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瑞德西韦和法匹拉韦治疗新冠肺炎患者的疗效与安全性——一项系统评价与荟萃分析

Efficacy and safety of remdesivir and favipiravir in COVID-19 patients - A systematic review and meta-analysis.

作者信息

Vatsha Piyush, Vardhan Gyan, Kumari Tanuja, Kanwar Navjot, Kanwal Abhinav, Deshmukh Rahul

机构信息

Department of Pharmaceutical Sciences and Technology, MRSPTU, Bathinda, Punjab, India.

Department of Pharmacology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.

出版信息

J Family Med Prim Care. 2025 May;14(5):1604-1616. doi: 10.4103/jfmpc.jfmpc_1694_24. Epub 2025 May 31.

Abstract

Coronavirus-2019 (Covid-19) has led to a severe medical, social and economic crisis globally. The use of antivirals has given inconsistent results; thus, systematic summaries of available evidence may help us to understand its effectiveness. The current investigation was planned to conduct a systematic review and meta-analysis on the use of antivirals for Covid-19. Using 'MeSH' term databases were searched on Google Scholar, PubMed, Web of Science, SCOPUS, OVID, Cochrane Library, and Limits- English Language only. Title/abstract screening, full-text screening and data extraction were carried out by three authors. Pooled effect sizes and 95% confidence intervals (CI) were calculated using the Mantel-Haenszel method of random effects for meta-analysis. Ten studies were found eligible for inclusion: randomized controlled trials Moderate-quality evidence suggests a likely clinical benefit from the use of remdesivir in improving the number of recoveries (OR 1.46; 95% CI 1.23-1.74; I2=0%). A possibility of a higher mortality rate is also suggested by high-quality evidence with remdesivir (OR 0.78; 95% CI 0.57-1.05, I2=14%). Favipiravir also showed patient's higher mortality outcome (OR 0.69;95% CI 0.24-2.01, I2 = 0%). Although the need for oxygen therapy (OR 0.70 95% CI 0.40-1.23; I2= 72%) was highly significant p < 0.001** and Remdesivir/Favipiravir was determined to be beneficial overall for male gender data across all studies (OR 0.77; 95% CI;0.37-1.60;I2=90%) and highly significant < 0.0001***. Worsening of comorbidities (OR 0.94; 95% CI 0.81-1.08; I2= 0%), Ferritin level measured (OR-19.80 95% CI -56.51-16.92; I2 = 0 %) and Transferred to ICU/ Mechanical Ventilation (OR 0.85 95% CI 0.25 -2.91; I2 = 52 %) were observed in both the anti-viral. This meta-analysis found mixed efficacy for Remdesivir and negative outcomes for Favipiravir.

摘要

2019冠状病毒病(Covid-19)在全球引发了严重的医学、社会和经济危机。抗病毒药物的使用效果参差不齐;因此,对现有证据进行系统总结可能有助于我们了解其有效性。本项调查旨在对抗病毒药物用于治疗Covid-19进行系统评价和荟萃分析。使用“医学主题词表(MeSH)”术语,在谷歌学术、PubMed、科学网、Scopus、OVID、考克兰图书馆中进行检索,并限定仅检索英文文献。由三位作者进行标题/摘要筛选、全文筛选和数据提取。采用随机效应的曼特尔-亨塞尔方法计算合并效应量和95%置信区间(CI),以进行荟萃分析。发现有10项研究符合纳入标准:随机对照试验。中等质量的证据表明,使用瑞德西韦可能在临床上有利于提高康复人数(比值比[OR]1.46;95%CI 1.23 - 1.74;I2 = 0%)。高质量证据还表明,使用瑞德西韦可能有更高的死亡率(OR 0.78;95%CI 0.57 - 1.05,I2 = 14%)。法匹拉韦也显示出患者更高的死亡结局(OR 0.69;95%CI 0.24 - 2.01,I2 = 0%)。尽管氧疗需求(OR 0.70,95%CI 0.40 - 1.23;I2 = 72%)具有高度显著性(p < 0.001**),且在所有研究中,瑞德西韦/法匹拉韦总体上对男性数据有益(OR 0.77;95%CI;0.37 - 1.60;I2 = 90%),具有高度显著性(< 0.0001***)。在两种抗病毒药物治疗中均观察到合并症恶化(OR 0.94;95%CI 0.81 - 1.08;I2 = %)、铁蛋白水平测量值(OR - 19.80,95%CI - 56.51 - 16.92;I2 = 0%)以及转入重症监护病房/机械通气(OR 0.85;95%CI 0.25 - 2.91;I2 = 52%)。这项荟萃分析发现,瑞德西韦疗效不一,法匹拉韦则有负面结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b45/12178481/8f02efa70f9f/JFMPC-14-1604-g001.jpg

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