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长期COVID的最低数据集的开发:一个Delphi研究协议

Adelaide Amah^1,2, Pawan Kumar², Hammed Ejalonibu^2,3

¹Research Department, Saskatchewan Health Authority, Saskatoon, Saskatchewan, Canada.

|November 28, 2024

概括

这项研究优先考虑了长期COVID护理,生活质量和症状的关键概念. 调查结果将为全国患者登记处提供信息,以标准化加拿大长期COVID患者的数据收集.

科学领域:

公共卫生公共卫生
医疗保健服务研究医疗服务研究
患者参与患者参与

背景情况:

之前的长期COVID研究集中在优先事项和定义上.
这项研究旨在通过涉及各方利益相关者,在现有工作的基础上进行构建.
为了标准化数据收集,需要建立长期COVID的国家患者登记册.

研究的目的:

优先考虑长期COVID的护理,生活质量和症状的概念.
为加拿大长期COVID国家患者登记册的发展提供信息.
建立标准化数据收集的最低数据集.

主要方法:

将与经历或与长期COVID工作的加拿大人进行Delphi过程.
100名不同的参与者将完成三轮匿名在线调查.
调查问题将优先确定注册表的核心数据点.

主要成果:

优先考虑与长期COVID护理,生活质量和症状相关的基本概念.
为标准化数据收集制定最低数据集.
关于国家长期COVID患者登记册的建议.

结论:

该研究将提供优先考虑的概念列表,以告知国家长期COVID患者登记册.
通过最低数据集进行标准化数据收集将改善对长期COVID的理解和管理.
通过出版物和会议传播发现将支持国家在长期COVID研究和护理方面的努力.

关键词:

后急性COVID-19综合征是什么登记处登记处登记处登记处研究设计研究研究设计在SARS-CoV-2感染.

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