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Decoding upper limb residual muscle activity in severe chronic stroke

OBJECTIVE: Stroke is a leading cause of long-term motor disability. Stroke patients with severe hand weakness do not profit from rehabilitative treatments. Recently, brain-controlled robotics and sequential functional electrical stimulation allowed some improvement. However, for such therapies to su...

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Autores principales: Ramos-Murguialday, Ander, García-Cossio, Eliana, Walter, Armin, Cho, Woosang, Broetz, Doris, Bogdan, Martin, Cohen, Leonardo G, Birbaumer, Niels
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301668/
https://www.ncbi.nlm.nih.gov/pubmed/25642429
http://dx.doi.org/10.1002/acn3.122
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author Ramos-Murguialday, Ander
García-Cossio, Eliana
Walter, Armin
Cho, Woosang
Broetz, Doris
Bogdan, Martin
Cohen, Leonardo G
Birbaumer, Niels
author_facet Ramos-Murguialday, Ander
García-Cossio, Eliana
Walter, Armin
Cho, Woosang
Broetz, Doris
Bogdan, Martin
Cohen, Leonardo G
Birbaumer, Niels
author_sort Ramos-Murguialday, Ander
collection PubMed
description OBJECTIVE: Stroke is a leading cause of long-term motor disability. Stroke patients with severe hand weakness do not profit from rehabilitative treatments. Recently, brain-controlled robotics and sequential functional electrical stimulation allowed some improvement. However, for such therapies to succeed, it is required to decode patients' intentions for different arm movements. Here, we evaluated whether residual muscle activity could be used to predict movements from paralyzed joints in severely impaired chronic stroke patients. METHODS: Muscle activity was recorded with surface-electromyography (EMG) in 41 patients, with severe hand weakness (Fugl-Meyer Assessment [FMA] hand subscores of 2.93 ± 2.7), in order to decode their intention to perform six different motions of the affected arm, required for voluntary muscle activity and to control neuroprostheses. Decoding of paretic and nonparetic muscle activity was performed using a feed-forward neural network classifier. The contribution of each muscle to the intended movement was determined. RESULTS: Decoding of up to six arm movements was accurate (>65%) in more than 97% of nonparetic and 46% of paretic muscles. INTERPRETATION: These results demonstrate that some level of neuronal innervation to the paretic muscle remains preserved and can be used to implement neurorehabilitative treatments in 46% of patients with severe paralysis and extensive cortical and/or subcortical lesions. Such decoding may allow these patients for the first time after stroke to control different motions of arm prostheses through muscle-triggered rehabilitative treatments.
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spelling pubmed-43016682015-01-30 Decoding upper limb residual muscle activity in severe chronic stroke Ramos-Murguialday, Ander García-Cossio, Eliana Walter, Armin Cho, Woosang Broetz, Doris Bogdan, Martin Cohen, Leonardo G Birbaumer, Niels Ann Clin Transl Neurol Research Articles OBJECTIVE: Stroke is a leading cause of long-term motor disability. Stroke patients with severe hand weakness do not profit from rehabilitative treatments. Recently, brain-controlled robotics and sequential functional electrical stimulation allowed some improvement. However, for such therapies to succeed, it is required to decode patients' intentions for different arm movements. Here, we evaluated whether residual muscle activity could be used to predict movements from paralyzed joints in severely impaired chronic stroke patients. METHODS: Muscle activity was recorded with surface-electromyography (EMG) in 41 patients, with severe hand weakness (Fugl-Meyer Assessment [FMA] hand subscores of 2.93 ± 2.7), in order to decode their intention to perform six different motions of the affected arm, required for voluntary muscle activity and to control neuroprostheses. Decoding of paretic and nonparetic muscle activity was performed using a feed-forward neural network classifier. The contribution of each muscle to the intended movement was determined. RESULTS: Decoding of up to six arm movements was accurate (>65%) in more than 97% of nonparetic and 46% of paretic muscles. INTERPRETATION: These results demonstrate that some level of neuronal innervation to the paretic muscle remains preserved and can be used to implement neurorehabilitative treatments in 46% of patients with severe paralysis and extensive cortical and/or subcortical lesions. Such decoding may allow these patients for the first time after stroke to control different motions of arm prostheses through muscle-triggered rehabilitative treatments. BlackWell Publishing Ltd 2015-01 2014-12-09 /pmc/articles/PMC4301668/ /pubmed/25642429 http://dx.doi.org/10.1002/acn3.122 Text en © 2014 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Ramos-Murguialday, Ander
García-Cossio, Eliana
Walter, Armin
Cho, Woosang
Broetz, Doris
Bogdan, Martin
Cohen, Leonardo G
Birbaumer, Niels
Decoding upper limb residual muscle activity in severe chronic stroke
title Decoding upper limb residual muscle activity in severe chronic stroke
title_full Decoding upper limb residual muscle activity in severe chronic stroke
title_fullStr Decoding upper limb residual muscle activity in severe chronic stroke
title_full_unstemmed Decoding upper limb residual muscle activity in severe chronic stroke
title_short Decoding upper limb residual muscle activity in severe chronic stroke
title_sort decoding upper limb residual muscle activity in severe chronic stroke
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301668/
https://www.ncbi.nlm.nih.gov/pubmed/25642429
http://dx.doi.org/10.1002/acn3.122
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