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

被引:3
作者
Gastine, Silke E. E. [1 ]
Rauwolf, Kerstin K. K. [2 ,3 ]
Pieper, Stephanie [2 ,3 ]
Hempel, Georg [1 ]
Lehrnbecher, Thomas [4 ]
Tragiannidis, Athanasios [2 ,3 ,5 ]
Groll, Andreas H. H. [2 ,3 ,6 ,7 ]
机构
[1] Westphalian Wilhelms Univ Munster, Inst Pharmaceut & Med Chem, Dept Clin Pharm, Munster, Germany
[2] Childrens Univ Hosp Munster, Ctr Bone Marrow Transplantat, Infect Dis Res Program, Munster, Germany
[3] Childrens Univ Hosp Munster, Dept Pediat Hematol Oncol, Munster, Germany
[4] Goethe Univ Frankfurt, Hosp Children & Adolescents, Div Pediat Hematol & Oncol, Frankfurt, Germany
[5] Aristotle Univ Thessaloniki, AHEPA Hosp, Dept Pediat 2, Thessaloniki, Greece
[6] Childrens Univ Hosp, Ctr Bone Marrow Transplantat, Infect Dis Res Program, Albert Schweitzer Campus 1,Bldg A1, D-48149 Munster, Germany
[7] Childrens Univ Hosp, Dept Pediat Hematol Oncol, Albert Schweitzer Campus 1,Bldg A1, D-48149 Munster, Germany
关键词
drug monitoring; mycoses; pediatrics; prophylaxis; treatment; voriconazole; INVASIVE FUNGAL DISEASE; PULMONARY ASPERGILLOSIS; CHILDREN YOUNGER; MANAGEMENT; PHARMACOKINETICS; DIAGNOSIS; EFFICACY; SAFETY; INFECTIONS; GUIDELINES;
D O I
10.1111/myc.13643
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Voriconazole (VCZ) is an important first-line option for management of invasive fungal diseases and approved in paediatric patients & GE;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.
引用
收藏
页码:969 / 976
页数:8
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