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首页> 外文期刊>Health expectations: an international journal of public participation in health care and health policy >Developing quality criteria for patient‐directed knowledge tools related to clinical practice guidelines. A development and consensus study
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Developing quality criteria for patient‐directed knowledge tools related to clinical practice guidelines. A development and consensus study

机译:为与临床实践指南相关的以患者为导向的知识工具制定质量标准。发展与共识研究

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Background Patient‐directed knowledge tools such as patient versions of guidelines and patient decision aids are increasingly developed to facilitate shared decision making. In this paper, we report how consensus was reached within the Netherlands on quality criteria for development, content and governance of these tools. Method A 12‐month development and consensus study. The consortium worked on four work packages: (a) reviewing existing criteria; (b) drafting the quality criteria; (c) safe‐guarding the acceptability and feasibility of the draft criteria by participatory research in on‐going tool development projects; and (d) gaining formal support from national stakeholders on the quality criteria. Results We reached consensus on a 8‐step guidance; describing minimal quality criteria for (a) the team composition; (b) setting the scope; (c) identifying needs; (d) the content and format; (e) testing the draft; (f) finalizing and approval; (g) dissemination and application, and (h) ownership and revision. The participants of the on‐going tool development projects were positive about the quality criteria in general, but divided as to the degree of detail. Whereas some expressed a clear desire for procedural standards, others felt that it would be sufficient to provide only general directions. Despite the different views as to the degree of detail, consensus was reached in three stakeholder meetings. Discussion We successfully collaborated with all stakeholders and achieved formal support from national stakeholders on a set of minimum criteria for the development process, content and governance of patient‐directed knowledge tools.
机译:背景技术以患者为导向的知识工具(例如患者版本的指南和患者决策辅助工具)正在不断发展,以促进共同的决策制定。在本文中,我们报告了荷兰内部如何就这些工具的开发,内容和治理的质量标准达成共识。方法一个为期12个月的开发和共识研究。该财团制定了四个工作包:(a)审查现有标准; (b)起草质量标准; (c)通过正在进行的工具开发项目中的参与性研究来维护标准草案的可接受性和可行性; (d)在质量标准上获得国家利益相关者的正式支持。结果我们就8步指南达成了共识;描述(a)团队组成的最低质量标准; (b)确定范围; (c)确定需求; (d)内容和格式; (e)测试草案; (f)敲定并批准; (g)传播和应用,以及(h)所有权和修订。正在进行的工具开发项目的参与者总体上对质量标准持肯定态度,但在细节程度上存在分歧。尽管有些人对程序标准表达了明确的要求,但其他人则认为仅提供一般性指导就足够了。尽管对详细程度存在不同意见,但在三个利益相关者会议上达成了共识。讨论我们成功地与所有利益相关者合作,并获得了国家利益相关者的正式支持,以一套针对患者导向的知识工具的开发过程,内容和治理的最低标准。

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