Policy responses to COVID-19, particularly those related to non-pharmaceutical interventions, are unprecedented in scale and scope. Researchers and policymakers are striving to understand the impact of these policies on a variety of outcomes. Policy impact evaluations always require a complex combination of circumstance, study design, data, statistics, and analysis. Beyond the issues that are faced for any policy, evaluation of COVID-19 policies is complicated by additional challenges related to infectious disease dynamics and lags, lack of direct observation of key outcomes, and a multiplicity of interventions occurring on an accelerated time scale. The volume, speed, and methodological complications of policy evaluations can make it difficult for decision-makers and researchers to synthesize and evaluate strength of evidence in COVID-19 health policy papers. In this paper, we (1) introduce the basic suite of policy impact evaluation designs for observational data, including cross-sectional analyses, pre/post, interrupted time-series, and difference-in-differences analysis, (2) demonstrate key ways in which the requirements and assumptions underlying these designs are often violated in the context of COVID-19, and (3) provide decision-makers and reviewers a conceptual and graphical guide to identifying these key violations. The overall goal of this paper is to help policy-makers, journal editors, journalists, researchers, and other research consumers understand and weigh the strengths and limitations of evidence that is essential to decision-making.
翻译:对COVID-19的政策反应,特别是与非药物干预有关的政策反应,在规模和范围上都是前所未有的。研究人员和决策者正在努力了解这些政策对各种结果的影响。政策影响评价总是需要情况、研究设计、数据、统计和分析的复杂组合。除了对任何政策所面临的问题外,对COVID-19政策的评价由于与传染病动态和滞后有关的额外挑战、对关键结果缺乏直接观察以及加速时间规模的干预活动的多样性而变得复杂。政策评价的数量、速度和方法复杂,可能使决策者和研究人员难以综合和评价COVID-19卫生政策文件中证据的力度。在本文件中,我们(1) 介绍观察数据的政策影响评价设计的基本组合,包括跨部门分析、前后、中断的时间序列和差异分析;(2) 说明在COVID-19背景下这些设计所依据的要求和假设经常遭到违反的主要方式;(3) 向决策者和研究人员提供一份概念和图表性指南,用以确定这些关键的违反情况。