Entropy mapping approach for functional reentry detection in atrial fibrillation: An in-silico study

Catheter ablation of critical electrical propagation sites is a promising tool for reducing the recurrence of atrial fibrillation (AF). The spatial identification of the arrhythmogenic mechanisms sustaining AF requires the evaluation of electrograms (EGMs) recorded over the atrial surface. This work...

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2019
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Universidad de Medellín
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Repositorio UDEM
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eng
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id REPOUDEM2_b3b7e6528a55670c774617aa29bb0f7f
oai_identifier_str oai:repository.udem.edu.co:11407/6072
network_acronym_str REPOUDEM2
network_name_str Repositorio UDEM
repository_id_str
dc.title.none.fl_str_mv Entropy mapping approach for functional reentry detection in atrial fibrillation: An in-silico study
title Entropy mapping approach for functional reentry detection in atrial fibrillation: An in-silico study
spellingShingle Entropy mapping approach for functional reentry detection in atrial fibrillation: An in-silico study
title_short Entropy mapping approach for functional reentry detection in atrial fibrillation: An in-silico study
title_full Entropy mapping approach for functional reentry detection in atrial fibrillation: An in-silico study
title_fullStr Entropy mapping approach for functional reentry detection in atrial fibrillation: An in-silico study
title_full_unstemmed Entropy mapping approach for functional reentry detection in atrial fibrillation: An in-silico study
title_sort Entropy mapping approach for functional reentry detection in atrial fibrillation: An in-silico study
description Catheter ablation of critical electrical propagation sites is a promising tool for reducing the recurrence of atrial fibrillation (AF). The spatial identification of the arrhythmogenic mechanisms sustaining AF requires the evaluation of electrograms (EGMs) recorded over the atrial surface. This work aims to characterize functional reentries using measures of entropy to track and detect a reentry core. To this end, different AF episodes are simulated using a 2D model of atrial tissue. Modified Courtemanche human action potential and Fenton-Karma models are implemented. Action potential propagation is modeled by a fractional diffusion equation, and virtual unipolar EGM are calculated. Episodes with stable and meandering rotors, figure-of-eight reentry, and disorganized propagation with multiple reentries are generated. Shannon entropy (ShEn), approximate entropy (ApEn), and sample entropy (SampEn) are computed from the virtual EGM, and entropy maps are built. Phase singularity maps are implemented as references. The results show that ApEn and SampEn maps are able to detect and track the reentry core of rotors and figure-of-eight reentry, while the ShEn results are not satisfactory. Moreover, ApEn and SampEn consistently highlight a reentry core by high entropy values for all of the studied cases, while the ability of ShEn to characterize the reentry core depends on the propagation dynamics. Such features make the ApEn and SampEn maps attractive tools for the study of AF reentries that persist for a period of time that is similar to the length of the observation window, and reentries could be interpreted as AF-sustaining mechanisms. Further research is needed to determine and fully understand the relation of these entropy measures with fibrillation mechanisms other than reentries. © 2019 by the authors.
publishDate 2019
dc.date.accessioned.none.fl_str_mv 2021-02-05T14:59:07Z
dc.date.available.none.fl_str_mv 2021-02-05T14:59:07Z
dc.date.none.fl_str_mv 2019
dc.type.eng.fl_str_mv Article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.driver.none.fl_str_mv info:eu-repo/semantics/article
dc.identifier.issn.none.fl_str_mv 10994300
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/11407/6072
dc.identifier.doi.none.fl_str_mv 10.3390/e21020194
identifier_str_mv 10994300
10.3390/e21020194
url http://hdl.handle.net/11407/6072
dc.language.iso.none.fl_str_mv eng
language eng
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dc.relation.citationvolume.none.fl_str_mv 21
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dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_16ec
rights_invalid_str_mv http://purl.org/coar/access_right/c_16ec
dc.publisher.none.fl_str_mv MDPI AG
dc.publisher.faculty.spa.fl_str_mv Facultad de Ciencias Básicas
publisher.none.fl_str_mv MDPI AG
dc.source.none.fl_str_mv Entropy
institution Universidad de Medellín
repository.name.fl_str_mv Repositorio Institucional Universidad de Medellin
repository.mail.fl_str_mv repositorio@udem.edu.co
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spelling 20192021-02-05T14:59:07Z2021-02-05T14:59:07Z10994300http://hdl.handle.net/11407/607210.3390/e21020194Catheter ablation of critical electrical propagation sites is a promising tool for reducing the recurrence of atrial fibrillation (AF). The spatial identification of the arrhythmogenic mechanisms sustaining AF requires the evaluation of electrograms (EGMs) recorded over the atrial surface. This work aims to characterize functional reentries using measures of entropy to track and detect a reentry core. To this end, different AF episodes are simulated using a 2D model of atrial tissue. Modified Courtemanche human action potential and Fenton-Karma models are implemented. Action potential propagation is modeled by a fractional diffusion equation, and virtual unipolar EGM are calculated. Episodes with stable and meandering rotors, figure-of-eight reentry, and disorganized propagation with multiple reentries are generated. Shannon entropy (ShEn), approximate entropy (ApEn), and sample entropy (SampEn) are computed from the virtual EGM, and entropy maps are built. Phase singularity maps are implemented as references. The results show that ApEn and SampEn maps are able to detect and track the reentry core of rotors and figure-of-eight reentry, while the ShEn results are not satisfactory. Moreover, ApEn and SampEn consistently highlight a reentry core by high entropy values for all of the studied cases, while the ability of ShEn to characterize the reentry core depends on the propagation dynamics. Such features make the ApEn and SampEn maps attractive tools for the study of AF reentries that persist for a period of time that is similar to the length of the observation window, and reentries could be interpreted as AF-sustaining mechanisms. Further research is needed to determine and fully understand the relation of these entropy measures with fibrillation mechanisms other than reentries. © 2019 by the authors.engMDPI AGFacultad de Ciencias Básicashttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85061976167&doi=10.3390%2fe21020194&partnerID=40&md5=760fcf45b8c581b3d7c36bc996a9a214212Kirchhof, P., Benussi, S., Kotecha, D., Ahlsson, A., Atar, D., Casadei, B., Castella, M., Hendriks, J., 2016 ESC Guidelines for the management of atrial fibrillation developed in collaboration with EACTS (2016) Europace, 18, pp. 1609-1678Björck, S., Palaszewski, B., Friberg, L., Bergfeldt, L., Atrial fibrillation, stroke risk, and warfarin therapy revisited: A population-based study (2013) Stroke, 44, pp. 3103-3108Zaman, J.A.B., Harling, L., Ashrafian, H., Darzi, A., Gooderham, N., Athanasiou, T., Peters, N.S., Post-operative atrial fibrillation is associated with a pre-existing structural and electrical substrate in human right atrial myocardium (2016) Int. 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Eng, 65, pp. 273-281Arunachalam, S., Kapa, S., Mulpuru, S., Friedman, P., Tolkacheva, E., Rotor pivot point identification using recurrence period density entropy (2017) Proceedings of the 54th Annual Rocky Mountain Bioengineering Symposium, Denver, CO, USA, 31 March-1 April 2017 In Proceedings of the 54th International ISA Biomedical Sciences Instrumentation Symposium 2017, , Denver:CO, USA, 31 March-1 AprilEntropyEntropy mapping approach for functional reentry detection in atrial fibrillation: An in-silico studyArticleinfo:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1Ugarte, J.P., Grupo de Investigación en Modelamiento y Simulación Computacional (GIMSC), Universidad de San Buenaventura, Medellín, 050010, ColombiaTobón, C., Materiales Nanoestructurados y Biomodelación (MATBIOM), Universidad de Medellín, Medellín, 050026, ColombiaOrozco-Duque, A., Grupo de Investigación e Innovación Biomédica (GI2B), Instituto Tecnológico Metropolitano, Medellín, 050034, Colombiahttp://purl.org/coar/access_right/c_16ecUgarte J.P.Tobón C.Orozco-Duque A.11407/6072oai:repository.udem.edu.co:11407/60722021-02-05 09:59:07.955Repositorio Institucional Universidad de Medellinrepositorio@udem.edu.co