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2019/20 季节欧洲特定品牌流感疫苗效果估计 - DRIVE EU 研究平台的结果。

Brand-specific influenza vaccine effectiveness estimates during 2019/20 season in Europe - Results from the DRIVE EU study platform.

机构信息

P95 Pharmacovigilance and Epidemiology, Leuven, Belgium.

FISABIO Public Health, Valencia, Spain.

出版信息

Vaccine. 2021 Jun 29;39(29):3964-3973. doi: 10.1016/j.vaccine.2021.05.059. Epub 2021 Jun 3.

Abstract

DRIVE (Development of Robust and Innovative Vaccine Effectiveness) is an IMI funded public-private platform that aims to annually estimate brand-specific influenza vaccine effectiveness (IVE), for public health and regulatory purposes. IVE analyses and reporting are conducted by public partners in the consortium. In 2019/20, four primary care-based test-negative design (TND) studies (Austria, England, Italy (n = 2)), eight hospital-based TND studies (Finland, France, Italy, Romania, Spain (n = 4)), and one population-based cohort study (Finland) were conducted. The COVID-19 pandemic affected influenza surveillance in all participating study sites, therefore the study period was truncated on February 29, 2020. Age-stratified (6 m-17y, 18-64y, ≥65y), confounder-adjusted, site-specific adjusted IVE estimates were calculated and pooled through meta-analysis. Parsimonious confounder-adjustment was performed, adjusting the estimates for age, sex and calendar time. TND studies included 3531 cases (351 vaccinated) and 5546 controls (1415 vaccinated) of all ages. IVE estimates were available for 8/11 brands marketed in Europe in 2019. Most children and adults < 64y were captured in primary care setting and the most frequently observed vaccine brand was Vaxigrip Tetra. The estimate against any influenza for Vaxigrip Tetra in primary care setting was 61% (95%CI 38-77) in children and 32% (95%CI -13-59) in adults up to 64y. Most adults ≥ 65y were captured in hospital setting and the most frequently observed brand was Fluad, with an estimate of 52% (95%CI 27-68). The population-based cohort covered 511,854 person-years and two vaccine brands. In children aged 2-6y, the IVE against any influenza was 68% (95%CI 58-75) for Fluenz Tetra and 71% (56-80) for Vaxigrip Tetra. In adults ≥ 65y, IVE against any influenza was 29% (20-36) for Vaxigrip Tetra. DRIVE is a growing platform. Public health institutes with surveillance data and hospitals in countries with high influenza vaccine coverage are encouraged to join DRIVE.

摘要

DRIVE(疫苗有效性的创新和稳健发展)是一个 IMI 资助的公私合作平台,旨在每年评估特定品牌的流感疫苗有效性(IVE),以用于公共卫生和监管目的。IVE 分析和报告由联盟中的公共合作伙伴进行。在 2019/20 年,进行了四项基于初级保健的测试阴性设计(TND)研究(奥地利、英国、意大利(n=2))、八项基于医院的 TND 研究(芬兰、法国、意大利、罗马尼亚、西班牙(n=4))和一项基于人群的队列研究(芬兰)。COVID-19 大流行影响了所有参与研究地点的流感监测,因此研究期于 2020 年 2 月 29 日截止。对年龄分层(6m-17y、18-64y、≥65y)、混杂因素调整、特定地点调整的 IVE 估计值进行了计算,并通过荟萃分析进行了汇总。进行了简约混杂因素调整,根据年龄、性别和日历时间调整了估计值。TND 研究包括来自所有年龄段的 3531 例病例(351 例接种)和 5546 例对照(1415 例接种)。2019 年在欧洲销售的 11 个品牌中有 8 个品牌提供了 IVE 估计值。大多数儿童和<64 岁的成年人在初级保健机构中被捕获,最常观察到的疫苗品牌是 Vaxigrip Tetra。在初级保健机构中,针对任何流感的 Vaxigrip Tetra 的估计值在儿童中为 61%(95%CI 38-77),在 18-64 岁的成年人中为 32%(95%CI-13-59)。大多数≥65 岁的成年人在医院环境中被捕获,最常观察到的品牌是 Fluad,估计值为 52%(95%CI 27-68)。基于人群的队列覆盖了 511,854 人年和两个疫苗品牌。在 2-6 岁的儿童中,针对任何流感的 IVE 对 Fluenz Tetra 为 68%(95%CI 58-75),对 Vaxigrip Tetra 为 71%(56-80)。在≥65 岁的成年人中,针对任何流感的 IVE 对 Vaxigrip Tetra 为 29%(20-36)。DRIVE 是一个不断发展的平台。鼓励有监测数据的公共卫生机构和流感疫苗覆盖率高的国家的医院加入 DRIVE。

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