Tramadol intoxication in children: An emerging issue.

CYP2D6 Children Overdose Pharmacogenetics Tramadol

Journal

Therapie
ISSN: 1958-5578
Titre abrégé: Therapie
Pays: France
ID NLM: 0420544

Informations de publication

Date de publication:
03 Jun 2024
Historique:
received: 28 03 2024
revised: 14 05 2024
accepted: 27 05 2024
medline: 14 6 2024
pubmed: 14 6 2024
entrez: 13 6 2024
Statut: aheadofprint

Résumé

Prescribing tramadol in children raises safety concerns. In Europe, tramadol is still approved and licensed for use in children over 1-3 years of age, depending on the country. In this context, the authors report a case of a tramadol overdose in a 5-year-old-child with a medical history of homozygous sickle cell disease. Tramadol and M1 were quantified using liquid chromatography with a diode array detection method. CYP2D6 genotype was determined using a next generation sequencing platform (MISeq, Illumina). Tramadol and M1 were quantified in blood respectively at 5.48 and 1.32μg/mL at admission, at 0.77 and 0.35μg/mL 12hours later, and at 0.32 and 0.18μg/mL 20hours later. The patient was predicted as a CYP2D6 normal metabolizer (*35/*29). One of the most important difficulties with the use of tramadol in children relates to its pharmacokinetic (PK) properties. Indeed, tramadol's PK is characterized by a great variability related to: (i) anatomical/physiological factors that impact the volume of distribution (Vd); (ii) CYP2D6 genetic polymorphisms. Considering such an issue is particularly relevant to prevent poisoning. In the reported case, the plasma elimination half-life was estimated at 6.3h, significantly more than those reported in 2-8 year-old children (about 3h). This discrepancy does not seem related to genetic polymorphisms but rather to the Vd. Indeed, the patient was predicted to be a CYP2D6 normal metabolizer (*35/*29). The case presented here highlights the risk associated with the tramadol use in children and emphasizes the importance of considering PK variability among this population. Such variability necessitates greater caution in prescribing tramadol in children and highlights the importance of therapeutic education for families of children treated with this painkiller.

Sections du résumé

BACKGROUND BACKGROUND
Prescribing tramadol in children raises safety concerns. In Europe, tramadol is still approved and licensed for use in children over 1-3 years of age, depending on the country. In this context, the authors report a case of a tramadol overdose in a 5-year-old-child with a medical history of homozygous sickle cell disease.
METHODS METHODS
Tramadol and M1 were quantified using liquid chromatography with a diode array detection method. CYP2D6 genotype was determined using a next generation sequencing platform (MISeq, Illumina).
RESULTS RESULTS
Tramadol and M1 were quantified in blood respectively at 5.48 and 1.32μg/mL at admission, at 0.77 and 0.35μg/mL 12hours later, and at 0.32 and 0.18μg/mL 20hours later. The patient was predicted as a CYP2D6 normal metabolizer (*35/*29).
CONCLUSION CONCLUSIONS
One of the most important difficulties with the use of tramadol in children relates to its pharmacokinetic (PK) properties. Indeed, tramadol's PK is characterized by a great variability related to: (i) anatomical/physiological factors that impact the volume of distribution (Vd); (ii) CYP2D6 genetic polymorphisms. Considering such an issue is particularly relevant to prevent poisoning. In the reported case, the plasma elimination half-life was estimated at 6.3h, significantly more than those reported in 2-8 year-old children (about 3h). This discrepancy does not seem related to genetic polymorphisms but rather to the Vd. Indeed, the patient was predicted to be a CYP2D6 normal metabolizer (*35/*29). The case presented here highlights the risk associated with the tramadol use in children and emphasizes the importance of considering PK variability among this population. Such variability necessitates greater caution in prescribing tramadol in children and highlights the importance of therapeutic education for families of children treated with this painkiller.

Identifiants

pubmed: 38871543
pii: S0040-5957(24)00067-2
doi: 10.1016/j.therap.2024.05.005
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Société française de pharmacologie et de thérapeutique. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

Guillaume Drevin (G)

Service de pharmacologie-toxicologie et pharmacovigilance, centre hospitalo-universitaire d'Angers, 49000 Angers, France. Electronic address: Guillaume.Drevin@chu-angers.fr.

Nicolas Picard (N)

Service de pharmacologie, toxicologie et pharmacovigilance, centre hospitalo-universitaire de Limoges, 87000 Limoges, France.

Antoine Baudriller (A)

Service de pharmacologie-toxicologie et pharmacovigilance, centre hospitalo-universitaire d'Angers, 49000 Angers, France; Université d'Angers, 49000 Angers, France.

Maria Pena-Martin (M)

Service de pharmacologie-toxicologie et pharmacovigilance, centre hospitalo-universitaire d'Angers, 49000 Angers, France.

Séverine Ferec (S)

Service de pharmacologie-toxicologie et pharmacovigilance, centre hospitalo-universitaire d'Angers, 49000 Angers, France.

Laurent Leuger (L)

Service de pharmacologie-toxicologie et pharmacovigilance, centre hospitalo-universitaire d'Angers, 49000 Angers, France.

Marie Briet (M)

Service de pharmacologie-toxicologie et pharmacovigilance, centre hospitalo-universitaire d'Angers, 49000 Angers, France; Université d'Angers, 49000 Angers, France; Unité MitoVasc, Team Carme, SFR ICAT, UMR CNRS 6015, Inserm U1083, University Angers, 49000 Angers, France.

Chadi Abbara (C)

Service de pharmacologie-toxicologie et pharmacovigilance, centre hospitalo-universitaire d'Angers, 49000 Angers, France.

Classifications MeSH