Improved Risk Stratification for Ventricular Arrhythmias and Sudden Death in Patients With Nonischemic Dilated Cardiomyopathy

2021 ◽  
Vol 77 (23) ◽  
pp. 2890-2905
Author(s):  
Andrea Di Marco ◽  
Pamela Frances Brown ◽  
Joshua Bradley ◽  
Gaetano Nucifora ◽  
Eduard Claver ◽  
...  
Author(s):  
Marianna Leopoulou ◽  
Jo Ann LeQuang ◽  
Joseph V. Pergolizzi ◽  
Peter Magnusson

Dilated cardiomyopathy (DCM) is characterized by the phenotype of a dilated left ventricle with systolic dysfunction. It is classified as hereditary when it is deemed of genetic origin; more than 50 genes are reported to be related to the condition. Symptoms include, among others, dyspnea, fatigue, arrhythmias, and syncope. Unfortunately, sudden cardiac death may be the first manifestation of the disease. Risk stratification regarding sudden death in hereditary DCM as well as preventive management poses a challenge due to the heterogeneity of the disease. The purpose of this chapter is to present the epidemiology, risk stratification, and preventive strategies of sudden cardiac death in hereditary DCM.


2006 ◽  
Vol 97 (3) ◽  
pp. 416-420 ◽  
Author(s):  
Robert S. Phang ◽  
David Kang ◽  
Hocine Tighiouart ◽  
N.A. Mark Estes ◽  
Mark S. Link

2007 ◽  
Vol 13 (9) ◽  
pp. 752-758 ◽  
Author(s):  
Tomoaki Ohtsuka ◽  
Kazuhisa Nishimura ◽  
Akira Kurata ◽  
Akiyoshi Ogimoto ◽  
Hideki Okayama ◽  
...  

2020 ◽  
Vol 68 (2) ◽  
Author(s):  
Cinzia Crescenzi ◽  
Germana Panattoni ◽  
Alessandra Stazi ◽  
Annamaria Martino ◽  
Marianna Sgueglia ◽  
...  

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