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Normalized skin conductance level could differentiate physical pain stimuli from other sympathetic stimuli

Skin conductance monitoring is one of the promising methods for objectively evaluating pain. However, skin conductance might possibly increase in response to sympathetic stimulation other than pain. In this study, we aimed to test whether skin conductance monitoring can distinguish physical pain sti...

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Autores principales: Sugimine, Satomi, Saito, Shigeru, Takazawa, Tomonori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331661/
https://www.ncbi.nlm.nih.gov/pubmed/32616939
http://dx.doi.org/10.1038/s41598-020-67936-0
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author Sugimine, Satomi
Saito, Shigeru
Takazawa, Tomonori
author_facet Sugimine, Satomi
Saito, Shigeru
Takazawa, Tomonori
author_sort Sugimine, Satomi
collection PubMed
description Skin conductance monitoring is one of the promising methods for objectively evaluating pain. However, skin conductance might possibly increase in response to sympathetic stimulation other than pain. In this study, we aimed to test whether skin conductance monitoring can distinguish physical pain stimulation (heat, mechanical and cold stimulation) from other sympathetic stimuli (stimulation by noise and painful images). Twenty-three healthy volunteers participated in this prospective observational study. The number of fluctuations in skin conductance (NFSC) and normalized skin conductance level (nSCL) were measured and compared with pain scores on a self-reported pain scale (numerical pain scale [NPS]). Both NFSC and nSCL increased during mechanical stimulation. Further, nSCL, but not NFSC, well reflected heat stimulus intensity, suggesting its ability to quantitatively evaluate pain. nSCLs during physical pain stimulation were greater than those during other sympathetic stimulations. However, NFSC was not able to completely distinguish between the stimuli. These results suggest that nSCL could better differentiate physical pain stimuli from other sympathetic stimuli than NFSC. In comparisons between subjective and objective pain assessment in the same individual, nSCL correlated better with NPS score, indicating the possibility of being able to monitor the transition of pain. Monitoring changes in skin conductance using nSCL might be useful for objectively detecting physical pain.
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spelling pubmed-73316612020-07-06 Normalized skin conductance level could differentiate physical pain stimuli from other sympathetic stimuli Sugimine, Satomi Saito, Shigeru Takazawa, Tomonori Sci Rep Article Skin conductance monitoring is one of the promising methods for objectively evaluating pain. However, skin conductance might possibly increase in response to sympathetic stimulation other than pain. In this study, we aimed to test whether skin conductance monitoring can distinguish physical pain stimulation (heat, mechanical and cold stimulation) from other sympathetic stimuli (stimulation by noise and painful images). Twenty-three healthy volunteers participated in this prospective observational study. The number of fluctuations in skin conductance (NFSC) and normalized skin conductance level (nSCL) were measured and compared with pain scores on a self-reported pain scale (numerical pain scale [NPS]). Both NFSC and nSCL increased during mechanical stimulation. Further, nSCL, but not NFSC, well reflected heat stimulus intensity, suggesting its ability to quantitatively evaluate pain. nSCLs during physical pain stimulation were greater than those during other sympathetic stimulations. However, NFSC was not able to completely distinguish between the stimuli. These results suggest that nSCL could better differentiate physical pain stimuli from other sympathetic stimuli than NFSC. In comparisons between subjective and objective pain assessment in the same individual, nSCL correlated better with NPS score, indicating the possibility of being able to monitor the transition of pain. Monitoring changes in skin conductance using nSCL might be useful for objectively detecting physical pain. Nature Publishing Group UK 2020-07-02 /pmc/articles/PMC7331661/ /pubmed/32616939 http://dx.doi.org/10.1038/s41598-020-67936-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sugimine, Satomi
Saito, Shigeru
Takazawa, Tomonori
Normalized skin conductance level could differentiate physical pain stimuli from other sympathetic stimuli
title Normalized skin conductance level could differentiate physical pain stimuli from other sympathetic stimuli
title_full Normalized skin conductance level could differentiate physical pain stimuli from other sympathetic stimuli
title_fullStr Normalized skin conductance level could differentiate physical pain stimuli from other sympathetic stimuli
title_full_unstemmed Normalized skin conductance level could differentiate physical pain stimuli from other sympathetic stimuli
title_short Normalized skin conductance level could differentiate physical pain stimuli from other sympathetic stimuli
title_sort normalized skin conductance level could differentiate physical pain stimuli from other sympathetic stimuli
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331661/
https://www.ncbi.nlm.nih.gov/pubmed/32616939
http://dx.doi.org/10.1038/s41598-020-67936-0
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