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Deviations in continuously monitored electrodermal activity before severe clinical complications: a clinical prospective observational explorative cohort study

Monitoring of high-risk patients in hospital wards is crucial in identifying and preventing clinical deterioration. Sympathetic nervous system activity measured continuously and non-invasively by Electrodermal activity (EDA) may relate to complications, but the clinical use remains untested. The aim...

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Autores principales: Johansen, Andreas Ohrt, Mølgaard, Jesper, Rasmussen, Søren Straarup, Gu, Ying, Grønbæk, Katja Kjær, Sørensen, Helge B. D., Aasvang, Eske Kvanner, Meyhoff, Christian Sylvest
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651525/
https://www.ncbi.nlm.nih.gov/pubmed/37195623
http://dx.doi.org/10.1007/s10877-023-01030-4
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author Johansen, Andreas Ohrt
Mølgaard, Jesper
Rasmussen, Søren Straarup
Gu, Ying
Grønbæk, Katja Kjær
Sørensen, Helge B. D.
Aasvang, Eske Kvanner
Meyhoff, Christian Sylvest
author_facet Johansen, Andreas Ohrt
Mølgaard, Jesper
Rasmussen, Søren Straarup
Gu, Ying
Grønbæk, Katja Kjær
Sørensen, Helge B. D.
Aasvang, Eske Kvanner
Meyhoff, Christian Sylvest
author_sort Johansen, Andreas Ohrt
collection PubMed
description Monitoring of high-risk patients in hospital wards is crucial in identifying and preventing clinical deterioration. Sympathetic nervous system activity measured continuously and non-invasively by Electrodermal activity (EDA) may relate to complications, but the clinical use remains untested. The aim of this study was to explore associations between deviations of EDA and subsequent serious adverse events (SAE). Patients admitted to general wards after major abdominal cancer surgery or with acute exacerbation of chronic obstructive pulmonary disease were continuously EDA-monitored for up to 5 days. We used time-perspectives consisting of 1, 3, 6, and 12 h of data prior to first SAE or from start of monitoring. We constructed 648 different EDA-derived features to assess EDA. The primary outcome was any SAE and secondary outcomes were respiratory, infectious, and cardiovascular SAEs. Associations were evaluated using logistic regressions with adjustment for relevant confounders. We included 714 patients and found a total of 192 statistically significant associations between EDA-derived features and clinical outcomes. 79% of these associations were EDA-derived features of absolute and relative increases in EDA and 14% were EDA-derived features with normalized EDA above a threshold. The highest F1-scores for primary outcome with the four time-perspectives were 20.7–32.8%, with precision ranging 34.9–38.6%, recall 14.7–29.4%, and specificity 83.1–91.4%. We identified statistically significant associations between specific deviations of EDA and subsequent SAE, and patterns of EDA may be developed to be considered indicators of upcoming clinical deterioration in high-risk patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10877-023-01030-4.
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spelling pubmed-106515252023-05-17 Deviations in continuously monitored electrodermal activity before severe clinical complications: a clinical prospective observational explorative cohort study Johansen, Andreas Ohrt Mølgaard, Jesper Rasmussen, Søren Straarup Gu, Ying Grønbæk, Katja Kjær Sørensen, Helge B. D. Aasvang, Eske Kvanner Meyhoff, Christian Sylvest J Clin Monit Comput Original Research Monitoring of high-risk patients in hospital wards is crucial in identifying and preventing clinical deterioration. Sympathetic nervous system activity measured continuously and non-invasively by Electrodermal activity (EDA) may relate to complications, but the clinical use remains untested. The aim of this study was to explore associations between deviations of EDA and subsequent serious adverse events (SAE). Patients admitted to general wards after major abdominal cancer surgery or with acute exacerbation of chronic obstructive pulmonary disease were continuously EDA-monitored for up to 5 days. We used time-perspectives consisting of 1, 3, 6, and 12 h of data prior to first SAE or from start of monitoring. We constructed 648 different EDA-derived features to assess EDA. The primary outcome was any SAE and secondary outcomes were respiratory, infectious, and cardiovascular SAEs. Associations were evaluated using logistic regressions with adjustment for relevant confounders. We included 714 patients and found a total of 192 statistically significant associations between EDA-derived features and clinical outcomes. 79% of these associations were EDA-derived features of absolute and relative increases in EDA and 14% were EDA-derived features with normalized EDA above a threshold. The highest F1-scores for primary outcome with the four time-perspectives were 20.7–32.8%, with precision ranging 34.9–38.6%, recall 14.7–29.4%, and specificity 83.1–91.4%. We identified statistically significant associations between specific deviations of EDA and subsequent SAE, and patterns of EDA may be developed to be considered indicators of upcoming clinical deterioration in high-risk patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10877-023-01030-4. Springer Netherlands 2023-05-17 2023 /pmc/articles/PMC10651525/ /pubmed/37195623 http://dx.doi.org/10.1007/s10877-023-01030-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Research
Johansen, Andreas Ohrt
Mølgaard, Jesper
Rasmussen, Søren Straarup
Gu, Ying
Grønbæk, Katja Kjær
Sørensen, Helge B. D.
Aasvang, Eske Kvanner
Meyhoff, Christian Sylvest
Deviations in continuously monitored electrodermal activity before severe clinical complications: a clinical prospective observational explorative cohort study
title Deviations in continuously monitored electrodermal activity before severe clinical complications: a clinical prospective observational explorative cohort study
title_full Deviations in continuously monitored electrodermal activity before severe clinical complications: a clinical prospective observational explorative cohort study
title_fullStr Deviations in continuously monitored electrodermal activity before severe clinical complications: a clinical prospective observational explorative cohort study
title_full_unstemmed Deviations in continuously monitored electrodermal activity before severe clinical complications: a clinical prospective observational explorative cohort study
title_short Deviations in continuously monitored electrodermal activity before severe clinical complications: a clinical prospective observational explorative cohort study
title_sort deviations in continuously monitored electrodermal activity before severe clinical complications: a clinical prospective observational explorative cohort study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651525/
https://www.ncbi.nlm.nih.gov/pubmed/37195623
http://dx.doi.org/10.1007/s10877-023-01030-4
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