Personalized Models of Human Atrial Electrophysiology Derived From Endocardial Electrograms
Objective : Computational models represent a novel framework for understanding the mechanisms behind atrial fibrillation (AF) and offer a pathway for personalizing and optimizing treatment. The characterization of local electrophysiological properties across the atria during procedures remains a cha...
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Published in | IEEE transactions on biomedical engineering Vol. 64; no. 4; pp. 735 - 742 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
IEEE
01.04.2017
The Institute of Electrical and Electronics Engineers, Inc. (IEEE) |
Subjects | |
Online Access | Get full text |
ISSN | 0018-9294 1558-2531 |
DOI | 10.1109/TBME.2016.2574619 |
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Summary: | Objective : Computational models represent a novel framework for understanding the mechanisms behind atrial fibrillation (AF) and offer a pathway for personalizing and optimizing treatment. The characterization of local electrophysiological properties across the atria during procedures remains a challenge. The aim of this work is to characterize the regional properties of the human atrium from multielectrode catheter measurements. Methods : We propose a novel method that characterizes regional electrophysiology properties by fitting parameters of an ionic model to conduction velocity and effective refractory period restitution curves obtained by a <inline-formula><tex-math notation="LaTeX">s_\text{1}\_ s_\text{2}</tex-math></inline-formula> pacing protocol applied through a multielectrode catheter. Using an in-silico dataset we demonstrate that the fitting method can constrain parameters with a mean error of <inline-formula><tex-math notation="LaTeX">21.9\pm 16.1\%</tex-math></inline-formula> and can replicate conduction velocity and effective refractory curves not used in the original fitting with a relative error of <inline-formula><tex-math notation="LaTeX">4.4\pm 6.9\%</tex-math></inline-formula>. Results : We demonstrate this parameter estimation approach on five clinical datasets recorded from AF patients. Recordings and parametrization took approx. 5 and 6 min, respectively. Models fitted restitution curves with an error of <inline-formula><tex-math notation="LaTeX">\sim 5\%</tex-math></inline-formula> and identify a unique parameter set. Tissue properties were predicted using a two-dimensional atrial tissue sheet model. Spiral wave stability in each case was predicted using tissue simulations, identifying distinct stable (2/5), meandering and breaking up (2/5), and unstable self-terminating (1/5) spiral tip patterns for different cases. Conclusion and significance : We have developed and demonstrated a robust and rapid approach for personalizing local ionic models from a clinically tractable protocol to characterize cellular properties and predict tissue electrophysiological function. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0018-9294 1558-2531 |
DOI: | 10.1109/TBME.2016.2574619 |