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

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 ter...

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Autores principales: Keij, Fleur M, Schouwenburg, Stef, Kornelisse, René F, Preijers, Tim, Mir, Fatima, Degraeuwe, Pieter, Stolk, Leo M, van Driel, Arianne, Kenter, Sandra, van der Sluijs, Jacqueline, Heidema, Jojanneke, den Butter, Paul C P, Reiss, Irwin K M, Allegaert, Karel, Tramper-Stranders, Gerdien A, Koch, Birgit C P, Flint, Robert B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686957/
https://www.ncbi.nlm.nih.gov/pubmed/37757471
http://dx.doi.org/10.1093/cid/ciad432
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author Keij, Fleur M
Schouwenburg, Stef
Kornelisse, René F
Preijers, Tim
Mir, Fatima
Degraeuwe, Pieter
Stolk, Leo M
van Driel, Arianne
Kenter, Sandra
van der Sluijs, Jacqueline
Heidema, Jojanneke
den Butter, Paul C P
Reiss, Irwin K M
Allegaert, Karel
Tramper-Stranders, Gerdien A
Koch, Birgit C P
Flint, Robert B
author_facet Keij, Fleur M
Schouwenburg, Stef
Kornelisse, René F
Preijers, Tim
Mir, Fatima
Degraeuwe, Pieter
Stolk, Leo M
van Driel, Arianne
Kenter, Sandra
van der Sluijs, Jacqueline
Heidema, Jojanneke
den Butter, Paul C P
Reiss, Irwin K M
Allegaert, Karel
Tramper-Stranders, Gerdien A
Koch, Birgit C P
Flint, Robert B
author_sort Keij, Fleur M
collection PubMed
description 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 MIC(ECOFF) 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.
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spelling pubmed-106869572023-12-01 Oral and Intravenous Amoxicillin Dosing Recommendations in Neonates: A Pooled Population Pharmacokinetic Study Keij, Fleur M Schouwenburg, Stef Kornelisse, René F Preijers, Tim Mir, Fatima Degraeuwe, Pieter Stolk, Leo M van Driel, Arianne Kenter, Sandra van der Sluijs, Jacqueline Heidema, Jojanneke den Butter, Paul C P Reiss, Irwin K M Allegaert, Karel Tramper-Stranders, Gerdien A Koch, Birgit C P Flint, Robert B Clin Infect Dis Major Article 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 MIC(ECOFF) 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. Oxford University Press 2023-09-27 /pmc/articles/PMC10686957/ /pubmed/37757471 http://dx.doi.org/10.1093/cid/ciad432 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Keij, Fleur M
Schouwenburg, Stef
Kornelisse, René F
Preijers, Tim
Mir, Fatima
Degraeuwe, Pieter
Stolk, Leo M
van Driel, Arianne
Kenter, Sandra
van der Sluijs, Jacqueline
Heidema, Jojanneke
den Butter, Paul C P
Reiss, Irwin K M
Allegaert, Karel
Tramper-Stranders, Gerdien A
Koch, Birgit C P
Flint, Robert B
Oral and Intravenous Amoxicillin Dosing Recommendations in Neonates: A Pooled Population Pharmacokinetic Study
title Oral and Intravenous Amoxicillin Dosing Recommendations in Neonates: A Pooled Population Pharmacokinetic Study
title_full Oral and Intravenous Amoxicillin Dosing Recommendations in Neonates: A Pooled Population Pharmacokinetic Study
title_fullStr Oral and Intravenous Amoxicillin Dosing Recommendations in Neonates: A Pooled Population Pharmacokinetic Study
title_full_unstemmed Oral and Intravenous Amoxicillin Dosing Recommendations in Neonates: A Pooled Population Pharmacokinetic Study
title_short Oral and Intravenous Amoxicillin Dosing Recommendations in Neonates: A Pooled Population Pharmacokinetic Study
title_sort oral and intravenous amoxicillin dosing recommendations in neonates: a pooled population pharmacokinetic study
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686957/
https://www.ncbi.nlm.nih.gov/pubmed/37757471
http://dx.doi.org/10.1093/cid/ciad432
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