Cargando…

Motor outcome and electrode location in deep brain stimulation in Parkinson's disease

OBJECTIVES: To evaluate the efficacy and adverse effects of subthalamic deep brain stimulation (STN‐DBS) in patients with advanced Parkinson's disease (PD) and the possible correlation between electrode location and clinical outcome. METHODS: We retrospectively reviewed 87 PD‐related STN‐DBS op...

Descripción completa

Detalles Bibliográficos
Autores principales: Koivu, Maija, Huotarinen, Antti, Scheperjans, Filip, Laakso, Aki, Kivisaari, Riku, Pekkonen, Eero
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043715/
https://www.ncbi.nlm.nih.gov/pubmed/29851316
http://dx.doi.org/10.1002/brb3.1003
_version_ 1783339340500303872
author Koivu, Maija
Huotarinen, Antti
Scheperjans, Filip
Laakso, Aki
Kivisaari, Riku
Pekkonen, Eero
author_facet Koivu, Maija
Huotarinen, Antti
Scheperjans, Filip
Laakso, Aki
Kivisaari, Riku
Pekkonen, Eero
author_sort Koivu, Maija
collection PubMed
description OBJECTIVES: To evaluate the efficacy and adverse effects of subthalamic deep brain stimulation (STN‐DBS) in patients with advanced Parkinson's disease (PD) and the possible correlation between electrode location and clinical outcome. METHODS: We retrospectively reviewed 87 PD‐related STN‐DBS operations at Helsinki University Hospital (HUH) from 2007 to 2014. The changes of Unified Parkinson's Disease Rating Scale (UPDRS) part III score, Hoehn & Yahr stage, antiparkinson medication, and adverse effects were studied. We estimated the active electrode location in three different coordinate systems: direct visual analysis of MRI correlated to brain atlas, location in relation to the nucleus borders and location in relation to the midcommisural point. RESULTS: At 6 months after operation, both levodopa equivalent doses (LEDs; 35%, Wilcoxon signed‐rank test = 0.000) and UPDRS part III scores significantly decreased (38%, Wilcoxon signed‐rank test = 0.000). Four patients (5%) suffered from moderate DBS‐related dysarthria. The generator and electrodes had to be removed in one patient due to infection (1%). Electrode coordinates in the three coordinate systems correlated well with each other. On the left side, more ventral location of the active contact was associated with greater LED decrease. CONCLUSIONS: STN‐DBS improves motor function and enables the reduction in antiparkinson medication with an acceptable adverse effect profile. More ventral location of the active contact may allow stronger LED reduction. Further research on the correlation between contact location, clinical outcome, and LED reduction is warranted.
format Online
Article
Text
id pubmed-6043715
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-60437152018-07-15 Motor outcome and electrode location in deep brain stimulation in Parkinson's disease Koivu, Maija Huotarinen, Antti Scheperjans, Filip Laakso, Aki Kivisaari, Riku Pekkonen, Eero Brain Behav Original Research OBJECTIVES: To evaluate the efficacy and adverse effects of subthalamic deep brain stimulation (STN‐DBS) in patients with advanced Parkinson's disease (PD) and the possible correlation between electrode location and clinical outcome. METHODS: We retrospectively reviewed 87 PD‐related STN‐DBS operations at Helsinki University Hospital (HUH) from 2007 to 2014. The changes of Unified Parkinson's Disease Rating Scale (UPDRS) part III score, Hoehn & Yahr stage, antiparkinson medication, and adverse effects were studied. We estimated the active electrode location in three different coordinate systems: direct visual analysis of MRI correlated to brain atlas, location in relation to the nucleus borders and location in relation to the midcommisural point. RESULTS: At 6 months after operation, both levodopa equivalent doses (LEDs; 35%, Wilcoxon signed‐rank test = 0.000) and UPDRS part III scores significantly decreased (38%, Wilcoxon signed‐rank test = 0.000). Four patients (5%) suffered from moderate DBS‐related dysarthria. The generator and electrodes had to be removed in one patient due to infection (1%). Electrode coordinates in the three coordinate systems correlated well with each other. On the left side, more ventral location of the active contact was associated with greater LED decrease. CONCLUSIONS: STN‐DBS improves motor function and enables the reduction in antiparkinson medication with an acceptable adverse effect profile. More ventral location of the active contact may allow stronger LED reduction. Further research on the correlation between contact location, clinical outcome, and LED reduction is warranted. John Wiley and Sons Inc. 2018-05-30 /pmc/articles/PMC6043715/ /pubmed/29851316 http://dx.doi.org/10.1002/brb3.1003 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Koivu, Maija
Huotarinen, Antti
Scheperjans, Filip
Laakso, Aki
Kivisaari, Riku
Pekkonen, Eero
Motor outcome and electrode location in deep brain stimulation in Parkinson's disease
title Motor outcome and electrode location in deep brain stimulation in Parkinson's disease
title_full Motor outcome and electrode location in deep brain stimulation in Parkinson's disease
title_fullStr Motor outcome and electrode location in deep brain stimulation in Parkinson's disease
title_full_unstemmed Motor outcome and electrode location in deep brain stimulation in Parkinson's disease
title_short Motor outcome and electrode location in deep brain stimulation in Parkinson's disease
title_sort motor outcome and electrode location in deep brain stimulation in parkinson's disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043715/
https://www.ncbi.nlm.nih.gov/pubmed/29851316
http://dx.doi.org/10.1002/brb3.1003
work_keys_str_mv AT koivumaija motoroutcomeandelectrodelocationindeepbrainstimulationinparkinsonsdisease
AT huotarinenantti motoroutcomeandelectrodelocationindeepbrainstimulationinparkinsonsdisease
AT scheperjansfilip motoroutcomeandelectrodelocationindeepbrainstimulationinparkinsonsdisease
AT laaksoaki motoroutcomeandelectrodelocationindeepbrainstimulationinparkinsonsdisease
AT kivisaaririku motoroutcomeandelectrodelocationindeepbrainstimulationinparkinsonsdisease
AT pekkoneneero motoroutcomeandelectrodelocationindeepbrainstimulationinparkinsonsdisease