» Articles » PMID: 39118052

Real-world Evaluation of Early Remdesivir in High-risk COVID-19 Outpatients During Omicron Including BQ.1/BQ.1.1/XBB.1.5

Abstract

Background: A trial performed among unvaccinated, high-risk outpatients with COVID-19 during the delta period showed remdesivir reduced hospitalization. We used our real-world data platform to determine the effectiveness of remdesivir on reducing 28-day hospitalization among outpatients with mild-moderate COVID-19 during an Omicron period including BQ.1/BQ.1.1/XBB.1.5.

Methods: We did a propensity-matched, retrospective cohort study of non-hospitalized adults with SARS-CoV-2 infection between April 7, 2022, and February 7, 2023. Electronic healthcare record data from a large health system in Colorado were linked to statewide vaccination and mortality data. We included patients with a positive SARS-CoV-2 test or outpatient remdesivir administration. Exclusion criteria were other SARS-CoV-2 treatments or positive SARS-CoV-2 test more than seven days before remdesivir. The primary outcome was all-cause hospitalization up to day 28. Secondary outcomes included 28-day COVID-related hospitalization and 28-day all-cause mortality.

Results: Among 29,270 patients with SARS-CoV-2 infection, 1,252 remdesivir-treated patients were matched to 2,499 untreated patients. Remdesivir was associated with lower 28-day all-cause hospitalization (1.3% vs. 3.3%, adjusted hazard ratio (aHR) 0.39 [95% CI 0.23-0.67], p < 0.001) than no treatment. All-cause mortality at 28 days was numerically lower among remdesivir-treated patients (0.1% vs. 0.4%; aOR 0.32 [95% CI 0.03-1.40]). Similar benefit of RDV treatment on 28-day all-cause hospitalization was observed across Omicron periods, aOR (95% CI): BA.2/BA2.12.1 (0.77[0.19-2.41]), BA.4/5 (0.50[95% CI 0.50-1.01]), BQ.1/BQ.1.1/XBB.1.5 (0.21[95% CI 0.08-0.57].

Conclusion: Among outpatients with SARS-CoV-2 during recent Omicron surges, remdesivir was associated with lower hospitalization than no treatment, supporting current National Institutes of Health Guidelines.

References
1.
Focosi D, McConnell S, Casadevall A, Cappello E, Valdiserra G, Tuccori M . Monoclonal antibody therapies against SARS-CoV-2. Lancet Infect Dis. 2022; 22(11):e311-e326. PMC: 9255948. DOI: 10.1016/S1473-3099(22)00311-5. View

2.
Lim S, Tignanelli C, Hoertel N, Boulware D, Usher M . Prevalence of Medical Contraindications to Nirmatrelvir/Ritonavir in a Cohort of Hospitalized and Nonhospitalized Patients With COVID-19. Open Forum Infect Dis. 2022; 9(8):ofac389. PMC: 9384640. DOI: 10.1093/ofid/ofac389. View

3.
Heinze G, Schemper M . A solution to the problem of separation in logistic regression. Stat Med. 2002; 21(16):2409-19. DOI: 10.1002/sim.1047. View

4.
Cao Z, Gao W, Bao H, Feng H, Mei S, Chen P . VV116 versus Nirmatrelvir-Ritonavir for Oral Treatment of Covid-19. N Engl J Med. 2022; 388(5):406-417. PMC: 9812289. DOI: 10.1056/NEJMoa2208822. View

5.
Piccicacco N, Zeitler K, Ing A, Montero J, Faughn J, Silbert S . Real-world effectiveness of early remdesivir and sotrovimab in the highest-risk COVID-19 outpatients during the Omicron surge. J Antimicrob Chemother. 2022; 77(10):2693-2700. PMC: 9384598. DOI: 10.1093/jac/dkac256. View