4.7 Article

Clinical Improvement, Outcomes, Antiviral Activity, and Costs Associated With Early Treatment With Remdesivir for Patients With Coronavirus Disease 2019 (COVID-19)

Journal

CLINICAL INFECTIOUS DISEASES
Volume 74, Issue 8, Pages 1450-1458

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciab631

Keywords

antiviral activity; clinical improvement; cost; COVID-19; remdesivir

Funding

  1. Health and Medical Research Fund, The Food and Health Bureau, The Government of the Hong Kong Special Administrative Region, China [COVID190210]

Ask authors/readers for more resources

Early initiation of remdesivir in hospitalized patients with moderate COVID-19, who do not require oxygen therapy, is associated with significantly shorter time to clinical improvement, low viral load and positive IgG antibody, a shorter length of hospital stay, and a significantly lower risk of in-hospital death.
Among hospitalized patients with moderate COVID-19, early initiation of remdesivir was associated with significantly shorter time to clinical improvement, low viral load and positive IgG antibody, a shorter length of hospital stay, and a significantly lower risk of in-hospital death. Background Evidence remains inconclusive on any significant benefits of remdesivir in patients with mild-to-moderate COVID-19. This study explored the disease progression, various clinical outcomes, changes in viral load, and costs associated with early remdesivir treatment among COVID-19 patients. Methods A territory-wide retrospective cohort of 10 419 patients with COVID-19 hospitalized from 21 January 2020 to 31 January 2021 in Hong Kong was identified. Early remdesivir users were matched with controls using propensity-score matching in a ratio <= 1:4. Study outcomes were time to clinical improvement of at least 1 point on WHO clinical progression scale, hospital discharge, recovery, viral clearance, low viral load, positive IgG antibody, in-hospital death, and composite outcomes of in-hospital death requiring invasive ventilation or intensive care. Results After multiple imputation and propensity-score matching, median follow-up was 14 days for both remdesivir (n = 352) and control (n = 1347) groups. Time to clinical improvement was significantly shorter in the remdesivir group than that of control (HR: 1.14; 95% CI: 1.01-1.29; P = .038), as well as for achieving low viral load (1.51; 1.24-1.83; P < .001) and positive IgG antibody (1.50; 1.31-1.70; P < .001). Early remdesivir treatment was associated with lower risk of in-hospital death (HR: .58; 95% CI: .34-.99; P = .045), in addition to a significantly shorter length of hospital stay (difference: -2.56 days; 95% CI: -4.86 to -.26; P = .029), without increasing risks of composite outcomes for clinical deterioration. Conclusions Early remdesivir treatment could be extended to hospitalized patients with moderate COVID-19 not requiring oxygen therapy on admission.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available