Arrhythmogenic Cardiomyopathy: Diagnosis, Evolution, Risk Stratification and Pediatric Population-Where Are We?

J Cardiovasc Dev Dis. 2022 Mar 27;9(4):98. doi: 10.3390/jcdd9040098.

Abstract

Arrhythmogenic cardiomyopathy (ACM) is a cardiomyopathy characterized by the occurrence of a high risk of life-threatening ventricular arrhythmias and sudden cardiac death even at presentation. Diagnosis, evolution and outcomes in adults have been extensively reported, but little data in pediatric population are available. Risk stratification in this particular setting is still a matter of debate and new risk factors are needed in a model of an ever more "individualized medicine".

Keywords: arrhythmogenic cardiomyopathy; children; heart failure; premature ventricular contractions; sudden cardiac death.

Publication types

  • Review