Effect of topiramate on intractable seizures in Taiwanese children

Sung-Tse Li1, Ein-Yiao Shen, Nan-Chang Chiu

  • 1Department of Pediatrics, Mackay Memorial Hospital, Taipei, Taiwan.

Insights

Topiramate effectively reduced seizures in Taiwanese children with difficult-to-treat epilepsy. This adjunctive therapy showed promise for both partial and generalized epilepsy, with a good safety profile.

Area of Science:

  • Pediatric Neurology
  • Clinical Pharmacology
  • Epileptology

Background:

  • Intractable epilepsy in children poses significant treatment challenges.
  • Existing antiepileptic drug (AED) regimens are often insufficient for severe cases.
  • Need for effective adjunctive therapies in pediatric epilepsy populations.

Purpose of the Study:

  • To prospectively evaluate topiramate as an adjunctive therapy for intractable epilepsy in Taiwanese children.
  • To assess the efficacy and safety of topiramate in pediatric patients with partial and generalized epilepsy.
  • To determine seizure reduction rates and identify adverse effects associated with topiramate treatment.

Main Methods:

  • Prospective study involving 30 Taiwanese children (2-16 years) with intractable epilepsy.
  • Topiramate initiated at 1 mg/kg/day, titrated up to 10 mg/kg/day over 4+ weeks.
  • Patients received stable background AEDs; seizure frequency monitored pre- and post-treatment.

Main Results:

  • In partial epilepsy (n=18): 33.3% achieved ≥50% seizure frequency reduction; 44.4% became seizure-free.
  • In generalized epilepsy (n=12): 33.3% achieved ≥50% seizure frequency reduction; 41.7% became seizure-free.
  • Most common adverse effect was poor appetite (10.0%); no idiosyncratic reactions observed.

Conclusions:

  • Topiramate demonstrates efficacy as an adjunctive treatment for intractable partial and generalized epilepsy in Taiwanese children.
  • The drug is generally well-tolerated, with a favorable safety profile in this pediatric cohort.
  • Topiramate represents a viable therapeutic option for children with refractory epilepsy.

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