评估两种涉及残疾患者的方法在制定临床指南中的可接受性、可行性和结果:交叉试点研究。

Q2 Medicine
Marie-Eve Lamontagne, Marie-Pierre Gagnon, Kadija Perreault, Véronique Gauthier
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引用次数: 0

摘要

背景:让患者和公众参与临床实践指南(CPG)的制定被认为对指南质量有重大贡献,但各种共同设计策略的优势尚未得到实证比较,因此很难选择一种策略。目的:本初步研究旨在探讨两种患者参与CPG概述的可接受性、可行性和结果。方法:对外伤性脑损伤患者进行单盲交叉实用研究。患者试验了两种产生临床实践建议的替代方法(即,讨论组和wiki)。参与者对两种方法的可接受性进行评分,并使用完成两种方法的参与者人数和所需支持干预的数量等指标评估可行性。对该方法不知情的专家独立地对参与者的结果建议的清晰度、准确性、适当性和有用性进行评级。结果:我们招募了20名参与者,其中16人完成了研究。两种方法的可接受性几乎没有变化,定性评论表达了对焦点小组的社会性质的轻微偏好。因此,让患者参与CPG开发的两种方法似乎都是可行的,专家对改编后的建议的意见都是积极的,尽管通过焦点小组提出的建议被认为与支持临床实践更相关。结论:我们的研究结果证实了焦点小组和wiki让创伤性脑损伤患者参与临床实践指南制作的可接受性和可行性。本研究为科学文献做出了贡献,表明这两种方法是可接受的、可行的,并产生了积极的结果。试验注册:ClinicalTrials.gov NCT02023138;https://clinicaltrials.gov/ct2/show/NCT02023138。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluating the Acceptability, Feasibility, and Outcomes of Two Methods Involving Patients With Disability in Developing Clinical Guidelines: Crossover Pilot Study.

Evaluating the Acceptability, Feasibility, and Outcomes of Two Methods Involving Patients With Disability in Developing Clinical Guidelines: Crossover Pilot Study.

Background: Engaging patients and the public in clinical practice guideline (CPG) development is believed to contribute significantly to guideline quality, but the advantages of the various co-design strategies have not been empirically compared, making it difficult to choose one strategy over another.

Objective: This pilot study aims to document the acceptability, feasibility, and outcomes of 2 methods of involving patients in outlining CPG.

Methods: A single-blind crossover pragmatic study was performed with patients with traumatic brain injury. The patients experimented with 2 alternative methods of producing clinical practice recommendations (ie, a discussion group and a wiki). The participants rated the acceptability of the 2 methods, and feasibility was assessed using indicators, such as the number of participants who completed the 2 methods and the number of support interventions required. Experts, blinded to the method, independently rated the participants' outcome recommendations for clarity, accuracy, appropriateness, and usefulness.

Results: We recruited 20 participants, and 16 completed the study. The acceptability of the 2 methods showed little variation, with qualitative comments expressing a slight preference for the social nature of focus groups. Thus, both methods of involving patients in CPG development appeared feasible, and the experts' opinions of the adapted recommendations were both positive, although the recommendations produced through focus groups were deemed more relevant to support clinical practice.

Conclusions: Our results confirm the acceptability and feasibility of focus groups and wikis to allow patients with traumatic brain injury to participate in clinical practice guideline production. This study contributes to the scientific literature by suggesting that the 2 methods were acceptable, feasible, and produced positive outcomes.

Trial registration: ClinicalTrials.gov NCT02023138; https://clinicaltrials.gov/ct2/show/NCT02023138.

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来源期刊
Journal of Participatory Medicine
Journal of Participatory Medicine Medicine-Medicine (miscellaneous)
CiteScore
3.20
自引率
0.00%
发文量
8
审稿时长
12 weeks
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