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Rufinamide in children and adults in routine clinical practice
S Jaraba1,2, E Santamarina3, J Miró1
1Epilepsy Unit, Neurology Department, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.
Rufinamide effectively reduced seizure frequency in patients with Lennox-Gastaut Syndrome (LGS) and other refractory epilepsies. While generally well-tolerated, some patients discontinued treatment due to lack of effectiveness.
Area of Science:
- Neurology
- Clinical Pharmacology
- Epileptology
Background:
- Lennox-Gastaut Syndrome (LGS) and other epileptic encephalopathies are severe forms of epilepsy.
- Intractable focal epilepsies present significant treatment challenges.
- Long-term effectiveness data for rufinamide in real-world clinical practice are limited.
Purpose of the Study:
- To evaluate the long-term effectiveness and tolerability of rufinamide.
- To assess rufinamide's efficacy in managing LGS, other epileptic encephalopathies, and intractable focal epilepsies.
- To analyze seizure frequency reduction and side effects in adult and pediatric patients.
Main Methods:
- Multicentre, retrospective chart review.
- Involved seven Spanish epilepsy centers.
- Assessed patients at 6 and 12 months post-initiation of adjunctive rufinamide.
Main Results:
- 58 patients (7-57 years) with LGS, epileptic encephalopathies, or focal epilepsies were included.
- Rufinamide significantly reduced generalized tonic-clonic, tonic/atonic, and focal seizures.
- Common side effects included nausea, vomiting, and weight loss; 43.1% discontinued treatment, primarily due to lack of effectiveness.
Conclusions:
- Rufinamide demonstrated effectiveness in reducing seizure frequency in severe refractory epilepsies.
- The drug was generally well-tolerated in both children and adults.
- Rufinamide is a viable treatment option for LGS and other refractory epilepsy types.
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