Evidence map›Paper›PMID 41664408›Full record

ArticleAmerican journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists2026

Real-world effectiveness of remdesivir in immunocompromised patients hospitalized due to SARS-CoV-2 Infection: Insights to inform pharmacy practice.

Andre C Kalil, Chidinma Chima-Melton, Emi Naslazi, Heribert Ramroth, Alpesh N Amin, Natasha N Pettit, Robert L Gottlieb

Abstract read
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Article in American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Andre C KalilDivision of Infectious Diseases, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
Chidinma Chima-MeltonCardiopulmonary Division, Pipeline Health, Los Angeles, CA.
Emi NaslaziEvidence and Access, Certara, The Netherlands.
Heribert RamrothMedical Affairs, Gilead Sciences, Foster City, CA, USA.
Alpesh N AminDepartment of Medicine, School of Medicine, University of California Irvine, Irvine, CA, USA.
Natasha N PettitDepartment of Pharmacy, UChicago Medicine, Chicago, IL, USA.
Robert L GottliebDepartment of Internal Medicine, Baylor University Medical Center, Baylor Scott & White Health, Dallas, TX.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeImmunocompromised adults hospitalized for coronavirus disease 2019 (COVID-19) remain at high risk for morbidity. Despite remdesivir's approval for treatment of COVID-19, real-world evidence on its early use, particularly in patients infected with evolving Omicron-era subvariants, remains limited. Contemporary evidence is essential to support hospital pharmacy practice and antiviral stewardship.

methodsWe conducted a retrospective cohort study using the Premier Healthcare Database. Adult immunocompromised patients hospitalized for COVID-19 from December 2021 to December 2024 were included. Patients with COVID-19 present-on-admission who received remdesivir within the first 2 hospital days were compared to untreated patients using 1:1 propensity score matching. The outcomes assessed were 14- and 28-day all-cause mortality. Subgroup analyses assessed outcomes stratified by oxygen requirements and specific immunocompromising conditions.

resultsAmong 22,808 matched patients, early remdesivir use was associated with significantly lower 14-day (hazard ratio [HR], 0.75; 95% CI, 0.69-0.82; P < 0.0001) and 28-day mortality (HR, 0.80; 95% CI, 0.74-0.86; P < 0.0001). Mortality reductions were observed across early and later Omicron periods and among patients with or without supplemental oxygen requirements. Subgroup analyses showed similar survival benefit in patients with cancer, including hematologic malignancies, as well as transplant recipients.

conclusionsEarly remdesivir initiation was associated with clinically meaningful and significant survival benefits in immunocompromised patients hospitalized for COVID-19, with these associations persisting in the Omicron subvariant era. These findings highlight the potential benefit of early antiviral treatment in this vulnerable population while underscoring the need for further prospective studies, including randomized controlled trials, to confirm causal effects and refine treatment strategies. Clinical pharmacists have a pivotal role in ensuring institutional protocols remain aligned with current evidence so that eligible high-risk patients consistently receive appropriate therapy.

Indexed as

Adenosine MonophosphateAlanineAntiviral AgentsCOVID-19COVID-19 Drug TreatmentImmunocompromised HostPharmacy Service, HospitalAgedFemaleHospitalizationHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAdenosine MonophosphateAlanineAntiviral Agentsremdesivirantiviral therapyCOVID-19early remdesivirhospital pharmacyimmunocompromisedmortality

Identifiers

PMID41664408
PMCPMC13070692

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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.