[Therapeutic drug monitoring of antidepressants: Why venlafaxine is the most monitored drug? A review of literature].

Suivi thérapeutique pharmacologique des antidépresseurs : pourquoi la venlafaxine est le médicament le plus surveillé ? Une revue de la littérature.
Antidepressive agents Antidépresseurs CYP2D6 Cytochrome P-450 CYP2D6 Drug monitoring Suivi thérapeutique pharmacologique Venlafaxine hydrochloride

Journal

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

Informations de publication

Date de publication:
Historique:
received: 12 10 2020
revised: 02 01 2021
accepted: 18 01 2021
pubmed: 9 2 2021
medline: 24 11 2021
entrez: 8 2 2021
Statut: ppublish

Résumé

Venlafaxine is the third most frequently prescribed antidepressant in France the last decade, with about 400,000 daily doses. Therapeutic drug monitoring (TDM) of this medication, by measuring the active moiety venlafaxine (V) and O-desmethylvenlafaxine (ODV), is recommended (level of recommendation 2). However, this antidepressant seems to be the one for which clinicians most often use TDM, much more frequently than escitalopram, which is more prescribed and for which TDM is also recommended. The main goal of this review is to provide an update on the TDM of venlafaxine: its therapeutic interval, its level of recommendation and the origin of its "success". From the literature does not enable to define a therapeutic interval for the active moiety V+ODV, that is to say a steady-state trough concentration allowing a clinical response without toxicity. Nevertheless, a target concentration from 100 to 400μg/L is certainly relevant for the majority of patients without any pharmacodynamic resistance ; though a greater concentration could result in an earlier response or could be required for a clinical response in a minority of patients. A patient with no clinical response despite a concentration greater than 1000μg/L should be proposed another antidepressant. Measurement of the ODV/V ratio is also a useful tool, values below 0.3 usually reflecting a slow metabolizer phenotype for cytochrome P-450 2D6, which is more at risk of adverse effects. Research for this phenotype probably explains many prescriptions for TDM.

Identifiants

pubmed: 33551091
pii: S0040-5957(21)00061-5
doi: 10.1016/j.therap.2021.01.052
pii:
doi:

Substances chimiques

Antidepressive Agents 0
Pharmaceutical Preparations 0
Venlafaxine Hydrochloride 7D7RX5A8MO
Cytochrome P-450 CYP2D6 EC 1.14.14.1
Desvenlafaxine Succinate ZB22ENF0XR

Types de publication

Journal Article Review

Langues

fre

Sous-ensembles de citation

IM

Pagination

725-733

Informations de copyright

Copyright © 2021 Société française de pharmacologie et de thérapeutique. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

Sylvain Couderc (S)

Service de pharmacologie toxicologie et pharmacovigilance, CHU de Limoges, 87000 Limoges, France. Electronic address: Sylvain.COUDERC@chu-limoges.fr.

Celine Mory (C)

Service de pharmacologie toxicologie et pharmacovigilance, CHU de Limoges, 87000 Limoges, France.

Léa Darnaud (L)

Service de pharmacologie toxicologie et pharmacovigilance, CHU de Limoges, 87000 Limoges, France.

Franck Saint-Marcoux (F)

Service de pharmacologie toxicologie et pharmacovigilance, CHU de Limoges, 87000 Limoges, France.

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Classifications MeSH