Abstract
Among drug-resistant epilepsies, epileptic syndromes, characterized by combination of several types of seizures, are considered to be the most difficult in terms of treatment. Lennox–Gastaut syndrome is one of them. It manifests with polymorphic seizures (tonic axial, myatonic, atypical absence seizures, status epilepticus of minor motor seizures, myoclonic, generalized convulsive, and focal seizures). This is a heterogeneous disease, represented by a complex of clinical and electroencephalographic manifestations with various etiology. Current review is devoted to a novel antiepileptic drug rufinamide, which has a new mechanism of action. The drug has been registered in Russia in 2015. The authors also describe their own experience of rufinamide usage in the treatment of drug-resistant focal epilepsy as a part of multicomponent therapy for polymorphic seizures. One patient achieved clinical remission for 16 months; the second one had more than 50 % decrease in seizures frequency with a remission of drop-attacks.
Highlights
Наибольшие трудности в терапии фармакорезистентной эпилепсии представляют эпилептические синдромы, при которых отмечается сочетание нескольких типов приступов
Lennox–Gastaut syndrome is one of them. It manifests with polymorphic seizures
Current review is devoted to a novel antiepileptic drug rufinamide, which has a new mechanism of action
Summary
Наибольшие трудности в терапии фармакорезистентной эпилепсии представляют эпилептические синдромы, при которых отмечается сочетание нескольких типов приступов. EFFICACY OF RUFINAMIDE IN THE TREATMENT OF DRUG-RESISTANT FOCAL EPILEPSIES IN PAEDIATRIC PRACTICE
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have