Abstract | BACKGROUND: METHODS: Thirty-eight patients (19 males, 19 females), aged between 4 and 34 (mean 13.7 ± 8.3, median 12.5), all affected by different types of childhood-onset refractory epileptic encephalopathies other than Lennox-Gastaut syndrome, were treated with rufinamide as adjunctive drug for a mean period of 11.4 months (range 3-26 months). RESULTS: Fifteen of 38 patients (39.5%) had a ≥ 50% seizure reduction in countable seizures. Complete seizure freedom was achieved in one of these patients (2.6%). Three patients (7.9%) had a 25-49% seizure reduction, whilst seizure frequency remained unchanged in 15 (39.5%) and increased in five patients (13.1%). Eleven patients (28.9%) reported adverse side effects. Vomiting was reported in five patients (13.1%); drowsiness, decreased appetite and irritability with migraine manifested in other four patients. They were transient and mild in all cases. CONCLUSION:
|
Authors | G Coppola, S Grosso, E Franzoni, P Veggiotti, N Zamponi, P Parisi, A Spalice, F Habetswallner, A Fels, A Verrotti, A D'Aniello, S Mangano, A Balestri, P Curatolo, A Pascotto |
Journal | European journal of neurology
(Eur J Neurol)
Vol. 18
Issue 2
Pg. 246-251
(Feb 2011)
ISSN: 1468-1331 [Electronic] England |
PMID | 20666837
(Publication Type: Clinical Trial, Journal Article, Multicenter Study)
|
Copyright | © 2010 The Author(s). European Journal of Neurology © 2010 EFNS. |
Chemical References |
- Anticonvulsants
- Triazoles
- rufinamide
|
Topics |
- Adolescent
- Adult
- Anticonvulsants
(therapeutic use)
- Brain Diseases
(complications, drug therapy)
- Child
- Child, Preschool
- Epilepsy
(drug therapy, etiology)
- Female
- Humans
- Male
- Triazoles
(therapeutic use)
- Young Adult
|