Speckle-tracking echocardiography for arrhythmic risk. Assessment in hypertrophic and Fabry cardiomyopathy
Abstract
Data di Pubblicazione:
2022
Abstract:
Hypertrophic Cardiomyopathy (HCM) is burdened by sudden cardiac death (SCD) risk of 0.9%/year, and is the most common cause of SCD in young adults. It is an autosomal dominant inherited disease caused by mutations in cardiac sarcomere genes, but the hypertrophic phenotype can also be an expression of cardiac involvement in multiorgan metabolic storage diseases, such as Anderson-Fabry disease (AFD). Mechanical Dispersion (MD) by Speckle-Tracking Echocardiography (STE) has recently emerged as an additional arrhythmic risk marker.
Tipologia CRIS:
01.05 Abstract in rivista
Keywords:
fabry disease; holter electrocardiography; hypertrophic cardiomyopathy; phenotype; ventricular fibrillation; echocardiography; sudden cardiac death; cardiomyopathy; mutation; left ventricular hypertrophy; genetic disorder; diastole; gadolinium; genes; risk assessment; sarcomeres; systole; heart; patient prognosis; non-sustained ventricular tachycardia; ventricular arrhythmia; storage disease; ejection fraction; cardiac mri; young adult; cardiovascular findings; two-dimensional speckle tracking; longitudinal strain
Elenco autori:
Rodolico, MARGHERITA STEFANIA
Link alla scheda completa:
Pubblicato in: