Back to Search Start Over

Treatment of myoclonic seizures in patients with juvenile myoclonic epilepsy

Authors :
Stéphane Auvin
Source :
Neuropsychiatric Disease and Treatment, Vol 2007, Iss Issue 6, Pp 729-734 (2007)
Publication Year :
2007
Publisher :
Dove Medical Press, 2007.

Abstract

Stéphane AuvinDepartment of Pediatric Neurology, Lille University Hospital, Lille, France; Pharmacology Laboratory, Lille Medical School, Lille, FranceAbstract: Drug treatment of Juvenile myoclonic epilepsy (JME) is mainly based on clinical experience and prospective and retrospective studies, with little evidence from randomized clinical trials. There are no head-to-head comparisons between old and new antiepileptic drugs (AEDs) and no drugs licensed specifically for JME. Valproate is unquestionably the drug of the first choice in men with JME. In women, lamotrigine should be preferred regarding teratogenicity and side effects of valproate. In addition, levetiracetam and topiramate are effective and can be use in combination or as second line treatment. Some AEDs can aggravate JME. In addition of AEDs, non-pharmacological treatments are important in JME. JME usually require lifelong treatment because seizures nearly always return after withdrawal of therapy.Keywords: myoclonic seizure, myoclonic epilepsy, antiepileptic drugs

Details

Language :
English
ISSN :
11766328 and 11782021
Volume :
2007
Issue :
Issue 6
Database :
Directory of Open Access Journals
Journal :
Neuropsychiatric Disease and Treatment
Publication Type :
Academic Journal
Accession number :
edsdoj.9b04f17b927043a79727885a2605500e
Document Type :
article