Abstract
Purpose: A 34-year-old woman with progressive myoclonus epilepsy of Unverricht-Lundborg type was considered for vagus nerve stimulation (VNS) therapy. Methods: After demonstration of intractability to multiple antiepileptic regimens and progressive deterioration in cerebellar function, the patient was implanted with a vagus nerve stimulator and followed for 1 year. Neurological status, seizure frequency, and parameter changes were analyzed. Results: VNS therapy resulted in reduction of seizures (more than 90%) and a significant improvement in cerebellar function demonstrated on neurological examination. The patient reported improved quality of life based in part on her ability to perform activities of daily living. Conclusions: VNS therapy may be considered a treatment option for progressive myoclonus epilepsy. The effects of VNS on seizure control and cerebellar dysfunction may provide clues to the underlying mechanism(s) of action.
Original language | English |
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Pages (from-to) | 1046-1048 |
Number of pages | 3 |
Journal | Epilepsia |
Volume | 41 |
Issue number | 8 |
DOIs | |
State | Published - 2000 |
Externally published | Yes |
Keywords
- Electrical stimulation
- Epilepsy
- Progressive myoclonus epilepsy
- Seizure
- Vagus nerve