Evidence map›Paper›PMID 41152810›Full record

Observational studyBMC infectious diseases2025

Association of remdesivir treatment with long-term mortality after COVID-19 hospitalization.

Trisha Agarwal, Laurel E Beaty, Nichole E Carlson, Tellen D Bennett, Lindsey E Fish, David A Mayer, Kyle C Molina, Jennifer L Peers, Brandon J Webb, Mengli Xiao and 2 more

Abstract readObservational Study
In one paragraph

Observational study in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Trisha AgarwalUniversity of Colorado School of Medicine, 13001 E 17th Pl, Aurora, CO, 80045, USA. trisha.agarwal@cuanschutz.edu.
Laurel E BeatyDepartment of Biostatistics and Informatics, Colorado School of Public Health, Aurora, CO, 80045, USA.
Nichole E CarlsonDepartment of Biostatistics and Informatics, Colorado School of Public Health, Aurora, CO, 80045, USA.
Tellen D BennettDepartments of Biomedical Informatics and Pediatrics, University of Colorado School of Medicine, Aurora, CO, 80045, USA.
Lindsey E FishDepartment of General Internal Medicine, Denver Health, Denver, CO, 80204, USA.
David A MayerDepartment of Biostatistics and Informatics, Colorado School of Public Health, Aurora, CO, 80045, USA.
Kyle C MolinaDepartment of Emergency Medicine, University of Colorado School of Medicine, Aurora, CO, 80045, USA.
Jennifer L PeersDepartment of Emergency Medicine, University of Colorado School of Medicine, Aurora, CO, 80045, USA.
Brandon J WebbDivision of Infectious Diseases and Clinical Epidemiology, Intermountain Health, Salt Lake City, UT, 84107, USA.
Mengli XiaoDepartment of Biostatistics and Informatics, Colorado School of Public Health, Aurora, CO, 80045, USA.
Adit A Ginde *Department of Emergency Medicine, University of Colorado School of Medicine, Aurora, CO, 80045, USA.
Neil R Aggarwal *Department of Medicine, Division of Pulmonary, Allergy, and Critical Care, University of Colorado School of Medicine, 12700 E 19th Ave, RC2, Mail Stop C272, Aurora, CO, 80045, USA. neil.aggarwal@cuanschutz.edu.ORCID http://orcid.org/0000-0002-0922-8824

Funding

NIH Prior Approval Process ProfessionalUL1TR002535 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2018 to 2022
$51.1M
NCATS NIH HHS L40 TR002525NCATS NIH HHS UL1TR002525NCATS NIH HHS UL1 TR002535
6 · The paper itself

Abstract

backgroundEffectiveness of remdesivir (RDV) treatment on short-term mortality and other outcomes has been well-studied, yet the impact of RDV on long-term outcomes is less well-known. The objective of this study was to determine if inpatient RDV use in survivors of COVID-19 hospitalization is associated with reduced mortality after discharge.

methodsThis is a retrospective observational cohort study of patients hospitalized with COVID-19 between November 2020 and October 2022 in three health systems in Colorado and Utah. Real-world data were identified from electronic health records and state-level vaccination and mortality records. Our primary cohort were patients hospitalized with COVID-19, either treated or not treated with RDV, who survived to hospital discharge. Unadjusted and adjusted Cox proportional hazard models were used to estimate the hazard ratio of all-cause mortality following hospital discharge for those administered vs. not administered inpatient RDV. Sensitivity analyses included propensity-matching the primary cohort with in-hospital mortality as a competing risk. Secondary outcomes, including hospital and ED readmissions respectively, within 28 days after index hospitalization discharge, were also evaluated using Cox proportional hazard models.

resultsThe primary cohort consisted of 9760 patients who survived index hospitalization and had between 6 and 29 months of post-hospital follow up. Of the primary cohort, 4771 (48.8%) were treated with inpatient RDV, inpatient RDV was associated with a decreased mortality hazard (aHR 0.73; 95% confidence interval (CI) 0.61-0.87) among survivors with up to two and a half years of follow-up. Results from a sensitivity analysis using in-hospital mortality as a competing risk were similar to the primary model (aHR 0.76; CI 0.63-0.92). RDV treatment was also associated with decreased re-hospitalization (aHR 0.77; CI 0.67-0.89) and ED readmission rates (aHR 0.79; CI 0.67-0.92). Most subgroups appear to benefit from RDV, with possible exceptions for patients infected during the first Omicron wave, having received at least 1 vaccine dose, and those not requiring supplemental oxygen during index hospitalization.

conclusionsIn this real-world analysis of three large health systems in Colorado and Utah, RDV use was associated with decreased long-term mortality among survivors of initial COVID-19 hospitalization. Inpatient RDV treatment may provide a mortality benefit after COVID-19 hospitalization.

Indexed as

Adenosine MonophosphateAlanineAntiviral AgentsCOVID-19COVID-19 Drug TreatmentAdultAgedColoradoFemaleHospitalizationHospital MortalityHumansMaleMiddle AgedProportional Hazards ModelsRetrospective StudiesAdenosine MonophosphateAlanineAntiviral AgentsremdesivirCOVID-19Long-term mortalityRemdesivir

Identifiers

PMID41152810
PMCPMC12560357

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.