Prospective study of first-choice topiramate therapy in newly diagnosed infantile spasms

Clin Neuropharmacol. 2006 Nov-Dec;29(6):343-9. doi: 10.1097/01.WNF.0000236768.54150.8C.

Abstract

Objective: This was a prospective open study to establish the efficacy, tolerability, and problems associated with the use of topiramate as first-choice drug in children with infantile spasms.

Methods: Open-label follow-up study, ranging from 24 to 36 months, of the cases of 54 patients with infantile spasms treated initially with topiramate as first-choice drug.

Results: Thirty-one patients (57.4%) were seizure free for more than 24 months; 9 patients were treated with topiramate alone and 22 patients with topiramate plus nitrazepam and/or valproate. In 44 cases (81.4%), the reduction of seizure frequency from baseline was greater than 30%, whereas in 10 cases (18.6%), there was poor or no response. The average dosage applied was 5.2 mg/kg per day (maximum dosage, 26 mg/kg per day; minimum dosage, 1.56 mg/kg per day). Adverse events occurred in 14 patients (26%). They included poor appetite leading to anorexia, absence of sweating, and sleeplessness.

Conclusions: Topiramate proves to be an effective and safe first-choice drug not only as adjunctive but also as monotherapy of infantile spasms in children younger than 2 years.

Publication types

  • Comparative Study
  • Evaluation Study

MeSH terms

  • Anticonvulsants / therapeutic use*
  • Drug Administration Schedule
  • Electroencephalography / methods
  • Follow-Up Studies
  • Fructose / analogs & derivatives*
  • Fructose / therapeutic use
  • Humans
  • Infant
  • Prospective Studies
  • Retrospective Studies
  • Spasms, Infantile / diagnosis
  • Spasms, Infantile / drug therapy*
  • Topiramate
  • Treatment Outcome*

Substances

  • Anticonvulsants
  • Topiramate
  • Fructose