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迈向基于结果的分析性能规格框架:评估测量不确定度对临床结果影响的间接方法的方法学综述。

Toward a Framework for Outcome-Based Analytical Performance Specifications: A Methodology Review of Indirect Methods for Evaluating the Impact of Measurement Uncertainty on Clinical Outcomes.

机构信息

Test Evaluation Group, Academic Unit of Health Economics, University of Leeds, Leeds, UK;

NIHR Leeds In Vitro Diagnostic (IVD) Co-operative, Leeds, UK.

出版信息

Clin Chem. 2019 Nov;65(11):1363-1374. doi: 10.1373/clinchem.2018.300954. Epub 2019 Aug 23.

Abstract

BACKGROUND

For medical tests that have a central role in clinical decision-making, current guidelines advocate analytical performance specifications. Given that empirical (clinical trial-style) analyses are often impractical or unfeasible in this context, the ability to set such specifications is expected to rely on indirect studies to calculate the impact of test measurement uncertainty on downstream clinical, operational, and economic outcomes. Currently, however, a lack of awareness and guidance concerning available alternative indirect methods is limiting the production of outcome-based specifications. Therefore, our aim was to review available indirect methods and present an analytical framework to inform future outcome-based performance goals.

CONTENT

A methodology review consisting of database searches and extensive citation tracking was conducted to identify studies using indirect methods to incorporate or evaluate the impact of test measurement uncertainty on downstream outcomes (including clinical accuracy, clinical utility, and/or costs). Eighty-two studies were identified, most of which evaluated the impact of imprecision and/or bias on clinical accuracy. A common analytical framework underpinning the various methods was identified, consisting of 3 key steps: () calculation of "" test values; () calculation of test values (incorporating uncertainty); and () calculation of the of discrepancies between () and () on specified outcomes. A summary of the methods adopted is provided, and key considerations are discussed.

CONCLUSIONS

Various approaches are available for conducting indirect assessments to inform outcome-based performance specifications. This study provides an overview of methods and key considerations to inform future studies and research in this area.

摘要

背景

对于在临床决策中起核心作用的医学检验,目前的指南主张制定分析性能规范。鉴于在这种情况下进行经验(临床试验式)分析通常不切实际或不可行,因此,制定此类规范的能力预计将依赖于间接研究来计算检验测量不确定性对下游临床、运营和经济结果的影响。然而,目前,对于可用的替代间接方法缺乏认识和指导,限制了基于结果的规范的制定。因此,我们的目的是回顾现有的间接方法,并提出一个分析框架,为未来基于结果的性能目标提供信息。

内容

进行了一项方法学综述,包括数据库搜索和广泛的引文追踪,以确定使用间接方法来纳入或评估检验测量不确定性对下游结果(包括临床准确性、临床实用性和/或成本)影响的研究。确定了 82 项研究,其中大多数评估了不精密度和/或偏倚对临床准确性的影响。确定了一个支撑各种方法的共同分析框架,包括 3 个关键步骤:()计算“检验值;()计算(纳入不确定性)的检验值;以及()计算()和()在指定结果上差异的概率。提供了所采用方法的摘要,并讨论了关键考虑因素。

结论

有多种方法可用于进行间接评估,以提供基于结果的性能规范。本研究提供了方法和关键考虑因素的概述,以为该领域的未来研究提供信息。

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