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Timing and dosage of FES cycling early after acute spinal cord injury: A case series report

OBJECTIVE: To understand the progression in parameters of functional electrical stimulation (FES) cycling dosage (including duration, velocity, stimulation amplitudes, power output), and the resulting changes in muscle mass early after acute spinal cord injury (SCI). METHODS: Three participants, 24–...

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Autores principales: Everaert, Dirk G., Okuma, Yoshino, Abdollah, Vahid, Ho, Chester
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604517/
https://www.ncbi.nlm.nih.gov/pubmed/34292125
http://dx.doi.org/10.1080/10790268.2021.1953323
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author Everaert, Dirk G.
Okuma, Yoshino
Abdollah, Vahid
Ho, Chester
author_facet Everaert, Dirk G.
Okuma, Yoshino
Abdollah, Vahid
Ho, Chester
author_sort Everaert, Dirk G.
collection PubMed
description OBJECTIVE: To understand the progression in parameters of functional electrical stimulation (FES) cycling dosage (including duration, velocity, stimulation amplitudes, power output), and the resulting changes in muscle mass early after acute spinal cord injury (SCI). METHODS: Three participants, 24–38 years old, with neurological injury level C4–T4, severity AIS (American Spinal Injury Association Impairment Scale) A–C, started FES cycling 16–20 days post injury while admitted at a level-1 trauma center in Canada, and continued for 8–13 weeks in a rehabilitation hospital. They performed three sessions/week of 15–45 min FES cycling, supine or sitting. FES parameters, cycling performance, and muscle cross-sectional area (CSA) in thighs and calves were measured every 2 weeks. RESULTS: Progression in power output, but not in session duration, was limited in two participants who experienced stimulation-associated referred pain or apprehension, requiring limitation of stimulation amplitudes for up to 65 days after the start of FES cycling. Participants started with 15 min cycling at 20 RPM with no resistance (0 W), and progressed to 30–45 min at 30 RPM producing 8.8–19.0 W average power/session after 2–3 months. Initially, muscle CSA decreased in all 3 participants (up to 16% after 6 weeks), and recovered later after a variable period of FES cycling (up to 16% at 13.3 weeks). CONCLUSION: Progression of FES cycling in the first 3 months after injury required a highly individualized approach, guided by participant response, rather than standardized increments in stimulation intensity or duration. Changes in muscle CSA did not always correspond with the dose of FES cycling.
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spelling pubmed-86045172022-03-03 Timing and dosage of FES cycling early after acute spinal cord injury: A case series report Everaert, Dirk G. Okuma, Yoshino Abdollah, Vahid Ho, Chester J Spinal Cord Med Research Articles OBJECTIVE: To understand the progression in parameters of functional electrical stimulation (FES) cycling dosage (including duration, velocity, stimulation amplitudes, power output), and the resulting changes in muscle mass early after acute spinal cord injury (SCI). METHODS: Three participants, 24–38 years old, with neurological injury level C4–T4, severity AIS (American Spinal Injury Association Impairment Scale) A–C, started FES cycling 16–20 days post injury while admitted at a level-1 trauma center in Canada, and continued for 8–13 weeks in a rehabilitation hospital. They performed three sessions/week of 15–45 min FES cycling, supine or sitting. FES parameters, cycling performance, and muscle cross-sectional area (CSA) in thighs and calves were measured every 2 weeks. RESULTS: Progression in power output, but not in session duration, was limited in two participants who experienced stimulation-associated referred pain or apprehension, requiring limitation of stimulation amplitudes for up to 65 days after the start of FES cycling. Participants started with 15 min cycling at 20 RPM with no resistance (0 W), and progressed to 30–45 min at 30 RPM producing 8.8–19.0 W average power/session after 2–3 months. Initially, muscle CSA decreased in all 3 participants (up to 16% after 6 weeks), and recovered later after a variable period of FES cycling (up to 16% at 13.3 weeks). CONCLUSION: Progression of FES cycling in the first 3 months after injury required a highly individualized approach, guided by participant response, rather than standardized increments in stimulation intensity or duration. Changes in muscle CSA did not always correspond with the dose of FES cycling. Taylor & Francis 2021-07-22 /pmc/articles/PMC8604517/ /pubmed/34292125 http://dx.doi.org/10.1080/10790268.2021.1953323 Text en © 2021 The Author(s). Published with license by Taylor & Francis Group, LLC https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Articles
Everaert, Dirk G.
Okuma, Yoshino
Abdollah, Vahid
Ho, Chester
Timing and dosage of FES cycling early after acute spinal cord injury: A case series report
title Timing and dosage of FES cycling early after acute spinal cord injury: A case series report
title_full Timing and dosage of FES cycling early after acute spinal cord injury: A case series report
title_fullStr Timing and dosage of FES cycling early after acute spinal cord injury: A case series report
title_full_unstemmed Timing and dosage of FES cycling early after acute spinal cord injury: A case series report
title_short Timing and dosage of FES cycling early after acute spinal cord injury: A case series report
title_sort timing and dosage of fes cycling early after acute spinal cord injury: a case series report
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604517/
https://www.ncbi.nlm.nih.gov/pubmed/34292125
http://dx.doi.org/10.1080/10790268.2021.1953323
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