Oral favipiravir for patients with delayed SARS-CoV-2 viral RNA clearance: a case series
Critical Care volume 24, Article number: 578 (2020)
The COVID-19 pandemic has caused 14,893,706 infections and 613,879 deaths in 188 countries worldwide as of July 22, 2020, posing the largest world health crisis . Although the pandemic is well controlled in China and the incidence is currently very low, we have observed a number of patients with delayed SARS-CoV-2 viral RNA clearance in the upper respiratory tract (more than 30 days), which combined with asymptomatic carriers, limits the prospect of eliminating the disease. The emergence of patients with delayed viral RNA clearance and healthy viral carriers is a major concern, not only in terms of disease control, but also due to the possible long-term damage to the patients’ health. Previously, we have reported that favipiravir, a broad-spectrum antiviral drug approved in Japan and China, potently inhibits SARS-CoV-2 with a 50% effective concentration (EC50) of 61.88 μM in vitro, indicating its antiviral potential . Notably, favipiravir significantly reduced the time to viral clearance in an open-label nonrandomized controlled trial . Here, we report a series of patients with considerably delayed SARS-CoV-2 RNA clearance and the treatment efficacy of favipiravir in this population.
From March 26, 2020, we administered oral favipiravir (two doses of 1600 mg on day 1 and 600 mg twice per day on days 2–10 or until SARS-CoV-2 RNA negative) to nine asymptomatic rehabilitation patients. Eight patients were analyzed, and one patient was lost to follow-up due to transfer to another hospital. Of the eight patients included in this analysis, one received the full 10-day course of favipiravir, and seven received 4 to 9 days of favipiravir treatment.
The demographic and clinical characteristics of the eight patients are shown in Table 1. The median duration of positive detection of SARS-CoV-2 viral RNA in patients before the initiation of favipiravir treatment was 61.0 days (interquartile range, 52.8 to 67.3 days). Coexisting conditions included hypertension (four patients), diabetes (two patients), coronary heart disease (one patient), and malignant tumor (two patients). No interruption of treatment occurred due to adverse reactions.
Over the 14-day follow-up period, the median duration of viral shedding was 3 days (interquartile range, 2 to 6 days) and one patient remained SARS-CoV-2 RNA-positive after 14 days (Fig. 1a). Notably, seven of eight patients showed a rapid viral clearance within 6 days. One patient kept sustained positive detection of SARS-CoV-2 viral RNA in the upper respiratory tract during the 14-day follow-up (Fig. 1b). The persistence of viral RNA detection in individual patients is shown in Fig. 1c. Seven patients were discharged after two consecutive negative viral RNA tests performed at least 24 h apart. The patients were followed for about 1–2 months for the detection of viral nuclear acid in the throat swabs, and the patients remained negative (Fig. 1d).
It has been reported that the persistence of intestinal SARS-CoV-2 shedding in some patients has led to their re-admission after their pneumonia had resolved . Antiviral therapies appear to be an important means to resolve the problem of viral persistence. Our study suggests that favipiravir is worth further investigation as a common and widely used method of treating asymptomatic convalescent patients and carriers. The small size of this cohort and the relatively short period of follow-up limit the strength of evidence obtained by this study, and the results should be interpreted with caution. However, the rapid elimination of viral RNA in seven of the eight patients strongly suggests that administration of favipiravir may have played a role in terminating the viral RNA persistence. Randomized controlled trials are required to determine the efficacy of favipiravir for terminating SARS-CoV-2 shedding in convalescent patients and healthy carriers with delayed viral clearance.
Availability of data and materials
The datasets generated and/or analyzed during the current study are available from the corresponding authors on request.
Coronavirus disease 2019
Severe acute respiratory syndrome coronavirus 2
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We thank the COVID-19 Huoshenshan Study Group and medical care personnel, who assisted in the care of the patients in this program:
Xiaoli Xu, Xinyi Xia, Tangfeng Lv, Jiong Liu, Songqing He, Jingjing Liang, Yulong Cai, Min Xu, and Zhenhua Gan (Jinling Hospital, Nanjing University School of Medicine, Nanjing, China); Yunhu Pan and Guang Chen (The 907th Hospital of Chinese People’s Liberation Army Joint Logistics Support Force, Nanping, China); Xiao Wang and Min Tang (The 904th Hospital of Chinese People’s Liberation Army Joint Logistics Support Force, Wuxi, China); Guoji Xia, Yongchun Xu, Xiaochun Ouyang, Xi Ma, Qiang Wang, and Qianyong Yang (The 908th Hospital of Chinese People’s Liberation Army Joint Logistics Support Force, Nanchang, China); Maozeng Lin (The 909th Hospital of Chinese People’s Liberation Army Joint Logistics Support Force, Zhangzhou, China); and Yuancheng Hong (The 910th Hospital of Chinese People’s Liberation Army Joint Logistics Support Force, Quanzhou, China).
This work was supported by the National Science and Technology Major Project (2018ZX09711003) and the National Key R&D Program of China (2020YFC0841700).
Ethics approval and consent to participate
All studies were approved by the institutional review board of the Huoshenshan Hospital (HSSLL008). Trial registration: ChiCTR2000033491. Registered on 2 June 2020. All patients provided written informed consent to participate in the study.
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The authors declare that they have no competing interests.
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Fu, D., Cao, R., Zhao, L. et al. Oral favipiravir for patients with delayed SARS-CoV-2 viral RNA clearance: a case series. Crit Care 24, 578 (2020). https://doi.org/10.1186/s13054-020-03288-5