Frontiers in Pharmacology (Sep 2022)

Efficacy and safety of chinese herbal medicine for treating mild or moderate COVID-19: A systematic review and meta-analysis of randomized controlled trials and observational studies

  • Hongfei Zhu,
  • Hongfei Zhu,
  • Mengting Li,
  • Mengting Li,
  • Chen Tian,
  • Chen Tian,
  • Honghao Lai,
  • Honghao Lai,
  • Yuqing Zhang,
  • Yuqing Zhang,
  • Yuqing Zhang,
  • Yuqing Zhang,
  • Jiaheng Shi,
  • Jiaheng Shi,
  • Nannan Shi,
  • Hui Zhao,
  • Kehu Yang,
  • Kehu Yang,
  • Kehu Yang,
  • Hongcai Shang,
  • Hongcai Shang,
  • Xin Sun,
  • Jie Liu,
  • Jie Liu,
  • Long Ge,
  • Long Ge,
  • Long Ge,
  • Long Ge,
  • Luqi Huang,
  • Luqi Huang

DOI
https://doi.org/10.3389/fphar.2022.988237
Journal volume & issue
Vol. 13

Abstract

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Background: The coronavirus disease 2019 (COVID-19) is still a pandemic globally, about 80% of patients infected with COVID-19 were mild and moderate. Chinese herbal medicine (CHM) has played a positive role in the treatment of COVID-19, with a certain number of primary studies focused on CHM in managing COVID-19 published. This study aims to systematically review the currently published randomized controlled trials (RCTs) and observational studies (OBs), and summarize the effectiveness and safety of CHM in the treatment of mild/moderate COVID-19 patients.Methods: We searched 9 databases up to 19 March 2022. Pairs of reviewers independently screened literature, extracted data and assessed risk of bias. For overall effect, we calculated the absolute risk difference (ARD) of weighted averages of different estimates, and certainty of evidence was assessed using the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) system.Results: We included 35 RCTs and 24 OBs enrolling 16,580 mild/moderate patients. The certainty of evidence was very low to low. Compared with usual supportive treatments, most effect estimates of CHM treatments were consistent in direction. CHMs presented significant benefits in reducing rate of conversion to severe cases (ARD = 99 less per 1000 patients in RCTs and 131 less per 1000 patients in OBs, baseline risk: 16.52%) and mortality (ARD = 3 less per 1000 patients in RCTs and OBs, baseline risk: 0.40%); shortening time to symptom resolution (3.35 days in RCTs and 2.94 days in OBs), length of hospital stay (2.36 days in RCTs and 2.12 days in OBs) and time to viral clearance (2.64 days in RCTs and 4.46 days in OBs); increasing rate of nucleic acid conversion (ARD = 73 more per 1000 patients in OBs, baseline risk: 16.30%). No serious adverse reactions were found and the differences between CHM and usual supportive care were insignificant.Conclusion: Encouraging evidence showed that CHMs were beneficial in treating mild or moderate patients. CHMs have been proved to possess a safety profile that is comparable to that of usual supportive treatment alone. More rigorously designed clinical trials and mechanism studies are still warranted to further confirm the present findings.

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