Abstract |
Few randomized, controlled trials evaluating antiepileptic drug (AED) efficacy and tolerability have focused solely on patients with juvenile myoclonic epilepsy (JME). We conducted a pilot, randomized controlled trial comparing topiramate (N=19) and valproate (N=9) in adolescents/adults with JME to evaluate clinical response when these broad-spectrum agents are titrated to optimal effect. Rating scales were used to systematically assess tolerability. Among patients completing 26 weeks of treatment, 8 of 12 (67%) in the topiramate group and 4 of 7 (57%) in the valproate group were seizure-free during the 12-week maintenance period. Median daily dose was 250mg topiramate or 750mg valproate. Two (11%) topiramate-treated patients and one (11%) valproate-treated patient discontinued due to adverse events. Systemic toxicity scores, but not neurotoxicity scores, differed substantially between the two groups; greater systemic toxicity was associated with valproate. Our preliminary findings that topiramate may be an effective, well-tolerated alternative to valproate warrant validation in a double-blind trial.
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Authors | Paul M Levisohn, Katherine D Holland |
Journal | Epilepsy & behavior : E&B
(Epilepsy Behav)
Vol. 10
Issue 4
Pg. 547-52
(Jun 2007)
ISSN: 1525-5050 [Print] United States |
PMID | 17482520
(Publication Type: Comparative Study, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Anticonvulsants
- Topiramate
- Fructose
- Valproic Acid
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Topics |
- Adolescent
- Adult
- Aged
- Anticonvulsants
(adverse effects, therapeutic use)
- Child
- Double-Blind Method
- Female
- Fructose
(adverse effects, analogs & derivatives, therapeutic use)
- Humans
- Magnetic Resonance Imaging
- Male
- Middle Aged
- Myoclonic Epilepsy, Juvenile
(drug therapy)
- Neurotoxicity Syndromes
(epidemiology)
- Pilot Projects
- Seizures
(epidemiology, prevention & control)
- Tomography, X-Ray Computed
- Topiramate
- Valproic Acid
(adverse effects, therapeutic use)
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