Mostrar el registro sencillo del ítem
dc.contributor.author
Tauber, Pablo E.
dc.contributor.author
Mansilla, Virginia
dc.contributor.author
Brugada, Pedro
dc.contributor.author
Sanchez, Sara Serafina del V.
dc.contributor.author
Honore, Stella Maris
dc.contributor.author
Elizari, Marcelo
dc.contributor.author
Chain Molina, Sergio
dc.contributor.author
Albano, Felix A.
dc.contributor.author
Corbalán, Ricardo R.
dc.contributor.author
Figueroa Castellanos, Federico
dc.contributor.author
Alzugaray Bioeng, Damian
dc.contributor.other
Lakshmanadoss, Umashankar
dc.date.available
2023-06-08T12:23:16Z
dc.date.issued
2018
dc.identifier.citation
Tauber, Pablo E.; Mansilla, Virginia; Brugada, Pedro; Sanchez, Sara Serafina del V.; Honore, Stella Maris; et al.; Endocardial approach for substrate ablation in Brugada Syndrome; IntechOpen; 2018; 121-143
dc.identifier.isbn
978-1-78923-303-2
dc.identifier.uri
http://hdl.handle.net/11336/199965
dc.description.abstract
Radiofrequency ablation (RFA) in Brugada syndrome (BrS) has been performed by both endocardial and epicardial. The substrate in BrS is not completely understood. We investigate the functional endocardial substrate and its correlation with clinical, electrophysiological and ECG findings in order to guide an endocardial ablation. Two patients agreed to undergo an endocardial biopsy and the samples were examined with transmission electron microscopy (TEM) to investigate the correlation between functional and ultrastructural alterations. About 13 patients (38.7 ± 12.3 years old) with spontaneous type 1 ECG BrS pattern, inducible VF with programmed ventricular stimulation (PVS) and syncope without prodromes were enrolled. Before endocardial mapping, the patients underwent flecainide testing with the purpose of measuring the greatest ST-segment elevation for to be correlated with the size and location of substrate in the electro-anatomic map. Patients underwent endocardial bipolar and electro-anatomic mapping with the purpose of identify areas of abnormal electrograms (EGMs) as target for RFA and determine the location and size of the substrate. When the greatest ST-segment elevation was in the third intercostal space (ICS), the substrate was located upper in the longitudinal plane of the right ventricular outflow tract (RVOT) and a greatest ST-segment elevation in fourth ICS correspond with a location of substrate in lower region of longitudinal plane of RVOT. A QRS complex widening on its initial and final part, with prolonged transmural and regional depolarization time of RVOT corresponded to the substrate located in the anterior-lateral region of RVOT. A QRS complex widening rightwards and only prolonged transmural depolarization time corresponded with a substrate located in the anterior, anterior-septal or septal region of RVOT. RFA of endocardial substrate suppressed the inducibility and ECG BrS pattern during 34.7 ± 15.5 months. After RFA, flecainide testing confirmed elimination of the ECG BrS pattern. Endocardial biopsy showed a correlation between functional and ultrastructural alterations. Endocardial RFA can eliminate the BrS phenotype and inducibility during programmed ventricular stimulation (PVS).
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
IntechOpen
dc.relation
https://ri.conicet.gov.ar/handle/11336/101940
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/
dc.subject
Brugada syndrome
dc.subject
Mapping
dc.subject
Radiofrequency catheter ablation
dc.subject
Electrocardiography
dc.subject.classification
Bioquímica y Biología Molecular
dc.subject.classification
Ciencias Biológicas
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS
dc.title
Endocardial approach for substrate ablation in Brugada Syndrome
dc.type
info:eu-repo/semantics/publishedVersion
dc.type
info:eu-repo/semantics/bookPart
dc.type
info:ar-repo/semantics/parte de libro
dc.date.updated
2022-04-20T19:36:59Z
dc.journal.pagination
121-143
dc.journal.pais
Estados Unidos
dc.description.fil
Fil: Tauber, Pablo E.. Model Heart Center. Electrophysiology Division; Argentina
dc.description.fil
Fil: Mansilla, Virginia. Model Heart Center. Electrophysiology Division; Argentina
dc.description.fil
Fil: Brugada, Pedro. Université Libre de Bruxelles; Bélgica
dc.description.fil
Fil: Sanchez, Sara Serafina del V.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto Superior de Investigaciones Biológicas. Universidad Nacional de Tucumán. Instituto Superior de Investigaciones Biológicas; Argentina
dc.description.fil
Fil: Honore, Stella Maris. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto Superior de Investigaciones Biológicas. Universidad Nacional de Tucumán. Instituto Superior de Investigaciones Biológicas; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia; Argentina
dc.description.fil
Fil: Elizari, Marcelo. Academia Nacional de Medicina de Buenos Aires; Argentina
dc.description.fil
Fil: Chain Molina, Sergio. Model Heart Center. Electrophysiology Division; Argentina
dc.description.fil
Fil: Albano, Felix A.. Model Heart Center. Electrophysiology Division; Argentina
dc.description.fil
Fil: Corbalán, Ricardo R.. Model Heart Center. Electrophysiology Division; Argentina
dc.description.fil
Fil: Figueroa Castellanos, Federico. Clinica Mayo de UMCB; Argentina
dc.description.fil
Fil: Alzugaray Bioeng, Damian. Abbott; Argentina
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.intechopen.com/chapters/61238
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.5772/intechopen.75932
dc.conicet.paginas
193
dc.source.titulo
Cardiac Arrhythmias
Archivos asociados