Suppr超能文献

诊断准确性研究质量评估方法的开发与验证

Development and validation of methods for assessing the quality of diagnostic accuracy studies.

作者信息

Whiting P, Rutjes A W S, Dinnes J, Reitsma J, Bossuyt P M M, Kleijnen J

机构信息

Centre for Reviews and Dissemination, University of York, UK.

出版信息

Health Technol Assess. 2004 Jun;8(25):iii, 1-234. doi: 10.3310/hta8250.

Abstract

OBJECTIVES

To develop a quality assessment tool which will be used in systematic reviews to assess the quality of primary studies of diagnostic accuracy.

DATA SOURCES

Electronic databases including MEDLINE, EMBASE, BIOSIS and the methodological databases of both CRD and the Cochrane Collaboration.

REVIEW METHODS

Three systematic reviews were conducted to provide an evidence base for the development of the quality assessment tool. A Delphi procedure was used to develop the quality assessment tool and the information provided by the reviews was incorporated into this. A panel of nine experts in the area of diagnostic accuracy studies took part in the Delphi procedure to agree on the items to be included in the tool. Panel members were also asked to provide feedback on various other items and whether they would like to see the development of additional topic and design specific items. The Delphi procedure produced the quality assessment tool, named the QUADAS tool, which consisted of 14 items. A background document was produced describing each item included in the tool and how each of the items should be scored.

RESULTS

The reviews produced 28 possible items for inclusion in the quality assessment tool. It was found that the sources of bias supported by the most empirical evidence were variation by clinical and demographic subgroups, disease prevalence/severity, partial verification bias, clinical review bias and observer/instrument variation. There was also some evidence of bias for the effects of distorted selection of participants, absent or inappropriate reference standard, differential verification bias and review bias. The evidence for the effects of other sources of bias was insufficient to draw conclusions. The third review found that only one item, the avoidance of review bias, was included in more than 75% of tools. Spectrum composition, population recruitment, absent or inappropriate reference standard and verification bias were each included in 50-75% of tools. Other items were included in less than 50% of tools. The second review found that the quality assessment tool should have the potential to be discussed narratively, reported in a tabular summary, used as recommendations for future research, used to conduct sensitivity or regression analyses and used as criteria for inclusion in the review or a primary analysis. This suggested that some distinction is needed between high- and low-quality studies. Component analysis was considered the best approach to incorporate quality into systematic reviews of diagnostic studies and this was taken into consideration when developing the tool.

CONCLUSIONS

This project produced an evidence-based quality assessment tool to be used in systematic reviews of diagnostic accuracy studies. Through the various stages of the project the current lack of such a tool and the need for a systematically developed validated tool were demonstrated. Further work to validate the tool continues beyond the scope of this project. The further development of the tool by the addition of design- and topic-specific criteria is proposed.

摘要

目的

开发一种质量评估工具,用于系统评价中评估诊断准确性的原始研究的质量。

数据来源

电子数据库,包括MEDLINE、EMBASE、BIOSIS以及CRD和Cochrane协作网的方法学数据库。

综述方法

进行了三项系统评价,为质量评估工具的开发提供证据基础。采用德尔菲法开发质量评估工具,并将评价提供的信息纳入其中。由九名诊断准确性研究领域的专家组成的小组参与了德尔菲法,以商定工具中应包含的条目。还要求小组成员对其他各种条目以及是否希望看到开发更多特定主题和设计的条目提供反馈。德尔菲法产生了名为QUADAS工具的质量评估工具,该工具由14个条目组成。编制了一份背景文件,描述工具中包含的每个条目以及每个条目应如何评分。

结果

评价产生了28个可能纳入质量评估工具的条目。发现有最多实证证据支持的偏倚来源是临床和人口亚组的差异、疾病患病率/严重程度、部分验证偏倚、临床审查偏倚以及观察者/仪器差异。也有一些证据表明存在因参与者选择扭曲、缺乏或不适当的参考标准、差异验证偏倚和审查偏倚而产生的偏倚。其他偏倚来源的影响证据不足以得出结论。第三次评价发现,只有一个条目,即避免审查偏倚,在超过75%的工具中被纳入。谱构成、人群招募、缺乏或不适当的参考标准以及验证偏倚在50%-75%的工具中被纳入。其他条目在不到50%的工具中被纳入。第二次评价发现,质量评估工具应具有进行叙述性讨论、以表格汇总形式报告、用作未来研究建议、用于进行敏感性或回归分析以及用作纳入评价或初步分析的标准的潜力。这表明需要区分高质量和低质量研究。成分分析被认为是将质量纳入诊断研究系统评价的最佳方法,在开发工具时已考虑到这一点。

结论

本项目产生了一种基于证据的质量评估工具,用于诊断准确性研究的系统评价。通过项目的各个阶段,证明了目前缺乏这样一种工具以及需要一个系统开发的经过验证的工具。在本项目范围之外,验证该工具的进一步工作仍在继续。建议通过增加特定设计和主题的标准来进一步开发该工具。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验