Arrhythmogenic Cardiomyopathy—Current Treatment and Future Options
Arrhythmogenic cardiomyopathy (ACM) is an inheritable heart muscle disease characterised pathologically by fibrofatty myocardial replacement and clinically by ventricular arrhythmias (VAs) and sudden cardiac death (SCD). Although, in its original description, the disease was believed to predominantl...
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doaj-6efe2f3376be49fb9b80842dd23cbca02021-07-15T15:38:47ZengMDPI AGJournal of Clinical Medicine2077-03832021-06-01102750275010.3390/jcm10132750Arrhythmogenic Cardiomyopathy—Current Treatment and Future OptionsFederico Migliore0Giulia Mattesi1Alessandro Zorzi2Barbara Bauce3Ilaria Rigato4Domenico Corrado5Alberto Cipriani6Department of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padova, Via Giustiniani 2, 35128 Padova, ItalyDepartment of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padova, Via Giustiniani 2, 35128 Padova, ItalyDepartment of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padova, Via Giustiniani 2, 35128 Padova, ItalyDepartment of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padova, Via Giustiniani 2, 35128 Padova, ItalyDepartment of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padova, Via Giustiniani 2, 35128 Padova, ItalyDepartment of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padova, Via Giustiniani 2, 35128 Padova, ItalyDepartment of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padova, Via Giustiniani 2, 35128 Padova, ItalyArrhythmogenic cardiomyopathy (ACM) is an inheritable heart muscle disease characterised pathologically by fibrofatty myocardial replacement and clinically by ventricular arrhythmias (VAs) and sudden cardiac death (SCD). Although, in its original description, the disease was believed to predominantly involve the right ventricle, biventricular and left-dominant variants, in which the myocardial lesions affect in parallel or even mostly the left ventricle, are nowadays commonly observed. The clinical management of these patients has two main purposes: the prevention of SCD and the control of arrhythmic and heart failure (HF) events. An implantable cardioverter defibrillator (ICD) is the only proven lifesaving treatment, despite significant morbidity because of device-related complications and inappropriate shocks. Selection of patients who can benefit the most from ICD therapy is one of the most challenging issues in clinical practice. Risk stratification in ACM patients is mostly based on arrhythmic burden and ventricular dysfunction severity, although other clinical features resulting from electrocardiogram and imaging modalities such as cardiac magnetic resonance may have a role. Medical therapy is crucial for treatment of VAs and the prevention of negative ventricular remodelling. In this regard, the efficacy of novel anti-HF molecules and drugs acting on the inflammatory pathway in patients with ACM is, to date, unknown. Catheter ablation represents an effective strategy to treat ventricular tachycardia relapses and recurrent ICD shocks. The present review will address the current strategies for prevention of SCD and treatment of VAs and HF in patients with ACM.https://www.mdpi.com/2077-0383/10/13/2750arrhythmogenic cardiomyopathyrisk stratificationdrug therapyimplantable cardioverter defibrillatorcatheter ablationtreatment |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Federico Migliore Giulia Mattesi Alessandro Zorzi Barbara Bauce Ilaria Rigato Domenico Corrado Alberto Cipriani |
spellingShingle |
Federico Migliore Giulia Mattesi Alessandro Zorzi Barbara Bauce Ilaria Rigato Domenico Corrado Alberto Cipriani Arrhythmogenic Cardiomyopathy—Current Treatment and Future Options Journal of Clinical Medicine arrhythmogenic cardiomyopathy risk stratification drug therapy implantable cardioverter defibrillator catheter ablation treatment |
author_facet |
Federico Migliore Giulia Mattesi Alessandro Zorzi Barbara Bauce Ilaria Rigato Domenico Corrado Alberto Cipriani |
author_sort |
Federico Migliore |
title |
Arrhythmogenic Cardiomyopathy—Current Treatment and Future Options |
title_short |
Arrhythmogenic Cardiomyopathy—Current Treatment and Future Options |
title_full |
Arrhythmogenic Cardiomyopathy—Current Treatment and Future Options |
title_fullStr |
Arrhythmogenic Cardiomyopathy—Current Treatment and Future Options |
title_full_unstemmed |
Arrhythmogenic Cardiomyopathy—Current Treatment and Future Options |
title_sort |
arrhythmogenic cardiomyopathy—current treatment and future options |
publisher |
MDPI AG |
series |
Journal of Clinical Medicine |
issn |
2077-0383 |
publishDate |
2021-06-01 |
description |
Arrhythmogenic cardiomyopathy (ACM) is an inheritable heart muscle disease characterised pathologically by fibrofatty myocardial replacement and clinically by ventricular arrhythmias (VAs) and sudden cardiac death (SCD). Although, in its original description, the disease was believed to predominantly involve the right ventricle, biventricular and left-dominant variants, in which the myocardial lesions affect in parallel or even mostly the left ventricle, are nowadays commonly observed. The clinical management of these patients has two main purposes: the prevention of SCD and the control of arrhythmic and heart failure (HF) events. An implantable cardioverter defibrillator (ICD) is the only proven lifesaving treatment, despite significant morbidity because of device-related complications and inappropriate shocks. Selection of patients who can benefit the most from ICD therapy is one of the most challenging issues in clinical practice. Risk stratification in ACM patients is mostly based on arrhythmic burden and ventricular dysfunction severity, although other clinical features resulting from electrocardiogram and imaging modalities such as cardiac magnetic resonance may have a role. Medical therapy is crucial for treatment of VAs and the prevention of negative ventricular remodelling. In this regard, the efficacy of novel anti-HF molecules and drugs acting on the inflammatory pathway in patients with ACM is, to date, unknown. Catheter ablation represents an effective strategy to treat ventricular tachycardia relapses and recurrent ICD shocks. The present review will address the current strategies for prevention of SCD and treatment of VAs and HF in patients with ACM. |
topic |
arrhythmogenic cardiomyopathy risk stratification drug therapy implantable cardioverter defibrillator catheter ablation treatment |
url |
https://www.mdpi.com/2077-0383/10/13/2750 |
work_keys_str_mv |
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