Add-on lamotrigine treatment in children and young adults with severe partial epilepsy: an open, prospective, long-term study

J Child Neurol. 2000 Oct;15(10):671-4. doi: 10.1177/088307380001501006.

Abstract

We evaluated the efficacy and safety of lamotrigine in 41 children and young adults (age range, 3-25 years; mean, 12 years) with drug-resistant, partial epilepsies, based on a prospective, add-on study. Patients had severe symptomatic/cryptogenic partial epilepsies (mean seizure frequency = 3.6/day), resistant to one to four major antiepileptic drugs. Mean seizure frequency significantly decreased (P < .001) throughout the period of treatment. A good response (>50% seizure reduction) was observed in 15 patients of whom 6 were seizure-free (follow-up: 12-48 months). Higher responder rate was found among cryptogenic epilepsies and epilepsies symptomatic of cerebral malformation, whereas patients with posthypoxic-ischemic perinatal damage were poor responders. Lamotrigine discontinuation was mainly due to lack of efficacy (46% of patients), whereas only 2 patients developed a transient skin rash and did not drop out. Lamotrigine represents a valuable treatment for severe partial epilepsies of childhood that have proved resistant to previous antiepileptic drugs.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Drug Therapy, Combination
  • Epilepsies, Partial / diagnosis
  • Epilepsies, Partial / drug therapy*
  • Epilepsies, Partial / etiology
  • Female
  • Follow-Up Studies
  • Humans
  • Lamotrigine
  • Male
  • Prospective Studies
  • Severity of Illness Index
  • Treatment Outcome
  • Triazines / administration & dosage
  • Triazines / adverse effects
  • Triazines / therapeutic use*

Substances

  • Triazines
  • Lamotrigine