Lamotrigine for Generalized Seizures Associated with the LennoxGastaut Syndrome
Jacques Motte, M.D., Edwin Trevathan, M.D., M.P.H., Jan F.V. Arvidsson, M.D., Manuel Nieto Barrera, M.D., E. Lynette Mullens, M.D., Penelope Manasco, M.D., for The Lamictal LennoxGastaut Study Group
Background The LennoxGastaut syndrome, a severe formof epilepsy that usually begins in early childhood, is difficultto treat. Dose-related drug toxicity is common.
Methods We conducted a double-blind, placebo-controlled trialof the antiepileptic drug lamotrigine in patients with the LennoxGastautsyndrome. Eligible patients had more than one type of predominantlygeneralized seizure, including tonicclonic, atonic, tonic,and major myoclonic, and had seizures on average at least everyother day. After a 4-week base-line period in which all participantsreceived placebo, we randomly assigned 169 patients (age range,3 to 25 years) to 16 weeks of lamotrigine (n = 79) or placebo(n = 90) in addition to their other antiepileptic drugs.
Results The median frequency of all major seizures changed frombase-line levels of 16.4 and 13.5 per week in the lamotrigineand placebo groups, respectively, to 9.9 and 14.2 per week after16 weeks of treatment (P = 0.002). Thirty-three percent of thepatients in the lamotrigine group and 16 percent of those inthe placebo group had a reduction of at least 50 percent inthe frequency of seizures (P = 0.01). There were no significantdifferences between groups in the incidence of adverse events,except for colds or viral illnesses, which were more commonin the lamotrigine group (P = 0.05).
Conclusions Lamotrigine was an effective and well-toleratedtreatment for seizures associated with the LennoxGastautsyndrome.
Source Information
From the American Memorial Hospital, Hôpital d'Enfants, Reims, France (J.M.); the Department of Neurology, Comprehensive Epilepsy Center, University of Kentucky College of Medicine, Lexington (E.T.); the Pediatric Clinic, Central County Hospital Ryhov, Jonkoping, Sweden (J.F.V.A.); Infantil Virgen del Rocio Hospital, Seville, Spain (M.N.B.); Central Nervous System Clinical Research, Glaxo Wellcome Research and Development, Greenford, Middlesex, United Kingdom (E.L.M.); and Central Nervous System Clinical Research, Glaxo Wellcome Research and Development, Research Triangle Park, N.C. (P.M.).
Address reprint requests to Dr. Trevathan at the Comprehensive Epilepsy Center, University of Kentucky College of Medicine, Kentucky Clinic L445, Lexington, KY 40536-0284.
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