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Efficiency and safety of oxcarbazepine in mood disorders: A naturalistic study exploring the interest of plasma dosages

Published online by Cambridge University Press:  16 April 2020

David Misdrahi*
Affiliation:
Pôle 347 de Psychiatrie Adulte, Centre Hospitalier Charles Perrens, 121 rue de la Béchade, 33076Bordeaux Cedex, France
Marie Tournier
Affiliation:
INSERM U657, Université Victor Segalen Bordeaux 2, 146 rue Léo Saignat, 33076Bordeaux Cedex, France Service Universitaire de Psychiatrie, Centre Hospitalier Charles Perrens, 121 rue de la Béchade, 33076Bordeaux Cedex, France
Tiphaine Droulout
Affiliation:
Service Universitaire de Psychiatrie, Centre Hospitalier Charles Perrens, 121 rue de la Béchade, 33076Bordeaux Cedex, France
Adeline Grolleau
Affiliation:
INSERM U657, Université Victor Segalen Bordeaux 2, 146 rue Léo Saignat, 33076Bordeaux Cedex, France
Karine Titier
Affiliation:
INSERM U657, Université Victor Segalen Bordeaux 2, 146 rue Léo Saignat, 33076Bordeaux Cedex, France
Mathieu Molimard
Affiliation:
INSERM U657, Université Victor Segalen Bordeaux 2, 146 rue Léo Saignat, 33076Bordeaux Cedex, France
Helene Verdoux
Affiliation:
INSERM U657, Université Victor Segalen Bordeaux 2, 146 rue Léo Saignat, 33076Bordeaux Cedex, France Service Universitaire de Psychiatrie, Centre Hospitalier Charles Perrens, 121 rue de la Béchade, 33076Bordeaux Cedex, France
*
*Corresponding author. Pôle de Psychiatrie adulte, Hôpital Charles Perrens, 121 rue de la Béchade, 33076 Bordeaux Cedex, France. Tel.: +33 5 56 56 34 50; fax: +33 5 56 56 35 46. E-mail address: dmisdrahi@ch-perrens.fr (D. Misdrahi).
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Abstract

Objective

To investigate whether measurement of plasma levels can predict tolerance to oxcarbazepine (OXC).

Methods

We reviewed medical records to identify all inpatients consecutively treated by OXC at the University Department of Psychiatry in Bordeaux. Adverse effects were rated before treatment onset, at day 3, then every week and at discharge or at discontinuation. Residual hydroxy-OXC concentrations were measured on blood samples at the same periods.

Results

OXC was prescribed to 20 patients with bipolar (n = 18) or schizoaffective bipolar-type disorder (n = 2). Reported side effects were transient and occurred mostly at the beginning of the treatment. Three patients stopped OXC because of severe cutaneous side effects. Residual hydroxy-OXC plasma levels were similar in patients with or without occurrence of side effects at all times of assessment.

Conclusion

Our data suggest that the occurrence of severe side-effects is relatively high with OXC. Measurement of plasma OXC levels does not appear to be of interest in clinical practice since plasma concentrations are not predictive of the occurrence of side effects.

Type
Original article
Copyright
Copyright © Elsevier Masson SAS 2008

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