{Reference Type}: Journal Article
{Title}: Current role of rufinamide in the treatment of childhood epilepsy: literature review and treatment guidelines.
{Author}: Coppola G;Besag F;Cusmai R;Dulac O;Kluger G;Moavero R;Nabbout R;Nikanorova M;Pisani F;Verrotti A;von Stülpnagel C;Curatolo P;
{Journal}: Eur J Paediatr Neurol
{Volume}: 18
{Issue}: 6
{Year}: Nov 2014
{Factor}: 3.692
{DOI}: 10.1016/j.ejpn.2014.05.008
{Abstract}: <B>OBJECTIVE: </B>The literature on the efficacy and safety of rufinamide in childhood-onset epilepsy syndromes currently includes approximately 600 paediatric patients. This paper summarizes the views of a panel of experienced European epileptologists with regard to the current role of rufinamide in the treatment of childhood epilepsies.<BR><B>RESULTS: </B>Rufinamide is effective in decreasing the seizure frequency in the Lennox-Gastaut syndrome (LGS), especially tonic and atonic seizures. It might consequently be preferred to other drugs as a second-line treatment for LGS when drop-attacks are frequent. The mean responder rate in the published studies is 38% with seizure freedom achieved in 2.4% of patients. Rufinamide has shown some efficacy in epileptic encephalopathies other than LGS. It can be also effective as adjunctive therapy in children and adolescents with drug-resistant partial seizures. The available data suggest that rufinamide has an acceptable risk/benefit ratio with quite a low risk of aggravating seizures. Common adverse effects (somnolence, nausea and vomiting) are usually mild and self-limiting; they are more frequently observed during titration than in the maintenance phase, suggesting that low escalation rates might be associated with fewer adverse effects. Rufinamide appears to have a favourable cognitive profile compared with other antiepileptic drugs.<BR><B>CONCLUSIONS: </B>Rufinamide is only approved for adjunctive treatment of seizures associated with LGS in children 4 years of age and older. There are very few data on rufinamide treatment at the onset of LGS or early in the course of the disorder; whether early treatment will improve outcome has yet to be determined.