» Articles » PMID: 37243828

The Kinetics of SARS-CoV-2 Viremia in COVID-19 Patients Receiving Remdesivir

Overview
Publisher Springer
Date 2023 May 27
PMID 37243828
Authors
Affiliations
Soon will be listed here.
Abstract

Detection of SARS-CoV-2 RNA in serum, viremia, has been linked to disease severity and outcome. The kinetics of viremia in patients receiving remdesivir has not been thoroughly studied and could help predict treatment response and outcome. We investigated the kinetics of SARS-CoV-2 viremia and factors associated with baseline viremia, viral clearance and 30-day mortality in patients receiving remdesivir. An observational study including 378 hospitalised patients (median age 67 years, 67% male) sampled with serum SARS-CoV-2 RT-PCR within ± 24 h of initiation of remdesivir treatment. Baseline viremia was present in 206 (54%) patients with a median Ct value of 35.3 (IQR = 33.3-37.1). In patients with baseline viremia, the estimated probability of viral clearance was 72% by day 5. Ct values decreased significantly during remdesivir treatment for viremic patients, indicating an increase in viral load. In total, 44 patients (12%) died within 30 days, and mortality was significantly associated with viremia at baseline (OR = 2.45, p = 0.01) and lack of viral clearance by day 5 (OR = 4.8, p =  < 0.01). Viral clearance was not associated with any individual risk factor. Viremia appears to be a prognostic marker before and during remedesivir treatment. The resolution of viremia was similar to patients not receiving remdesivir in other studies, and the decrease in Ct values during treatment questions the antiviral capacity of remdesivir in vivo. Prospective studies are warranted to confirm our findings.

Citing Articles

Occurrence and clinical correlates of SARS-CoV-2 viremia in two German patient cohorts.

Grikscheit K, Berger A, Rabenau H, Kohmer N, Appel K, Scherer M Emerg Microbes Infect. 2025; 14(1):2459137.

PMID: 39868965 PMC: 11812106. DOI: 10.1080/22221751.2025.2459137.


Nasopharyngeal SARS-CoV-2 viral load kinetics using digital PCR.

Hastie E, Amogan H, Looney D, Mehta S Heliyon. 2023; 9(10):e20739.

PMID: 37876488 PMC: 10590800. DOI: 10.1016/j.heliyon.2023.e20739.


SARS-CoV-2 RNAemia and Disease Severity in COVID-19 Patients.

Lawrence Panchali M, Kim C, Seo J, Kim D, Yun N, Kim D Viruses. 2023; 15(7).

PMID: 37515246 PMC: 10386401. DOI: 10.3390/v15071560.

References
1.
Yek C, Warner S, Wiltz J, Sun J, Adjei S, Mancera A . Risk Factors for Severe COVID-19 Outcomes Among Persons Aged ≥18 Years Who Completed a Primary COVID-19 Vaccination Series - 465 Health Care Facilities, United States, December 2020-October 2021. MMWR Morb Mortal Wkly Rep. 2022; 71(1):19-25. PMC: 8735560. DOI: 10.15585/mmwr.mm7101a4. View

2.
Wang M, Cao R, Zhang L, Yang X, Liu J, Xu M . Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-nCoV) in vitro. Cell Res. 2020; 30(3):269-271. PMC: 7054408. DOI: 10.1038/s41422-020-0282-0. View

3.
Li Y, Schneider A, Mehta A, Sade-Feldman M, Kays K, Gentili M . SARS-CoV-2 viremia is associated with distinct proteomic pathways and predicts COVID-19 outcomes. J Clin Invest. 2021; 131(13). PMC: 8245177. DOI: 10.1172/JCI148635. View

4.
Vangeel L, Chiu W, De Jonghe S, Maes P, Slechten B, Raymenants J . Remdesivir, Molnupiravir and Nirmatrelvir remain active against SARS-CoV-2 Omicron and other variants of concern. Antiviral Res. 2022; 198:105252. PMC: 8785409. DOI: 10.1016/j.antiviral.2022.105252. View

5.
Cardenoso Domingo L, Roy Vallejo E, Zurita Cruz N, Chicot Llano M, Perez-Urria E, Barrios A . Relevant SARS-CoV-2 viremia is associated with COVID-19 severity: Prospective cohort study and validation cohort. J Med Virol. 2022; 94(11):5260-5270. PMC: 9349374. DOI: 10.1002/jmv.27989. View