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Implantation Surgery for Abdominal Vagus Nerve Stimulation and Recording Studies in Awake Rats
Published on: January 19, 2024
Vagus nerve stimulation (VNS) is effective in treating catastrophic 1 epilepsy in very young children
Nelia Zamponi1, Franco Rychlicki, Ludovica Corpaci
1Pediatric Neurology Department, Azienda Ospedaliera-Universitaria, Ospedali Riuniti, Presidio G Salesi, Ancona, Italy. n.zamponi@tin.it
Insights
Vagus nerve stimulation (VNS) effectively controlled seizures in very young children with severe epilepsy. This treatment improved quality of life and developmental milestones, offering a viable option when other treatments fail.
Area of Science:
- Pediatric Neurology
- Neurosurgery
- Epileptology
Background:
- Catastrophic epilepsy in infants presents significant treatment challenges.
- Established therapies often prove insufficient for severe pediatric epilepsy cases.
Observation:
- Six children under 3 years old with severe epilepsy and cognitive impairment received vagus nerve stimulation (VNS).
- Three patients with life-threatening status epilepticus were implanted during intensive care unit (ICU) admission.
- The VNS implantation procedure involved a single cervical incision with no observed complications.
Findings:
- Four out of six children experienced significant and persistent seizure control improvement (60-90%).
- VNS facilitated early cessation of status epilepticus and discharge from the ICU for affected patients.
- Improvements in quality of life, parental satisfaction, and some developmental milestones were noted.
Implications:
- Vagus nerve stimulation (VNS) is a safe and effective treatment option for severe epilepsy in toddlers when resective surgery is not feasible.
- VNS offers a well-tolerated alternative for infants with catastrophic epilepsy and multiple developmental disabilities.
- This study supports considering VNS for very young children facing intractable seizures and associated complications.
Abstract:
The objective of this study is to evaluate the safety and efficacy of vagus nerve stimulation (VNS) in very young children suffering from catastrophic epilepsy and status epilepticus. We reviewed files of 60 VNS-implanted children at our institution and we selected six very young patients, less than 3 years old (mean age at implant 1.6 years). All patients suffered from severe cognitive impairment and catastrophic epilepsy with underlying diagnosis of hemimegalencephaly (1), hypoxic-ischemic encephalopathy (1), tuberous sclerosis complex (1), and malignant migrating partial epilepsy of infancy (3). Three patients were VNS-implanted during admission at intensive care unit (ICU) after developing life-threatening status epilepticus. The mean follow-up time was 41.6 months. The VNS was implanted using a single cervical incision. No surgery-related complications were observed. Four of six children have shown a significant, persistent improvement in seizure control (range, 60-90%). In patients with status, insertion of the vagal nerve stimulator allowed early cessation of status and discharge from ICU. Quality of life and parental satisfaction improved and for three children there was some milestone evolution. Catastrophic epilepsy in infancy can be devastating and difficult to treat with drugs and surgery. If resective surgery is inappropriate or refused, VNS can be considered as a well-tolerated and effective procedure even in toddlers affected by severe epilepsy and multiple developmental disabilities.
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