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Dose evaluation of intravenous metamizole (dipyrone) in infants and children: a prospective population pharmacokinetic study.

Authors :
Ziesenitz VC
Rodieux F
Atkinson A
Borter C
Bielicki JA
Haschke M
Duthaler U
Bachmann F
Erb TO
Gürtler N
Holland-Cunz S
van den Anker JN
Gotta V
Pfister M
Source :
European journal of clinical pharmacology [Eur J Clin Pharmacol] 2019 Nov; Vol. 75 (11), pp. 1491-1502. Date of Electronic Publication: 2019 Aug 07.
Publication Year :
2019

Abstract

Purpose: The prodrug metamizole is prescribed intravenously for postoperative pain in children, including off-label use in infants < 1 year. We aimed to assess the pharmacokinetics of the main metabolites of metamizole in children aged 3-72 months.<br />Methods: A single dose of 10 mg/kg metamizole was administered intravenously for postoperative analgesia. Pharmacokinetic samples were drawn at predefined time points. Pharmacokinetics of the main active metabolite 4-methylaminoantipyrine and three other metabolites was characterized by both non-compartmental and population pharmacokinetic analysis. AUC <subscript>0-inf</subscript> of 4-methylaminoantipyrine was calculated by non-compartmental analysis for two age cohorts (3-23 months, 2-6 years) and compared with the 80-125% range of adult dose-adjusted reference exposure (AUC <subscript>ref</subscript> ). Population pharmacokinetic analysis investigated age and weight dependency of the pharmacokinetics and optimal dosing strategies to achieve equivalent adult exposure.<br />Results: A total of 25 children aged 5 months-5.8 years (7.8-24.8 kg) with at least one concentration sample were included; 19 children had ≥ 5 predefined samples up to 10 h after metamizole dose administration. AUC <subscript>0-inf</subscript> of 4-methylaminoantipyrine in children 2-6 years was 29.9 mg/L/h (95% CI 23.4-38.2), significantly lower than AUC <subscript>ref</subscript> (80-125% range 39.2-61.2 mg/L/h). AUC <subscript>0-inf</subscript> of 4-methylaminoantipyrine in infants < 2 years was 43.6 mg/L/h (95% CI 15.8-119.0), comparable with AUC <subscript>ref</subscript> , while infants < 12 months showed increased exposure. Observed variability could be partially explained by covariates weight and age.<br />Conclusions: Age-related changes in pharmacokinetics of 4-methylaminoantipyrine requires reduced weight-based IV dosing in infants < 1 year compared with infants and children up to 6 years (5 versus 10-20 mg/kg) to achieve equivalent adult exposure.<br />Trial Registration: ClinicalTrials.gov identifier: NCT02660177 .

Details

Language :
English
ISSN :
1432-1041
Volume :
75
Issue :
11
Database :
MEDLINE
Journal :
European journal of clinical pharmacology
Publication Type :
Academic Journal
Accession number :
31388703
Full Text :
https://doi.org/10.1007/s00228-019-02720-2