Oral and Intravenous Amoxicillin Dosing Recommendations in Neonates: A Pooled Population Pharmacokinetic Study

Author:

Keij Fleur M12ORCID,Schouwenburg Stef34,Kornelisse René F1,Preijers Tim34,Mir Fatima5,Degraeuwe Pieter6,Stolk Leo M7,van Driel Arianne8,Kenter Sandra2,van der Sluijs Jacqueline9,Heidema Jojanneke10,den Butter Paul C P11,Reiss Irwin K M1,Allegaert Karel31213,Tramper-Stranders Gerdien A12,Koch Birgit C P34,Flint Robert B134

Affiliation:

1. Department of Paediatrics, Division of Neonatology, Erasmus University Medical Centre–Sophia Children's Hospital , Rotterdam , The Netherlands

2. Department of Paediatrics, Franciscus Gasthuis & Vlietland , Rotterdam , The Netherlands

3. Department of Hospital Pharmacy, Erasmus University Medical Centre , Rotterdam , The Netherlands

4. Rotterdam Clinical Pharmacometrics Group, Erasmus University Medical Centre , Rotterdam , The Netherlands

5. Section of Paediatric Infectious Disease, Paediatrics and Child Health, Aga Khan University , Karachi , Pakistan

6. Department of Paediatrics, Division of Neonatology, Maastricht University Medical Centre , Maastricht , The Netherlands

7. Department of Clinical Pharmacy, Maastricht University Medical Centre , The Netherlands

8. Department of Paediatrics, IJsselland Hospital , Capelle a/d IJssel , The Netherlands

9. Department of Paediatrics, Division of Neonatology, Maxima Medical Centre , Veldhoven , The Netherlands

10. Department of Paediatrics, St. Antonius Hospital , Nieuwegein , The Netherlands

11. Department of Paediatrics, Ikazia Hospital , Rotterdam , The Netherlands

12. Department of Development and Regeneration, KU Leuven , Leuven , Belgium

13. Department of Pharmaceutical and Pharmacological Sciences, KU Leuven , Leuven , Belgium

Abstract

Abstract Background There is a lack of evidence on oral amoxicillin pharmacokinetics and exposure in neonates with possible serious bacterial infection (pSBI). We aimed to describe amoxicillin disposition following oral and intravenous administration and to provide dosing recommendations for preterm and term neonates treated for pSBI. Methods In this pooled-population pharmacokinetic study, 3 datasets were combined for nonlinear mixed-effects modeling. In order to evaluate amoxicillin exposure following oral and intravenous administration, pharmacokinetic profiles for different dosing regimens were simulated with the developed population pharmacokinetic model. A target of 50% time of the free fraction above the minimal inhibitory concentration (MIC) with an MICECOFF of 8 mg/L (to cover gram-negative bacteria such as Escherichia coli) was used. Results The cohort consisted of 261 (79 oral, 182 intravenous) neonates with a median (range) gestational age of 35.8 weeks (range, 24.9–42.4) and bodyweight of 2.6 kg (range, 0.5–5). A 1-compartment model with first-order absorption best described amoxicillin pharmacokinetics. Clearance (L/h/kg) in neonates born after 30 weeks’ gestation increased with increasing postnatal age (PNA day 10, 1.25-fold; PNA day 20, 1.43-fold vs PNA day 3). Oral bioavailability was 87%. We found that a twice-daily regimen of 50 mg/kg/day is superior to a 3- or 4-times daily schedule in the first week of life for both oral and intravenous administration. Conclusions This pooled population pharmacokinetic description of intravenous and oral amoxicillin in neonates provides age-specific dosing recommendations. We conclude that neonates treated with oral amoxicillin in the first weeks of life reach adequate amoxicillin levels following a twice-daily dosing regimen. Oral amoxicillin therapy could therefore be an adequate, cost-effective, and more patient-friendly alternative for neonates worldwide.

Funder

the Netherlands Organization for Health Research and Development

ZonMw

Innovatiefonds Zorgverzekeraars

Sophia Foundation

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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