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Study Sensitivity: Evaluating the Ability to Detect Effects in Systematic Reviews of Chemical Exposures

机译:研究敏感性:评估在化学暴露的系统评价中检测效应的能力

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摘要

A critical step in systematic reviews of potential health hazards is the structured evaluation of the strengths and weaknesses of the included studies; risk of bias is a term often used to represent this process, specifically with respect to the evaluation of systematic errors that can lead to inaccurate (biased) results (i.e. focusing on internal validity). Systematic review methods developed in the clinical medicine arena have been adapted for use in evaluating environmental health hazards; this expansion raises questions about the scope of risk of bias tools and the extent to which they capture the elements that can affect the interpretation of results from environmental and occupational epidemiology studies and in vivo animal toxicology studies, (the studies typically available for assessment of risk of chemicals). One such element, described here as “sensitivity”, is a measure of the ability of a study to detect a true effect or hazard. This concept is similar to the concept of the sensitivity of an assay; an insensitive study may fail to show a difference that truly exists, leading to a false conclusion of no effect. Factors relating to study sensitivity should be evaluated in a systematic manner with the same rigor as the evaluation of other elements within a risk of bias framework. We discuss the importance of this component for the interpretation of individual studies, examine approaches proposed or in use to address it, and describe how it relates to other evaluation components. The evaluation domains contained within a risk of bias tool can include, or can be modified to include, some features relating to study sensitivity; the explicit inclusion of these sensitivity criteria with the same rigor and at the same stage of study evaluation as other bias-related criteria can improve the evaluation process. In some cases, these and other features may be better addressed through a separate sensitivity domain. The combined evaluation of risk of bias and sensitivity can be used to identify the most informative studies, to evaluate the confidence of the findings from individual studies and to identify those study elements that may help to explain heterogeneity across the body of literature.
机译:系统审查潜在健康危害的关键步骤是对纳入研究的优缺点进行结构化评估;偏见风险是一个经常用来表示此过程的术语,尤其是在评估可能导致不准确(偏见)结果(即专注于内部有效性)的系统错误方面。临床医学领域开发的系统评价方法已被用于评估环境健康危害。这种扩展引发了有关偏倚工具风险范围以及它们在多大程度上捕获可能影响环境和职业流行病学研究以及体内动物毒理学研究结果解释的要素的问题(这些研究通常可用于评估风险)化学药品)。一个这样的要素,在这里被描述为“敏感性”,是对一项研究发现真实影响或危害的能力的一种度量。这个概念类似于测定灵敏度的概念。不敏感的研究可能无法显示出确实存在的差异,从而导致无效的错误结论。与研究敏感性相关的因素应与偏倚风险框架内的其他要素的评估一样严格地系统评估。我们讨论了该组件对单个研究的解释的重要性,研究了提出或正在使用的解决方法,并描述了它与其他评估组件的关系。偏倚风险工具中包含的评估域可以包括或可以修改为包括与研究敏感性相关的某些功能;与其他与偏倚相关的标准一样,以相同的严格度和相同的研究评估阶段明确包含这些敏感性标准可以改善评估过程。在某些情况下,可以通过单独的灵敏度域更好地解决这些和其他功能。偏倚风险和敏感性风险的综合评估可用于识别最有用的研究,评估单个研究结果的置信度,并识别可有助于解释整个文献异质性的那些研究要素。

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