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Unique Characteristics of the Dorsal Root Ganglion as a Target for Neuromodulation

OBJECTIVE: The dorsal root ganglion (DRG) is a novel target for neuromodulation, and DRG stimulation is proving to be a viable option in the treatment of chronic intractable neuropathic pain. Although the overall principle of conventional spinal cord stimulation (SCS) and DRG stimulation—in which an...

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Autores principales: Esposito, Michael F, Malayil, Rudy, Hanes, Michael, Deer, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544557/
https://www.ncbi.nlm.nih.gov/pubmed/31152179
http://dx.doi.org/10.1093/pm/pnz012
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author Esposito, Michael F
Malayil, Rudy
Hanes, Michael
Deer, Timothy
author_facet Esposito, Michael F
Malayil, Rudy
Hanes, Michael
Deer, Timothy
author_sort Esposito, Michael F
collection PubMed
description OBJECTIVE: The dorsal root ganglion (DRG) is a novel target for neuromodulation, and DRG stimulation is proving to be a viable option in the treatment of chronic intractable neuropathic pain. Although the overall principle of conventional spinal cord stimulation (SCS) and DRG stimulation—in which an electric field is applied to a neural target with the intent of affecting neural pathways to decrease pain perception—is similar, there are significant differences in the anatomy and physiology of the DRG that make it an ideal target for neuromodulation and may account for the superior outcomes observed in the treatment of certain chronic neuropathic pain states. This review highlights the anatomy of the DRG, its function in maintaining homeostasis and its role in neuropathic pain, and the unique value of DRG as a target in neuromodulation for pain. METHODS: A narrative literature review was performed. RESULTS: Overall, the DRG is a critical structure in sensory transduction and modulation, including pain transmission and the maintenance of persistent neuropathic pain states. Unique characteristics including selective somatic organization, specialized membrane characteristics, and accessible and consistent location make the DRG an ideal target for neuromodulation. Because DRG stimulation directly recruits the somata of primary sensory neurons and harnesses the filtering capacity of the pseudounipolar neural architecture, it is differentiated from SCS, peripheral nerve stimulation, and other neuromodulation options. CONCLUSIONS: There are several advantages to targeting the DRG, including lower energy usage, more focused and posture-independent stimulation, reduced paresthesia, and improved clinical outcomes.
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spelling pubmed-65445572019-06-12 Unique Characteristics of the Dorsal Root Ganglion as a Target for Neuromodulation Esposito, Michael F Malayil, Rudy Hanes, Michael Deer, Timothy Pain Med Review Articles OBJECTIVE: The dorsal root ganglion (DRG) is a novel target for neuromodulation, and DRG stimulation is proving to be a viable option in the treatment of chronic intractable neuropathic pain. Although the overall principle of conventional spinal cord stimulation (SCS) and DRG stimulation—in which an electric field is applied to a neural target with the intent of affecting neural pathways to decrease pain perception—is similar, there are significant differences in the anatomy and physiology of the DRG that make it an ideal target for neuromodulation and may account for the superior outcomes observed in the treatment of certain chronic neuropathic pain states. This review highlights the anatomy of the DRG, its function in maintaining homeostasis and its role in neuropathic pain, and the unique value of DRG as a target in neuromodulation for pain. METHODS: A narrative literature review was performed. RESULTS: Overall, the DRG is a critical structure in sensory transduction and modulation, including pain transmission and the maintenance of persistent neuropathic pain states. Unique characteristics including selective somatic organization, specialized membrane characteristics, and accessible and consistent location make the DRG an ideal target for neuromodulation. Because DRG stimulation directly recruits the somata of primary sensory neurons and harnesses the filtering capacity of the pseudounipolar neural architecture, it is differentiated from SCS, peripheral nerve stimulation, and other neuromodulation options. CONCLUSIONS: There are several advantages to targeting the DRG, including lower energy usage, more focused and posture-independent stimulation, reduced paresthesia, and improved clinical outcomes. Oxford University Press 2019-06 2019-06-01 /pmc/articles/PMC6544557/ /pubmed/31152179 http://dx.doi.org/10.1093/pm/pnz012 Text en © 2019 American Academy of Pain Medicine. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contactjournals.permissions@oup.com
spellingShingle Review Articles
Esposito, Michael F
Malayil, Rudy
Hanes, Michael
Deer, Timothy
Unique Characteristics of the Dorsal Root Ganglion as a Target for Neuromodulation
title Unique Characteristics of the Dorsal Root Ganglion as a Target for Neuromodulation
title_full Unique Characteristics of the Dorsal Root Ganglion as a Target for Neuromodulation
title_fullStr Unique Characteristics of the Dorsal Root Ganglion as a Target for Neuromodulation
title_full_unstemmed Unique Characteristics of the Dorsal Root Ganglion as a Target for Neuromodulation
title_short Unique Characteristics of the Dorsal Root Ganglion as a Target for Neuromodulation
title_sort unique characteristics of the dorsal root ganglion as a target for neuromodulation
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544557/
https://www.ncbi.nlm.nih.gov/pubmed/31152179
http://dx.doi.org/10.1093/pm/pnz012
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