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感兴趣的不良事件因流感疫苗类型和品牌而异:八个季节(2010 - 2018年)的哨点网络研究。

Adverse events of interest vary by influenza vaccine type and brand: Sentinel network study of eight seasons (2010-2018).

作者信息

Cross Joe W, Joy Mark, McGee Christopher, Akinyemi Oluwafunmi, Gatenby Piers, de Lusignan Simon

机构信息

University of Surrey Department of Clinical and Experimental Medicine, University of Surrey, Guildford GU2 7XH, United Kingdom; The Royal Surrey County Hospital, Egerton Road, Guildford GU2 7XX, United Kingdom.

University of Surrey Department of Clinical and Experimental Medicine, University of Surrey, Guildford GU2 7XH, United Kingdom.

出版信息

Vaccine. 2020 May 8;38(22):3869-3880. doi: 10.1016/j.vaccine.2020.03.034. Epub 2020 Apr 13.

Abstract

BACKGROUND

Influenza contributes significantly to the burden of disease worldwide; the United Kingdom has a policy of vaccination across all ages. Influenza vaccinations are known to be associated with common minor adverse events of interest (AEIs). The European Medicines Agency (EMA) recommends ongoing surveillance of AEIs following influenza vaccination to monitor common and detect infrequent but important AEIs.

METHODS

A retrospective cohort study using computerised medical record data from the Royal College of General Practitioners (RCGP) Research and Surveillance Centre (RSC) sentinel network database 2010-2018 (N = 848,375). We extracted data about vaccine exposure (n = 3,121,334) and consultations for AEIs within seven days of receiving vaccinations specified by the EMA (1,488,870 consultations by 430,029 unique individuals). We used a self-case series design which employs a likelihood estimation method using conditioning of observed adverse events. Such a model assumes non-homogenous Poisson intensity processes for each exposure period and age interval. We compared AEI between QIV and TIV reporting relative incidence (RI) of AEIs. A RI < 1 signified lower AEI rate compared to TIV.

RESULTS

QIV was associated with a RI of AEIs of 1.14 (95%CI, 1.10-1.18, p < 0.01), though the number of years exposure was limited. By way of contrast, LAIV had a lower rate 0.60 (95%CI 0.63-0.68, p < 0.001). Cellular manufacture was also associated with a lower rate 0.78 (95%CI 0.61-0.99, p = 0.04). AEIs varied by season: Rash and musculoskeletal conditions are particularly pronounced in the 2014/15 season and respiratory conditions in 2016/17. In an analysis of all seasons, we found an elevated relative incidence of AEIs of 1.78 (95%CI, 1.62-1.95) in pregnant women and 1.76 (95%CI, 1.56 - 1.99) in children under 5 years.

CONCLUSION

Routine sentinel network data can be used to contrast AEIs between vaccine types and may provide a consistent method of observation of vaccine benefit-risk over time.

摘要

背景

流感在全球疾病负担中占很大比重;英国实行全年龄段接种疫苗的政策。已知流感疫苗接种与常见的轻微不良事件相关。欧洲药品管理局(EMA)建议在流感疫苗接种后持续监测不良事件,以监测常见的不良事件并发现罕见但重要的不良事件。

方法

一项回顾性队列研究,使用来自皇家全科医师学院(RCGP)研究与监测中心(RSC)哨点网络数据库2010 - 2018年的计算机化医疗记录数据(N = 848,375)。我们提取了疫苗接种暴露数据(n = 3,121,334)以及在EMA规定的接种疫苗后7天内因不良事件进行的会诊数据(430,029名个体进行了1,488,870次会诊)。我们采用了自病例系列设计,该设计采用基于观察到的不良事件进行条件设定的似然估计方法。这种模型假设每个暴露期和年龄区间的泊松强度过程是非齐次的。我们比较了四价流感疫苗(QIV)和三价流感疫苗(TIV)报告的不良事件相对发病率(RI)。RI < 1表示与TIV相比不良事件发生率较低。

结果

尽管暴露年限有限,但QIV的不良事件RI为1.14(95%置信区间,1.10 - 1.18,p < 0.01)。相比之下,减毒活流感疫苗(LAIV)的发病率较低,为0.60(95%置信区间0.63 - 0.68,p < 0.001)。细胞培养生产的疫苗发病率也较低,为0.78(95%置信区间0.61 - 0.99,p = 0.04)。不良事件因季节而异:皮疹和肌肉骨骼疾病在2014/15季节尤为明显,呼吸道疾病在2016/17季节较为突出。在对所有季节的分析中,我们发现孕妇的不良事件相对发病率升高至1.78(95%置信区间,1.62 - 1.95),5岁以下儿童为1.76(95%置信区间,1.56 - 1.99)。

结论

常规哨点网络数据可用于对比不同疫苗类型的不良事件,并可能提供一种长期观察疫苗效益风险的一致方法。

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