<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(2)</volume><submitter>Seethapathy R</submitter><funding>Gilead Sciences</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>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.&lt;h4>Methods&lt;/h4>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.&lt;h4>Results&lt;/h4>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).&lt;h4>Conclusions&lt;/h4>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.</pubmed_abstract><journal>PloS one</journal><pagination>e0279765</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9970064</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effect of remdesivir on adverse kidney outcomes in hospitalized patients with COVID-19 and impaired kidney function.</pubmed_title><pmcid>PMC9970064</pmcid><pubmed_authors>Harden D</pubmed_authors><pubmed_authors>Moreno D</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhao S</pubmed_authors><pubmed_authors>Kadiyala VB</pubmed_authors><pubmed_authors>Sise ME</pubmed_authors><pubmed_authors>Seethapathy R</pubmed_authors><pubmed_authors>Strohbehn IA</pubmed_authors><pubmed_authors>Dinulos JE</pubmed_authors><pubmed_authors>Long JD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of remdesivir on adverse kidney outcomes in hospitalized patients with COVID-19 and impaired kidney function.</name><description>&lt;h4>Background&lt;/h4>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.&lt;h4>Methods&lt;/h4>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.&lt;h4>Results&lt;/h4>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).&lt;h4>Conclusions&lt;/h4>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.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-18T14:23:04.668Z</modification><creation>2025-04-07T00:33:03.935Z</creation></dates><accession>S-EPMC9970064</accession><cross_references><pubmed>36848366</pubmed><doi>10.1371/journal.pone.0279765</doi></cross_references></HashMap>