European Programme for Intervention Epidemiology Training (EPIET), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden.
Centre for Infectious Disease Control, National Institute for Public Health and Environment (RIVM), Bilthoven, the Netherlands.
Euro Surveill. 2022 Nov;27(45). doi: 10.2807/1560-7917.ES.2022.27.45.2200217.
BackgroundDifferential SARS-CoV-2 exposure between vaccinated and unvaccinated individuals may confound vaccine effectiveness (VE) estimates.AimWe conducted a test-negative case-control study to determine VE against SARS-CoV-2 infection and the presence of confounding by SARS-CoV-2 exposure.MethodsWe included adults tested for SARS-CoV-2 at community facilities between 4 July and 8 December 2021 (circulation period of the Delta variant). The VE against SARS-CoV-2 infection after primary vaccination with an mRNA (Comirnaty or Spikevax) or vector-based vaccine (Vaxzevria or Janssen) was calculated using logistic regression adjusting for age, sex and calendar week (Model 1). We additionally adjusted for comorbidity and education level (Model 2) and SARS-CoV-2 exposure (number of close contacts, visiting busy locations, household size, face mask wearing, contact with SARS-CoV-2 case; Model 3). We stratified by age, vaccine type and time since vaccination.ResultsVE against infection (Model 3) was 64% (95% CI: 50-73), only slightly lower than in Models 1 (68%; 95% CI: 58-76) and 2 (67%; 95% CI: 56-75). Estimates stratified by age group, vaccine and time since vaccination remained similar: mRNA VE (Model 3) among people ≥ 50 years decreased significantly (p = 0.01) from 81% (95% CI: 66-91) at < 120 days to 61% (95% CI: 22-80) at ≥ 120 days after vaccination. It decreased from 83% to 59% in Model 1 and from 81% to 56% in Model 2.ConclusionSARS-CoV-2 exposure did not majorly confound the estimated COVID-19 VE against infection, suggesting that VE can be estimated accurately using routinely collected data without exposure information.
接种疫苗和未接种疫苗个体之间 SARS-CoV-2 暴露的差异可能会使疫苗有效性(VE)估计产生偏倚。
我们开展了一项病例对照研究,旨在确定针对 SARS-CoV-2 感染的 VE,并确定 SARS-CoV-2 暴露是否存在混杂。
我们纳入了 2021 年 7 月 4 日至 12 月 8 日期间在社区场所接受 SARS-CoV-2 检测的成年人(Delta 变体流行期间)。使用逻辑回归调整年龄、性别和日历周(模型 1),计算 mRNA(Comirnaty 或 Spikevax)或基于载体的疫苗(Vaxzevria 或 Janssen)初次接种后针对 SARS-CoV-2 感染的 VE。我们还调整了合并症和教育水平(模型 2)以及 SARS-CoV-2 暴露(密切接触人数、前往繁忙地点、家庭规模、戴口罩、接触 SARS-CoV-2 病例;模型 3)。我们按年龄、疫苗类型和接种后时间进行分层。
感染的 VE(模型 3)为 64%(95%CI:50-73),略低于模型 1(68%;95%CI:58-76)和模型 2(67%;95%CI:56-75)。按年龄组、疫苗和接种后时间分层的估计值仍然相似:≥50 岁人群的 mRNA VE(模型 3)在接种后<120 天从 81%(95%CI:66-91)显著下降(p=0.01)至 61%(95%CI:22-80),在接种后≥120 天从 83%下降至 59%,在模型 1 中从 81%下降至 56%。
SARS-CoV-2 暴露并未显著混淆针对感染的 COVID-19 VE 的估计值,这表明可以使用常规收集的数据准确估计 VE,而无需暴露信息。