Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33074
Full metadata record
DC FieldValueLanguage
dc.contributor.authorTonroe, Thomas-
dc.contributor.authorMcDermott, Hugh-
dc.contributor.authorPearce, Patrick-
dc.contributor.authorAcevedo, Nicola-
dc.contributor.authorThevathasan, Wesley-
dc.contributor.authorXu, San San-
dc.contributor.authorBulluss, Kristian J-
dc.contributor.authorPerera, Thushara-
dc.date2023-
dc.date.accessioned2023-06-16T06:48:40Z-
dc.date.available2023-06-16T06:48:40Z-
dc.date.issued2023-06-08-
dc.identifier.citationJournal of Neuroimaging : Official journal of the American Society of Neuroimaging 2023en_US
dc.identifier.issn1552-6569-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33074-
dc.description.abstractIn deep brain stimulation (DBS), accurate electrode placement is essential for optimizing patient outcomes. Localizing electrodes enables insight into therapeutic outcomes and development of metrics for use in clinical trials. Methods of defining anatomical targets have been described with varying accuracy and objectivity. To assess variability in anatomical targeting, we compare four methods of defining an appropriate target for DBS of the subthalamic nucleus for Parkinson's disease. The methods compared are direct visualization, red nucleus-based indirect targeting, mid-commissural point-based indirect targeting, and automated template-based targeting. This study assessed 226 hemispheres in 113 DBS recipients (39 females, 73 males, 62.2 ± 7.7 years). We utilized the electrode placement error (the Euclidean distance between the defined target and closest DBS electrode) as a metric for comparative analysis. Pairwise differences in electrode placement error across the four methods were compared using the Kruskal-Wallis H-test and Wilcoxon signed-rank tests. Interquartile ranges of the differences in electrode placement error spanned 1.18-1.56 mm. A Kruskal-Wallis H-test reported a statistically significant difference in the median of at least two groups (H(5) = 41.052, p < .001). Wilcoxon signed-rank tests reported statistically significant difference in two comparisons: direct visualization versus red nucleus-based indirect, and direct visualization versus automated template-based methods (T < 9215, p < .001). All methods were similarly discordant in their relative accuracy, despite having significant technical differences in their application. The differing protocols and technical aspects of each method, however, have the implication that one may be more practical depending on the clinical or research application at hand.en_US
dc.language.isoeng-
dc.subjectParkinson's diseaseen_US
dc.subjectanatomical targetingen_US
dc.subjectautomationen_US
dc.subjectdeep brain stimulationen_US
dc.subjectelectrode localizationen_US
dc.subjectneuroimagingen_US
dc.subjectsubthalamic nucleusen_US
dc.titleAnatomical targeting for electrode localization in subthalamic nucleus deep brain stimulation: A comparative study.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Neuroimaging : Official journal of the American Society of Neuroimagingen_US
dc.identifier.affiliationBionics Institute, East Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDBS Technologies Pty Ltd, East Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Neurosurgery, Cabrini Hospital, Malvern, Victoria, Australiaen_US
dc.identifier.affiliationCentre for Mental Health, Swinburne University of Technology, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationNeurologyen_US
dc.identifier.affiliationMedical Bionics Department, The University of Melbourne, East Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Neurosurgery, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australiaen_US
dc.identifier.affiliationSchool of Engineering, RMIT University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Neurosurgery, Cabrini Hospital, Malvern, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Neurology, The Royal Melbourne Hospital, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, The University of Melbourne, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationNeurosurgeryen_US
dc.identifier.affiliationDepartment of Surgery, The University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.doi10.1111/jon.13133en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-4341-6033en_US
dc.identifier.orcid0000-0002-4237-8373en_US
dc.identifier.pubmedid37288952-
local.name.researcherBulluss, Kristian J
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptNeurosurgery-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

34
checked on Nov 24, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.