Xuanfei Baidu decoction, a Chinese herbal medicine for coronavirus disease 2019 (COVID-19): a randomized clinical trial

Tao Li, Mingfen Zhao, Mingjun Zhu, Shi-xiang Zhang, Jiarong He, He Pan, M. Shao, Zhen Wang, Yu-bing Fu, Ning Li, Long Zhao, Xinyao Jin, Fengwen Yang, Wentai Pang
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引用次数: 1

Abstract

Objective: To evaluate the efficacy and safety of Xuanfei Baidu decoction for treating coronavirus disease 2019 (COVID-19). Methods: Patients with COVID-19 were enrolled, and eligible patients were randomly allocated to three groups: group A (Xuanfei Baidu decoction combined with conventional treatment), group B (Ganlu Xiaodu decoction combined with conventional treatment), and group C (conventional treatment only). The duration of treatment was 14 days. The primary outcomes were the duration of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleic acid testing from positive to negative and hospitalization days. The secondary outcome was the rate of symptom resolution. The safety outcome was drug-related adverse events. Results: In total, 103 patients with ordinary-type COVID-19 were included and randomly allocated to groups A (34 cases), B (35 cases), and C (34 cases). Duration for SARS-CoV-2 nucleic acid testing from positive to negative was shortest in group A [(9.88 ± 3.62) days], followed by groups C [(11.20 ± 2.93) days] and B [(12.69 ± 4.11) days]; differences between the three groups were statistically significant (P = 0.010). The number of hospitalization days was the least in group A [(14.00 ± 6.55) days], followed by groups B [(15.40 ± 4.02) days] and C [(16.38 ± 5.73) days], and differences between groups were statistically significant (P = 0.019). There was no statistically significant difference in the rate of symptom resolution between groups (P > 0.05). No deaths or serious adverse events occurred in either of the groups. Conclusion: Considering the treatment of ordinary-type COVID-19, Xuanfei Baidu decoction can shorten the duration from a positive to negative SARS-CoV-2 nucleic acid test, as well as the duration of hospitalization. Moreover, there were no Xuanfei Baidu decoction-induced adverse reactions. Graphical abstract: http://links.lww.com/AHM/A44.
新型冠状病毒病(COVID-19)中药宣肺汤的随机临床试验
目的:评价宣肺百度汤治疗新型冠状病毒病2019 (COVID-19)的疗效和安全性。方法:纳入COVID-19患者,将符合条件的患者随机分为三组:A组(宣肺百度汤联合常规治疗)、B组(肝露消毒汤联合常规治疗)和C组(仅常规治疗)。疗程为14 d。主要观察指标为SARS-CoV-2核酸检测由阳性到阴性的持续时间和住院天数。次要观察指标为症状缓解率。安全性结果是药物相关不良事件。结果:共纳入103例普通型COVID-19患者,随机分为A组(34例)、B组(35例)、C组(34例)。SARS-CoV-2核酸检测由阳性到阴性持续时间最短的是A组[(9.88±3.62)d],其次是C组[(11.20±2.93)d]和B组[(12.69±4.11)d];三组间差异均有统计学意义(P = 0.010)。A组患者住院天数最少[(14.00±6.55)d],其次为B组[(15.40±4.02)d]、C组[(16.38±5.73)d],组间差异有统计学意义(P = 0.019)。两组患者症状缓解率比较,差异无统计学意义(P > 0.05)。两组均未发生死亡或严重不良事件。结论:与治疗普通型相比,宣肺百度汤可缩短SARS-CoV-2核酸检测阳性到阴性的时间,缩短住院时间。此外,宣肺百度煎剂未出现不良反应。图形摘要:http://links.lww.com/AHM/A44。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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