Successful application of vagus nerve stimulation in super refractory status epilepticus associated with MERRF syndrome

Myoclonic epilepsy with ragged red fibers (MERRF) syndrome is a rare mitochondrial disorder marked by myoclonus, ataxia, cognitive impairment, myopathy, and sensorineural hearing loss. Seizures in MERRF syndrome are often resistant to standard antiseizure medication. We present a unique case of an adult patient with MERRF syndrome, caused by the m.8344A > G point mutation, who developed super-refractory status epilepticus (SRSE), successfully managed by the initiation and rapid escalation of vagus nerve stimulation (VNS) therapy. Over a two-year follow-up period, the VNS therapy enabled a long-term control of generalized tonic-clonic seizures. A further status epilepticus has not yet occurred. VNS may therefore be a promising therapeutic option for managing SRSE in patients with mitochondrial epilepsy syndromes.

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Publication Details

Journal
Epilepsy & Behavior Reports
Published
2025-04-14
DOI
https://doi.org/10.1016/j.ebr.2025.100769
Primary Topic
EEG and Brain-Computer Interfaces
Type
article
Field-Weighted Citation Impact
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article

Successful application of vagus nerve stimulation in super refractory status epilepticus associated with MERRF syndrome

Leyla Baysal-Kıraç, Ann‐Kristin Helmers, Nils G. Margraf, S. Zimmermann et al.
1 links
Epilepsy & Behavior Reports
EEG and Brain-Computer Interfaces
article

Successful application of vagus nerve stimulation in super refractory status epilepticus associated with MERRF syndrome

Leyla Baysal-Kıraç, Ann‐Kristin Helmers, Nils G. Margraf, S. Zimmermann, Sabrina Jobi
article en

Abstract

Myoclonic epilepsy with ragged red fibers (MERRF) syndrome is a rare mitochondrial disorder marked by myoclonus, ataxia, cognitive impairment, myopathy, and sensorineural hearing loss. Seizures in MERRF syndrome are often resistant to standard antiseizure medication. We present a unique case of an adult patient with MERRF syndrome, caused by the m.8344A > G point mutation, who developed super-refractory status epilepticus (SRSE), successfully managed by the initiation and rapid escalation of vagus nerve stimulation (VNS) therapy. Over a two-year follow-up period, the VNS therapy enabled a long-term control of generalized tonic-clonic seizures. A further status epilepticus has not yet occurred. VNS may therefore be a promising therapeutic option for managing SRSE in patients with mitochondrial epilepsy syndromes.

Epilepsy & Behavior ReportsVol. 30
University Hospital Schleswig-Holstein (DE), University of Lübeck (DE)
Openalex Percentile: Top 93%
EEG and Brain-Computer Interfaces
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