Favipiravir for the treatment of patients with COVID-19: a systematic review and meta-analysis

被引:113
作者
Manabe, Toshie [1 ,2 ]
Kambayashi, Dan [1 ,3 ]
Akatsu, Hiroyasu [1 ]
Kudo, Koichiro [4 ,5 ]
机构
[1] Nagoya City Univ, Grad Sch Med, Mizuho Ku, 1 Kawasumi,Mizuho Cho, Nagoya, Aichi 4678601, Japan
[2] Nagoya City Univ, West Med Ctr, Nagoya, Aichi, Japan
[3] Showa Pharmaceut Univ, Tokyo, Japan
[4] Yurin Hosp, Tokyo, Japan
[5] Waseda Univ Reg & Interreg Org, Tokyo, Japan
关键词
Favipiravir; COVID-19; SARS-CoV-2; Viral clearance; Clinical improvement; T-705;
D O I
10.1186/s12879-021-06164-x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
BackgroundFavipiravir possesses high utility for treating patients with COVID-19. However, research examining the efficacy and safety of favipiravir for patients with COVID-19 is limited.MethodsWe conducted a systematic review of published studies reporting the efficacy of favipiravir against COVID-19. Two investigators independently searched PubMed, the Cochrane Database of Systematic Reviews, MedRxiv, and ClinicalTrials.gov (inception to September 2020) to identify eligible studies. A meta-analysis was performed to measure viral clearance and clinical improvement as the primary outcomes.ResultsAmong 11 eligible studies, 5 included a comparator group. Comparing to the comparator group, the favipiravir group exhibited significantly better viral clearance on day 7 after the initiation of treatment (odds ratio [OR]=2.49, 95% confidence interval [CI]=1.19-5.22), whereas no difference was noted on day 14 (OR=2.19, 95% CI=0.69-6.95). Although clinical improvement was significantly better in the favipiravir group on both days 7 and 14, the improvement was better on day 14 (OR=3.03, 95% CI=1.17-7.80) than on day 7 (OR=1.60, 95% CI=1.03-2.49). The estimated proportions of patients with viral clearance in the favipiravir arm on days 7 and 14 were 65.42 and 88.9%, respectively, versus 43.42 and 78.79%, respectively, in the comparator group. The estimated proportions of patients with clinical improvement on days 7 and 14 in the favipiravir group were 54.33 and 84.63%, respectively, compared with 34.40 and 65.77%, respectively, in the comparator group.ConclusionsFavipiravir induces viral clearance by 7days and contributes to clinical improvement within 14days. The results indicated that favipiravir has strong possibility for treating COVID-19, especially in patients with mild-to-moderate illness. Additional well-designed studies, including examinations of the dose and duration of treatment, are crucial for reaching definitive conclusions.
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页数:13
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