Voriconazole plasma concentrations and dosing in paediatric patients below 24 months of age

Author:

Gastine Silke E.1,Rauwolf Kerstin K.2ORCID,Pieper Stephanie2,Hempel Georg1,Lehrnbecher Thomas3,Tragiannidis Athanasios24,Groll Andreas H.2ORCID

Affiliation:

1. Institute of Pharmaceutical and Medical Chemistry – Department of Clinical Pharmacy Westphalian Wilhelms University Münster Münster Germany

2. Infectious Disease Research Program, Center for Bone Marrow Transplantation and Department of Pediatric Hematology/Oncology Children's University Hospital Münster Münster Germany

3. Division of Pediatric Hematology and Oncology, Hospital for Children and Adolescents Johann Wolfgang Goethe University Frankfurt Frankfurt Germany

4. 2nd Department of Pediatrics Aristotle University of Thessaloniki, AHEPA Hospital Thessaloniki Greece

Abstract

AbstractVoriconazole (VCZ) is an important first‐line option for management of invasive fungal diseases and approved in paediatric patients ≥24 months at distinct dosing schedules that consider different developmental stages. Information on dosing and exposures in children <24 months of age is scarce. Here we report our experience in children <24 months who received VCZ due to the lack of alternative treatment options. This retrospective analysis includes 50 distinct treatment episodes in 17 immunocompromised children aged between 3 and <24 months, who received VCZ between 2004 and 2022 as prophylaxis (14 patients; 47 episodes) or as empirical treatment (3 patients; 3 episodes) by mouth (46 episodes) or intravenously (4 episodes) based on contraindications, intolerance or lack of alternative options. Trough concentrations were measured as clinically indicated, and tolerability was assessed based on hepatic function parameters and discontinuations due to adverse events (AEs). VCZ was administered for a median duration of 10 days (range: 1–138). Intravenous doses ranged from 4.9 to 7.0 mg/kg (median: 6.5) twice daily, and oral doses from 3.8 to 29 mg/kg (median: 9.5) twice daily, respectively. The median trough concentration was 0.63 mg/L (range: 0.01–16.2; 38 samples). Only 34.2% of samples were in the recommended target range of 1–6 mg/L; 57.9% had lower and 7.9% higher trough concentrations. Hepatic function parameters analysed at baseline, during treatment and at end of treatment did not show significant changes during VCZ treatment. There was no correlation between dose and exposure or hepatic function parameters. In three episodes, VCZ was discontinued due to an AE (6%; three patients). In conclusion, this retrospective analysis reveals no signal for increased toxicity in paediatric patients <24 months of age. Empirical dosing resulted in mostly subtherapeutic exposures which emphasises the need for more systematic study of the pharmacokinetics of VCZ in this age group.

Publisher

Wiley

Subject

Infectious Diseases,Dermatology,General Medicine

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