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Current Directions in Deep Brain Stimulation for Parkinson’s Disease—Directing Current to Maximize Clinical Benefit

Several single-center studies and one large multicenter clinical trial demonstrated that directional deep brain stimulation (DBS) could optimize the volume of tissue activated (VTA) based on the individual placement of the lead in relation to the target. The ability to generate axially asymmetric fi...

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Autores principales: Merola, Aristide, Romagnolo, Alberto, Krishna, Vibhor, Pallavaram, Srivatsan, Carcieri, Stephen, Goetz, Steven, Mandybur, George, Duker, Andrew P., Dalm, Brian, Rolston, John D., Fasano, Alfonso, Verhagen, Leo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229063/
https://www.ncbi.nlm.nih.gov/pubmed/32157562
http://dx.doi.org/10.1007/s40120-020-00181-9
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author Merola, Aristide
Romagnolo, Alberto
Krishna, Vibhor
Pallavaram, Srivatsan
Carcieri, Stephen
Goetz, Steven
Mandybur, George
Duker, Andrew P.
Dalm, Brian
Rolston, John D.
Fasano, Alfonso
Verhagen, Leo
author_facet Merola, Aristide
Romagnolo, Alberto
Krishna, Vibhor
Pallavaram, Srivatsan
Carcieri, Stephen
Goetz, Steven
Mandybur, George
Duker, Andrew P.
Dalm, Brian
Rolston, John D.
Fasano, Alfonso
Verhagen, Leo
author_sort Merola, Aristide
collection PubMed
description Several single-center studies and one large multicenter clinical trial demonstrated that directional deep brain stimulation (DBS) could optimize the volume of tissue activated (VTA) based on the individual placement of the lead in relation to the target. The ability to generate axially asymmetric fields of stimulation translates into a broader therapeutic window (TW) compared to conventional DBS. However, changing the shape and surface of stimulating electrodes (directional segmented vs. conventional ring-shaped) also demands a revision of the programming strategies employed for DBS programming. Model-based approaches have been used to predict the shape of the VTA, which can be visualized on standardized neuroimaging atlases or individual magnetic resonance imaging. While potentially useful for optimizing clinical care, these systems remain limited by factors such as patient-specific anatomical variability, postsurgical lead migrations, and inability to account for individual contact impedances and orientation of the systems of fibers surrounding the electrode. Alternative programming tools based on the functional assessment of stimulation-induced clinical benefits and side effects allow one to collect and analyze data from each electrode of the DBS system and provide an action plan of ranked alternatives for therapeutic settings based on the selection of optimal directional contacts. Overall, an increasing amount of data supports the use of directional DBS. It is conceivable that the use of directionality may reduce the need for complex programming paradigms such as bipolar configurations, frequency or pulse width modulation, or interleaving. At a minimum, stimulation through directional electrodes can be considered as another tool to improve the benefit/side effect ratio. At a maximum, directionality may become the preferred way to program because of its larger TW and lower energy consumption. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40120-020-00181-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-72290632020-05-18 Current Directions in Deep Brain Stimulation for Parkinson’s Disease—Directing Current to Maximize Clinical Benefit Merola, Aristide Romagnolo, Alberto Krishna, Vibhor Pallavaram, Srivatsan Carcieri, Stephen Goetz, Steven Mandybur, George Duker, Andrew P. Dalm, Brian Rolston, John D. Fasano, Alfonso Verhagen, Leo Neurol Ther Review Several single-center studies and one large multicenter clinical trial demonstrated that directional deep brain stimulation (DBS) could optimize the volume of tissue activated (VTA) based on the individual placement of the lead in relation to the target. The ability to generate axially asymmetric fields of stimulation translates into a broader therapeutic window (TW) compared to conventional DBS. However, changing the shape and surface of stimulating electrodes (directional segmented vs. conventional ring-shaped) also demands a revision of the programming strategies employed for DBS programming. Model-based approaches have been used to predict the shape of the VTA, which can be visualized on standardized neuroimaging atlases or individual magnetic resonance imaging. While potentially useful for optimizing clinical care, these systems remain limited by factors such as patient-specific anatomical variability, postsurgical lead migrations, and inability to account for individual contact impedances and orientation of the systems of fibers surrounding the electrode. Alternative programming tools based on the functional assessment of stimulation-induced clinical benefits and side effects allow one to collect and analyze data from each electrode of the DBS system and provide an action plan of ranked alternatives for therapeutic settings based on the selection of optimal directional contacts. Overall, an increasing amount of data supports the use of directional DBS. It is conceivable that the use of directionality may reduce the need for complex programming paradigms such as bipolar configurations, frequency or pulse width modulation, or interleaving. At a minimum, stimulation through directional electrodes can be considered as another tool to improve the benefit/side effect ratio. At a maximum, directionality may become the preferred way to program because of its larger TW and lower energy consumption. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40120-020-00181-9) contains supplementary material, which is available to authorized users. Springer Healthcare 2020-03-09 /pmc/articles/PMC7229063/ /pubmed/32157562 http://dx.doi.org/10.1007/s40120-020-00181-9 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Review
Merola, Aristide
Romagnolo, Alberto
Krishna, Vibhor
Pallavaram, Srivatsan
Carcieri, Stephen
Goetz, Steven
Mandybur, George
Duker, Andrew P.
Dalm, Brian
Rolston, John D.
Fasano, Alfonso
Verhagen, Leo
Current Directions in Deep Brain Stimulation for Parkinson’s Disease—Directing Current to Maximize Clinical Benefit
title Current Directions in Deep Brain Stimulation for Parkinson’s Disease—Directing Current to Maximize Clinical Benefit
title_full Current Directions in Deep Brain Stimulation for Parkinson’s Disease—Directing Current to Maximize Clinical Benefit
title_fullStr Current Directions in Deep Brain Stimulation for Parkinson’s Disease—Directing Current to Maximize Clinical Benefit
title_full_unstemmed Current Directions in Deep Brain Stimulation for Parkinson’s Disease—Directing Current to Maximize Clinical Benefit
title_short Current Directions in Deep Brain Stimulation for Parkinson’s Disease—Directing Current to Maximize Clinical Benefit
title_sort current directions in deep brain stimulation for parkinson’s disease—directing current to maximize clinical benefit
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229063/
https://www.ncbi.nlm.nih.gov/pubmed/32157562
http://dx.doi.org/10.1007/s40120-020-00181-9
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