Risk factors for liver enzyme elevation with remdesivir use in the treatment of paediatric COVID‐19

Author:

Jinda Tsuyoshi1,Mizuno Shinsuke2ORCID,Tatami Shunsuke1,Kasai Masashi2,Ishida Tatsuhiko1

Affiliation:

1. Division of Infectious Diseases, Department of Pediatrics Hyogo Prefectural Kobe Children's Hospital Kobe Hyogo Japan

2. Department of Pharmacy Hyogo Prefectural Kobe Children's Hospital Kobe Hyogo Japan

Abstract

AimRemdesivir (RDV) causes liver enzyme elevation in adults; however, the frequency of this elevation in children and the associated risk factors are largely unknown. Therefore, we aimed to examine risk factors for liver enzyme elevation in hospitalised paediatric patients who received RDV.MethodsThis was a retrospective case–control study of all patients aged <18 years who were diagnosed with coronavirus disease 2019 and received RDV at a tertiary care hospital between February 2022 and September 2023. Demographic and clinical data were retrieved from the medical records and analysed. Patients with liver enzyme elevation were defined as cases, while those with no liver enzyme elevation were defined as controls. The two groups were compared and analysed for possible risk factors for liver enzyme elevation with RDV use.ResultsSixty‐six patients were treated with RDV, 12 (18.2%) of whom developed liver enzyme elevation. Liver enzyme elevation was associated with the median duration of RDV administration (7.5 days vs. 3 days, P = 0.012), median total RDV dose (17.7 mg/kg vs. 10.3 mg/kg, P = 0.017) and acetaminophen use (67% vs. 22%) (odds ratio = 4.34; 95% confidence interval, 1.05–19.97, P = 0.023). All patients showed improvement, except three who had no liver enzyme measurements after having the highest aspartate aminotransferase and alanine aminotransferase values during the observation period.ConclusionLiver enzyme elevation was reversible after discontinuing RDV use. Overall, RDV can be considered safe in children with careful monitoring.

Publisher

Wiley

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