Cargando…

Using evoked compound action potentials to quantify differential neural activation with burst and conventional, 40 Hz spinal cord stimulation in ovines

Unlike conventional dorsal spinal cord stimulation (SCS)—which uses single pulses at a fixed rate—burst SCS uses a fixed-rate, five-pulse stimuli cluster as a treatment for chronic pain; mechanistic explanations suggest burst SCS differentially modulate the medial and lateral pain pathways vs conven...

Descripción completa

Detalles Bibliográficos
Autores principales: Dinsmoor, David A., Usoro, Joshua O., Barka, Noah D., Billstrom, Tina M., Litvak, Leonid M., Poree, Lawrence R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663139/
https://www.ncbi.nlm.nih.gov/pubmed/36398199
http://dx.doi.org/10.1097/PR9.0000000000001047
_version_ 1784830804908572672
author Dinsmoor, David A.
Usoro, Joshua O.
Barka, Noah D.
Billstrom, Tina M.
Litvak, Leonid M.
Poree, Lawrence R.
author_facet Dinsmoor, David A.
Usoro, Joshua O.
Barka, Noah D.
Billstrom, Tina M.
Litvak, Leonid M.
Poree, Lawrence R.
author_sort Dinsmoor, David A.
collection PubMed
description Unlike conventional dorsal spinal cord stimulation (SCS)—which uses single pulses at a fixed rate—burst SCS uses a fixed-rate, five-pulse stimuli cluster as a treatment for chronic pain; mechanistic explanations suggest burst SCS differentially modulate the medial and lateral pain pathways vs conventional SCS. Neural activation differences between burst and conventional SCS are quantifiable with the spinal-evoked compound action potential (ECAP), an electrical measure of synchronous neural activation. METHODS: We implanted 7 sheep with a dorsal stimulation lead at T9/T10, a dorsal ECAP sensing lead at T6/T7, and a lead also at T9/T10 but adjacent to the anterolateral system (ALS). Both burst and conventional SCS with stimulation amplitudes up to the visual motor threshold (vMT) were delivered to 3 different dorsal spinal locations, and ECAP thresholds (ECAPTs) were calculated for all combinations. Then, changes in ALS activation were assessed with both types of SCS. RESULTS: Evoked compound action potential thresholds and vMTs were significantly higher (P < 0.05) with conventional vs burst SCS, with no statistical difference (P > 0.05) among stimulation sites. However, the vMT−ECAPT window (a proxy for the useable therapeutic dosing range) was significantly wider (P < 0.05) with conventional vs burst SCS. No significant difference (P > 0.05) in ALS activation was noted between conventional and burst SCS. CONCLUSION: When dosed equivalently, no differentially unique change in ALS activation results with burst SCS vs conventional SCS; in addition, sub-ECAPT burst SCS results in no discernable excitability changes in the neural pathways feeding pain relevant supraspinal sites.
format Online
Article
Text
id pubmed-9663139
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Wolters Kluwer
record_format MEDLINE/PubMed
spelling pubmed-96631392022-11-16 Using evoked compound action potentials to quantify differential neural activation with burst and conventional, 40 Hz spinal cord stimulation in ovines Dinsmoor, David A. Usoro, Joshua O. Barka, Noah D. Billstrom, Tina M. Litvak, Leonid M. Poree, Lawrence R. Pain Rep Basic Science Unlike conventional dorsal spinal cord stimulation (SCS)—which uses single pulses at a fixed rate—burst SCS uses a fixed-rate, five-pulse stimuli cluster as a treatment for chronic pain; mechanistic explanations suggest burst SCS differentially modulate the medial and lateral pain pathways vs conventional SCS. Neural activation differences between burst and conventional SCS are quantifiable with the spinal-evoked compound action potential (ECAP), an electrical measure of synchronous neural activation. METHODS: We implanted 7 sheep with a dorsal stimulation lead at T9/T10, a dorsal ECAP sensing lead at T6/T7, and a lead also at T9/T10 but adjacent to the anterolateral system (ALS). Both burst and conventional SCS with stimulation amplitudes up to the visual motor threshold (vMT) were delivered to 3 different dorsal spinal locations, and ECAP thresholds (ECAPTs) were calculated for all combinations. Then, changes in ALS activation were assessed with both types of SCS. RESULTS: Evoked compound action potential thresholds and vMTs were significantly higher (P < 0.05) with conventional vs burst SCS, with no statistical difference (P > 0.05) among stimulation sites. However, the vMT−ECAPT window (a proxy for the useable therapeutic dosing range) was significantly wider (P < 0.05) with conventional vs burst SCS. No significant difference (P > 0.05) in ALS activation was noted between conventional and burst SCS. CONCLUSION: When dosed equivalently, no differentially unique change in ALS activation results with burst SCS vs conventional SCS; in addition, sub-ECAPT burst SCS results in no discernable excitability changes in the neural pathways feeding pain relevant supraspinal sites. Wolters Kluwer 2022-11-11 /pmc/articles/PMC9663139/ /pubmed/36398199 http://dx.doi.org/10.1097/PR9.0000000000001047 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The International Association for the Study of Pain. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Basic Science
Dinsmoor, David A.
Usoro, Joshua O.
Barka, Noah D.
Billstrom, Tina M.
Litvak, Leonid M.
Poree, Lawrence R.
Using evoked compound action potentials to quantify differential neural activation with burst and conventional, 40 Hz spinal cord stimulation in ovines
title Using evoked compound action potentials to quantify differential neural activation with burst and conventional, 40 Hz spinal cord stimulation in ovines
title_full Using evoked compound action potentials to quantify differential neural activation with burst and conventional, 40 Hz spinal cord stimulation in ovines
title_fullStr Using evoked compound action potentials to quantify differential neural activation with burst and conventional, 40 Hz spinal cord stimulation in ovines
title_full_unstemmed Using evoked compound action potentials to quantify differential neural activation with burst and conventional, 40 Hz spinal cord stimulation in ovines
title_short Using evoked compound action potentials to quantify differential neural activation with burst and conventional, 40 Hz spinal cord stimulation in ovines
title_sort using evoked compound action potentials to quantify differential neural activation with burst and conventional, 40 hz spinal cord stimulation in ovines
topic Basic Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663139/
https://www.ncbi.nlm.nih.gov/pubmed/36398199
http://dx.doi.org/10.1097/PR9.0000000000001047
work_keys_str_mv AT dinsmoordavida usingevokedcompoundactionpotentialstoquantifydifferentialneuralactivationwithburstandconventional40hzspinalcordstimulationinovines
AT usorojoshuao usingevokedcompoundactionpotentialstoquantifydifferentialneuralactivationwithburstandconventional40hzspinalcordstimulationinovines
AT barkanoahd usingevokedcompoundactionpotentialstoquantifydifferentialneuralactivationwithburstandconventional40hzspinalcordstimulationinovines
AT billstromtinam usingevokedcompoundactionpotentialstoquantifydifferentialneuralactivationwithburstandconventional40hzspinalcordstimulationinovines
AT litvakleonidm usingevokedcompoundactionpotentialstoquantifydifferentialneuralactivationwithburstandconventional40hzspinalcordstimulationinovines
AT poreelawrencer usingevokedcompoundactionpotentialstoquantifydifferentialneuralactivationwithburstandconventional40hzspinalcordstimulationinovines