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Add-on therapy with topiramate in progressive myoclonic epilepsy.

Abstract
We evaluated the clinical responses to add-on therapy with topiramate in eight patients with progressive myoclonic epilepsy (PME). Severe myoclonic seizures disturbing daily activities were persistent despite adequate trials of various combinations of antiepileptic drugs in all patients. After the initiation of topiramate therapy, five patients had a marked decrease in myoclonic seizure frequency, prominent improvement of daily functioning, and recovery from previous drug-related side effects such as weight gain and irregularities of menstruation due to polycystic ovary syndrome. However, we had to discontinue topiramate in three patients because of side effects. Topiramate seems to be a useful alternative agent in the treatment of PME. The antimyoclonic effect provides some independence in daily activities and decreases the side effects related to other antiepileptic drugs, which are clear benefits for this grave disease, although having a short-term effect in some patients.
AuthorsEbru Aykutlu, Betül Baykan, Candan Gürses, Nerses Bebek, Nesimi Büyükbabani, Ayşen Gökyigit
JournalEpilepsy & behavior : E&B (Epilepsy Behav) Vol. 6 Issue 2 Pg. 260-3 (Mar 2005) ISSN: 1525-5050 [Print] United States
PMID15710314 (Publication Type: Clinical Trial, Comparative Study, Journal Article)
Chemical References
  • Anticonvulsants
  • Topiramate
  • Fructose
Topics
  • Adolescent
  • Adult
  • Anticonvulsants (therapeutic use)
  • Disability Evaluation
  • Drug Therapy, Combination
  • Female
  • Follow-Up Studies
  • Fructose (analogs & derivatives, therapeutic use)
  • Humans
  • Male
  • Myoclonic Epilepsies, Progressive (drug therapy)
  • Time Factors
  • Topiramate
  • Treatment Outcome

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