Effect of remdesivir on adverse kidney outcomes in hospitalized patients with COVID-19 and impaired kidney function.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2023
Historique:
received: 20 04 2022
accepted: 14 12 2022
entrez: 27 2 2023
pubmed: 28 2 2023
medline: 3 3 2023
Statut: epublish

Résumé

Chronic kidney disease (CKD) is an important risk factor for mortality from COVID-19. Remdesivir has been shown to shorten time to recovery in patients with severe COVID-19. However, exclusion of patients with severe kidney function impairment in clinical trials has led to concerns about kidney safety of remdesivir in patients with pre-existing kidney disease. Retrospective propensity score matched cohort study of hospitalized patients with COVID-19 admitted with estimated glomerular filtration rate (eGFR) between 15 - 60 mL/min/1.73m2. Remdesivir-treated patients were 1:1 matched to historical comparators admitted during the first wave of COVID-19 (between March-April 2020) prior to emergency use authorization of remdesivir using propensity scores accounting for factors predicting treatment assignment. Dependent outcomes included in-hospital peak creatinine, incidence of doubling of creatine, rate of kidney replacement therapy initiation and eGFR among surviving patients at day 90. 175 remdesivir-treated patients were 1:1 matched to untreated historical comparators. Mean age was 74.1 (SD 12.8), 56.9% were male, 59% patients were white, and the majority (83.1%) had at least one co-morbidity. There were no statistically significant differences in peak creatinine during hospitalization (2.3mg/dL vs. 2.5 mg/dL, P = 0.34), incidence of doubling of creatinine (10.3% vs. 13.1%, P = 0.48), and rate of kidney replacement therapy initiation (4.6% vs. 6.3%, P = 0.49) in remdesivir-treated patients versus matched untreated historical comparators, respectively. Among surviving patients, there was no difference of the average eGFR at day 90 (54.7 ± 20.0 mL/min/1.73m2 for remdesivir-treated patients vs. 51.7 ± 19.5 mL/min/1.73m2 for untreated comparators, P = 0.41). Remdesivir use in patients with impaired kidney function (eGFR between 15 - 60 mL/min/1.73m2) who present to the hospital with COVID-19 is not associated with increased risk of adverse kidney outcomes.

Sections du résumé

BACKGROUND
Chronic kidney disease (CKD) is an important risk factor for mortality from COVID-19. Remdesivir has been shown to shorten time to recovery in patients with severe COVID-19. However, exclusion of patients with severe kidney function impairment in clinical trials has led to concerns about kidney safety of remdesivir in patients with pre-existing kidney disease.
METHODS
Retrospective propensity score matched cohort study of hospitalized patients with COVID-19 admitted with estimated glomerular filtration rate (eGFR) between 15 - 60 mL/min/1.73m2. Remdesivir-treated patients were 1:1 matched to historical comparators admitted during the first wave of COVID-19 (between March-April 2020) prior to emergency use authorization of remdesivir using propensity scores accounting for factors predicting treatment assignment. Dependent outcomes included in-hospital peak creatinine, incidence of doubling of creatine, rate of kidney replacement therapy initiation and eGFR among surviving patients at day 90.
RESULTS
175 remdesivir-treated patients were 1:1 matched to untreated historical comparators. Mean age was 74.1 (SD 12.8), 56.9% were male, 59% patients were white, and the majority (83.1%) had at least one co-morbidity. There were no statistically significant differences in peak creatinine during hospitalization (2.3mg/dL vs. 2.5 mg/dL, P = 0.34), incidence of doubling of creatinine (10.3% vs. 13.1%, P = 0.48), and rate of kidney replacement therapy initiation (4.6% vs. 6.3%, P = 0.49) in remdesivir-treated patients versus matched untreated historical comparators, respectively. Among surviving patients, there was no difference of the average eGFR at day 90 (54.7 ± 20.0 mL/min/1.73m2 for remdesivir-treated patients vs. 51.7 ± 19.5 mL/min/1.73m2 for untreated comparators, P = 0.41).
CONCLUSIONS
Remdesivir use in patients with impaired kidney function (eGFR between 15 - 60 mL/min/1.73m2) who present to the hospital with COVID-19 is not associated with increased risk of adverse kidney outcomes.

Identifiants

pubmed: 36848366
doi: 10.1371/journal.pone.0279765
pii: PONE-D-22-11192
pmc: PMC9970064
doi:

Substances chimiques

remdesivir 3QKI37EEHE
Creatinine AYI8EX34EU

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0279765

Informations de copyright

Copyright: © 2023 Seethapathy et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

I have read the journal’s policy and the authors of this manuscript have the following competing interests:Dr. Sise has received research grants to institution from Gilead in the area of COVID-19 and Hepatitis C, and has served as a scientific advisory board member to Gilead in the area of Hepatitis B. All remaining authors have nothing to disclose.

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Auteurs

Rituvanthikaa Seethapathy (R)

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.

Qiyu Wang (Q)

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.

Sophia Zhao (S)

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.

Ian A Strohbehn (IA)

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.

Joshua D Long (JD)

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.

James E Dinulos (JE)

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.

Destiny Harden (D)

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.

Vinay B Kadiyala (VB)

Department of Medicine, Mass General Brigham Salem Hospital, Salem, MA, United States of America.

Daiana Moreno (D)

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.

Meghan E Sise (ME)

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.

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