Evidence map›Paper›PMID 40999188›Full record

ArticleClinical pharmacokinetics2025

Evaluation of Fentanyl-Emerged Adverse Events and Pharmacokinetics in Neonates: A Physiologically Based Pharmacokinetic Modeling Approach.

Walaa Yousef Bassyouni Mahdy, Kazuhiro Yamamoto, Risa Joji, Mari Hashimoto, Ruka Nakasone, Kazumichi Fujioka, Kotaro Itohara, Yumi Kitahiro, Tomohiro Omura, Ikuko Yano

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Article in Clinical pharmacokinetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Walaa Yousef Bassyouni MahdyDepartment of Pharmacy, Kobe University Hospital, Kobe, Japan.
Kazuhiro YamamotoDepartment of Pharmacy, Kobe University Hospital, Kobe, Japan. yamakz@okayama-u.ac.jp.ORCID 0000-0002-7513-6725
Risa JojiDepartment of Pharmacy, Kobe University Hospital, Kobe, Japan.
Mari HashimotoDepartment of Pharmacy, Kobe University Hospital, Kobe, Japan.
Ruka NakasoneDepartment of Pediatrics, Graduate School of Medicine, Kobe University, Kobe, Japan.
Kazumichi FujiokaDepartment of Pediatrics, Graduate School of Medicine, Kobe University, Kobe, Japan.
Kotaro ItoharaDepartment of Pharmacy, Kobe University Hospital, Kobe, Japan.
Yumi KitahiroDepartment of Pharmacy, Kobe University Hospital, Kobe, Japan.
Tomohiro OmuraDepartment of Pharmacy, Kobe University Hospital, Kobe, Japan.
Ikuko YanoDepartment of Pharmacy, Kobe University Hospital, Kobe, Japan.

Funding

Japan Society for the Promotion of Science 20H00102Japan Society for the Promotion of Science 22K06697
6 · The paper itself

Abstract

backgroundDespite its common use for analgesia in neonatal intensive care units, the optimal dosing and safety profile of fentanyl, particularly regarding suspected fentanyl-emerged adverse events (FEAEs), such as hypotension, desaturation, and oliguria, are not well-defined.

objectiveThis study aimed to develop an optimal therapeutic monitoring and dosing strategy for fentanyl for neonates. A physiologically based pharmacokinetic (PBPK) model for predicting fentanyl pharmacokinetics across various populations, including preterm and term neonates, was developed, and the relationship between predicted fentanyl exposure and FEAE incidence in neonates was assessed.

methodsA PBPK model was developed and validated against the observed values in the literature. The model's predictive accuracy for fentanyl pharmacokinetics and association with FEAE incidence in an external retrospective cohort of Japanese neonates was evaluated using the predicted concentrations and pharmacokinetic parameters estimated by PBPK simulation.

resultsThe PBPK model exhibited reasonable predictive performance for serum fentanyl concentrations in actual neonatal patients (mean error: 9.27% [standard error: 5.06%], root mean squared error: 54.7%). The incidence of any FEAE, particularly oxygen desaturation, was associated with the fentanyl concentration-to-dose ratio, but not with some exposure parameters, such as the area under the curve and maximum concentration. The recommended reduced infusion rate allowed serum fentanyl concentrations to fall within the ranges established by the reported values and our data.

conclusionsOur PBPK model and proposed dosing strategy may contribute to safer and more effective fentanyl use in neonates.

Indexed as

Analgesics, OpioidFentanylModels, BiologicalDrug MonitoringFemaleHumansInfant, NewbornIntensive Care Units, NeonatalJapanMaleRetrospective StudiesAnalgesics, OpioidFentanyl

Identifiers

PMID40999188
PMCPMC12715038

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