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Scalable and Accurate ECG Simulation for Reaction-Diffusion Models of the Human Heart
Realistic electrocardiogram (ECG) simulation with numerical models is important for research linking cellular and molecular physiology to clinically observable signals, and crucial for patient tailoring of numerical heart models. However, ECG simulation with a realistic torso model is computationall...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920200/ https://www.ncbi.nlm.nih.gov/pubmed/29731720 http://dx.doi.org/10.3389/fphys.2018.00370 |
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author | Potse, Mark |
author_facet | Potse, Mark |
author_sort | Potse, Mark |
collection | PubMed |
description | Realistic electrocardiogram (ECG) simulation with numerical models is important for research linking cellular and molecular physiology to clinically observable signals, and crucial for patient tailoring of numerical heart models. However, ECG simulation with a realistic torso model is computationally much harder than simulation of cardiac activity itself, so that many studies with sophisticated heart models have resorted to crude approximations of the ECG. This paper shows how the classical concept of electrocardiographic lead fields can be used for an ECG simulation method that matches the realism of modern heart models. The accuracy and resource requirements were compared to those of a full-torso solution for the potential and scaling was tested up to 14,336 cores with a heart model consisting of 11 million nodes. Reference ECGs were computed on a 3.3 billion-node heart-torso mesh at 0.2 mm resolution. The results show that the lead-field method is more efficient than a full-torso solution when the number of simulated samples is larger than the number of computed ECG leads. While the initial computation of the lead fields remains a hard and poorly scalable problem, the ECG computation itself scales almost perfectly and, even for several hundreds of ECG leads, takes much less time than the underlying simulation of cardiac activity. |
format | Online Article Text |
id | pubmed-5920200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59202002018-05-04 Scalable and Accurate ECG Simulation for Reaction-Diffusion Models of the Human Heart Potse, Mark Front Physiol Physiology Realistic electrocardiogram (ECG) simulation with numerical models is important for research linking cellular and molecular physiology to clinically observable signals, and crucial for patient tailoring of numerical heart models. However, ECG simulation with a realistic torso model is computationally much harder than simulation of cardiac activity itself, so that many studies with sophisticated heart models have resorted to crude approximations of the ECG. This paper shows how the classical concept of electrocardiographic lead fields can be used for an ECG simulation method that matches the realism of modern heart models. The accuracy and resource requirements were compared to those of a full-torso solution for the potential and scaling was tested up to 14,336 cores with a heart model consisting of 11 million nodes. Reference ECGs were computed on a 3.3 billion-node heart-torso mesh at 0.2 mm resolution. The results show that the lead-field method is more efficient than a full-torso solution when the number of simulated samples is larger than the number of computed ECG leads. While the initial computation of the lead fields remains a hard and poorly scalable problem, the ECG computation itself scales almost perfectly and, even for several hundreds of ECG leads, takes much less time than the underlying simulation of cardiac activity. Frontiers Media S.A. 2018-04-20 /pmc/articles/PMC5920200/ /pubmed/29731720 http://dx.doi.org/10.3389/fphys.2018.00370 Text en Copyright © 2018 Potse. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Potse, Mark Scalable and Accurate ECG Simulation for Reaction-Diffusion Models of the Human Heart |
title | Scalable and Accurate ECG Simulation for Reaction-Diffusion Models of the Human Heart |
title_full | Scalable and Accurate ECG Simulation for Reaction-Diffusion Models of the Human Heart |
title_fullStr | Scalable and Accurate ECG Simulation for Reaction-Diffusion Models of the Human Heart |
title_full_unstemmed | Scalable and Accurate ECG Simulation for Reaction-Diffusion Models of the Human Heart |
title_short | Scalable and Accurate ECG Simulation for Reaction-Diffusion Models of the Human Heart |
title_sort | scalable and accurate ecg simulation for reaction-diffusion models of the human heart |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920200/ https://www.ncbi.nlm.nih.gov/pubmed/29731720 http://dx.doi.org/10.3389/fphys.2018.00370 |
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