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A Valid Warning or Clinical Lore: an Evaluation of Safety Outcomes of Remdesivir in Patients with Impaired Renal Function from a Multicenter Matched Cohort.
Ackley, Tyler W; McManus, Dayna; Topal, Jeffrey E; Cicali, Brian; Shah, Sunish.
  • Ackley TW; Department of Pharmacy, Yale New Haven Health System, New Haven, Connecticut, USA.
  • McManus D; Department of Pharmacy, Yale New Haven Health System, New Haven, Connecticut, USA.
  • Topal JE; Department of Pharmacy, Yale New Haven Health System, New Haven, Connecticut, USA.
  • Cicali B; Yale University School of Medicine, Department of Internal Medicine, Section of Infectious Diseases, New Haven, Connecticut, USA.
  • Shah S; Center for Pharmacometrics and Systems Pharmacology, Department of Pharmaceutics, University of Florida College of Pharmacy, Orlando, Florida, USA.
Antimicrob Agents Chemother ; 65(2)2021 01 20.
Article in English | MEDLINE | ID: covidwho-1040788
ABSTRACT
Per prescribing guidance, remdesivir is not recommended for SARS-CoV-2 in patients with renal disease given the absence of safety data in this patient population. This study was a multicenter, retrospective chart review of hospitalized patients with SARS-CoV-2 who received remdesivir. Safety outcomes were compared between patients with an estimated creatinine clearance (eCrCl) of <30 ml/min and an eCrCl of ≥30 ml/min. The primary endpoint was acute kidney injury (AKI) at the end of treatment (EOT). Of 359 patients who received remdesivir, 347 met inclusion criteria. Patients with an eCrCl of <30 ml/min were older {median, 80 years (interquartile range [IQR], 63.8 to 89) versus 62 (IQR, 54 to 74); P < 0.001}, were more likely to be on vasopressors on the day of remdesivir administration (30% versus 12.7%; P = 0.003), and were more likely to be mechanically ventilated during remdesivir therapy (27.5% versus 12.4%; P = 0.01) than those with an eCrCl of ≥30 ml/min. Despite these confounders, there was no significant difference in the frequency of EOT AKI (5% versus 2.3%; P = 0.283) or early discontinuation due to abnormal liver function tests (LFTs) (0% versus 3.9%; P = 0.374). Of the 5% of patients who developed EOT AKI on remdesivir with an eCrCl <30 ml/min, no cases were attributable to remdesivir administration per the treating physician. Comparable safety outcomes were observed when 11 nearest neighbor matching was applied to account for baseline confounders. In conclusion, remdesivir administration was not significantly associated with increased EOT AKI in patients with an eCrCl of <30 ml/min compared to patients with an eCrCl of ≥30 ml/min.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Adenosine Monophosphate / Alanine / Renal Insufficiency / SARS-CoV-2 / COVID-19 Drug Treatment Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Limits: Aged / Humans / Middle aged Language: English Year: 2021 Document Type: Article Affiliation country: AAC.02290-20

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Adenosine Monophosphate / Alanine / Renal Insufficiency / SARS-CoV-2 / COVID-19 Drug Treatment Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Limits: Aged / Humans / Middle aged Language: English Year: 2021 Document Type: Article Affiliation country: AAC.02290-20