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循证临床实践指南(CPGs)的制定:方法比较。

Development of evidence-based clinical practice guidelines (CPGs): comparing approaches.

机构信息

Centre for Clinical Effectiveness, Southern Health, Locked Bag 29, Clayton, Victoria, 3168, Australia.

出版信息

Implement Sci. 2008 Oct 27;3:45. doi: 10.1186/1748-5908-3-45.

Abstract

BACKGROUND

While the potential of clinical practice guidelines (CPGs) to support implementation of evidence has been demonstrated, it is not currently being achieved. CPGs are both poorly developed and ineffectively implemented. To improve clinical practice and health outcomes, both well-developed CPGs and effective methods of CPG implementation are needed. We sought to establish whether there is agreement on the fundamental characteristics of an evidence-based CPG development process and to explore whether the level of guidance provided in CPG development handbooks is sufficient for people using these handbooks to be able to apply it.

METHODS

CPG development handbooks were identified through a broad search of published and grey literature. Documents published in English produced by national or international organisations purporting to support development of evidence-based CPGs were included. A list of 14 key elements of a CPG development process was developed. Two authors read each handbook. For each handbook a judgement was made as to how it addressed each element; assigned as: 'mentioned and clear guidance provided', 'mentioned but limited practical detail provided ', or 'not mentioned'.

RESULTS

Six CPG development handbooks were included. These were produced by the Council of Europe, the National Health and Medical Research Council of Australia, the National Institute for Health and Clinical Excellence in the UK, the New Zealand Guidelines Group, the Scottish Intercollegiate Guideline Network, and the World Health Organization (WHO).There was strong concordance between the handbooks on the key elements of an evidence-based CPG development process. All six of the handbooks require and provide guidance on establishment of a multidisciplinary guideline development group, involvement of consumers, identification of clinical questions or problems, systematic searches for and appraisal of research evidence, a process for drafting recommendations, consultation with others beyond the guideline development group, and ongoing review and updating of the CPG.

CONCLUSION

The key elements of an evidence-based CPG development process are addressed with strong concordance by existing CPG development handbooks. Further research is required to determine why these key elements are often not addressed by CPG developers.

摘要

背景

虽然临床实践指南(CPG)在支持证据实施方面具有潜力,但目前尚未实现。CPG 的制定不够完善,实施效果也不佳。为了改善临床实践和健康结果,需要制定完善的 CPG 并采取有效的 CPG 实施方法。我们试图确定在循证 CPG 制定过程的基本特征方面是否存在共识,并探讨 CPG 制定手册中提供的指导水平是否足以让使用这些手册的人能够应用这些指导。

方法

通过广泛搜索已发表和灰色文献,确定了 CPG 制定手册。纳入了以支持循证 CPG 制定为目的、由国家或国际组织以英文出版的手册。制定了 CPG 制定过程的 14 个关键要素清单。两位作者阅读了每本手册。对于每本手册,都根据其如何处理每个要素进行了判断;分配为:“提及并有明确的指导”、“提及但提供的实用细节有限”或“未提及”。

结果

纳入了 6 本 CPG 制定手册,分别由欧洲理事会、澳大利亚国家卫生和医学研究委员会、英国国家卫生与临床优化研究所、新西兰指南小组、苏格兰校际指南网络和世界卫生组织(WHO)出版。这些手册在循证 CPG 制定过程的关键要素方面具有很强的一致性。这 6 本手册都要求并提供了关于建立多学科指南制定小组、纳入消费者、确定临床问题或问题、系统搜索和评估研究证据、起草建议的过程、与指南制定小组以外的人进行咨询、以及对 CPG 的持续审查和更新的指导。

结论

现有的 CPG 制定手册在循证 CPG 制定过程的关键要素方面具有很强的一致性。需要进一步研究为什么这些关键要素经常未被 CPG 制定者所考虑。

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