Qiu Ruijin, Han Songjie, Wei Xuxu, Zhong Changming, Li Min, Hu Jiayuan, Wang Pengqian, Zhao Chen, Chen Jing, Shang Hongcai
Key Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing, Beijing University of Chinese Medicine Affiliated Dongzhimen Hospital, Beijing, China.
Beijing University of Chinese Medicine Third Affiliated Hospital, Beijing, China.
Front Med (Lausanne). 2021 May 7;8:677068. doi: 10.3389/fmed.2021.677068. eCollection 2021.
To identify a minimum set of efficacy and adverse events for patients with acute heart failure (AHF) among different stakeholders in clinical trials of traditional Chinese medicine and Western medicine. First, we will develop a preliminary long list of outcomes that includes efficacy and adverse events/reactions via three steps: (i) systematic reviews of efficacy and safety outcomes for clinical trials of AHF; (ii) drugs included in the National Medical Insurance Catalog, the National Essential Medicines Catalog, and the WHO Essential Medicines List will be collected and safety outcomes extracted from the package inserts; and (iii) patients' or caregivers' semi-structured interviews will be carried out to add new viewpoints to the list. Second, after merging outcomes and grouping them under different outcome domains, questionnaires for health professionals and patients will be separately developed. Further, two rounds of Delphi survey for health professionals and a survey for patients and the public will be carried out. Third, different stakeholders will discuss and determine the final core outcome set (COS) for AHF in a consensus meeting. The entire project has been approved by the Ethics Committee of the main institution. After the final COS is developed, it will be published and discussed widely in conferences. This study is registered with the Core Outcome Measures in Effectiveness Trials database as study 1566 (available at: https://www.cometinitiative.org/Studies/Details/1566).
在中西医结合治疗急性心力衰竭(AHF)的临床试验中,确定不同利益相关者对AHF患者疗效和不良事件的最小数据集。首先,我们将通过三个步骤制定一份初步的结果长清单,包括疗效和不良事件/反应:(i)对AHF临床试验的疗效和安全性结果进行系统评价;(ii)收集纳入国家医保目录、国家基本药物目录和世界卫生组织基本药物清单的药物,并从药品说明书中提取安全性结果;(iii)对患者或护理人员进行半结构化访谈,为清单增添新观点。其次,合并结果并将其分组到不同的结果领域后,将分别为卫生专业人员和患者制定问卷。此外,将对卫生专业人员进行两轮德尔菲调查,并对患者和公众进行调查。第三,不同利益相关者将在共识会议上讨论并确定AHF的最终核心结局集(COS)。整个项目已获得主要机构伦理委员会的批准。最终的COS制定完成后,将在会议上广泛发表和讨论。本研究已在有效性试验核心结局指标数据库中注册,编号为1566(可在:https://www.cometinitiative.org/Studies/Details/1566获取)。