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制定使用模拟患者方法进行研究报告的清单(CRiSP):一项共识研究。

Developing a checklist for reporting research using simulated patient methodology (CRiSP): a consensus study.

机构信息

Discipline of Pharmacy, The University of Western Australia, Crawley, Western Australia, Australia.

School of Allied Health, The University of Western Australia, Crawley, Western Australia, Australia.

出版信息

Int J Pharm Pract. 2021 May 25;29(3):218-227. doi: 10.1093/ijpp/riaa002.

Abstract

OBJECTIVES

Simulated patients are increasingly used to measure outcomes in health services but reporting is suboptimal. This study aims to create a checklist for the reporting of simulated patient (SP) methodology.

METHODS

This was a Delphi study. The authors of health service research studies using SP methodology were invited to participate. Round 1 questionnaire assessed the applicability of the TIDieR (Template for Intervention Description and Replication) reporting checklist for SP methodology and asked for rewording of/additional items. Responses were thematically analysed to generate Round 2 items in which participants rated each item for importance (seven-point Likert scale) and median, mode and IQR were calculated. In Round 3, participants were invited to rescore their Round 2 responses. Consensus was defined as an IQR ≤ 1 (Extremely important) and median ≤ 2 (Very important). All consensus items were considered for inclusion in the checklist. Similarly, worded items were rationalised and items not specific to SP methodology or other existing checklists were excluded.

KEY FINDINGS

Twenty-nine authors participated in Round 1 and a further seven for Rounds 2 and 3. Twenty-six responses were analysed for Round 1, 30 for Round 2 and 28 for Round 3. There was consensus on 29 of 54 items in Round 2 and 45 of 63 items in Round 3. The final checklist comprised 28 items.

CONCLUSIONS

A new reporting checklist to guide the reporting of studies, using simulated patients, complementary to CONSORT or STROBE, has been developed and will now be tested for usability.

摘要

目的

模拟患者越来越多地用于衡量医疗服务的结果,但报告情况并不理想。本研究旨在为模拟患者(SP)方法学的报告创建一个清单。

方法

这是一项德尔菲研究。邀请使用 SP 方法学的卫生服务研究的作者参与。第一轮问卷评估了 TIDieR(干预描述和复制模板)报告清单对 SP 方法学的适用性,并要求改写/添加项目。对答复进行主题分析,以生成第二轮的项目,参与者对每个项目的重要性进行评分(七点李克特量表),并计算中位数、模式和 IQR。在第三轮中,参与者被邀请重新评分第二轮的答复。一致性定义为 IQR≤1(非常重要)和中位数≤2(非常重要)。所有达成一致的项目都被认为包含在清单中。同样,对措辞相同的项目进行了合理化处理,并排除了不适用于 SP 方法学或其他现有清单的项目。

主要发现

29 位作者参加了第一轮,另外 7 位参加了第二轮和第三轮。第一轮分析了 26 次回复,第二轮分析了 30 次回复,第三轮分析了 28 次回复。第二轮有 29 项达成共识,第三轮有 45 项达成共识。最终清单包括 28 个项目。

结论

已经开发了一个新的报告清单,用于指导使用模拟患者的研究报告,补充 CONSORT 或 STROBE,现在将测试其可用性。

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