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Vagus nerve stimulation for refractory status epilepticus
Veerle De Herdt1, Liesbeth Waterschoot, Kristl Vonck
1Department of Neurology, Reference Center for Refractory Epilepsy, Ghent University Hospital, Belgium. veerle.deherdt@ugent.be
Insights
Vagus nerve stimulation (VNS) effectively treated refractory non-convulsive status epilepticus (SE) in a pediatric patient. This intervention led to sustained seizure reduction and allowed for tapering of anti-epileptic drugs.
Area of Science:
- Neurology
- Pediatric Epilepsy
- Neurostimulation
Background:
- Refractory non-convulsive status epilepticus (SE) presents significant treatment challenges in pediatric patients.
- Previous treatments for this patient included thiopental-induced coma, highlighting the severity and resistance to standard therapies.
Purpose of the Study:
- To report the long-term follow-up of a pediatric patient with refractory non-convulsive SE treated with vagus nerve stimulation (VNS).
- To evaluate the acute and sustained efficacy of VNS in seizure control and medication management.
Main Methods:
- A 7-year-old girl with a history of neurological complications and epilepsy presented with refractory non-convulsive SE.
- Vagus nerve stimulator (VNS) implantation was performed after prolonged coma induced by thiopental.
- Patient's response was monitored via electroencephalography (EEG) and clinical seizure frequency.
Main Results:
- VNS implantation facilitated the successful withdrawal of thiopental-induced coma within three days.
- EEG normalization was observed one week after initiating VNS therapy.
- The patient remained seizure-free for 13 months post-implantation, with partial tapering of anti-epileptic drugs (AEDs).
Conclusions:
- Vagus nerve stimulation (VNS) demonstrated an acute abortive effect and sustained long-term seizure reduction in a pediatric case of refractory non-convulsive SE.
- VNS offers a promising therapeutic option for managing severe, treatment-resistant epilepsy in children.
- This case underscores the potential of VNS as an adjunctive therapy for improving seizure control and quality of life in pediatric epilepsy patients.
Abstract:
We report on the long-term follow-up of a patient with refractory non-convulsive SE who was successfully treated with VNS. A 7-year old girl with a medical history of thrombosis in the right internal cerebral vein and right thalamic bleeding 8 days after birth, developed epilepsy at the age of 13 months. At the age of 6 she presented with a refractory non-convulsive SE. A vagus nerve stimulator was placed after 11 days of thiopental-induced coma. Three days after VNS implantation, the thiopental-induced coma was successfully withdrawn and electroencephalography showed normalization one week after start of VNS. After a follow-up of 13 months she remains seizure-free and AEDs have been partially tapered. This case illustrates a potential acute abortive effect with sustained long-term seizure reduction of VNS in a 7-year old girl who presented with refractory non-convulsive SE.
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