Treatment of psychoses in patients with epilepsy: an update.

antiepileptic drugs antipsychotic drugs epilepsy interaction psychoses schizophrenia seizures

Journal

Therapeutic advances in psychopharmacology
ISSN: 2045-1253
Titre abrégé: Ther Adv Psychopharmacol
Pays: England
ID NLM: 101555693

Informations de publication

Date de publication:
2019
Historique:
received: 29 03 2019
accepted: 14 06 2019
entrez: 19 7 2019
pubmed: 19 7 2019
medline: 19 7 2019
Statut: epublish

Résumé

Psychotic disorders represent a relatively rare but serious comorbidity in epilepsy. Current epidemiological studies are showing a point prevalence of 5.6% in unselected samples of people with epilepsy going up to 7% in patients with temporal lobe epilepsy, with a pooled odds ratio of 7.8 as compared with the general population. This is a narrative review of the most recent updates in the management of psychotic disorders in epilepsy, taking into account the clinical scenarios where psychotic symptoms occur in epilepsy, interactions with antiepileptic drugs (AEDs) and the risk of seizures with antipsychotics. Psychotic symptoms in epilepsy can arise in a number of different clinical scenarios from peri-ictal symptoms, to chronic interictal psychoses, comorbid schizophrenia and related disorders to the so-called forced normalization phenomenon. Data on the treatment of psychotic disorders in epilepsy are still limited and the management of these problems is still based on individual clinical experience. For this reason, guidelines of treatment outside epilepsy should be adopted taking into account epilepsy-related issues including interactions with AEDs and seizure risk. Second-generation antipsychotics, especially risperidone, can represent a reasonable first-line option because of the low propensity for drug-drug interactions and the low risk of seizures. Quetiapine is burdened by a clinically significant pharmacokinetic interaction with enzyme-inducing drugs leading to undetectable levels of the antipsychotic, even for dosages up to 700 mg per day.

Identifiants

pubmed: 31316747
doi: 10.1177/2045125319862968
pii: 10.1177_2045125319862968
pmc: PMC6620723
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

2045125319862968

Déclaration de conflit d'intérêts

Conflict of interest statement: The authors declare that there is no conflict of interest with the present paper. Outside the submitted work, Dr Mula has received consultancy fees from UCB Pharma, Eisai Europe Limited, Bial and Elsevier. Dr Mula also has intellectual property rights with Elsevier and Springer.

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Auteurs

Niruj Agrawal (N)

Atkinson Morley Regional Neuroscience Centre, St George's University Hospitals NHS Foundation Trust, London, UK.

Marco Mula (M)

Institute of Medical and Biomedical Education, St George's University of London, UK.

Classifications MeSH