Please use this identifier to cite or link to this item:
https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4975
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Shah, U. | en |
dc.contributor.author | Yates, C. F. | en |
dc.contributor.author | Riney, K. | en |
dc.contributor.author | Coulthard, L. G. | en |
dc.contributor.author | Wood, M. | en |
dc.contributor.author | Malone, S. | en |
dc.contributor.author | Wallace, G. | en |
dc.contributor.author | Campbell, R. | en |
dc.date.accessioned | 2022-11-07T23:58:11Z | - |
dc.date.available | 2022-11-07T23:58:11Z | - |
dc.date.issued | 2022 | en |
dc.identifier.citation | 164, (1), 2022, p. 219-227 | en |
dc.identifier.other | RIS | en |
dc.identifier.uri | http://dora.health.qld.gov.au/qldresearchjspui/handle/1/4975 | - |
dc.description.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 <br />2022-01-31 <br /> | en |
dc.language.iso | en | en |
dc.relation.ispartof | Acta Neurochirurgica | en |
dc.title | Vagus nerve stimulation: a 20-year Australian experience | en |
dc.type | Article | en |
dc.identifier.doi | 10.1007/s00701-021-05046-0 | en |
dc.subject.keywords | clinical assessment | en |
dc.subject.keywords | clinical feature | en |
dc.subject.keywords | clinical outcome | en |
dc.subject.keywords | cohort analysis | en |
dc.subject.keywords | controlled study | en |
dc.subject.keywords | coughing | en |
dc.subject.keywords | demography | en |
dc.subject.keywords | device failure | en |
dc.subject.keywords | dysphagia | en |
dc.subject.keywords | dysphonia | en |
dc.subject.keywords | encephalitis | en |
dc.subject.keywords | epilepsy | en |
dc.subject.keywords | family history | en |
dc.subject.keywords | female | en |
dc.subject.keywords | follow up | en |
dc.subject.keywords | gestalt psychology | en |
dc.subject.keywords | human | en |
dc.subject.keywords | impedance | en |
dc.subject.keywords | intractable epilepsy | en |
dc.subject.keywords | major clinical study | en |
dc.subject.keywords | male | en |
dc.subject.keywords | nausea | en |
dc.subject.keywords | outcome assessment | en |
dc.subject.keywords | patient counseling | en |
dc.subject.keywords | private hospital | en |
dc.subject.keywords | Queensland | en |
dc.subject.keywords | recurrent laryngeal nerve palsy | en |
dc.subject.keywords | reoperation | en |
dc.subject.keywords | retrospective study | en |
dc.subject.keywords | school child | en |
dc.subject.keywords | sleep disordered breathing | en |
dc.subject.keywords | tonic clonic seizure | en |
dc.subject.keywords | treatment duration | en |
dc.subject.keywords | treatment response | en |
dc.subject.keywords | vagus nerve stimulation | en |
dc.subject.keywords | vomiting | en |
dc.subject.keywords | wound infection | en |
dc.subject.keywords | AspireSR 106 | en |
dc.subject.keywords | implanted vagus nerve stimulator | en |
dc.subject.keywords | AspireSR 101AspireSR 102 | en |
dc.subject.keywords | AspireSR 103 | en |
dc.subject.keywords | article | en |
dc.subject.keywords | child | en |
dc.relation.url | https://www.embase.com/search/results?subaction=viewrecord&id=L2014160534&from=exporthttp://dx.doi.org/10.1007/s00701-021-05046-0 | | en |
dc.identifier.risid | 496 | en |
dc.description.pages | 219-227 | en |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
Appears in Sites: | Children's Health Queensland Publications Queensland Health Publications |
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