{"id":70192,"date":"2018-03-09T23:14:41","date_gmt":"2018-03-09T23:14:41","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/seguimiento-electrocardiografico-a-largo-plazo-en-la-displasia-arritmogenica-ventricular-derecha\/"},"modified":"2018-03-09T23:14:41","modified_gmt":"2018-03-09T23:14:41","slug":"seguimiento-electrocardiografico-a-largo-plazo-en-la-displasia-arritmogenica-ventricular-derecha","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/seguimiento-electrocardiografico-a-largo-plazo-en-la-displasia-arritmogenica-ventricular-derecha\/","title":{"rendered":"Seguimiento electrocardiografico a largo plazo en la displasia arritmogenica ventricular derecha"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Jos\u00e9 Manuel Rubio Campal <\/strong><\/h2>\n<p>La displasia arritmog\u00e9nica ventricular derecha (davd) es una entidad que se caracteriza por la sustituci\u00f3n progresiva de los miocitos por tejido graso y fibroso. Aunque afecta predominantemente al ventr\u00edculo derecho, con el tiempo muchos pacientes desarrollan diversos grados de afectaci\u00f3n ventricular izquierda. Cl\u00ednicamente se caracteriza por el desarrollo de arritmias ventriculares, con s\u00edntomas que suelen comenzar en la adolescencia y juventud, aunque puede manifestarse a cualquier edad. En los casos en los que hay afectaci\u00f3n muy extensa en ambos ventr\u00edculos, pueden desarrollarse grados diversos de insuficiencia cardiaca. Se transmite gen\u00e9ticamente y hay historia familiar en un 30 &#8211; 40 % de los casos. El diagn\u00f3stico no siempre es f\u00e1cil, y se basa en la demostraci\u00f3n histol\u00f3gica del reemplazo fibro-adiposo , en la cl\u00ednica del paciente, en el electrocardiograma (ecg) , y en las diferentes t\u00e9cnicas de imagen (ventriculograf\u00eda, eco, rm cardiaca) que identifiquen alteraciones de la motilidad o en la estructura parietal del vd y del vi. Su evoluci\u00f3n es progresiva, pudiendo haber diversas fases de la enfermedad con diferentes manifestaciones cl\u00ednicas. Los estudios sobre dicha progresi\u00f3n son escasos,  y generalmente hacen hincapi\u00e9 en la evoluci\u00f3n anat\u00f3mica de la misma, sin que se identifiquen los cambios electrocardiogr\u00e1ficos o la relaci\u00f3n de los mismos con diferentes par\u00e1metros cl\u00ednicos. En el presente trabajo hemos hecho un seguimiento a largo plazo de 60 pacientes diagnosticados de davd de tres centros terciarios de espa\u00f1a, dos de la comunidad de Madrid y uno de la comunidad Valenciana. La edad media de los pacientes en el momento del diagn\u00f3stico era de 41 \u00c2\u00b1 17 a\u00f1os, y al final del seguimiento, de 52 \u00c2\u00b1 17 a\u00f1os. El 73 % de los pacientes eran varones y el 17 % ten\u00edan afectaci\u00f3n familiar. Todos ten\u00edan diversas manifestaciones cl\u00ednicas de arritmias ventriculares, documentadas cl\u00ednicamente en el 62 %. Veinticinco<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Seguimiento electrocardiografico a largo plazo en la displasia arritmogenica ventricular derecha<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Seguimiento electrocardiografico a largo plazo en la displasia arritmogenica ventricular derecha <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Jos\u00e9 Manuel Rubio Campal <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Aut\u00f3noma de Madrid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 21\/09\/2004<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li>Jeronimo Farre Muncharaz<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: manuel Oya otero <\/li>\n<li>Jes\u00fas Almendral garrote (vocal)<\/li>\n<li>concepcion Moro serrano (vocal)<\/li>\n<li>Carlos Macaya Miguel (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Jos\u00e9 Manuel Rubio Campal La displasia arritmog\u00e9nica ventricular derecha (davd) es una entidad que se caracteriza por [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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