Impact of Implementing More Restrictive Remdesivir Criteria Across a Multi-Hospital Health System

Nicholson et al., Am. J. Health-Syst. Pharm., doi:10.1093/ajhp/zxaf258, Mar 2026
Retrospective 2,249 hospitalized COVID-19 patients showing lower mortality after restricting remdesivir use. Mortality reduced from 7.6% to 5.6% (p = 0.12) after restriction. No baseline details are provided and results are subject to confounding by time, however both periods were post-pandemic with comparable risk.
Gérard, Zhou, Wu, Kamo, Choi, Kim show increased risk of acute kidney injury, Leo, Briciu, Muntean, Petrov, Arch show increased risk of liver injury, Negru, Cheng, Mohammed, Kwok, Zhu show increased risk of cardiac disorders, and Kwok, Merches, Akinci, Tang, Bagheri show increased risk of mitochondrial toxicity with remdesivir.
Nicholson et al., 6 Mar 2026, retrospective, USA, peer-reviewed, 3 authors.
Abstract: PROFESSIONAL POSTERS Impact of Implementing More Restrictive Remdesivir Criteria Across a Multi-Hospital Health System Type: Professional Posters Topic: Infectious Diseases/HIV Category: Evaluative Study Primary Author: James P. Nicholson, PharmD, BCPS, Clinical Pharmacy Manager, Methodist Medical Center of Oak Ridge Conclusion: The implementation of more restrictive remdesivir criteria at Covenant Health led to a signi"cant reduction in drug utilization and generated over $500,000!in cost savings. Importantly, these changes did not negatively impact clinical outcomes, including length of stay, mortality, and 30-day readmissions. The cost savings were consistent compared to a national benchmark, underscoring the e#ectiveness of targeted stewardship interventions in optimizing resource utilization in Covid-19!patients. Co-Author(s): John W. Gilliam, Jesse T. Doers Purpose: During the COVID-19!pandemic, Covenant Health initially aligned its remdesivir use criteria with NIH guidelines. In May 2024, the System Pharmacy and Therapeutics Committee, following a recommendation from the COVID-19!Subcommittee, approved more restrictive criteria. These limited remdesivir use to immunocompromised patients with oxygen requirements within 48!hours of admission and within 10!days of symptom onset. The updated criteria were implemented in the electronic medical record in July 2024. This study aimed to evaluate the clinical and "nancial impact of this change across the health system. Methods: This retrospective, multi-center study compared remdesivir use across eight acute care hospitals during two nine-month periods: pre- (July 2023!to March 2024) and post- (July 2024!to March 2025) implementation of more restrictive criteria. COVID-19!patients were identi"ed using ICD-10!codes. Remdesivir data collected included the number of patients that received the drug, the quantity of 100!mg vials charged, and associated costs. Pharmacists reviewed remdesivir orders and contacted providers to discontinue therapy when patients did not meet the updated criteria. Clinical outcomes assessed included length of stay, mortality, and 30-day readmission rates. Two cost analyses were conducted: one adjusted total remdesivir costs in the pre-implementation group to match the patient volume of the post-implementation group, and the other compared remdesivir cost per pharmacy-adjusted patient day with a national benchmark of approximately 120!healthcare facilities. Data were obtained from analytics platforms, and statistical analysis was performed using the Student’s t-test. Results: The pre-implementation group included 1,249!COVID19!patients, compared to 1,000!in the post-implementation group. There were no statistically signi"cant di#erences in clinical outcomes between the two groups. The average length of stay was 5.96!days in the pre-implementation group versus 5.72!days in the postimplementation group (p!=!0.34). Mortality rates were 7.57% and 5.61% (p!=!0.12), respectively, and 30-day readmission rates were 18.3% and 20.3% (p!=!0.30), respectively. In contrast, remdesivir utilization signi"cantly decreased. The number of patients receiving remdesivir dropped from 414!to 147!(p <!0.001), and the number of 100!mg vials charged decreased from 1,960!to 629!(p <!0.001). The percentage of COVID-19!patients receiving remdesivir declined from 32.8% to 15.5% (p..
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Late treatment
is less effective
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