Results 11 to 20 of about 2,014 (112)
Shortness of breath on a mustard patient: multidisciplinary approach improves outcomes. [PDF]
Background Dextro-transposition of the great arteries post-atrial switch patients may experience complications like baffle stenosis. While percutaneous interventions are the standard treatment, severe calcification can require uncommon alternatives such ...
Casallas-Gutierrez I +6 more
europepmc +2 more sources
Los adultos con cardiopatía congénita compleja, con fisiología univentricular y flujo pulmonar disminuido, constituyen un reto terapéutico. Muchos de ellos reciben tratamiento paliativo con fístula sistémico-pulmonar desde la etapa pediátrica.
José M. Torres-Martel +7 more
doaj +1 more source
Isomorfismo cardiaco: Una perspectiva multidisciplinaria
El isomorfismo cardiaco describe hallazgos anatómicos complejos con defectos en la determinación de la lateralización. Es una situación poco frecuente, con prevalencia de 1 en cada 10,000 a 20,000 nacidos vivos, con incidencia hasta del 4% de todas las ...
Diego B. Ortega-Zhindón +5 more
doaj +1 more source
Initial experience with the new percutaneous pulmonary self-expandable Venus P-valve
Introduction and objectives: Percutaneous pulmonary valve implantation is currently a common procedure in patients with congenital heart disease with a dysfunctional right ventricular outflow tract.
María Álvarez-Fuente +8 more
doaj +1 more source
Experiencia inicial con la nueva válvula pulmonar percutánea autoexpandible Venus P
RESUMEN Introducción y objetivos: El implante percutáneo de válvula pulmonar es, actualmente, un procedimiento habitual en pacientes con cardiopatías congénitas con un tracto de salida del ventrículo derecho ...
María Álvarez-Fuente +8 more
doaj +1 more source
Resumen: La conexión anómala total de venas pulmonares es una anomalía cardíaca rara, que ocurre del 1% al 3% en niños que nacen con defectos cardíacos congénitos.
Iris P. Flores-Sarria +4 more
doaj +1 more source
Implications of fetal premature atrial contractions: systematic review
ABSTRACT Objective Fetal heart‐rate irregularities occur in 1–2% of pregnancies and are usually caused by premature atrial contractions (PAC). Although PAC are considered benign, they may be associated with cardiac defects and tachyarrhythmia. We aimed to determine the incidence of congenital heart defects (CHDs) and complications in fetuses with PAC ...
B. B. Bet +6 more
wiley +1 more source
Hypokinetic hypertrophic cardiomyopathy: clinical phenotype, genetics, and prognosis
Abstract Aims To describe the phenotype, genetics, and events associated with the development of hypertrophic cardiomyopathy (HCM) with reduced ventricular function (HCMr). Heart failure in HCM is usually associated with preserved ejection fraction, yet some HCM patients develop impaired systolic function that is associated with worse outcomes. Methods
Yishay Wasserstrum +10 more
wiley +1 more source
Abstract Aims To describe the natural history of SARS‐CoV‐2 infection in patients with hypertrophic cardiomyopathy (HCM) compared with a control group and to identify predictors of adverse events. Methods and results Three hundred and five patients [age 56.6 ± 16.9 years old, 191 (62.6%) male patients] with HCM and SARS‐Cov‐2 infection were enrolled ...
Juan R. Gimeno +53 more
wiley +1 more source
Non‐ischaemic dilated cardiomyopathy (NI DCM) patients with positive genotype and/or late gadolinium enhancement (LGE) show increased risk of ventricular arrhythmias and end‐stage heart failure (ESHF) during follow‐up. CI, confidence interval; HR, hazard ratio; LVEF, left ventricular ejection fraction; MVA, malignant ventricular arrhythmia.
Jesús G. Mirelis +27 more
wiley +1 more source

