The new generation of antiepileptic drugs: advantages and disadvantages
Open Access
- 1 November 1996
- journal article
- review article
- Published by Wiley in British Journal of Clinical Pharmacology
- Vol. 42 (5) , 531-543
- https://doi.org/10.1111/j.1365-2125.1996.tb00107.x
Abstract
1. After a hiatus of over 20 years, several new antiepileptic drugs (vigabatrin, lamotrigine, gabapentin, oxcarbazepine, topiramate, felbamate, zonisamide and tiagabine) have reached or approached the registration phase. 2. Compared with older agents, many new drugs exhibit simpler pharmacokinetics. This is especially true for vigabatrin and gabapentin, which are renally eliminated and have a low interaction potential. 3. Unlike most of the older agents, vigabatrin, lamotrigine, gabapentin and tiagabine are devoid of significant enzyme inducing or inhibiting properties. Topiramate, oxcarbazepine and felbamate may induce the metabolism of steroid oral contraceptives. In addition, felbamate also acts as a metabolic inhibitor. 4. To date, the efficacy of new drugs has been evaluated extensively only under add-on conditions in patients with partial seizures (with or without secondary generalization) refractory to conventional treatment. However, there is evidence that lamotrigine, zonisamide, felbamate and, possibly, topiramate may also be effective in generalized epilepsies. 5. In placebo-controlled studies, typically between 15 and 40% of patients with difficult-to-treat partial epilepsy have shown an improvement (defined as a 50% or greater decrease in seizure frequency) after addition of a new drug. Only a small minority of these patients achieved complete seizure control. 6. Compared with older agents, some of the new drugs may have a better tolerability profile. Felbamate, however, has been associated with a high risk of aplastic anaemia and hepatotoxicity. 7. At present, the main use of the new agents is in patients refractory to first-line drugs such as carbamazepine or valproate, and further studies are required to characterize their activity spectrum as well as their potential value in monotherapy. In most patients, new drugs cannot be recommended for first-line use until evidence is obtained that potential advantages in tolerability or ease of use outweigh the drawback of their high cost.Keywords
This publication has 51 references indexed in Scilit:
- Pharmacological principles as a basis for polytherapyActa Neurologica Scandinavica, 2009
- Antiepileptic DrugsNew England Journal of Medicine, 1996
- The Management of Epilepsy in the 1990sDrugs, 1995
- Mechanisms of action of new antiepileptic drugs: rational design and serendipitous findingsTrends in Pharmacological Sciences, 1994
- The Clinical Pharmacology of the New Antiepileptic DrugsPharmacological Research, 1993
- Studies on the mechanism of action of the novel anticonvulsant lamotrigine (Lamictal) using primary neuroglial cultures from rat cortexBrain Research, 1993
- Interaction of lamotrigine with sodium valproateThe Lancet, 1993
- Interaction of lamotrigine with sodium valproateThe Lancet, 1993
- New Antiepileptic Drugs: From Serendipity to Rational DiscoveryEpilepsia, 1992
- Valproate-Ethosuximide Combination Therapy for Refractory Absence SeizuresArchives of Neurology, 1983