Jin Xinyao, Pang Bo, Zhang Junhua, Liu Qingquan, Yang Zhongqi, Feng Jihong, Liu Xuezheng, Zhang Lei, Wang Baohe, Huang Yuhong, Josephine Fauci Alice, Ma Yuling, Soo Lee Myeong, Yuan Wei'an, Xie Yanming, Tang Jianyuan, Gao Rui, Du Liang, Zhang Shuo, Qi Hanmei, Sun Yu, Zheng Wenke, Yang Fengwen, Chua Huizi, Wang Keyi, Ou Yi, Huang Ming, Zhu Yan, Yu Jiajie, Tian Jinhui, Zhao Min, Hu Jingqing, Yao Chen, Li Youping, Zhang Boli
Evidence-Based Medicine Center, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China.
Chinese Clinical Trials Core Outcome Set Research Center, Tianjin 301617, China.
Engineering (Beijing). 2020 Oct;6(10):1147-1152. doi: 10.1016/j.eng.2020.03.002. Epub 2020 Mar 18.
Since its outbreak in December 2019, a series of clinical trials on coronavirus disease 2019 (COVID-19) have been registered or carried out. However, the significant heterogeneity and less critical outcomes of such trials may be leading to a waste of research resources. This study aimed to develop a core outcome set (COS) for clinical trials on COVID-19 in order to tackle the outcome issues. The study was conducted according to the Core Outcome Measures in Effectiveness Trials (COMET) Handbook: Version 1.0, a guideline for COS development. A research group was set up that included experts in respiratory and critical medicine, traditional Chinese medicine (TCM), evidence-based medicine, clinical pharmacology, and statistics, in addition to medical journal editors. Clinical trial registry websites (www.chictr.org.cn and clinicaltrials.gov) were searched to retrieve clinical trial protocols and outcomes in order to form an outcome pool. A total of 78 clinical trial protocols on COVID-19 were included and 259 outcomes were collected. After standardization, 132 outcomes were identified within seven different categories, of which 58 were selected to develop a preliminary outcome list for further consensus. After two rounds of Delphi survey and one consensus meeting, the most important outcomes for the different clinical classifications of COVID-19 were identified and determined to constitute the COS for clinical trials on COVID-19 (COS-COVID). The COS-COVID includes one outcome for the mild type (time to 2019 novel coronavirus (2019-nCoV) reverse transcription-polymerase chain reaction (RT-PCR) negativity), four outcomes for the ordinary type (length of hospital stay, composite events, score of clinical symptoms, and time to 2019-nCoV RT-PCR negativity), five outcomes for the severe type (composite events, length of hospital stay, arterial oxygen partial pressure (PaO)/fraction of inspired oxygen (FiO), duration of mechanical ventilation, and time to 2019-nCoV RT-PCR negativity), one outcome for critical type (all-cause mortality), and one outcome for rehabilitation period (pulmonary function). The COS-COVID is currently the most valuable and practical clinical outcome set for the evaluation of intervention effect, and is useful for evidence assessment and decision-making. With a deepening understanding of COVID-19 and application feedback, the COS-COVID should be continuously updated.
自2019年12月爆发以来,针对2019冠状病毒病(COVID-19)已开展了一系列临床试验登记或试验。然而,这些试验显著的异质性和不太关键的结果可能导致研究资源的浪费。本研究旨在制定COVID-19临床试验的核心结局集(COS),以解决结局问题。该研究按照有效性试验核心结局指标(COMET)手册:第1.0版(COS制定指南)进行。成立了一个研究小组,成员包括呼吸与重症医学、中医、循证医学、临床药理学和统计学领域的专家,以及医学期刊编辑。检索临床试验注册网站(www.chictr.org.cn和clinicaltrials.gov)以获取临床试验方案和结局,从而形成一个结局库。共纳入78项COVID-19临床试验方案,收集到259个结局。标准化后,在七个不同类别中确定了132个结局,从中选择58个制定初步结局清单以进一步达成共识。经过两轮德尔菲调查和一次共识会议,确定了COVID-19不同临床分类的最重要结局,并确定其构成COVID-19临床试验的COS(COS-COVID)。COS-COVID包括轻型的1个结局(新型冠状病毒2019(2019-nCoV)逆转录-聚合酶链反应(RT-PCR)转阴时间)、普通型的4个结局(住院时间、复合事件、临床症状评分、2019-nCoV RT-PCR转阴时间)、重型的5个结局(复合事件、住院时间、动脉血氧分压(PaO)/吸入氧分数(FiO)、机械通气时间、2019-nCoV RT-PCR转阴时间)、危重型的1个结局(全因死亡率)以及康复期的1个结局(肺功能)。COS-COVID是目前评估干预效果最有价值、最实用的临床结局集,有助于证据评估和决策制定。随着对COVID-19认识的深入和应用反馈,COS-COVID应不断更新。