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在诊断试验准确性系统评价中使用似然比散点矩阵确定定性效应量等级。

Determining qualitative effect size ratings using a likelihood ratio scatter matrix in diagnostic test accuracy systematic reviews.

作者信息

Rubinstein Matthew L, Kraft Colleen S, Parrott J Scott

机构信息

Department of Clinical Laboratory and Medical Imaging Sciences, Rutgers University, School of Health Professions, Newark, NJ, USA.

Department of Interdisciplinary Studies, Rutgers University, School of Health Professions, Newark, NJ, USA.

出版信息

Diagnosis (Berl). 2018 Nov 27;5(4):205-214. doi: 10.1515/dx-2018-0061.

Abstract

Background Diagnostic test accuracy (DTA) systematic reviews (SRs) characterize a test's potential for diagnostic quality and safety. However, interpreting DTA measures in the context of SRs is challenging. Further, some evidence grading methods (e.g. Centers for Disease Control and Prevention, Division of Laboratory Systems Laboratory Medicine Best Practices method) require determination of qualitative effect size ratings as a contributor to practice recommendations. This paper describes a recently developed effect size rating approach for assessing a DTA evidence base. Methods A likelihood ratio scatter matrix will plot positive and negative likelihood ratio pairings for DTA studies. Pairings are graphed as single point estimates with confidence intervals, positioned in one of four quadrants derived from established thresholds for test clinical validity. These quadrants support defensible judgments on "substantial", "moderate", or "minimal" effect size ratings for each plotted study. The approach is flexible in relation to a priori determinations of the relative clinical importance of false positive and false negative test results. Results and conclusions This qualitative effect size rating approach was operationalized in a recent SR that assessed effectiveness of test practices for the diagnosis of Clostridium difficile. Relevance of this approach to other methods of grading evidence, and efforts to measure diagnostic quality and safety are described. Limitations of the approach arise from understanding that a diagnostic test is not an isolated element in the diagnostic process, but provides information in clinical context towards diagnostic quality and safety.

摘要

背景 诊断试验准确性(DTA)系统评价(SRs)描述了一项试验在诊断质量和安全性方面的潜力。然而,在系统评价的背景下解释DTA指标具有挑战性。此外,一些证据分级方法(如疾病控制与预防中心实验室系统司实验室医学最佳实践方法)要求确定定性效应大小评级,作为实践建议的一个因素。本文介绍了一种最近开发的用于评估DTA证据基础的效应大小评级方法。方法 似然比散点矩阵将绘制DTA研究的阳性和阴性似然比配对。配对以带有置信区间的单点估计值进行绘制,位于从已确立的试验临床有效性阈值得出的四个象限之一中。这些象限支持对每个绘制研究的“实质性”、“中等”或“最小”效应大小评级做出合理判断。该方法在假阳性和假阴性试验结果的相对临床重要性的先验确定方面具有灵活性。结果与结论 这种定性效应大小评级方法在最近一项评估艰难梭菌诊断试验实践有效性的系统评价中得到了应用。描述了该方法与其他证据分级方法的相关性,以及为衡量诊断质量和安全性所做的努力。该方法的局限性源于这样一种认识,即诊断试验不是诊断过程中的一个孤立要素,而是在临床背景下为诊断质量和安全性提供信息。

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