Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4975
Title: Vagus nerve stimulation: a 20-year Australian experience
Authors: Shah, U.
Yates, C. F.
Riney, K.
Coulthard, L. G.
Wood, M.
Malone, S. 
Wallace, G.
Campbell, R.
Issue Date: 2022
Source: 164, (1), 2022, p. 219-227
Pages: 219-227
Journal: Acta Neurochirurgica
Abstract: 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.L20141605342021-11-12
2022-01-31
DOI: 10.1007/s00701-021-05046-0
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L2014160534&from=exporthttp://dx.doi.org/10.1007/s00701-021-05046-0 |
Keywords: clinical assessment;clinical feature;clinical outcome;cohort analysis;controlled study;coughing;demography;device failure;dysphagia;dysphonia;encephalitis;epilepsy;family history;female;follow up;gestalt psychology;human;impedance;intractable epilepsy;major clinical study;male;nausea;outcome assessment;patient counseling;private hospital;Queensland;recurrent laryngeal nerve palsy;reoperation;retrospective study;school child;sleep disordered breathing;tonic clonic seizure;treatment duration;treatment response;vagus nerve stimulation;vomiting;wound infection;AspireSR 106;implanted vagus nerve stimulator;AspireSR 101AspireSR 102;AspireSR 103;article;child
Type: Article
Appears in Sites:Children's Health Queensland Publications

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