Literature DB >> 26076853

Carbamazepine and oxcarbazepine in adult patients with Dravet syndrome: Friend or foe?

F M Snoeijen-Schouwenaars1, M J B M Veendrick2, P van Mierlo3, G van Erp3, A J A de Louw3, B U Kleine3, H J Schelhaas3, I Y Tan2.   

Abstract

PURPOSE: In newly diagnosed patients with Dravet syndrome sodium channel blockers are usually avoided. However, in many adult patients the diagnosis was made long after the initiation of therapy. The purpose of our study was to acquire information concerning the potential risks and benefits of (ox)carba(ma)zepine withdrawal in adult patients with genetically confirmed Dravet syndrome.
METHOD: We identified 16 adults with Dravet syndrome, living in a tertiary care facility for people with epilepsy and an intellectual disability. We reviewed clinical history, genetic findings, the type and duration of sodium channels blockers that were used, seizure types and frequency, and the effect of a change in these medications.
RESULTS: The study population consisted of 9 men and 7 women. Median age was 35 years (range 20-61 years). An attempt to withdraw carbamazepine (CBZ) was made in 9 patients. In 3 of these patients an increase in tonic-clonic seizures was observed. An attempt to withdraw oxcarbazepine (OXC) was made in 3 patients, leading to a complete stop in 2 patients. 3 of the 4 deaths in the withdrawal-group were related to epilepsy.
CONCLUSION: In adult patients with Dravet syndrome withdrawal of CBZ or OXC is not without risks. We suggest that (ox)carba(ma)zepine withdrawal should be considered in these patients but only if there is a good reason to do so and only if they are closely monitored.
Copyright © 2015 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Adults; Carbamazepine; Dravet syndrome; Epilepsy; Oxcarbazepine; Withdrawal

Mesh:

Substances:

Year:  2015        PMID: 26076853     DOI: 10.1016/j.seizure.2015.03.010

Source DB:  PubMed          Journal:  Seizure        ISSN: 1059-1311            Impact factor:   3.184


  6 in total

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Authors:  Kelly G Knupp; Elaine C Wirrell
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Review 2.  Recent advances in epilepsy.

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Review 3.  Recent Advances in the Drug Treatment of Dravet Syndrome.

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Journal:  CNS Drugs       Date:  2019-09       Impact factor: 5.749

4.  Dravet syndrome and Dravet syndrome-like phenotype: a systematic review of the SCN1A and PCDH19 variants.

Authors:  Ana Carla Mondek Rampazzo; Rafael Rodrigues Pinheiro Dos Santos; Fernando Arfux Maluf; Renata Faria Simm; Fernando Augusto Lima Marson; Manoela Marques Ortega; Paulo Henrique Pires de Aguiar
Journal:  Neurogenetics       Date:  2021-05-03       Impact factor: 2.660

Review 5.  Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening.

Authors:  Aliesha Griffin; Kyla R Hamling; SoonGweon Hong; Mana Anvar; Luke P Lee; Scott C Baraban
Journal:  Front Pharmacol       Date:  2018-06-04       Impact factor: 5.810

6.  The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function.

Authors:  Laura B Jones; Colin H Peters; Richard E Rosch; Maxine Owers; Elaine Hughes; Deb K Pal; Peter C Ruben
Journal:  Front Pharmacol       Date:  2021-12-02       Impact factor: 5.810

  6 in total

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