case-control study was used to estimate vaccine effectiveness (VE) in vaccine-eligible children aged 2-16 years of age in preventing laboratory-confirmed influenza hospitalisation in England in the 2015-2016 season using a national sentinel laboratory surveillance system. Logistic regression was used to estimate the VE with adjustment for sex, risk-group, age group, region, ethnicity, deprivation and month of sample collection. A total of 977 individuals were included in the study (348 cases and 629 controls). The overall adjusted VE for all study ages and vaccine types was 33.4% (95% confidence interval (CI) 2.3-54.6) after adjusting for age group, sex, index of multiple deprivation, ethnicity, region, sample month and risk group. Risk group was shown to be an important confounder. The adjusted VE for all influenza types for the live-attenuated vaccine was 41.9% (95% CI 7.3-63.6) and 28.8% (95% CI -31.1 to 61.3) for the inactivated vaccine. The study provides evidence of the effectiveness of influenza vaccination in preventing hospitalisation due to laboratory-confirmed influenza in children in 2015-2016 and continues to support the rollout of the LAIV childhood programme.

摘要

英国最近启动了一项新的儿科流感疫苗计划,使用减毒活流感疫苗(LAIV)。对于该疫苗在预防更严重终点方面的保护效果存在不确定性。本研究采用了病例对照研究方法,利用全国哨点实验室监测系统,估计了在 2015-2016 年英国季节中,2-16 岁疫苗合格儿童中,LAIV 预防实验室确诊流感住院的疫苗有效性(VE)。采用逻辑回归进行估计,并对性别、风险组、年龄组、地区、种族、贫困程度和样本采集月份进行了调整。本研究共纳入了 977 名个体(348 例病例和 629 例对照)。对所有研究年龄和疫苗类型进行总体调整后,所有年龄组的总体调整 VE 为 33.4%(95%置信区间 2.3-54.6),调整了年龄组、性别、多重剥夺指数、种族、地区、采样月份和风险组。风险组是一个重要的混杂因素。对于减毒活疫苗,所有流感类型的调整 VE 为 41.9%(95%置信区间 7.3-63.6),对于灭活疫苗为 28.8%(95%置信区间 -31.1 至 61.3)。本研究为 2015-2016 年流感疫苗在预防儿童实验室确诊流感住院方面的有效性提供了证据,并继续支持 LAIV 儿童计划的推广。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e45c/6624859/618f02aabbc9/S0950268819000876_fig1.jpg

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