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基于社区的双相情感障碍试验中核心结局集的制定:一项定性研究和改良 Delphi 法。

Development of a core outcome set for use in community-based bipolar trials-A qualitative study and modified Delphi.

机构信息

Centre for Patient Reported Outcomes Research (CPROR), Institute of Applied Health Research, and Birmingham Health Partners Centre for Regulatory Science and Innovation, University of Birmingham, Birmingham, United Kingdom.

The McPin Foundation, London, United Kingdom.

出版信息

PLoS One. 2020 Oct 28;15(10):e0240518. doi: 10.1371/journal.pone.0240518. eCollection 2020.

Abstract

BACKGROUND

A core outcome set (COS) is a standardised collection of outcomes to be collected and reported in all trials within a research area. A COS can reduce reporting bias and facilitate evidence synthesis. This is currently unavailable for use in community-based bipolar trials. This research aimed to develop such a COS, with input from a full range of stakeholders.

METHODS

A co-production approach was used throughout. A longlist of outcomes was derived from focus groups with people with a bipolar diagnosis and carers, interviews with healthcare professionals and a rapid review of outcomes listed in bipolar trials on the Cochrane database. An expert panel with personal and/or professional experience of bipolar participated in a modified Delphi process and the COS was finalised at a consensus meeting.

RESULTS

Fifty participants rated the importance of each outcome. Sixty-six outcomes were included in Round 1 of the questionnaire; 13 outcomes were added by Round 1 participants and were rated in Round 2. Seventy-six percent of participants (n = 38) returned to Round 2 and 60 outcomes, including 4 outcomes added by participants in Round 1, received a rating of 7-9 by >70% and 1-3 by <25% of the sample. Fourteen participants finalised a COS containing 11 outcomes at the consensus meeting: personal recovery; connectedness; clinical recovery of bipolar symptoms; mental health and wellbeing; physical health; self-monitoring and management; medication effects; quality of life; service outcomes; experience of care; and use of coercion.

CONCLUSIONS

This COS is recommended for use in community-based bipolar trials to ensure stakeholder-relevant outcomes, facilitate data synthesis, and transparent reporting. The COS includes guidance notes for each outcome to allow the identification of suitable measurement instruments. Further validation is recommended for use with a wide range of communities and to achieve standardised measurement.

摘要

背景

核心结局集(COS)是一套标准化的结局集合,旨在在研究领域内的所有试验中收集和报告。COS 可以减少报告偏倚并促进证据综合。目前,在基于社区的双相情感障碍试验中尚未使用。本研究旨在通过广泛的利益相关者的参与,开发这样一个 COS。

方法

在整个研究过程中采用了共同制定的方法。通过对有双相诊断和照顾者的人进行焦点小组讨论、对医疗保健专业人员进行访谈以及对 Cochrane 数据库中列出的双相情感障碍试验的快速审查,得出了一份长名单的结局。一个具有双相情感障碍个人和/或专业经验的专家小组参与了一项修改后的 Delphi 流程,COS 在共识会议上最终确定。

结果

五十名参与者对每个结局的重要性进行了评分。第一轮问卷包括 66 个结局;第一轮参与者增加了 13 个结局,并在第二轮进行了评分。76%的参与者(n=38)返回第二轮,60 个结局,包括第一轮参与者增加的 4 个结局,得到了>70%的参与者的 7-9 分,而<25%的参与者的得分在 1-3 分之间。十四名参与者在共识会议上最终确定了包含 11 个结局的 COS:个人康复;联系;双相症状的临床康复;心理健康和幸福感;身体健康;自我监测和管理;药物效果;生活质量;服务结局;护理体验;以及使用强制手段。

结论

这个 COS 推荐在基于社区的双相情感障碍试验中使用,以确保相关的利益相关者结局,促进数据综合和透明报告。COS 包括每个结局的指导说明,以允许识别合适的测量工具。建议进一步验证该 COS 在广泛的社区中的使用情况,并实现标准化测量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac8c/7592842/0266198356be/pone.0240518.g001.jpg

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