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Common issues raised during the quality assurance process of WHO guidelines: a cross-sectional study

机译:在世卫组织指导方针的质量保证过程中提出的常见问题:横断面研究

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In 2007, WHO established the Guidelines Review Committee (GRC) to ensure that WHO guidelines adhere to the highest international standards. The GRC reviews guideline proposals and final guidelines. The objectives of this study were to examine the rates of and reasons for conditional approval and non-approval of documents submitted for the first time to the GRC, and calculate the time intervals and numbers of submissions to achieve approval for documents conditionally approved or not approved at first submission. All initial submissions to the GRC between 2014 and 2017 were examined. Data were extracted from the GRC's records of written comments and discussions. Of a total of 85 proposals and 88 final guidelines, 32 (37.6%) proposals and 37 (42.0%) final guidelines were conditionally approved, and 15 (17.6%) proposals and 28 (31.8%) final guidelines were not. For both conditionally approved and not approved proposals, the most frequent reasons were suboptimal composition or inadequate description of the guideline contributor groups (in all proposals), followed by inadequate formulation of key questions (in 90.6% of conditionally approved proposals and all not approved proposals). For both conditionally approved and not approved final guidelines, the most frequent reasons were problems with recommendations (in all final guidelines), followed by inappropriate methods for evidence retrieval or an inadequate description thereof (in all conditionally approved final guidelines and 75.0% of not approved final guidelines). The median time to achieve approval was 2 months for proposals and 1-2 months for final guidelines. The median number of submissions was 2 for proposals and 2-2.5 for final guidelines. The GRC implements a rigorous quality assurance process and identifies problems with a significant percentage of initial submissions. WHO needs to continuously evaluate its guideline development processes to inform effective quality improvement measures and optimise the quality of its guidelines.
机译:2007年,世卫组织建立了指导方针审查委员会(GRC),以确保世卫组织指导方针遵守最高的国际标准。 GRC评论指南提案和最终指南。本研究的目标是审查条件批准的率和原因,并不批准首次向GRC提交的文件,并计算出于有条件批准或未批准的文件批准的提交时间间隔和数量首先提交。审查了2014年至2017年间GRC的所有初步提交。从GRC的书面评论和讨论记录中提取数据。共有85个提案和88个最终指南,32个(37.6%)提案和37(42.0%)最终指南有条件批准,15(17.6%)提案和28(31.8%)的最终指南并非如此。对于有条件批准和未批准的提案,最常见的原因是次优构图或对指南贡献者群体的描述(在所有提案中)的描述,其次是对关键问题的不足(在90.6%的有条件批准的提案中,并非批准的提案) )。对于有条件批准和未批准的最终指导方针,最常见的原因是建议(在所有最终指南中)的问题,其次是证据检索的不适当的方法或其不足的描述(在所有有条件批准的最终指南和75.0%的未经批准的75.0%)最终指南)。达到批准的中位时间为建议和最终指南的1-2个月为2个月。提交的中位数为2次提案,最终指南为2-2.5。 GRC实现了严格的质量保证过程,并确定了初始提交百分比的问题。谁需要不断评估其指导发展流程,以提供有效的质量改进措施,并优化其指导方针的质量。

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