Evolution of juvenile myoclonic epilepsy treated from the outset with sodium valproate

Seizure. 2001 Sep;10(6):424-7. doi: 10.1053/seiz.2000.0530.

Abstract

Sodium valproate (VPA) is considered the first choice drug in juvenile myoclonic epilepsy (JME). We have analysed the long-term evolution of 22 patients treated from the outset with VPA. The following inclusion criteria were applied: (1) unequivocal diagnosis of JME; (2) treatment should be initiated with VPA monotherapy; and (3) follow-up for more than 5 years. Twenty-two patients (15 females, seven males) were studied and their EEG recordings were analysed. Their mean age was 28 years (range: 20-40 years) and their mean follow-up was 7.7 years (range: 5-17 years). Four of them suffered persistent seizures despite optimal VPA dosage and needed the addition of a second drug (lamotrigine in three cases, clobazam in one case). All of our patients who continued their treatment are seizure-free. VPA effectively controlled all seizures in 80% of patients. The discontinuation of drug therapy lead to a very high rate of relapses. With accurate diagnosis and appropriate therapy, seizures in JME can be effectively controlled. VPA is a very effective antiepileptic drug in controlling the seizures of JME, but many patients relapse after VPA discontinuation. Thus, JME may require lifelong therapy.

MeSH terms

  • Adolescent
  • Adult
  • Age of Onset
  • Anticonvulsants / administration & dosage
  • Anticonvulsants / therapeutic use*
  • Child
  • Dose-Response Relationship, Drug
  • Electroencephalography
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Myoclonic Epilepsy, Juvenile / drug therapy*
  • Myoclonic Epilepsy, Juvenile / physiopathology
  • Prospective Studies
  • Recurrence
  • Treatment Outcome
  • Valproic Acid / administration & dosage
  • Valproic Acid / therapeutic use*

Substances

  • Anticonvulsants
  • Valproic Acid