4.5 Article

Antiviral drugs arbidol and interferon alpha-1b contribute to reducing the severity of COVID-19 patients: a retrospective cohort study

Journal

VIROLOGY JOURNAL
Volume 18, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12985-021-01617-w

Keywords

Arbidol; Interferon alpha-1b; Severity rate; COVID-19; Antiviral agents

Categories

Funding

  1. National Natural Science Foundation of China [11801542]
  2. Shenzhen Fundamental Research Project [JCYJ20180703145002040]
  3. Strategic Priority Research Program of Chinese Academy of Sciences [XDB 38040200]
  4. Shenzhen Scientific and Technological Project [JSGG20200225150702770, JSGG20200225153023511]
  5. Guangdong Scientific and Technological Project [2020B1111340076]
  6. Shenzhen Bay Laboratory Open Research Program [SZBL202002271003]

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The study evaluated the role of antiviral drugs in reducing the severity of illness in patients with moderate COVID-19 pneumonia. The use of arbidol and interferon alpha-1b was associated with lower severity rates, while early use of arbidol within 7 days of symptom onset reduced patients' recovery time.
Objectives The aim of this study was to evaluate the role of antiviral drugs in reducing the risk of developing severe illness in patients with moderate COVID-19 pneumonia. Methods This retrospective cohort study included 403 adult patients with moderate COVID-19 pneumonia who were admitted to Shenzhen Third People's Hospital, China. The antiviral drugs arbidol, interferon alpha-1b, lopinavir-ritonavir and ribavirin were distributed to the patients for treatment. The primary endpoint of this study was the time to develop severe illness. Results Of the 462 patients admitted, 403 had moderate COVID-19 symptoms at hospital admission and were included in this study. 90 of the 403 (22.3%) patients progressed to severe illness. The use of arbidol was associated with a lower severity rate 3.5% compared to control group 30.5%, p-value < 0.0001; the adjusted hazard ratio was 0.28 (95% CI: 0.084-0.90, p = 0.033). The use of interferon alpha-1b was associated with a lower severity rate 15.5% compared to control group 29.3%, with p-value < 0.0001; the adjusted hazard ratio was 0.30 (95% CI: 0.15-0.58, p = 0.0005). The use of lopinavir-itonavir and ribavirin did not show significant differences in adjusted regression models. Early use of arbidol within 7 days of symptom onset was significantly associated with a reduced recovery time of - 5.2 days (IQR - 3.0 to - 7.5, p = 4e-06) compared with the control group. Conclusion Treatment with arbidol and interferon alpha-1b contributes to reducing the severity of illness in patients with moderate COVID-19 pneumonia. Early use of arbidol may reduce patients' recovery time.

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