Jackson Michael L
Kaiser Permanente Washington Health Research Institute, Seattle, WA, United States.
Vaccine X. 2018 Dec 29;1:100003. doi: 10.1016/j.jvacx.2018.100003. eCollection 2019 Apr 11.
A number of national/multi-national networks provide annual estimates of influenza vaccine effectiveness (VE) based on the test-negative design. Most of these networks use subject self-reports to define influenza vaccination history. In this study, we used simulations to estimate the degree to which self-reported vaccination status can bias test-negative VE estimates.
We simulated a population whose members are at risk for acute respiratory illness (ARI) due to influenza and for ARI due to other respiratory pathogens. Vaccination was assumed to reduce the risk of influenza but not of non-influenza ARI. We simulated a range of possible values for VE and for vaccine coverage. Across simulations, we varied the sensitivity and specificity of self-reported vaccination status relative to true vaccination. We estimated bias as the percent difference in VE in the presence of misclassification relative to true simulated VE.
Assuming self-report has sensitivity of 95% and specificity of 90%, estimated VE underestimated true VE by 16% (95% confidence interval, 4-30%). Decreasing specificity of self-reports resulted in greater bias than decreasing sensitivity of self-reports. Bias also increased as vaccine coverage decreased.
The use of self-reported influenza vaccination history can meaningfully bias influenza VE in test-negative studies. Researchers using test-negative designs should attempt to supplement or validate self-reported vaccination history using additional data sources.
一些国家/跨国网络基于检测阴性设计提供流感疫苗效力(VE)的年度估计值。这些网络大多使用受试者自我报告来确定流感疫苗接种史。在本研究中,我们使用模拟方法来估计自我报告的疫苗接种状态对检测阴性VE估计值产生偏差的程度。
我们模拟了一个人群,其成员因流感和其他呼吸道病原体而有患急性呼吸道疾病(ARI)的风险。假设接种疫苗可降低患流感的风险,但不能降低患非流感ARI的风险。我们模拟了一系列可能的VE值和疫苗接种覆盖率。在所有模拟中,我们改变了自我报告的疫苗接种状态相对于真实疫苗接种状态的敏感性和特异性。我们将偏差估计为存在错误分类时的VE与真实模拟VE的百分比差异。
假设自我报告的敏感性为95%,特异性为90%,估计的VE比真实的VE低16%(95%置信区间,4 - 30%)。自我报告特异性的降低导致的偏差比敏感性的降低更大。随着疫苗接种覆盖率的降低,偏差也会增加。
在检测阴性研究中,使用自我报告的流感疫苗接种史会对流感VE产生显著偏差。采用检测阴性设计的研究人员应尝试使用其他数据源来补充或验证自我报告的疫苗接种史。