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Exploring Deep Physiological Models for Nociceptive Pain Recognition
Standard feature engineering involves manually designing measurable descriptors based on some expert knowledge in the domain of application, followed by the selection of the best performing set of designed features for the subsequent optimisation of an inference model. Several studies have shown tha...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833075/ https://www.ncbi.nlm.nih.gov/pubmed/31627305 http://dx.doi.org/10.3390/s19204503 |
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author | Thiam, Patrick Bellmann, Peter Kestler, Hans A. Schwenker, Friedhelm |
author_facet | Thiam, Patrick Bellmann, Peter Kestler, Hans A. Schwenker, Friedhelm |
author_sort | Thiam, Patrick |
collection | PubMed |
description | Standard feature engineering involves manually designing measurable descriptors based on some expert knowledge in the domain of application, followed by the selection of the best performing set of designed features for the subsequent optimisation of an inference model. Several studies have shown that this whole manual process can be efficiently replaced by deep learning approaches which are characterised by the integration of feature engineering, feature selection and inference model optimisation into a single learning process. In the following work, deep learning architectures are designed for the assessment of measurable physiological channels in order to perform an accurate classification of different levels of artificially induced nociceptive pain. In contrast to previous works, which rely on carefully designed sets of hand-crafted features, the current work aims at building competitive pain intensity inference models through autonomous feature learning, based on deep neural networks. The assessment of the designed deep learning architectures is based on the BioVid Heat Pain Database (Part A) and experimental validation demonstrates that the proposed uni-modal architecture for the electrodermal activity (EDA) and the deep fusion approaches significantly outperform previous methods reported in the literature, with respective average performances of [Formula: see text] and [Formula: see text] for the binary classification experiment consisting of the discrimination between the baseline and the pain tolerance level ([Formula: see text] vs. [Formula: see text]) in a Leave-One-Subject-Out (LOSO) cross-validation evaluation setting. Moreover, the experimental results clearly show the relevance of the proposed approaches, which also offer more flexibility in the case of transfer learning due to the modular nature of deep neural networks. |
format | Online Article Text |
id | pubmed-6833075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68330752019-11-25 Exploring Deep Physiological Models for Nociceptive Pain Recognition Thiam, Patrick Bellmann, Peter Kestler, Hans A. Schwenker, Friedhelm Sensors (Basel) Article Standard feature engineering involves manually designing measurable descriptors based on some expert knowledge in the domain of application, followed by the selection of the best performing set of designed features for the subsequent optimisation of an inference model. Several studies have shown that this whole manual process can be efficiently replaced by deep learning approaches which are characterised by the integration of feature engineering, feature selection and inference model optimisation into a single learning process. In the following work, deep learning architectures are designed for the assessment of measurable physiological channels in order to perform an accurate classification of different levels of artificially induced nociceptive pain. In contrast to previous works, which rely on carefully designed sets of hand-crafted features, the current work aims at building competitive pain intensity inference models through autonomous feature learning, based on deep neural networks. The assessment of the designed deep learning architectures is based on the BioVid Heat Pain Database (Part A) and experimental validation demonstrates that the proposed uni-modal architecture for the electrodermal activity (EDA) and the deep fusion approaches significantly outperform previous methods reported in the literature, with respective average performances of [Formula: see text] and [Formula: see text] for the binary classification experiment consisting of the discrimination between the baseline and the pain tolerance level ([Formula: see text] vs. [Formula: see text]) in a Leave-One-Subject-Out (LOSO) cross-validation evaluation setting. Moreover, the experimental results clearly show the relevance of the proposed approaches, which also offer more flexibility in the case of transfer learning due to the modular nature of deep neural networks. MDPI 2019-10-17 /pmc/articles/PMC6833075/ /pubmed/31627305 http://dx.doi.org/10.3390/s19204503 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Thiam, Patrick Bellmann, Peter Kestler, Hans A. Schwenker, Friedhelm Exploring Deep Physiological Models for Nociceptive Pain Recognition |
title | Exploring Deep Physiological Models for Nociceptive Pain Recognition |
title_full | Exploring Deep Physiological Models for Nociceptive Pain Recognition |
title_fullStr | Exploring Deep Physiological Models for Nociceptive Pain Recognition |
title_full_unstemmed | Exploring Deep Physiological Models for Nociceptive Pain Recognition |
title_short | Exploring Deep Physiological Models for Nociceptive Pain Recognition |
title_sort | exploring deep physiological models for nociceptive pain recognition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833075/ https://www.ncbi.nlm.nih.gov/pubmed/31627305 http://dx.doi.org/10.3390/s19204503 |
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