Electrocardiogram in arrhytmogenic cardiomyopathy

Author:

Calò Leonardo1,Oliviero Giada1,Crescenzi Cinzia1,Romeo Fabiana1,Martino Annamaria1,Bressi Edoardo1,Stefanini Matteo2,Silvetti Elisa1,Danza Ludovica1,Rebecchi Marco1,Canestrelli Stefano1,Fedele Elisa1,Lanzillo Chiara1,Fusco Armando2,De Ruvo Ermenegildo1

Affiliation:

1. Division of Cardiology, Policlinico Casilino , Via Casilina 1049, 00169 Rome , Italy

2. Division of Radiology, Policlinico Casilino , Via Casilina 1049, 00169 Rome , Italy

Abstract

Abstract Criteria for diagnosis of arrhythmogenic cardiomyopathy (ACM) were first proposed in 1994 and subsequently revised in 2010 and in 2020 by an international task force. According to the last consensus of 2020, ACM is defined as a heart muscle disease affecting right ventricle, left ventricle or both, whose principal pathologic feature is fibrofatty myocardial replacement that impairs systolic ventricular function and predisposes to lethal ventricular arrhythmias. ECG findings not only could help to early recognize affected patients but also could identify the ones with maximum risk of ventricular arrhythmias and sudden cardiac death.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Translation of Electrocardiography and Genetics in Arrhythmogenic Left Ventricular Cardiomyopathy;International Journal of Cardiology and Cardiovascular Disorder;2024-06-03

2. Arrhythmogenic Left Ventricular Cardiomyopathy: From Diagnosis to Risk Management;Journal of Clinical Medicine;2024-03-22

3. Inherited Arrhythmias in the Pediatric Population: An Updated Overview;Medicina;2024-01-03

4. The pivotal role of ECG in cardiomyopathies;Frontiers in Cardiovascular Medicine;2023-06-19

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