Mostrar el registro sencillo del ítem
dc.contributor.author | Sebastian, Rafael | es_ES |
dc.contributor.author | Heidenreich, Elvio | es_ES |
dc.contributor.author | Dux-Santoy Hurtado, Lydia | es_ES |
dc.contributor.author | Rodriguez, Jose F. | es_ES |
dc.contributor.author | Ferrero De Loma-Osorio, José María | es_ES |
dc.contributor.author | Saiz Rodríguez, Francisco Javier | es_ES |
dc.date.accessioned | 2018-09-17T06:51:24Z | |
dc.date.available | 2018-09-17T06:51:24Z | |
dc.date.issued | 2010 | es_ES |
dc.identifier.issn | 0302-9743 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/107322 | |
dc.description.abstract | [EN] The use of anti-arrhythmic drugs is common to treat heart rhythm disorders. Computational modeling and simulation are powerful tools that can be used to investigate the effects of specific drugs on cardiac electrophysiology. In this work a patient-specific anatomical heart model is built to study the effects of dofetilide, a drug that affects IKr current in cardiac cells. We study the multi-scale effects of the drug, from cellular to organ level, by simulating electrical propagation on tissue coupled cellular ion kinetics for several heart beats. Different cell populations configurations namely endocardial, midmyocardial and epicardial are used to test the effect of tissue heterogeneity. Results confirmed the expected effects of dofetilide at cellular level, increasing the action potential duration. Pseudo-ECGs obtained for each heart beat correlated well with cellular results showing prolongation of QT segment. These techniques can be applied over the development of more complex drugs that affect multiple cellular currents. | es_ES |
dc.description.sponsorship | This work has been partially funded by the Ministerio de Ciencia e Innovacion,TEC-2008-02090. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | Springer-Verlag | es_ES |
dc.relation.ispartof | Lecture Notes in Computer Science | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject.classification | TECNOLOGIA ELECTRONICA | es_ES |
dc.title | Modelling drug effects on personalized 3D models of the heart: a simulation study | es_ES |
dc.type | Artículo | es_ES |
dc.type | Comunicación en congreso | es_ES |
dc.identifier.doi | 10.1007/978-3-642-15835-3_23 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//TEC2008-02090/ES/MODELO MULTI-ESCALA DEL CORAZON. APLICACION EN LA PREVENCION, DIAGNOSTICO Y TRATAMIENTO DE ARRITMIAS CARDIACAS/ | es_ES |
dc.rights.accessRights | Cerrado | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Ingeniería Electrónica - Departament d'Enginyeria Electrònica | es_ES |
dc.description.bibliographicCitation | Sebastian, R.; Heidenreich, E.; Dux-Santoy Hurtado, L.; Rodriguez, JF.; Ferrero De Loma-Osorio, JM.; Saiz Rodríguez, FJ. (2010). Modelling drug effects on personalized 3D models of the heart: a simulation study. Lecture Notes in Computer Science. 6364:222-231. https://doi.org/10.1007/978-3-642-15835-3_23 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.conferencename | 1st International Workshop on Statistical Atlases and Computational Models of the Heart | es_ES |
dc.relation.conferencedate | Septiembre 10-10,2010 | es_ES |
dc.relation.conferenceplace | Beijing, China | es_ES |
dc.relation.publisherversion | https://doi.org/10.1007/978-3-642-15835-3_23 | es_ES |
dc.description.upvformatpinicio | 222 | es_ES |
dc.description.upvformatpfin | 231 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 6364 | es_ES |
dc.relation.pasarela | S\222458 | es_ES |
dc.contributor.funder | Ministerio de Ciencia e Innovación | es_ES |
dc.description.references | Yap, Y.G., Camm, A.J.: Drug induced qt prolongation and torsades de pointes. Heart 89(11), 1363–1372 (2003) | es_ES |
dc.description.references | Recanatini, M., Poluzzi, E., Masetti, M., Cavalli, A., Ponti, F.D.: Qt prolongation through herg k(+) channel blockade: current knowledge and strategies for the early prediction during drug development. Med. Res. Rev. 25(2), 133–166 (2005) | es_ES |
dc.description.references | Gintant, G.A., Su, Z., Martin, R.L., Cox, B.F.: Utility of herg assays as surrogate markers of delayed cardiac repolarization and qt safety. Toxicol. Pathol. 34(1), 81–90 (2006) | es_ES |
dc.description.references | Tusscherten, K.H.W.J., Panfilov, A.V.: Eikonal formulation of the minimal principle for scroll wave filaments. Phys. Rev. Lett. 93(10), 108106 (2004) | es_ES |
dc.description.references | Helm, P.: A novel technique for quantifying variability of cardiac anatomy applica- tion to the dyssynchronous failing heart, Ph.D. thesis, Johns Hopkins University (2005) | es_ES |
dc.description.references | Heidenreich, E., Ferrero, J.M., Doblare, M., Rodriguez Jose, F.: Adaptive macro finite elements for the numerical solution of monodomain equation in cardiac electrophysiology. Annals of Biomedical Engineering 38, 2331–2345 (2010) | es_ES |
dc.description.references | Drouin, E., Charpentier, F., Gauthier, C., Laurent, K., Marec, H.L.: Electrophysiologic characteristics of cells spanning the left ventricular wall of human heart: evidence for presence of m cells. J. Am. Coll. Cardiol. 26(1), 185–192 (1995) | es_ES |
dc.description.references | Antzelevitch, C., Sicouri, S., Litovsky, S.H., Lukas, A., Krishnan, S.C., Diego, J.M.D., Gintant, G.A., Liu, D.W.: Heterogeneity within the ventricular wall. electrophysiology and pharmacology of epicardial, endocardial, and m cells. Circ. Res. 69(6), 1427–1449 (1991) | es_ES |
dc.description.references | Sicouri, S., Fish, J., Antzelevitch, C.: Distribution of m cells in the canine ventricle. J. Cardiovasc. Electrophysiol. 5(10), 824–837 (1994) | es_ES |
dc.description.references | ten Tusscher, K.H.W.J., Noble, D., Noble, P.J., Panfilov, A.V.: A model for human ventricular tissue. Am. J. Physiol. Heart Circ. Physiol. 286(4), 1573–1589 (2004) | es_ES |
dc.description.references | Heidenreich, E.A.: Algoritmos para ecuaciones de reaccion difusion aplicados a electrofisiologia, Ph.D. thesis, Departamento de Ingenieria Mecanica, Universidad de Zaragoza (2009) | es_ES |
dc.description.references | Plonsey, R.: Bioelectric sources arising in excitable fibers (alza lecture). Ann. Biomed. Eng. 16(6), 519–546 (1988) | es_ES |
dc.description.references | Potse, M., Dub, B., Richer, J., Vinet, A., Gulrajani, R.M.: A comparison of monodomain and bidomain reaction-diffusion models for action potential propagation in the human heart. IEEE Trans. Biomed. Eng. 53(12 Pt 1), 2425–2435 (2006) | es_ES |
dc.description.references | Durrer, D., van Dam, R.T., Freud, G.E., Janse, M.J., Meijler, F.L., Arzbaecher, R.C.: Total excitation of the isolated human heart. Circulation 41(6), 899–912 (1970) | es_ES |
dc.description.references | Tusscher, K.H.W.J.T., Panfilov, A.V.: Cell model for efficient simulation of wave propagation in human ventricular tissue under normal and pathological conditions. Phys. Med. Biol. 51(23), 6141–6156 (2006) | es_ES |
dc.description.references | Yan, G.X., Wu, Y., Liu, T., Wang, J., Marinchak, R.A., Kowey, P.R.: Phase 2 early afterdepolarization as a trigger of polymorphic ventricular tachycardia in acquired long-qt syndrome: direct evidence from intracellular recordings in the intact left ventricular wall. Circulation 103(23), 2851–2856 (2001) | es_ES |
dc.description.references | Okada, Y., Ogawa, S., Sadanaga, T., Mitamura, H.: Assessment of reverse use-dependent blocking actions of class iii antiarrhythmic drugs by 24-hour holter electrocardiography. J. Am. Coll. Cardiol. 27(1), 84–89 (1996) | es_ES |