Topiramate for the treatment of intractable childhood epilepsy

Abeer A Hassan1, Mohammed M Jan, Ali O Shaabat

  • 1Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Jeddah, Kingdom of Saudi Arabia.

Insights

Topiramate (TPM) effectively treated pediatric intractable epilepsy, with over 60% of children achieving significant seizure reduction. Careful monitoring of body weight is advised due to potential transient side effects.

Area of Science:

  • Pediatric Neurology
  • Clinical Pharmacology
  • Epileptology

Background:

  • Intractable epilepsy in children poses significant therapeutic challenges.
  • Topiramate (TPM) is an antiepileptic drug with a broad spectrum of action.
  • Limited data exists on TPM's efficacy and safety in pediatric populations with refractory epilepsy.

Purpose of the Study:

  • To evaluate the effectiveness and safety of Topiramate (TPM) as an add-on therapy for children with intractable epilepsy.
  • To assess seizure reduction rates and identify potential adverse events associated with TPM treatment in pediatric patients.

Main Methods:

  • Prospective, open-label, add-on trial involving 62 children with intractable epilepsy.
  • Patients received Topiramate (TPM) as adjunctive therapy for up to 3 years.
  • Seizure frequency was monitored, and therapeutic response was categorized as complete, good, fair, or none.

Main Results:

  • 34% of children achieved complete seizure freedom, and 39% experienced >50% seizure reduction with Topiramate (TPM).
  • Daily seizures decreased significantly from 55% to 13% (p=0.0007) after TPM introduction.
  • Adverse events, including decreased appetite, weight loss, and sedation, occurred in 34% of children, mostly transient.

Conclusions:

  • Topiramate (TPM) demonstrates high efficacy in treating pediatric intractable epilepsy.
  • Most side effects associated with Topiramate (TPM) are transient, but weight monitoring is recommended.
  • Topiramate (TPM) offers a valuable therapeutic option for children with refractory seizures.
Abstract

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