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Electrophysiological Measurements and Analysis of Nociception in Human Infants
Published on: December 20, 2011
Clinical experience with open-label topiramate use in infants younger than 2 years of age
Nathan Watemberg1, Hadassah Goldberg-Stern, Bruria Ben-Zeev
1Pediatric Neurology Unit, Wolfson Medical Center, Holon, Israel. nwatemberg@pol.net
Insights
Topiramate is effective and well-tolerated for treating refractory epilepsy in infants under 24 months. This study found positive outcomes in infantile spasms and other seizure types, with minimal adverse effects.
Area of Science:
- Pediatric Neurology
- Clinical Pharmacology
Background:
- Infantile epilepsy requires effective and safe treatment options.
- Topiramate is an established antiepileptic drug, but its use in infants is less studied.
Purpose of the Study:
- To evaluate the efficacy, safety, and tolerability of topiramate in infants under 24 months with refractory epilepsy.
- To identify common epilepsy syndromes and seizure types treated with topiramate in this age group.
Main Methods:
- An open-label, multicenter chart review of 28 infants younger than 24 months receiving topiramate for refractory epilepsy.
- Data collected on epilepsy syndrome, seizure type, treatment regimen, response, duration, and adverse effects.
Main Results:
- Seven of eight infants with infantile spasms improved with topiramate.
- Half of infants with other seizure types responded to topiramate.
- Adverse effects were infrequent, with only two discontinuations.
Conclusions:
- Topiramate demonstrates efficacy and good tolerability in infants with refractory epilepsy.
- Further prospective studies are recommended to confirm these findings.
Abstract:
To assess the efficacy, safety, and tolerability of topiramate in infants younger than 24 months of age, we conducted an open-label, multicenter chart review study of infants who received topiramate. Twenty-eight patients were evaluated. All had refractory epilepsy. The mean age of seizure onset was 3.8 months (range 0-10 months). Refractory infantile spasms were the most common epilepsy syndrome. Among infants without infantile spasms, complex partial seizures were the prominent seizure type in eight, followed by simple partial seizures in six. Topiramate was prescribed as add-on therapy in 25 cases and a s monotherapy in 3 cases. Seven of the eight infantile spasms cases improved on topiramate therapy, attaining topiramate monotherapy in three infants. Half of the infants with other seizure types responded to topiramate. The average treatment duration among topiramate responders was 11 months. Topiramate was prescribed after a mean of 3.3 antiepilepsy drugs had been used in these infants. In no case was topiramate the first prescribed antiepilepsy drug. Adverse effects occurred only in five patients, leading to topiramate discontinuation in two patients. Topiramate was efficacious and well tolerated in infants younger than 24 months of age with refractory epilepsy. Prospective data are needed to corroborate this observation.
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