Advertisement
Review article| Volume 23, ISSUE 5, P277-283, August 2001

Download started.

Ok

Newer antiepileptic drugs: advantages and disadvantages

      Abstract

      The choice of an antiepileptic drug depends firstly on its efficacy in specific seizure types and epilepsies. However, it is imperative to consider whether possible adverse events will outweigh any benefits. The advantages and disadvantages of vigabatrin, lamotrigine, gabapentin, topiramate, tiagabine and felbamate are considered in some detail, and oxcarbazepine, stiripentol, remacemide, zonisamide and levetiracetam more briefly. Vigabatrin is effective for partial seizures and infantile spasms, but visual field defects are limiting its use. Lamotrigine has a wide spectrum, needs to be prescribed with care. Gabapentin is unlikely to cause adverse effects, but has relatively poor efficacy. Topiramate is widely effective, but can be poorly tolerated. Tiagabine is relatively untried in childhood epilepsies. The use of felbamate is restricted to severe refractory epilepsies. Stiripentol can be effective in severe myoclonic epilepsy in infancy. Zonisamide has a special place in the progressive myoclonus epilepsies. Levetiracetam, remacemide and oxcarbazepine have been used mainly for partial seizures: further studies of their roles in other circumstances are required.

      Keywords

      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Brain and Development
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Marson A.G.
        • Kadir Z.A.
        • Hutton J.L.
        • Chadwick D.W.
        The new antiepileptic drugs: a systematic review of their efficacy and tolerability.
        Epilepsia. 1997; 38: 859-880
        • Dalla Bernardina B.
        • Fontana E.
        • Vigevano F.
        • Fusco L.
        • Torelli D.
        • Galeone D.
        • et al.
        Efficacy and tolerability of vigabatrin in children with refractory partial seizures: a single-blind, dose-increasing study.
        Epilepsia. 1995; 36: 687-691
        • Appleton R.E.
        • Peters A.C.
        • Mumford J.P.
        • Shaw D.E.
        Randomised, placebo-controlled study of vigabatrin as first-line treatment of infantile spasms.
        Epilepsia. 1999; 40: 1627-1633
        • Hancock E.
        • Osborne J.P.
        Vigabatrin in the treatment of infantile spasms in tuberous sclerosis: literature review.
        J Child Neurol. 1999; 14: 71-74
        • Jambaque I.
        • Chiron C.
        • Dumas C.
        • Mumford J.
        • Dulac O.
        Mental and behavioural outcome of infantile epilepsy treated by vigabatrin in tuberous sclerosis patients.
        Epilepsy Res. 2000; 38: 151-160
        • Chiron C.
        • Dumas C.
        • Jambaque I.
        • Mumford J.
        • Dulac O.
        Randomized trial comparing vigabatrin and hydrocortisone in infantile spasms due to tuberous sclerosis.
        Epilepsy Res. 1997; 26: 389-395
        • Vigevano F.
        • Cilio C.
        Vigabatrin versus ACTH as first-line treatment for infantile spasms: a randomized prospective study.
        Epilepsia. 1997; 38: 1270-1274
        • Gidal B.E.
        • Privitera M.D.
        • Sheth R.D.
        • Gilman J.T.
        VGB: a novel therapy for seizure disorders.
        Ann Pharmacother. 1999; 33: 1277-1286
        • Aicardi J.
        • Mumford J.P.
        • Dumas C.
        • Wood S.
        • Sabril IS Investigator and Peer Review Groups
        Vigabatrin as initial therapy for infantile spasms: a European retrospective survey.
        Epilepsia. 1996; 37: 638-642
        • Gibbs J.M.
        • Appleton R.E.
        • Rosenbloom L.
        Vigabatrin in intractable childhood epilepsy: a retrospective study.
        Pediatr Neurol. 1992; 8: 338-340
        • Feucht M.
        • Brantner-Inthaler S.
        Gamma-vinyl GABA (vigabatrin) in the therapy of Lennox–Gastaut syndrome: an open study.
        Epilepsia. 1994; 35: 993-998
        • Lortie A.
        • Chiron C.
        • Mumford J.
        • Dulac O.
        The potential for increased seizure frequency, relapse and appearance of new seizure types with vigabatrin.
        Neurology. 1993; 43: S24-S27
        • Eke T.
        • Talbot J.F.
        • Lawden M.C.
        Severe persistent visual field constriction associated with vigabatrin.
        Br Med J. 1997; 314: 180-181
        • Harding G.F.
        • Wild J.M.
        • Robertson K.A.
        • Lawden M.C.
        • Betts T.A.
        • Barber C.
        • et al.
        Electro-oculography, electroretinography, visual evoked potentials and multifocal electroretinography in patients with vigabatrin-attributed visual field constriction.
        Epilepsia. 2000; 41: 1420-1431
        • Lawden M.C.
        • Eke T.
        • Degg C.
        • Harding G.F.A.
        • Wild J.M.
        Visual field defects associated with vigabatrin therapy.
        J Neurol Neurosurg Psychiatry. 1999; 67: 716-722
        • Wild J.M.
        • Martinez C.
        • Reinshagen G.
        • Harding G.F.A.
        Characteristics of a unique visual field defect attributed to vigabatrin.
        Epilepsia. 1999; 40: 1784-1794
        • Miller N.R.
        • Johnson M.A.
        • Paul S.R.
        • Girkin C.A.
        • Perry J.D.
        • Endres M.
        • et al.
        Visual dysfunction in patients receiving vigabatrin: clinical and electrophysiologic findings.
        Neurology. 1999; 53: 2082-2087
        • Farrell K.
        • Connolly M.B.
        • Munn R.
        • Peng S.
        • MacWilliam L.M.
        Prospective, open-label, add-on study of lamotrigine in 56 children with intractable generalized epilepsy.
        Pediatr Neurol. 1997; 16: 201-205
        • Belmonte A.
        • Ferrari R.
        • Battini R.
        • Guerrini R.
        Add-on lamotrigine treatment in children and young adults with severe partial epilepsy: an open prospective study.
        Epilepsia. 1999; 40: 236
        • Motte J.
        • Trevathan E.
        • Arvidsson J.F.
        • Barrera M.
        • Mullens E.L.
        • Manasco P.
        • et al.
        Lamotrigine for generalized seizures associated with the Lennox–Gastaut syndrome.
        N Engl J Med. 1997; 337: 1807-1812
        • Besag F.M.
        • Wallace S.J.
        • Dulac O.
        • Alving J.
        • Spencer S.C.
        • Hosking G.
        Lamotrigine for the treatment of epilepsy in childhood.
        J Pediatr. 1995; 127: 991-997
        • Frank L.M.
        • Enlow T.
        • Holmes G.L.
        • Manasco P.
        • Concannon S.
        • Chen C.
        • et al.
        Lamictal (lamotrigine) monotherapy for typical absence seizures in children.
        Epilepsia. 1999; 40: 973-979
        • Guerrini R.
        • Dravet C.
        • Genton P.
        • Belmonte A.
        • Kaminska A.
        • Dulac O.
        Lamotrigine and seizure aggravation in severe myoclonic epilepsy.
        Epilepsia. 1998; 39: 508-512
        • Gibbon F.M.
        • Wallace S.J.
        Lamotrigine in severe infantile epilepsies.
        Epilepsia. 1997; 38: 33
        • Besag F.
        Approaches to reducing the incidence of lamotrigine-induced rash.
        CNS Drugs. 2000; 13: 21-33
        • Guberman A.H.
        • Besag F.M.
        • Brodie M.J.
        • Dooley J.M.
        • Duchowney M.S.
        • Pellock J.M.
        • et al.
        Lamotrigine-associated rash: risk/benefit considerations in adults and children.
        Epilepsia. 1999; 40: 985-991
        • Schlienger R.G.
        • Shapiro L.E.
        • Shear N.H.
        Lamotrigine-associated severe cutaneous adverse reactions.
        Epilepsia. 1998; 39: S22-S26
        • Warner T.
        • Patsalos P.N.
        • Prevett M.
        Lamotrigine-induced carbamazepine toxicity: an interaction with carbamazepine-10, 11-epoxide.
        Epilepsy Res. 1992; 11: 147-150
        • Messenheimer J.
        • Giorgi L.
        • Risner M.
        The tolerability of lamotrigine in children.
        Drug Saf. 2000; 22: 303-312
        • Appleton R.
        • Fichtner K.
        • La Moreaux L.
        • Alexander J.
        • Halsall G.
        • Murray G.
        • et al.
        Gabapentin as add-on therapy in children with refractory partial seizures: a 12-week, multicentre, double-blind, placebo-controlled study.
        Epilepsia. 1999; 40: 1147-1154
        • Chadwick D.W.
        • Anhut H.
        • Greiner M.J.
        • Alexander J.
        • Murray J.H.
        • Garofalo E.A.
        • et al.
        A double-blind trial of gabapentin monotherapy for newly diagnosed partial seizures.
        Neurology. 1998; 51: 1282-1288
        • Vossler D.G.
        Exacerbation of seizures in Lennox–Gastaut syndrome by gabapentin.
        Neurology. 1996; 46: 852-853
        • Scheyer R.D.
        • Assaf B.A.
        • Spencer S.S.
        • Mattson R.H.
        Gabapentin-related myoclonus.
        Epilepsia. 1996; 37: 203
        • Wolf S.M.
        • Shinnar S.
        • Kang H.
        • Gil K.B.
        • Moshe S.L.
        Gabapentin toxicity in children manifesting as behavioral changes.
        Epilepsia. 1995; 36: 1203-1205
        • Lee D.O.
        • Steingard R.J.
        • Cesena M.
        • Helmers S.
        • Riviello J.
        • Mikati M.
        Behavioral side-effects of gabapentin in children.
        Epilepsia. 1996; 37: 87-90
        • Asconape J.
        • Collins T.
        Weight gain associated with the use of gabapentin.
        Epilepsia. 1995; 36: S72
        • King J.
        • Bayles R.L.
        Weight gain during add-on therapy using gabapentin (GBP).
        Epilepsia. 1995; 36: S72
        • Reife R.
        • Pledger G.
        • Wu S-C.
        Topiramate as add-on therapy: pooled analysis of randomized controlled trials in adults.
        Epilepsia. 2000; 41: S66-S71
        • Ritter F.
        • Glauser T.A.
        • Elterman R.D.
        • Wyllie E.
        • Topiramate YP Study Group
        Effectiveness, tolerability and safety of topiramate in children with partial-onset seizures.
        Epilepsia. 2000; 41: S82-S85
        • Glauser T.A.
        • Clark P.O.
        • McGee K.
        Long-term response to topiramate in patients with West syndrome.
        Epilepsia. 2000; 41: S91-S94
        • Glauser T.A.
        • Levisohn P.M.
        • Ritter F.
        • Sachdeo R.C.
        • Topiramate YL Study Group
        Topiramate in Lennox–Gastaut syndrome: open-label treatment of patients completing a randomized controlled trial.
        Epilepsia. 2000; 41: S86-S90
        • Leach J.P.
        • Brodie M.J.
        Tiagabine.
        Lancet. 1998; 351: 203-207
        • Boellner S.W.
        • Deaton R.
        • Sommerville K.W.
        Long-term treatment of partial seizures with tiagabine in children.
        Epilepsia. 1997; 38: 208
        • Uldall P.
        • Bulteau C.
        • Pedersen S.A.
        • Dulac O.
        • Meinild H.
        • Lassen L.C.
        Single-blind study of safety, tolerability and preliminary efficacy of tiagabine as adjunctive treatment of children with epilepsy.
        Epilepsia. 1995; 36: S147-S148
        • Pellock J.M.
        • Deaton R.
        • Sommerville K.W.
        Use of tiagabine as long-term therapy for complex partial seizures in adolescents.
        Epilepsia. 1997; 38: 105
        • Ettinger A.B.
        • Bernal O.G.
        • Andriola M.R.
        • Bagchi S.
        • Flores P.
        • Just C.
        • et al.
        Two cases of non-convulsive status epilepticus in association with tiagabine therapy.
        Epilepsia. 1999; 40: 1159-1162
        • Picinelli P.
        • Borgatti R.
        • Perucca E.
        • Tofani A.
        • Donati G.
        • Balottin U.
        Frontal non-convulsive status epilepticus associated with high-dose tiagabine therapy in a child with familial bilateral perisylvian polymicrogyria.
        Epilepsia. 2000; 41: 1485-1488
        • Theodore W.H.
        • Raubertas R.
        • Porter R.J.
        • Nice F.
        • Devinsky O.
        • Reeves P.
        • et al.
        Felbamate: a clinical trial for complex partial seizures.
        Epilepsia. 1991; 32: 392-397
        • Sachdeo R.
        • Kramer L.D.
        • Rosenberg A.
        • Sachdeo S.
        Felbamate monotherapy: controlled trial in patients with partial onset seizures.
        Ann Neurol. 1992; 32: 386-392
        • Felbamate Study Group in Lennox–Gastaut Syndrome
        Efficacy of felbamate in childhood epileptic encephalopathy (Lennox–Gastaut syndrome).
        N Engl J Med. 1993; 328: 29-33
        • Devinsky O.
        • Kothari M.
        • Rubin R.
        • Mercandetti R.
        • Luciano D.
        Felbamate for absence seizures.
        Epilepsia. 1992; 33: 84
        • Sachdeo R.C.
        • Murphy J.V.
        • Kamin M.
        Felbamate in juvenile myoclonic epilepsy.
        Epilepsia. 1992; 33: 118
        • Hurst D.L.
        • Rolan T.D.
        The use of felbamate to treat infantile spasms.
        J Child Neurol. 1995; 10: 134-136
        • Pellock J.M.
        Felbamate.
        Epilepsia. 1999; 40: S57-S62
        • Tecoma E.S.
        Oxcarbazepine.
        Epilepsia. 1999; 40: S37-S46
        • Gaily E.
        • Granstrom M.L.
        • Linkkonen E.
        Oxcarbazepine in the treatment of early childhood epilepsy.
        J Child Neurol. 1997; 12: 496-498
        • Guerreiro M.M.
        • Vigonius U.
        • Pohlmann H.
        • de Manreza M.L.
        • Fejerman N.
        • Antonuik S.A.
        • et al.
        A double-blind controlled clinical trial of oxcarbazepine versus phenytoin in children and adolescents with epilepsy.
        Epilepsy Res. 1997; 27: 205-213
        • Chiron C.
        • Marchand M.C.
        • Tran A.
        • Rey E.
        • d'Athis P.
        • Vincent J.
        • et al.
        Stiripentol in severe myoclonic epilepsy in infancy: a randomised placebo-controlled syndrome-dedicated trial.
        Lancet. 2000; 356: 1638-1642
        • Martinez-Lage J.M.
        • Loiseau P.
        • Levy R.H.
        • Gonzalez I.
        • Strube E.
        • Tor J.
        • et al.
        Clinical antiepileptic efficacy of stiripentol in resistant partial epilepsies.
        Epilepsia. 1984; 25: 673
        • Farwell J.R.
        • Anderson G.D.
        • Kerr D.M.
        • Tor J.A.
        • Levy R.H.
        Stiripentol in atypical absence seizures in children: an open trial.
        Epilepsia. 1993; 34: 305-311
        • Crawford P.
        • Richens A.
        • Mawer G.
        • Cooper P.
        • Hutchison J.B.
        A double-blind placebo controlled cross-over study of remacemide hydrochloride as adjunctive therapy in patients with refractory epilepsy.
        Seizure. 1992; 1: P7/013
        • Mawer G.E.
        • Jamieson V.
        • Lucas S.B.
        • Wild J.M.
        Adjustment of carbamazepine dose to offset the effects of the interaction with remacemide hydrochloride in a double-blind, multicentre, add-on drug trial (CR2237) in refractory epilepsy.
        Epilepsia. 1999; 40: 190-196
        • Leppik I.E.
        Zonisamide.
        Epilepsia. 1999; 40: S23-S29
        • Kimura S.
        Zonisamide-induced behavior disorder in two children.
        Epilepsia. 1994; 35: 403-405
        • Cereghino J.J.
        • Biton V.
        • Abou-Khalil B.
        • Dreifuss F.E.
        • Gauer L.J.
        • Leppik I.
        • et al.
        • United States Levetiracetam Study Group
        Levetiracetam for partial seizures: results of a double-blind randomized clinical trial.
        Neurology. 2000; 55: 236-242