Managing therapeutic uncertainty in the COVID-19 pandemic: rapid evidence syntheses and transparent decision-making

Trudy D. Leong, Andy L. Gray, Tamara Kredo, Renee de Waal, Karen Cohen, Andy G. Parrish, Halima Dawood
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引用次数: 1

Abstract

The outbreak of the COVID-19 pandemic posed challenges to the practice of evidence-informed decision-making. Soon after the index case was identified in South Africa, the first local clinical guidelines were developed, reliant on preliminary evidence. Quick decisions were essential to inform practice and procurement at a time of exceptional global demand for medicine supply. This chapter describes how a rapid review mechanism was implemented to enable the development of evidence-informed and context-specific clinical treatment and prevention recommendations for COVID-19 in South Africa. The chapter reflects on the extent to which there is evidence for the implementation of these recommendations in clinical practice, using medicinesutilisation data from the public sector. In order to manage the ‘infodemic’ of research evidence of variable quality, a robust mechanism of rapid evidence review, transparent decision-making, and dissemination of trustworthy, accurate and context-specific recommendations was developed. Rapid evidence syntheses were produced by a sub-committee of the National Essential Medicines List Committee, supported by the South African GRADE Network and SAMRC Cochrane Centre. A generic rapid review protocol was developed, relying on GRADE principles and an evidence-to-decision framework. Consensus recommendations informed the National Department of Health/National Institute for Communicable Diseases clinical guidelines. Reviews were published on the National Department of Health website to advance transparency and were updated as new evidence emerged. Medicinesutilisation data showed increased use of corticosteroids, but there was also evidence of increased use of medicines not recommended. Further investment in technical capacity and support is needed to strengthen implementation, monitoring, and evaluation of clinical guidelines.
管理COVID-19大流行期间治疗的不确定性:快速证据合成和透明决策
2019冠状病毒病大流行的爆发对循证决策的做法提出了挑战。在南非发现指示病例后不久,根据初步证据制定了第一个当地临床指南。在全球药品供应需求异常之时,快速决策对于为实践和采购提供信息至关重要。本章描述了南非如何实施快速审查机制,以制定针对COVID-19的循证和具体情况的临床治疗和预防建议。本章使用来自公共部门的药物利用数据,反映了在临床实践中实施这些建议的证据的程度。为了管理不同质量的研究证据的“信息学术”,建立了一个强有力的机制,用于快速审查证据、透明决策和传播可信、准确和具体情况的建议。在南非GRADE网络和SAMRC科克伦中心的支持下,国家基本药物清单委员会的一个小组委员会制作了快速证据合成。根据GRADE原则和从证据到决策的框架,制定了通用的快速审查方案。共识建议通报了国家卫生部/国家传染病研究所的临床指南。审查结果在国家卫生部网站上公布,以提高透明度,并随着新证据的出现而更新。药物利用数据显示,皮质类固醇的使用有所增加,但也有证据表明,不推荐药物的使用有所增加。需要对技术能力和支持进行进一步投资,以加强临床指南的实施、监测和评估。
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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