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hal.structure.identifierModélisation et calculs pour l'électrophysiologie cardiaque [CARMEN]
hal.structure.identifierInstitut de Mathématiques de Bordeaux [IMB]
hal.structure.identifierIHU-LIRYC
dc.contributor.authorDAVIDOVIĆ, Anđela
dc.date.accessioned2024-04-04T03:18:58Z
dc.date.available2024-04-04T03:18:58Z
dc.date.created2015-06-30
dc.date.issued2014-06-30
dc.date.conference2014-06-30
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/194460
dc.description.abstractEnIntroduction: The most used model in the elctrophysiology of the heart,known as the bidomain model, is the system of degenerate parabolic PDEs cou-pled with the non-linear ODE. Even though these equations provide quite ac-curate results, they are based on the fact that active cardiomyocytes are presenteverywhere in the heart, while it is known that non-small regions exist wherefibroblasts and other non-excitable cells or additional extracellular media takeplace. These regions, which play an important role in diseased hearts, are oftentaken into account through ad-hoc rough tuning of the tissue conductivities. Inthis work, we introduce a rigorous way to derive these conductivities from amicroscopic description of the heterogeneities in the tissue.Method: We assume a periodic alternation of the healthy tissue (bidomainmodel) and the fibrotic tissue (diffusive part). Such a microscopic model canbe simulated directly, at the price of a very fine discretization and a high com-putational cost. Instead we derive a homogenized model at the macroscopicscale, following a two-scale method technique. There are two problems risinghere. First one has to deal with the degeneracy of parabolic equations and sec-ond one comes from the non-linearity of the ionic model of the cardiac cells.In order to study the model and illustrate its relevance, we computed numeri-cal simulations of both the microscopic and homogenized models based on anon-physical linear model, and then on the Mitchell-Schaeffer ionic model.Results: Interestingly, we recover a bidomain type model, but with modifiedconductivities, that depend on the volume fraction of the diffusive inclusionsbut also on their geometries. The numerical results confirm the convergenceof the microscopic model to the homogenized equations in the linear case. Weare currently working on the numerical simulations for the non-linear case,where we expect to observe the influence of the diffusive inclusions on thepropagation of action potentials.Conclusion: With the final non-linear model, we shall provide cheap mod-eling tools to account for tissue heterogeneities at intermediate scales, as canbe observed, e.g., in the fibrotic tissue.
dc.language.isoen
dc.subject.enHomogenisation
dc.subject.enBidomain model
dc.subject.enCardiac Electrophysiology Modeling
dc.title.enRole and modelling of some heterogeneities for cardiac electrophysiology
dc.typeCommunication dans un congrès
dc.subject.halMathématiques [math]
bordeaux.hal.laboratoriesInstitut de Mathématiques de Bordeaux (IMB) - UMR 5251*
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionBordeaux INP
bordeaux.institutionCNRS
bordeaux.conference.titleFirst Joint International Meeting RSME-SCM-SEMA-SIMAI-UMI
bordeaux.countryES
bordeaux.conference.cityBilbao
bordeaux.peerReviewedoui
hal.identifierhal-01117276
hal.version1
hal.invitednon
hal.proceedingsnon
hal.conference.end2014-07-04
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01117276v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.date=2014-06-30&rft.au=DAVIDOVI%C4%86,%20An%C4%91ela&rft.genre=unknown


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