Abstract
Purpose
We discuss the effectiveness, tolerability, and safety of vagus nerve stimulation (VNS) as adjunctive therapy in 26 patients with refractory epileptic encephalopathies (EEs).
Material and methods
Twenty-six patients (17 male and 9 female) with electroclinical features compatible with Lennox–Gastaut syndrome (LGS) in 20 patients, Dravet syndrome (DS) in 3 patients, and epilepsy with myoclonic–astatic seizures (EMAS) in 3 patients implanted with the NCP system were analyzed.
Results
In our series of patients with LGS, 17 cases showed a significant improvement in seizure control, with a reduction in seizure frequency of at least 50%. Seven of them previously had epileptic spasms. Three patients with EMAS and two patients with DS showed a significant improvement in seizure control, with a reduction in seizure frequency of at least 50%. A good clinical response was evident early and efficacy progressively improved with the duration of treatment up to 36 months. In patients who had a reduction in seizure frequency of at least 50%, quality of life (QOL) and neuropsychological performance improved. VNS was well-tolerated in all patients.
Conclusion
VNS is an effective and well-tolerated treatment for patients with epileptic encephalopathies EEs, improving QOL and neuropsychological performance.
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Cersósimo, R.O., Bartuluchi, M., De Los Santos, C. et al. Vagus nerve stimulation: effectiveness and tolerability in patients with epileptic encephalopathies. Childs Nerv Syst 27, 787–792 (2011). https://doi.org/10.1007/s00381-010-1314-8
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DOI: https://doi.org/10.1007/s00381-010-1314-8