Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30190
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dc.contributor.authorXu, San San-
dc.contributor.authorLee, Wee-Lih-
dc.contributor.authorPerera, Thushara-
dc.contributor.authorSinclair, Nicholas C-
dc.contributor.authorBulluss, Kristian J-
dc.contributor.authorMcDermott, Hugh J-
dc.contributor.authorThevathasan, Wesley-
dc.date2022-
dc.date.accessioned2022-06-23T00:29:05Z-
dc.date.available2022-06-23T00:29:05Z-
dc.date.issued2022-05-19-
dc.identifier.citationJournal of Neurology, Neurosurgery, and Psychiatry 2022; jnnp-2021-327708en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30190-
dc.description.abstractSelecting the ideal contact to apply subthalamic nucleus deep brain stimulation (STN-DBS) in Parkinson's disease is time-consuming and reliant on clinical expertise. The aim of this cohort study was to assess whether neuronal signals (beta oscillations and evoked resonant neural activity (ERNA)), and the anatomical location of electrodes, can predict the contacts selected by long-term, expert-clinician programming of STN-DBS. We evaluated 92 hemispheres of 47 patients with Parkinson's disease receiving chronic monopolar and bipolar STN-DBS. At each contact, beta oscillations and ERNA were recorded intraoperatively, and anatomical locations were assessed. How these factors, alone and in combination, predicted the contacts clinically selected for chronic deep brain stimulation at 6 months postoperatively was evaluated using a simple-ranking method and machine learning algorithms. The probability that each factor individually predicted the clinician-chosen contact was as follows: ERNA 80%, anatomy 67%, beta oscillations 50%. ERNA performed significantly better than anatomy and beta oscillations. Combining neuronal signal and anatomical data did not improve predictive performance. This work supports the development of probability-based algorithms using neuronal signals and anatomical data to assist programming of deep brain stimulation.en
dc.language.isoeng
dc.subjectELECTRICAL STIMULATIONen
dc.subjectEVOKED POTENTIALSen
dc.subjectNEUROPHYSIOLOGYen
dc.subjectNEUROSURGERYen
dc.subjectPARKINSON'S DISEASEen
dc.titleCan brain signals and anatomy refine contact choice for deep brain stimulation in Parkinson's disease?en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Neurology, Neurosurgery, and Psychiatryen
dc.identifier.affiliationNeurosurgeryen
dc.identifier.affiliationNeurologyen
dc.identifier.affiliationDepartment of Surgery, The University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.affiliationDepartment of Neurology, The Royal Melbourne Hospital, Parkville, Victoria, Australiaen
dc.identifier.affiliationBionics Institute, East Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine, The University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.affiliationMedical Bionics Department, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Neurosurgery, St Vincent's Hospital, Fitzroy, Victoria, Australiaen
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35589375/en
dc.identifier.doi10.1136/jnnp-2021-327708en
dc.type.contentTexten
dc.identifier.orcid0000-0001-5338-5934en
dc.identifier.orcid0000-0002-6330-1607en
dc.identifier.orcid0000-0003-1465-1130en
dc.identifier.pubmedid35589375
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-
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