Department of Population Health Sciences, Albany College of Pharmacy and Health Sciences, Albany, New York, USA.
Precision Analytics, Montreal, Quebec, Canada.
Clin Infect Dis. 2022 Aug 24;75(1):e564-e571. doi: 10.1093/cid/ciac234.
The test-negative design is commonly used to estimate influenza and coronavirus disease 2019 (COVID-19) vaccine effectiveness (VE). In these studies, correlated COVID-19 and influenza vaccine behaviors may introduce a confounding bias where controls are included with the other vaccine-preventable acute respiratory illness (ARI). We quantified the impact of this bias on VE estimates in studies where this bias is not addressed.
We simulated study populations under varying vaccination probabilities, COVID-19 VE, influenza VE, and proportions of controls included with the other vaccine-preventable ARI. Mean bias was calculated as the difference between estimated and true VE. Absolute mean bias in VE estimates was classified as low (<10%), moderate (10% to <20%), and high (≥20%).
Where vaccination probabilities are positively correlated, COVID-19 and influenza VE test-negative studies with influenza and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ARI controls, respectively, underestimate VE. For COVID-19 VE studies, mean bias was low for all scenarios where influenza represented ≤25% of controls. For influenza VE studies, mean bias was low for all scenarios where SARS-CoV-2 represented ≤10% of controls. Although bias was driven by the conditional probability of vaccination, low VE of the vaccine of interest and high VE of the confounding vaccine increase its magnitude.
Where a low percentage of controls is included with the other vaccine-preventable ARI, bias in COVID-19 and influenza VE estimates is low. However, influenza VE estimates are likely more susceptible to bias. Researchers should consider potential bias and its implications in their respective study settings to make informed methodological decisions in test-negative VE studies.
病例对照设计常用于估计流感和 2019 年冠状病毒病(COVID-19)疫苗的有效性(VE)。在这些研究中,COVID-19 和流感疫苗的相关行为可能会引入混杂偏差,即对照中包含了其他可预防的急性呼吸道疾病(ARI)。我们量化了在未解决这种偏差的情况下进行这些研究对 VE 估计的影响。
我们在不同的疫苗接种概率、COVID-19 VE、流感 VE 和包含其他可预防的 ARI 的对照比例下模拟了研究人群。估计偏差是通过比较真实 VE 计算得出的。VE 估计的绝对平均偏差分为低(<10%)、中(10%至<20%)和高(≥20%)。
当疫苗接种概率呈正相关时,COVID-19 和流感 VE 测试阴性研究分别具有流感和严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)ARI 对照,低估了 VE。对于 COVID-19 VE 研究,在流感占对照的比例≤25%的所有情况下,平均偏差均较低。对于流感 VE 研究,在 SARS-CoV-2 占对照的比例≤10%的所有情况下,平均偏差均较低。尽管偏差是由疫苗接种的条件概率驱动的,但感兴趣疫苗的低 VE 和混杂疫苗的高 VE 会增加其幅度。
在只有一小部分对照包含在其他可预防的 ARI 中的情况下,COVID-19 和流感 VE 估计的偏差较低。然而,流感 VE 估计可能更容易受到偏差的影响。研究人员应考虑潜在的偏差及其在各自研究中的影响,以便在测试阴性 VE 研究中做出明智的方法学决策。