Application of machine-learning models to predict the ganciclovir and valganciclovir exposure in children using a limited sampling strategy.

Xgboost artificial intelligence children ganciclovir machine learning pharmacokinetics pharmacometrics transplantation valganciclovir

Journal

Antimicrobial agents and chemotherapy
ISSN: 1098-6596
Titre abrégé: Antimicrob Agents Chemother
Pays: United States
ID NLM: 0315061

Informations de publication

Date de publication:
28 Aug 2024
Historique:
medline: 28 8 2024
pubmed: 28 8 2024
entrez: 28 8 2024
Statut: aheadofprint

Résumé

Intravenous ganciclovir and oral valganciclovir display significant variability in ganciclovir pharmacokinetics, particularly in children. Therapeutic drug monitoring currently relies on the area under the concentration-time (AUC). Machine-learning (ML) algorithms represent an interesting alternative to Maximum-a-Posteriori Bayesian-estimators for AUC estimation. The goal of our study was to develop and validate an ML-based limited sampling strategy (LSS) approach to determine ganciclovir AUC

Identifiants

pubmed: 39194260
doi: 10.1128/aac.00860-24
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0086024

Auteurs

Laure Ponthier (L)

Pharmacology and Transplantation, INSERM U1248, Université de Limoges, Limoges, France.
Department of Pediatrics, University Hospital of Limoges, Limoges, France.

Bénédicte Franck (B)

Department of Clinical and Biological Pharmacology and Pharmacovigilance, Clinical Investigation Center CIC-P 1414, Rennes, France.

Julie Autmizguine (J)

Department of Pharmacology and Physiology, Université de Montréal, Montreal, Quebec, Canada.
Research Center, Center Hospitalier Universitaire Sainte-Justine, Montreal, Quebec, Canada.
Department of Pediatrics, Center Hospitalier Universitaire Sainte-Justine, Montreal, Quebec, Canada.

Marc Labriffe (M)

Pharmacology and Transplantation, INSERM U1248, Université de Limoges, Limoges, France.
Department of Pharmacology, Toxicology and Pharmacovigilance, University Hospital of Limoges, Limoges, France.

Philippe Ovetchkine (P)

Department of Pharmacology and Physiology, Université de Montréal, Montreal, Quebec, Canada.

Pierre Marquet (P)

Pharmacology and Transplantation, INSERM U1248, Université de Limoges, Limoges, France.
Department of Pharmacology, Toxicology and Pharmacovigilance, University Hospital of Limoges, Limoges, France.

Anders Åsberg (A)

Department of Transplantation Medicine, Oslo University Hospital-Rikshospitalet, Oslo, Norway.
Section of Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, Oslo, Norway.

Jean-Baptiste Woillard (J-B)

Pharmacology and Transplantation, INSERM U1248, Université de Limoges, Limoges, France.
Department of Pharmacology, Toxicology and Pharmacovigilance, University Hospital of Limoges, Limoges, France.

Classifications MeSH