Evaluation of a System-Specific Function To Describe the Pharmacokinetics of Benzylpenicillin in Term Neonates Undergoing Moderate Hypothermia

Author:

Bijleveld Yuma A.1,de Haan Timo R.2,van der Lee Johanna H.3,Groenendaal Floris45,Dijk Peter H.6,van Heijst Arno7,de Jonge Rogier C. J.8,Dijkman Koen P.9,van Straaten Henrica L. M.10,Rijken Monique11,Zonnenberg Inge A.12,Cools Filip13,Zecic Alexandra14,Nuytemans Debbie H. G. M.2,van Kaam Anton H.212,Mathôt Ron A. A.1

Affiliation:

1. Department of Pharmacy, Academic Medical Center, Amsterdam, The Netherlands

2. Department of Neonatology, Emma Children's Hospital, Academic Medical Center, Amsterdam, The Netherlands

3. Paediatric Clinical Research Office, Emma Children's Hospital, Academic Medical Center, University of Amsterdam, The Netherlands

4. Department of Neonatology, Wilhelmina Children's Hospital, Utrecht, The Netherlands

5. Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands

6. Department of Neonatology, University of Groningen, Groningen, The Netherlands

7. Department of Neonatology, Radboud University Medical Center, Nijmegen, The Netherlands

8. Department of Pediatrics, Division of Neonatology, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands

9. Department of Neonatology, Máxima Medical Center Veldhoven, Veldhoven, The Netherlands

10. Department of Neonatology, Isala Clinics, Zwolle, The Netherlands

11. Department of Neonatology, Leiden University Medical Center, Leiden, The Netherlands

12. Department of Neonatology, VU University Medical Center, Amsterdam, The Netherlands

13. Department of Neonatology, Vrije Universiteit Brussel, Brussels, Belgium

14. Department of Neonatology, University Hospital Gent, Ghent, Belgium

Abstract

ABSTRACT The pharmacokinetic (PK) properties of intravenous (i.v.) benzylpenicillin in term neonates undergoing moderate hypothermia after perinatal asphyxia were evaluated, as they have been unknown until now. A system-specific modeling approach was applied, in which our recently developed covariate model describing developmental and temperature-induced changes in amoxicillin clearance (CL) in the same patient study population was incorporated into a population PK model of benzylpenicillin with a priori birthweight (BW)-based allometric scaling. Pediatric population covariate models describing the developmental changes in drug elimination may constitute system-specific information and may therefore be incorporated into PK models of drugs cleared through the same pathway. The performance of this system-specific model was compared to that of a reference model. Furthermore, Monte-Carlo simulations were performed to evaluate the optimal dose. The system-specific model performed as well as the reference model. Significant correlations were found between CL and postnatal age (PNA), gestational age (GA), body temperature (TEMP), urine output (UO; system-specific model), and multiorgan failure (reference model). For a typical patient with a GA of 40 weeks, BW of 3,000 g, PNA of 2 days (TEMP, 33.5°C), and normal UO (2 ml/kg/h), benzylpenicillin CL was 0.48 liter/h (interindividual variability [IIV] of 49%) and the volume of distribution of the central compartment was 0.62 liter/kg (IIV of 53%) in the system-specific model. Based on simulations, we advise a benzylpenicillin i.v. dose regimen of 75,000 IU/kg/day every 8 h (q8h), 150,000 IU/kg/day q8h, and 200,000 IU/kg/day q6h for patients with GAs of 36 to 37 weeks, 38 to 41 weeks, and ≥42 weeks, respectively. The system-specific model may be used for other drugs cleared through the same pathway accelerating model development.

Funder

ZonMw

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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