Topiramate in intractable childhood onset epilepsy - A cautionary note

J. M. Dooley, P. R. Camfield, E. Smith, P. Langevin, G. Ronen

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

37 Citas (Scopus)

Resumen

Objectives: To study the effectiveness and safety of topiramate in clinical practice, for a group of patients with childhood onset epilepsy. Methods: All patients treated with topiramate at the three study centers between November 1995 and December 31, 1997 were analyzed retrospectively, using a standardized study protocol. Data were gathered on demographic features, seizure response and medication related adverse events. Results: Eighty-seven patients were treated with topiramate. Over 90% seizure reduction was achieved in 8 (9%) patients, 50%-90% in 21 (24%), <50% in 54 (62%) patients. Four patients (5%) had a deterioration in seizure control. Adverse events required topiramate discontinuation in 36 (41%). Of these 27 (31%) complained of unacceptable cognitive dulling. The rate of dose escalation and final dose in mg/kg were similar in those who remained on topiramate and those who were intolerant because of cognitive side effects. Conclusions: Although topiramate resulted in >50% seizure reduction in 29 (33%) of this group of patients with difficult epilepsy, its usefulness was limited by a high incidence of adverse effects. Adverse events prevented ongoing therapy for 36 (41%) and cognitive dulling resulted in topiramate discontinuation by 27 (31%) of the group.

Idioma originalEnglish
Páginas (desde-hasta)271-273
Número de páginas3
PublicaciónCanadian Journal of Neurological Sciences
Volumen26
N.º4
DOI
EstadoPublished - 1999
Publicado de forma externa

ASJC Scopus Subject Areas

  • Neurology
  • Clinical Neurology

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