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A Clinical Decision Support System for the Prediction of Quality of Life in ALS

Amyotrophic Lateral Sclerosis (ALS), also known as Motor Neuron Disease (MND), is a rare and fatal neurodegenerative disease. As ALS is currently incurable, the aim of the treatment is mainly to alleviate symptoms and improve quality of life (QoL). We designed a prototype Clinical Decision Support S...

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Autores principales: Antoniadi, Anna Markella, Galvin, Miriam, Heverin, Mark, Wei, Lan, Hardiman, Orla, Mooney, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955774/
https://www.ncbi.nlm.nih.gov/pubmed/35330435
http://dx.doi.org/10.3390/jpm12030435
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author Antoniadi, Anna Markella
Galvin, Miriam
Heverin, Mark
Wei, Lan
Hardiman, Orla
Mooney, Catherine
author_facet Antoniadi, Anna Markella
Galvin, Miriam
Heverin, Mark
Wei, Lan
Hardiman, Orla
Mooney, Catherine
author_sort Antoniadi, Anna Markella
collection PubMed
description Amyotrophic Lateral Sclerosis (ALS), also known as Motor Neuron Disease (MND), is a rare and fatal neurodegenerative disease. As ALS is currently incurable, the aim of the treatment is mainly to alleviate symptoms and improve quality of life (QoL). We designed a prototype Clinical Decision Support System (CDSS) to alert clinicians when a person with ALS is experiencing low QoL in order to inform and personalise the support they receive. Explainability is important for the success of a CDSS and its acceptance by healthcare professionals. The aim of this work isto announce our prototype (C-ALS), supported by a first short evaluation of its explainability. Given the lack of similar studies and systems, this work is a valid proof-of-concept that will lead to future work. We developed a CDSS that was evaluated by members of the team of healthcare professionals that provide care to people with ALS in the ALS/MND Multidisciplinary Clinic in Dublin, Ireland. We conducted a user study where participants were asked to review the CDSS and complete a short survey with a focus on explainability. Healthcare professionals demonstrated some uncertainty in understanding the system’s output. Based on their feedback, we altered the explanation provided in the updated version of our CDSS. C-ALS provides local explanations of its predictions in a post-hoc manner, using SHAP (SHapley Additive exPlanations). The CDSS predicts the risk of low QoL in the form of a probability, a bar plot shows the feature importance for the specific prediction, along with some verbal guidelines on how to interpret the results. Additionally, we provide the option of a global explanation of the system’s function in the form of a bar plot showing the average importance of each feature. C-ALS is available online for academic use.
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spelling pubmed-89557742022-03-26 A Clinical Decision Support System for the Prediction of Quality of Life in ALS Antoniadi, Anna Markella Galvin, Miriam Heverin, Mark Wei, Lan Hardiman, Orla Mooney, Catherine J Pers Med Article Amyotrophic Lateral Sclerosis (ALS), also known as Motor Neuron Disease (MND), is a rare and fatal neurodegenerative disease. As ALS is currently incurable, the aim of the treatment is mainly to alleviate symptoms and improve quality of life (QoL). We designed a prototype Clinical Decision Support System (CDSS) to alert clinicians when a person with ALS is experiencing low QoL in order to inform and personalise the support they receive. Explainability is important for the success of a CDSS and its acceptance by healthcare professionals. The aim of this work isto announce our prototype (C-ALS), supported by a first short evaluation of its explainability. Given the lack of similar studies and systems, this work is a valid proof-of-concept that will lead to future work. We developed a CDSS that was evaluated by members of the team of healthcare professionals that provide care to people with ALS in the ALS/MND Multidisciplinary Clinic in Dublin, Ireland. We conducted a user study where participants were asked to review the CDSS and complete a short survey with a focus on explainability. Healthcare professionals demonstrated some uncertainty in understanding the system’s output. Based on their feedback, we altered the explanation provided in the updated version of our CDSS. C-ALS provides local explanations of its predictions in a post-hoc manner, using SHAP (SHapley Additive exPlanations). The CDSS predicts the risk of low QoL in the form of a probability, a bar plot shows the feature importance for the specific prediction, along with some verbal guidelines on how to interpret the results. Additionally, we provide the option of a global explanation of the system’s function in the form of a bar plot showing the average importance of each feature. C-ALS is available online for academic use. MDPI 2022-03-10 /pmc/articles/PMC8955774/ /pubmed/35330435 http://dx.doi.org/10.3390/jpm12030435 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Antoniadi, Anna Markella
Galvin, Miriam
Heverin, Mark
Wei, Lan
Hardiman, Orla
Mooney, Catherine
A Clinical Decision Support System for the Prediction of Quality of Life in ALS
title A Clinical Decision Support System for the Prediction of Quality of Life in ALS
title_full A Clinical Decision Support System for the Prediction of Quality of Life in ALS
title_fullStr A Clinical Decision Support System for the Prediction of Quality of Life in ALS
title_full_unstemmed A Clinical Decision Support System for the Prediction of Quality of Life in ALS
title_short A Clinical Decision Support System for the Prediction of Quality of Life in ALS
title_sort clinical decision support system for the prediction of quality of life in als
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955774/
https://www.ncbi.nlm.nih.gov/pubmed/35330435
http://dx.doi.org/10.3390/jpm12030435
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