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Vagus nerve stimulation: a 20-year Australian experience.
Yates, Charles F; Riney, Kate; Malone, Stephen; Shah, Ubaid; Coulthard, Liam G; Campbell, Robert; Wallace, Geoff; Wood, Martin.
Affiliation
  • Yates CF; Department of Neurosurgery, Queensland Children's Hospital, Brisbane, QLD, Australia. Charles.Yates@health.qld.gov.au.
  • Riney K; Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia. Charles.Yates@health.qld.gov.au.
  • Malone S; School of Medicine, University of Queensland, Brisbane, QLD, Australia. Charles.Yates@health.qld.gov.au.
  • Shah U; School of Medicine, University of Queensland, Brisbane, QLD, Australia.
  • Coulthard LG; Neurosciences Unit, Queensland Children's Hospital, Brisbane, QLD, Australia.
  • Campbell R; School of Medicine, University of Queensland, Brisbane, QLD, Australia.
  • Wallace G; Neurosciences Unit, Queensland Children's Hospital, Brisbane, QLD, Australia.
  • Wood M; School of Medicine, University of Queensland, Brisbane, QLD, Australia.
Acta Neurochir (Wien) ; 164(1): 219-227, 2022 01.
Article in En | MEDLINE | ID: mdl-34755209
BACKGROUND: Vagus nerve stimulation (VNS) therapy was first approved in the mid-1990s in the USA, Europe and Australia, with demonstrable efficacy in paediatric populations. Benefit in seizure frequency reduction can be observed up to 2 years post-intervention; however, few studies assess outcomes beyond this period. Furthermore, paediatric cohort sizes are small, limiting generalisability of outcome assessments. We evaluate VNS insertion outcomes and complications or side-effects in a large paediatric cohort, over a 20-year period from Queensland's first VNS insertion. METHODS: A retrospective review was conducted of all paediatric VNS insertions at the Queensland Children's Hospital (QCH) and the Mater Children's Hospital/Mater Children's Private Hospital (MCH/MCPH) Brisbane. A minimum of 1-year follow-up from 1999 to 2020 was required for inclusion. Patients were assessed on demographics, epilepsy details, seizure outcomes and complications or side-effects. RESULTS: In this extended follow-up cohort (76 patients, 7.2 ± 5.3 years), 51.3% of patients had ≥ 50% seizure frequency reduction, while 73.7% experienced an Engel III outcome (worthwhile benefit) or better. Eleven patients (14.9%) were seizure-free at follow-up, and 81.6% retained long-term therapy. Stimulation-related side-effects are common (17.1%) but rarely result in stimulation cessation (3.9%). Cessation occurred in 14 patients (18.4%) and most commonly related to minimal benefit (13.2%). Demographics, aetiology, seizure nature and surgical factors did not influence outcomes. CONCLUSION: Over extended treatment periods, a large proportion of patients will benefit significantly from VNS therapy. Approximately 4 of 5 patients will retain VNS therapy, and in cases of cessation, this is most commonly related to minimal benefit. Underlying demographics, aetiology or seizure nature do not influence outcomes. This 20-year Queensland assessment of VNS therapy outcomes informs long-term expectation of VNS therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Vagus Nerve Stimulation Type of study: Observational_studies Limits: Child / Humans Country/Region as subject: Oceania Language: En Journal: Acta Neurochir (Wien) Year: 2022 Type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Vagus Nerve Stimulation Type of study: Observational_studies Limits: Child / Humans Country/Region as subject: Oceania Language: En Journal: Acta Neurochir (Wien) Year: 2022 Type: Article Affiliation country: Australia