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Rethinking multiscale cardiac electrophysiology with machine learning and predictive modelling
We review some of the latest approaches to analysing cardiac electrophysiology data using machine learning and predictive modelling. Cardiac arrhythmias, particularly atrial fibrillation, are a major global healthcare challenge. Treatment is often through catheter ablation, which involves the target...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334203/ https://www.ncbi.nlm.nih.gov/pubmed/30442428 http://dx.doi.org/10.1016/j.compbiomed.2018.10.015 |
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author | Cantwell, Chris D. Mohamied, Yumnah Tzortzis, Konstantinos N. Garasto, Stef Houston, Charles Chowdhury, Rasheda A. Ng, Fu Siong Bharath, Anil A. Peters, Nicholas S. |
author_facet | Cantwell, Chris D. Mohamied, Yumnah Tzortzis, Konstantinos N. Garasto, Stef Houston, Charles Chowdhury, Rasheda A. Ng, Fu Siong Bharath, Anil A. Peters, Nicholas S. |
author_sort | Cantwell, Chris D. |
collection | PubMed |
description | We review some of the latest approaches to analysing cardiac electrophysiology data using machine learning and predictive modelling. Cardiac arrhythmias, particularly atrial fibrillation, are a major global healthcare challenge. Treatment is often through catheter ablation, which involves the targeted localised destruction of regions of the myocardium responsible for initiating or perpetuating the arrhythmia. Ablation targets are either anatomically defined, or identified based on their functional properties as determined through the analysis of contact intracardiac electrograms acquired with increasing spatial density by modern electroanatomic mapping systems. While numerous quantitative approaches have been investigated over the past decades for identifying these critical curative sites, few have provided a reliable and reproducible advance in success rates. Machine learning techniques, including recent deep-learning approaches, offer a potential route to gaining new insight from this wealth of highly complex spatio-temporal information that existing methods struggle to analyse. Coupled with predictive modelling, these techniques offer exciting opportunities to advance the field and produce more accurate diagnoses and robust personalised treatment. We outline some of these methods and illustrate their use in making predictions from the contact electrogram and augmenting predictive modelling tools, both by more rapidly predicting future states of the system and by inferring the parameters of these models from experimental observations. |
format | Online Article Text |
id | pubmed-6334203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-63342032019-01-22 Rethinking multiscale cardiac electrophysiology with machine learning and predictive modelling Cantwell, Chris D. Mohamied, Yumnah Tzortzis, Konstantinos N. Garasto, Stef Houston, Charles Chowdhury, Rasheda A. Ng, Fu Siong Bharath, Anil A. Peters, Nicholas S. Comput Biol Med Article We review some of the latest approaches to analysing cardiac electrophysiology data using machine learning and predictive modelling. Cardiac arrhythmias, particularly atrial fibrillation, are a major global healthcare challenge. Treatment is often through catheter ablation, which involves the targeted localised destruction of regions of the myocardium responsible for initiating or perpetuating the arrhythmia. Ablation targets are either anatomically defined, or identified based on their functional properties as determined through the analysis of contact intracardiac electrograms acquired with increasing spatial density by modern electroanatomic mapping systems. While numerous quantitative approaches have been investigated over the past decades for identifying these critical curative sites, few have provided a reliable and reproducible advance in success rates. Machine learning techniques, including recent deep-learning approaches, offer a potential route to gaining new insight from this wealth of highly complex spatio-temporal information that existing methods struggle to analyse. Coupled with predictive modelling, these techniques offer exciting opportunities to advance the field and produce more accurate diagnoses and robust personalised treatment. We outline some of these methods and illustrate their use in making predictions from the contact electrogram and augmenting predictive modelling tools, both by more rapidly predicting future states of the system and by inferring the parameters of these models from experimental observations. Elsevier 2019-01 /pmc/articles/PMC6334203/ /pubmed/30442428 http://dx.doi.org/10.1016/j.compbiomed.2018.10.015 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cantwell, Chris D. Mohamied, Yumnah Tzortzis, Konstantinos N. Garasto, Stef Houston, Charles Chowdhury, Rasheda A. Ng, Fu Siong Bharath, Anil A. Peters, Nicholas S. Rethinking multiscale cardiac electrophysiology with machine learning and predictive modelling |
title | Rethinking multiscale cardiac electrophysiology with machine learning and predictive modelling |
title_full | Rethinking multiscale cardiac electrophysiology with machine learning and predictive modelling |
title_fullStr | Rethinking multiscale cardiac electrophysiology with machine learning and predictive modelling |
title_full_unstemmed | Rethinking multiscale cardiac electrophysiology with machine learning and predictive modelling |
title_short | Rethinking multiscale cardiac electrophysiology with machine learning and predictive modelling |
title_sort | rethinking multiscale cardiac electrophysiology with machine learning and predictive modelling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334203/ https://www.ncbi.nlm.nih.gov/pubmed/30442428 http://dx.doi.org/10.1016/j.compbiomed.2018.10.015 |
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