Institute of Information on Traditional Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Phytomedicine. 2022 Jul 20;102:154166. doi: 10.1016/j.phymed.2022.154166. Epub 2022 May 15.
Qingfei Paidu decoction (QFPDD) showed to be beneficial for the treatment of coronavirus disease 2019 (COVID-19) in China.
This study aimed to systematically assemble the evidence on the efficacy and safety of QFPDD combined with Western medicine treatments (WMT) for COVID-19.
Systematic review and meta-analysis.
A comprehensive literature search was conducted in PubMed, Embase, Cochrane Library, CNKI, CSTJ, CBM, Wanfang Data for clinical trials with a control arm until January 13, 2022. Studies matched the selection criteria were included. Data extraction and quality assessment of the included studies were independently conducted by two reviewers. Review Manager 5.4 was used for meta-analysis.
A total of 9 trials including 1108 COVID-19 patients met the selection criteria. Meta-analysis demonstrated that QFPDD combined with WMT reduced aggravation rate (AR) by 71% [risk ratio (RR) = 0.29, 95% confidence intervals (CI) (0.17, 0.51)], increased effective rate (ER) by 13% [RR = 1.13, 95%CI (1.04, 1.22)], shortened 4.78 days of viral shedding [95%CI (-5.79, -3.77)] and 4.45 days of hospital stay [95%CI (-6.05, -2.86)], also decreased the incidence of adverse events (AE) by 56% [RR = 0.44, 95%CI (0.22, 0.89)].
QFPDD combined with WMT might reduce the proportion of severe cases and the incidence of AE, shorten the duration of viral shedding and length of hospital stay. More randomized controlled trials (RCTs) are required to confirm our findings in the future.
清肺排毒汤(QFPDD)在中国被证明对治疗 2019 年冠状病毒病(COVID-19)有效。
本研究旨在系统收集 QFPDD 联合西药治疗 COVID-19 的疗效和安全性证据。
系统评价和荟萃分析。
对 PubMed、Embase、Cochrane 图书馆、中国知网、中国科技期刊数据库、中国生物医学文献数据库、万方数据等进行全面文献检索,检索时间截至 2022 年 1 月 13 日,收集有对照的临床试验。纳入符合选择标准的研究。两名评审员独立进行数据提取和质量评估。采用 Review Manager 5.4 进行荟萃分析。
共有 9 项试验(包括 1108 例 COVID-19 患者)符合选择标准。荟萃分析表明,QFPDD 联合 WMT 降低加重率(RR = 0.29,95%CI(0.17,0.51)),提高有效率(RR = 1.13,95%CI(1.04,1.22)),缩短病毒脱落时间 4.78 天[95%CI(-5.79,-3.77)]和住院时间 4.45 天[95%CI(-6.05,-2.86)],降低不良事件(AE)发生率 56%[RR = 0.44,95%CI(0.22,0.89)]。
QFPDD 联合 WMT 可能减少重症比例和 AE 发生率,缩短病毒脱落时间和住院时间。未来需要更多的随机对照试验(RCT)来证实我们的发现。