Fostering Shared Decision-Making Between Patients and Health Care Professionals in Clinical Practice Guidelines: Protocol for a Project to Develop and Test a Tool for Guideline Developers.

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
Lena Fischer, Fülöp Scheibler, Corinna Schaefer, Torsten Karge, Thomas Langer, Leon Vincent Schewe, Ivan D Florez, Andrew Hutchinson, Sheyu Li, Marta Maes-Carballo, Zachary Munn, Lilisbeth Perestelo-Perez, Livia Puljak, Anne Stiggelbout, Dawid Pieper
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引用次数: 0

Abstract

Background: Clinical practice guidelines (CPGs) are designed to assist health care professionals in medical decision-making, but they often lack effective integration of shared decision-making (SDM) principles to reflect patient values and preferences, particularly in the context of preference-sensitive CPG recommendations. To address this shortcoming and foster SDM through CPGs, the integration of patient decision aids (PDAs) into CPGs has been proposed as an important strategy. However, methods for systematically identifying and prioritizing CPG recommendations relevant to SDM and related decision support tools are currently lacking.

Objective: The aim of the project is to develop (1) a tool for systematically identifying and prioritizing CPG recommendations for which SDM is considered particularly relevant and (2) a platform for PDAs to support practical SDM implementation.

Methods: The project consists of 6 work packages (WPs). It is embedded in the German health care context but has an international focus. In WP 1, we will conduct a scoping review in bibliographic databases and gray literature sources to identify methods used to foster SDM via PDAs in the context of CPGs. In WP 2, we will conduct semistructured interviews with CPG experts to better understand the concepts of preference sensitivity and identify strategies for fostering SDM through CPGs. WP 3, a modified Delphi study including surveys and focus groups with SDM experts, aims to define and operationalize preference sensitivity. Based on the results of the Delphi study, we will develop a methodology for prioritizing key questions in CPGs. In WP 4, the tool will be developed. A list of relevant items to identify CPG recommendations for which SDM is most relevant will be created, tested, and iteratively refined, accompanied by the development of a user manual. In WP 5, a platform for creating and digitizing German-language PDAs will be developed to support the practical application of SDM during clinical encounters. WP 6 will conclude the project by testing the tool with newly developed and revised CPGs.

Results: The Brandenburg Medical School Ethics Committee approved the project (165122023-ANF). An international multidisciplinary advisory board is involved to guide the tool development on CPGs and SDM. Patient partners are involved throughout the project, considering the essential role of the patient perspective in SDM. As of February 20, 2024, we are currently assessing literature references to determine eligibility for inclusion in the scoping review (WP 1). We expect the project to be completed by December 31, 2026.

Conclusions: The tool will enable CPG developers to systematically incorporate aspects of SDM into CPG development, thereby providing guideline-based support for the patient-practitioner interaction. Together, the tool for CPGs and the platform for PDAs will create a systematic link between CPGs, SDM, and PDAs, which may facilitate SDM in clinical practice.

International registered report identifier (irrid): DERR1-10.2196/57611.

在临床实践指南中促进患者与医护人员共同决策:为指南制定者开发和测试工具的项目协议》(Protocol for a Project to Develop and Test a Tool for Guideline Developers)。
背景:临床实践指南(CPG)旨在协助医护人员进行医疗决策,但往往缺乏对共同决策(SDM)原则的有效整合,以反映患者的价值观和偏好,尤其是在对偏好敏感的 CPG 建议方面。为解决这一缺陷并通过 CPGs 促进 SDM,将患者决策辅助工具(PDAs)整合到 CPGs 中已被作为一项重要战略提出。然而,目前还缺乏系统识别和优先考虑与 SDM 相关的 CPG 建议和相关决策支持工具的方法:该项目的目标是开发(1)一种工具,用于系统地识别与 SDM 特别相关的 CPG 建议并对其进行优先排序;(2)一个 PDA 平台,以支持 SDM 的实际实施:该项目包括 6 个工作包(WPs)。方法:该项目由 6 个工作包(WPs)组成,既立足于德国的医疗环境,又着眼于国际。在 WP 1 中,我们将对文献数据库和灰色文献来源进行范围审查,以确定在 CPG 的背景下通过 PDA 促进 SDM 的方法。在工作方案 2 中,我们将对 CPG 专家进行半结构式访谈,以更好地理解偏好敏感性的概念,并确定通过 CPG 促进 SDM 的策略。第 3 工作组是一项经过修改的德尔菲研究,包括对 SDM 专家进行调查和焦点小组讨论,旨在定义偏好敏感性并使其具有可操作性。在德尔菲研究结果的基础上,我们将制定一种方法,用于确定国家方案指导文件中关键问题的优先次序。在工作方案 4 中,将开发该工具。我们将创建、测试和反复改进相关项目清单,以确定 SDM 最为相关的 CPG 建议,同时编制用户手册。在第 5 工作组中,将开发一个用于创建和数字化德语 PDA 的平台,以支持 SDM 在临床会诊中的实际应用。第 6 工作组将在项目结束时使用新开发和修订的 CPGs 对该工具进行测试:勃兰登堡医学院伦理委员会批准了该项目(165122023-ANF)。国际多学科咨询委员会参与指导 CPGs 和 SDM 工具的开发。考虑到患者视角在 SDM 中的重要作用,患者合作伙伴参与了整个项目。截至 2024 年 2 月 20 日,我们正在评估文献参考资料,以确定是否有资格纳入范围界定审查(WP 1)。我们预计该项目将于 2026 年 12 月 31 日前完成:该工具将使 CPG 开发人员能够系统地将 SDM 的各个方面纳入 CPG 开发,从而为患者与医生之间的互动提供基于指南的支持。CPG工具和PDA平台将在CPG、SDM和PDA之间建立系统联系,从而促进临床实践中的SDM:DERR1-10.2196/57611。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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