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Measurement of Vaccine Direct Effects Under the Test-Negative Design

机译:测试阴性设计下疫苗直接效应的测量

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摘要

Test-negative designs are commonplace in assessments of influenza vaccination effectiveness, estimating this value from the exposure odds ratio of vaccination among individuals treated for acute respiratory illness who test positive for influenza virus infection. This approach is widely believed to recover the vaccine direct effect by correcting for differential health-care-seeking behavior among vaccinated and unvaccinated persons. However, the relationship of the measured odds ratio to true vaccine effectiveness is poorly understood. We derived the odds ratio under circumstances of real-world test-negative studies. The odds ratio recovers the vaccine direct effect when 2 conditions are met: 1) Individuals’ vaccination decisions are uncorrelated with exposure or susceptibility to the test-positive or test-negative conditions, and 2) vaccination confers “all-or-nothing” protection (whereby certain individuals have no protection while others are perfectly protected). Biased effect-size estimates arise if either condition is unmet. Such bias might suggest misleading associations of vaccine effectiveness with time since vaccination or the force of infection of influenza. The test-negative design could also fail to correct for differential health-care-seeking behavior among vaccinated and unvaccinated persons without stringent criteria for enrollment and testing. Our findings demonstrate a need to reassess how data from test-negative studies can inform policy decisions.
机译:测试阴性的设计在评估流感疫苗接种效果时很常见,它是根据接受了急性呼吸道疾病治疗且流感病毒感染呈阳性的个体中疫苗接种的暴露比值比来估计该值的。人们普遍认为,该方法可通过纠正已接种疫苗者和未接种疫苗者之间寻求保健的不同行为来恢复疫苗的直接作用。然而,人们对测得的比值比与真正的疫苗效力之间的关系了解甚少。我们得出了真实世界中测试阴性研究情况下的优势比。当满足以下两个条件时,优势比可以恢复疫苗的直接作用:1)个人的疫苗接种决定与暴露于测试阳性或测试阴性条件的敏感性无关; 2)疫苗接种提供“全有或全无”保护(因此某些人没有保护,而其他人则受到完全保护)。如果任一条件均未满足,则会产生有偏差的效应大小估计。这种偏见可能提示疫苗有效性与自接种疫苗以来的时间或流感感染力之间存在误导性联系。如果没有严格的招募和测试标准,则阴性测试设计也可能无法纠正已接种疫苗者和未接种疫苗者之间寻求医疗保健行为的差异。我们的发现表明,有必要重新评估来自阴性测试研究的数据如何为政策决策提供依据。

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