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Influence of Fibrotic Tissue Arrangement on Intracardiac Electrograms During Persistent Atrial Fibrillation

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Influence of Fibrotic Tissue Arrangement on Intracardiac Electrograms During Persistent Atrial Fibrillation

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dc.contributor.author Sánchez, Jorge es_ES
dc.contributor.author Nothstein Mark es_ES
dc.contributor.author Unger, Laura es_ES
dc.contributor.author Saiz Rodríguez, Francisco Javier es_ES
dc.contributor.author Trenor Gomis, Beatriz Ana es_ES
dc.contributor.author Dossel, Olaf es_ES
dc.contributor.author Loewe, Axel es_ES
dc.date.accessioned 2022-02-17T07:20:55Z
dc.date.available 2022-02-17T07:20:55Z
dc.date.issued 2019-09-11 es_ES
dc.identifier.isbn 978-1-7281-6936-1 es_ES
dc.identifier.issn 2325-887X es_ES
dc.identifier.uri http://hdl.handle.net/10251/180930
dc.description.abstract [EN] Under persistent atrial fibrillation (peAF), cardiac tissue experiences electrophysiological and structural remodeling. Fibrosis in the atrial tissue has an important impact on the myocyte action potential and its propagation. The objective of this work is to explore the effect of heterogeneities present in the fibrotic tissue and their impact on the intracardiac electrogram (EGM). Human atrial myocyte and fibroblast electrophysiology was simulated using mathematical models proposed by Koivumäki et al. to represent electrical remodeling under peAF and the paracrine effect of the transforming grow factor ¿1 (TGF-¿1). 2D tissue simulations were computed varying the density of fibrosis (10%, 20% and 40%), myofibroblasts and collagen were randomly distributed with different ratios (0%-100%, 50%-50% and 100%- 0%). Results show that increasing the fibrosis density changes the re-entry dynamics from functional to anatomical due to a block in conduction in regions with high fibrosis density (40%). EGM morphology was affected by different ratios of myofibroblasts-collagen. For low myofibroblast densities (below 50%) the duration of active segments was shorter compared to higher myofibroblasts densities (above 50%). Our results show that fibrosis heterogeneities can alter the dynamics of the re-entry and the morphology of the EGM. es_ES
dc.description.sponsorship We gratefully acknowledge financial support by Deutsche Forschungsgemeinschaft (DFG) under grant LO 2093/1-1. es_ES
dc.language Inglés es_ES
dc.publisher IEEE es_ES
dc.relation.ispartof 2019 Computing in Cardiology (CinC). Proceedings es_ES
dc.rights Reserva de todos los derechos es_ES
dc.subject.classification TECNOLOGIA ELECTRONICA es_ES
dc.title Influence of Fibrotic Tissue Arrangement on Intracardiac Electrograms During Persistent Atrial Fibrillation es_ES
dc.type Comunicación en congreso es_ES
dc.type Artículo es_ES
dc.type Capítulo de libro es_ES
dc.identifier.doi 10.22489/CinC.2019.342 es_ES
dc.relation.projectID info:eu-repo/grantAgreement/DFG//LO2093%2F1-1/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement///PROMETEO%2F2016%2F088//MODELOS COMPUTACIONALES PERSONALIZADOS MULTI-ESCALA PARA LA OPTIMIZACION DEL DIAGNOSTICO Y TRATAMIENTO DE ARRITMIAS CARDIACAS (PERSONALISED DIGITAL HEART)/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/AEI//DPI2016-75799-R//TECNOLOGIAS COMPUTACIONALES PARA LA OPTIMIZACION DE TERAPIAS PERSONALIZADAS DE PATOLOGIAS AURICULARES Y VENTRICULARES/ es_ES
dc.rights.accessRights Abierto es_ES
dc.contributor.affiliation Universitat Politècnica de València. Departamento de Ingeniería Electrónica - Departament d'Enginyeria Electrònica es_ES
dc.description.bibliographicCitation Sánchez, J.; Nothstein Mark; Unger, L.; Saiz Rodríguez, FJ.; Trenor Gomis, BA.; Dossel, O.; Loewe, A. (2019). Influence of Fibrotic Tissue Arrangement on Intracardiac Electrograms During Persistent Atrial Fibrillation. IEEE. 1-4. https://doi.org/10.22489/CinC.2019.342 es_ES
dc.description.accrualMethod S es_ES
dc.relation.conferencename 46th Computing in Cardiology Conference (CinC 2019) es_ES
dc.relation.conferencedate Septiembre 08-11,2019 es_ES
dc.relation.conferenceplace Singapore es_ES
dc.relation.publisherversion https://doi.org/10.22489/CinC.2019.342 es_ES
dc.description.upvformatpinicio 1 es_ES
dc.description.upvformatpfin 4 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.relation.pasarela S\396361 es_ES
dc.contributor.funder Deutsche Forschungsgemeinschaft es_ES


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