低剂量艾美汀治疗COVID-19患者的临床疗效:一项现实世界研究

Q4 Biochemistry, Genetics and Molecular Biology
Journal of BioX Research Pub Date : 2021-06-01 Epub Date: 2020-12-03 DOI:10.1097/JBR.0000000000000076
Song Fan, Qi Zhen, Cheng Chen, Wenjun Wang, Qibing Wu, Huihui Ma, Chengyuan Zhang, Li Zhang, Baojing Lu, Huiyao Ge, Liang Yong, Bao Li, Yafen Yu, Weiwei Chen, Yiwen Mao, Guangbo Qu, Li Su, Aoli Wang, Zhen Ding, Haiwen Li, Jin Zhang, Yonglian Wang, Yufeng Gao, Xihai Xu, Zhongming Zhu, Jun Chen, Long Zhang, Hongqiang Liang, Song Wu, Meng Huang, Quan Xia, Ping Li, Yehuan Sun, Chaozhao Liang, Wei Wei, Qingsong Liu, Liangdan Sun
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引用次数: 12

摘要

目的:Emetine是一种在肺中高浓度富集的异喹啉生物碱,在体外显示出抗严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的有效活性。本研究的目的是更好地了解低剂量艾美汀对2019冠状病毒病(COVID-19)患者的有效性。方法:本研究于2020年2 - 3月在中国安徽省武汉市方仓方舱医院和5家COVID-19定点医院招募63例轻症或普通COVID-19患者。选取武汉市方仓方舱医院39例患者为务实随机对照临床试验,选取安徽省5家新冠肺炎定点医院24例患者为现实研究。艾美汀疗程均小于10天。观察并记录所有患者的主要症状及不良反应。主要结局指标是第10天出现SARS-CoV-2 RNA阴性结果所需的时间或阴性结果率。次要结果包括腋窝温度、经皮氧饱和度和呼吸频率恢复。本研究已于2019年2月20日获得安徽医科大学第一附属医院伦理委员会批准(批准号:PJ2020-03-19),已于2019年2月20日在中国临床试验注册中心注册(注册号:ChiCTR2000030022)。结果:在方仓方舱医院就诊的患者入组后第1天,治疗组血氧饱和度高于对照组。方仓方舱医院患者腋下体温、呼吸频率、血氧饱和度与干预措施的时间效应相关,与干预措施无关。安徽省定点医院患者的呼吸频率和血氧饱和度与干预措施有关,但与时间效果无关。安徽省定点医院患者腋窝体温与时间效应相关,与干预措施无关。结论:我们的初步研究显示,小剂量艾美汀联合基础常规抗病毒药物可改善轻、普通COVID-19患者的临床症状,且无明显不良反应,提示适度增加艾美汀剂量可能具有良好的治疗和预防潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical efficacy of low-dose emetine for patients with COVID-19: a real-world study.

Clinical efficacy of low-dose emetine for patients with COVID-19: a real-world study.

Objective: Emetine, an isoquinoline alkaloid that is enriched at high concentrations in the lung, has shown potent in vitro activity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The aim of this study was to better understand the effectiveness of low-dose emetine for patients with coronavirus disease 2019 (COVID-19).

Methods: In this real-world study, 63 patients with mild or common COVID-19 were recruited from Wuhan Fangcang Shelter Hospital and five COVID-19-designated hospitals in Anhui Province, China from February to March 2020. Thirty-nine patients from Wuhan Fangcang Shelter Hospital were assigned to a pragmatic randomized controlled clinical trial, and 24 patients from the 5 COVID-19-designated hospitals in Anhui Province underwent a real-world study. The medication course of emetine was less than 10 days. The main symptoms and adverse reactions of all patients were observed and recorded. The primary outcome measure was the time required for a negative SARS-CoV-2 RNA result or the negative result rate on day 10. Secondary outcomes included axillary temperature, transcutaneous oxygen saturation, and respiratory frequency recovery. The study was approved by the Ethics Committee of The First Affiliated Hospital of Anhui Medical University on February 20, 2019 (approval No. PJ2020-03-19) and was registered with the Chinese Clinical Trial Registry on February 20, 2019 (registration number: ChiCTR2000030022).

Results: The oxygen saturation values were higher in the treatment group than in the control group on the first day after enrollment for patients treated at Fangcang Shelter Hospital. The axillary body temperature, respiratory rate, and oxygen saturation among patients in Fangcang Shelter Hospital were related to the time effect but not to the intervention measures. The respiratory rate and oxygen saturation of patients in the Anhui designated hospitals were related to the intervention measures but not to the time effect. The axillary body temperature of patients in Anhui designated hospitals was related to the time effect but not to the intervention measures.

Conclusion: Our preliminary study shows that low-dose emetine combined with basic conventional antiviral drugs improves clinical symptoms in patients with mild and common COVID-19 without apparent adverse effects, suggesting that moderately increased doses of emetine may have good potential for treatment and prevention of COVID-19.

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CiteScore
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