Sudden death related cardiomyopathies - Arrhythmogenic right ventricular cardiomyopathy, arrhythmogenic cardiomyopathy, and exercise-induced cardiomyopathy.
Arrhythmogenic cardiomyopathy
Arrhythmogenic right ventricular cardiomyopathy
Cardiomyopathy
Exercise-induced cardiomyopathy
Implantable cardioverter defibrillator
Right ventricular dysplasia
Sudden cardiac death
Ventricular arrhythmias
Journal
Progress in cardiovascular diseases
ISSN: 1873-1740
Titre abrégé: Prog Cardiovasc Dis
Pays: United States
ID NLM: 0376442
Informations de publication
Date de publication:
Historique:
received:
15
04
2019
accepted:
15
04
2019
pubmed:
21
4
2019
medline:
3
10
2019
entrez:
21
4
2019
Statut:
ppublish
Résumé
Sudden cardiac death (SCD) is a devastating possible outcome of all cardiomyopathies. The risk of SCD is increased in patients with structural heart disease and continues to increase as ventricular dysfunction worsens. There is, however, a subset of cardiomyopathy, so-called "arrhythmogenic cardiomyopathy" (ACM), that carries an inherent propensity for arrhythmia in all stages of the disease, even preceding ventricular dysfunction. The aim of this review is to identify cardiomyopathies, other than ischemic and dilated cardiomyopathies, that are associated with ventricular arrhythmias (VAs) and SCD. We discuss prevalence, diagnosis, natural history and management of arrhythmogenic right ventricular dysplasia/cardiomyopathy, ACM, and exercise-induced cardiomyopathy, with emphasis on the morbidity and mortality of VAs associated with these cardiomyopathies and how they can be mitigated through lifestyle modification, medical management, and implantation of cardioverter defibrillators.
Identifiants
pubmed: 31004608
pii: S0033-0620(19)30073-8
doi: 10.1016/j.pcad.2019.04.002
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
217-226Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.