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Topiramate for the treatment of infantile spasms
Syed A Hosain1, Sabiha Merchant, Gail E Solomon
1Division of Pediatric Neurology, New York Presbyterian Hospital, Weill Medical College of Cornell University, Department of Pediatric Neurology, NY 10021, USA. sahosain@med.cornell.edu
Insights
Topiramate effectively reduced seizure rates in children with infantile spasms, showing a 41% median reduction. This antiepileptic drug was generally well-tolerated, with some patients becoming spasm-free.
Area of Science:
- Neurology
- Pediatrics
- Pharmacology
Background:
- Infantile spasms are a severe epilepsy syndrome in infants.
- Limited data exist on topiramate's efficacy for infantile spasms.
- Topiramate is a broad-spectrum antiepileptic drug.
Purpose of the Study:
- To prospectively evaluate the efficacy and tolerability of topiramate in treating infantile spasms.
- To assess seizure rate reduction and EEG changes in response to topiramate treatment.
Main Methods:
- 15 children with recently diagnosed infantile spasms were treated with topiramate.
- Dosing started at 3 mg/kg/day, titrated up to 27 mg/kg/day over 2-3 weeks.
- Seizure rates and EEGs were compared between baseline and the first 2 months of treatment.
Main Results:
- A 41% median reduction in seizure rate was observed (P = .002).
- 20% of patients became spasm-free, and 53% had >50% seizure reduction.
- Hypsarrhythmia cleared in 3 patients; irritability was the most common side effect.
Conclusions:
- Topiramate demonstrated efficacy in reducing seizure frequency in infantile spasms.
- The drug was generally well-tolerated in this pediatric population.
- Topiramate is a viable treatment option for infantile spasms, though not universally effective.
Abstract:
Topiramate is a new antiepileptic drug with a broad spectrum of efficacy. Reports on the use of topiramate for treatment of infantile spasms are limited. We prospectively followed 15 children with recently diagnosed infantile spasms treated with topiramate for efficacy and tolerability. Twelve patients had symptomatic infantile spasms, and two patients had cryptogenic infantile spasms. Topiramate was started at a dose of 3 mg/kg/day and titrated up to a dose of 27 mg/kg/day in 2 to 3 weeks. The primary efficacy measure was comparison of the seizure rate during the 2-week baseline with the median seizure rate during the first 2 months of treatment with topiramate. We also compared baseline electroencephalograms (EEGs) with post-treatment EEGs. The median seizure rate reduction during the first 2 months of treatment was 41% (P = .002). Three patients became spasm free (20%), five had > 50% reduction, and three had at least 25% reduction. Four patients did not respond. Three of 15 patients had clearing of hypsarrhythmia. Topiramate was generally well tolerated, with irritability being the most common side effect. Topiramate was efficacious and well tolerated; one patient discontinued the medication because of adverse effects. (J Child Neurol 2006;21:17-19).
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