Ebina-Shibuya Risa, Namkoong Ho, Horita Nobuyuki, Kato Hideaki, Hara Yu, Kobayashi Nobuaki, Kaneko Takeshi
Laboratory of Molecular Immunology, Immunology Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
J Thorac Dis. 2021 Jan;13(1):202-212. doi: 10.21037/jtd-20-2022.
Although the US government approved hydroxychloroquine (HCQ) and chloroquine (CQ) for hospitalized coronavirus disease 19 (COVID-19) patients, some studies denied efficacy of HCQ and CQ. We aimed to evaluate HCQ/CQ treatment for COVID-19.
Five databases were searched on April 15, 2020, without publication date restriction. We followed both Preferred Reporting Items for Systematic Reviews and Meta-analyses and Meta-analysis of Observational Studies in Epidemiology statement reporting recommendations. A random-model meta-analysis was conducted to pool odds ratio (OR) and hazard ratio (HR). The quality of evidence for each outcome and the final recommendation was assessed using the GRADE guidelines of the American College of Chest Physicians.
We identified four randomized controlled trials (RCTs) and four observational studies with 2,063 COVID-19 cases. All-cause mortality was not affected by the administration of HCQ/CQ [OR: 1.05, 95% confidence interval (CI): 0.53-2.09, P=0.89]. No improvement of viral clearance was found neither by time-to-event analysis (HR: 1.19, 95% CI: 0.74-1.94, P=0.47) nor frequency on day 7 (OR: 1.47, 95% CI: 0.33-6.63, P=0.62). HCQ/CQ treatment increased the risk of the any adverse event with OR of 3.56 (95% CI: 1.62-7.83, P=0.002).
HCQ/CQ failed to decrease the all-cause mortality (very low quality evidence) and did not improve viral clearance (low or very low quality evidence) but increased the risk of any adverse event (moderate quality evidence). Routine administration of HCQ/CQ for COVID-19 patients is not recommended (weak recommendation, Grade 2C).
尽管美国政府批准将羟氯喹(HCQ)和氯喹(CQ)用于住院的冠状病毒病19(COVID-19)患者,但一些研究否认了HCQ和CQ的疗效。我们旨在评估HCQ/CQ对COVID-19的治疗效果。
于2020年4月15日检索了五个数据库,无出版日期限制。我们遵循系统评价和Meta分析的首选报告项目以及流行病学观察性研究的Meta分析声明报告建议。进行随机模型Meta分析以汇总比值比(OR)和风险比(HR)。使用美国胸科医师学会的GRADE指南评估每个结局的证据质量和最终建议。
我们确定了四项随机对照试验(RCT)和四项观察性研究,共2063例COVID-19病例。HCQ/CQ的使用未影响全因死亡率[OR:1.05,95%置信区间(CI):0.53 - 2.09,P = 0.89]。无论是通过事件发生时间分析(HR:1.19,95%CI:0.74 - 1.94,P = 0.47)还是第7天的频率分析(OR:1.47,95%CI:0.33 - 6.63,P = 0.62),均未发现病毒清除情况有所改善。HCQ/CQ治疗增加了任何不良事件风险,OR为3.56(95%CI:1.62 - 7.83,P = 0.002)。
HCQ/CQ未能降低全因死亡率(极低质量证据),也未改善病毒清除情况(低或极低质量证据),但增加了任何不良事件风险(中等质量证据)。不建议对COVID-19患者常规使用HCQ/CQ(弱推荐,2C级)。