Your browser doesn't support javascript.
loading
Incidence and predisposing factors for flucloxacillin-related hepatotoxicity in children.
Coombs, Stefan; Pittet, Laure F; Tang, Kailey; Gwee, Amanda.
Afiliación
  • Coombs S; Department of Pharmacy and General Medicine, The Royal Children's Hospital Melbourne, 50 Flemington Road Parkville, Victoria 3052, Australia.
  • Pittet LF; Infectious Diseases Unit, Department of Paediatrics, Gynaecology and Obstetrics, Faculty of Medicine, University of Geneva and University Hospitals of Geneva, Geneva, Switzerland.
  • Tang K; Antimicrobials Group, Murdoch Children's Research Institute, Royal Children's Hospital Melbourne, 50 Flemington Road Parkville, Victoria 3052, Australia.
  • Gwee A; Department of Paediatrics, University of Melbourne, Reception Level 2, West Building, Royal Children's Hospital Melbourne, 50 Flemington Road Parkville, Victoria 3052, Australia.
J Antimicrob Chemother ; 78(11): 2667-2671, 2023 11 06.
Article en En | MEDLINE | ID: mdl-37699070
BACKGROUND: Flucloxacillin-induced hepatotoxicity is well established in adults. However, there are few paediatric studies of flucloxacillin-induced hepatotoxicity despite this drug being among the most commonly prescribed in children. We aimed to determine the incidence of flucloxacillin-induced hepatotoxicity in children receiving IV therapy as well as identify risk factors for this adverse drug reaction. METHODS: We undertook a 2 year retrospective audit of children aged 0-18 years admitted to the Royal Children's Hospital (March 2019 to March 2021) who had liver function tests determined before and after receiving IV flucloxacillin for at least 24 hours duration. Causality was assessed using the Roussel Uclaf Causality Assessment Method and Naranjo criteria. RESULTS: Overall, the incidence of hepatotoxicity was 66/393 (17%). The median age of children with hepatotoxicity was 1.1 years (IQR 0.3-11.9), 43 (65%) received two or more concomitant hepatotoxic medications and 23 (35%) were receiving total parenteral nutrition. The median timing of onset of hepatotoxicity after commencement of flucloxacillin was 4 days (range 2-7). Severe hepatotoxicity (Common Terminology Criteria for Adverse Events grade 3 or above) occurred in 9/66 (14%) for bilirubin, 13/66 (20%) for ALT and 10/66 (15%) for GGT. Predisposing factors for hepatotoxicity were increasing age (OR 1.06 per additional year, 95% CI 1.01-1.10, P = 0.02), with adolescents aged 12-18 years having the highest risk (OR 5.10, 95% CI 2.02-12.85, P = 0.001), and two or more concomitant hepatotoxic medications (OR 2.51, 95% CI 1.02-6.18, P = 0.05). The median time to resolution of hepatotoxicity after cessation of flucloxacillin was 5 days (range 2-10). CONCLUSIONS: In children, older patients and those receiving two or more concomitant hepatotoxic medications are at greater risk of flucloxacillin-induced hepatotoxicity.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos / Enfermedad Hepática Inducida por Sustancias y Drogas Tipo de estudio: Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant Idioma: En Revista: J Antimicrob Chemother Año: 2023 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos / Enfermedad Hepática Inducida por Sustancias y Drogas Tipo de estudio: Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant Idioma: En Revista: J Antimicrob Chemother Año: 2023 Tipo del documento: Article País de afiliación: Australia