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03.01.2019 | Original Research Article | Ausgabe 6/2019

Clinical Pharmacokinetics 6/2019

Developmental Pharmacokinetics and Age-Appropriate Dosing Design of Milrinone in Neonates and Infants with Acute Kidney Injury Following Cardiac Surgery

Zeitschrift:
Clinical Pharmacokinetics > Ausgabe 6/2019
Autoren:
Tomoyuki Mizuno, Katja M. Gist, Zhiqian Gao, Michael F. Wempe, Jeffrey Alten, David S. Cooper, Stuart L. Goldstein, Alexander A. Vinks
Wichtige Hinweise

Electronic supplementary material

The online version of this article (https://​doi.​org/​10.​1007/​s40262-018-0729-3) contains supplementary material, which is available to authorized users.
Tomoyuki Mizuno and Katja M. Gist contributed equally to this work.

Abstract

Background and Objective

Milrinone is used for the prevention of low cardiac output syndrome in pediatric patients after cardiac surgery. Milrinone is mainly eliminated by the kidneys; however, there is limited information on milrinone pharmacokinetics in infants who have acute kidney injury (AKI). The aim of this study was to develop a milrinone population pharmacokinetic model in neonates and infants with or without AKI. The developed milrinone pharmacokinetic model was utilized for a Monte Carlo simulation analysis to identify age-appropriate dosing regimens in neonates and infants.

Methods

Population pharmacokinetic analysis was performed with a total of 1088 serum milrinone concentrations obtained from 92 infants as part of a prospective clinical study in neonates and infants following cardiac surgery (ClinicalTrials.gov identifier NCT01966237). AKI stages were determined based on the Kidney Injury Improving Global Outcomes (KDIGO) Clinical Practice Guideline within the first three postoperative days.

Results

A two-compartment model was found to adequately describe the pharmacokinetic data. Allometrically scaled body weight, AKI stages, and maturation function were identified as significant predictors of milrinone clearance. The proposed dosing regimens for milrinone continuous infusions were determined based on a target concentration attainment of simulated steady-state concentration and covered three age groups across 0–12 months of age for each AKI stage.

Conclusion

This study provides a milrinone population pharmacokinetic model in neonates and infants and captures the developmental changes in clearance. Age-appropriate dosing regimens were determined based on the simulation analysis with the developed pharmacokinetic model. The findings will facilitate model-informed precision dosing of milrinone in infants with or without AKI.

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Zusatzmaterial
Supplementary material 1 (PDF 356 kb)
40262_2018_729_MOESM1_ESM.pdf
Literatur
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