Lamotrigine as an add-on drug in typical absence seizures
- 29 January 2009
- journal article
- research article
- Published by Hindawi Limited in Acta Neurologica Scandinavica
- Vol. 91 (3) , 200-202
- https://doi.org/10.1111/j.1600-0404.1995.tb00434.x
Abstract
Lamotrigine is licensed in many countries for use in patients with partial seizures. Evidence suggests that it may also be effective in generalised epilepsies. We analysed retrospectively our patients with idiopathic generalised epilepsy with refractory absences. Fifteen patients with idiopathic generalised epilepsies were identified who had been treated with lamotrigine for 3 months or more. All patients were also treated with sodium valproate. Fourteen patients had active absences. Nine (64%) had a total or virtual cessation of absences and in a further patient they became milder and less frequent. One patient reported an increase in seizures. The effective dose of lamotrigine was 1.6-3.0 mg/kg/day in children and 25-50 mg/day in adults. Patients who responded did so after the first or second dose. Lamotrigine was well tolerated. Low-dose lamotrigine added to sodium valproate appears to be effective in typical absence seizures. A therapeutic interaction of the two drugs seems likely.Keywords
This publication has 12 references indexed in Scilit:
- Therapeutic interaction of lamotrigine and sodium valproate in intractable myoclonic epilepsySeizure, 1994
- Interaction of lamotrigine with sodium valproateThe Lancet, 1993
- Lamotrigine for generalised epilepsiesThe Lancet, 1992
- Lamotrigine in primary generalised epilepsyThe Lancet, 1992
- Sodium valproate acutely inhibits lamotrigine metabolism.British Journal of Clinical Pharmacology, 1992
- Lamotrigine as an Add-On Drug in the Management of Lennox-Gastaut SyndromeEuropean Neurology, 1992
- Overview of the Clinical Efficacy of LamotrigineEpilepsia, 1991
- Proposal for Revised Classification of Epilepsies and Epileptic SyndromesEpilepsia, 1989
- DIFFERENTIATION OF TYPICAL ABSENCE SEIZURES IN EPILEPTIC SYNDROMESBrain, 1989
- Nosological Problems of Myoclonic Epilepsies in Childhood and AdolescenceDevelopmental Medicine and Child Neurology, 1977