Hypertrophic, Dilated, and Arrhythmogenic Cardiomyopathy: Where Are We?

Cardiomyopathies are a heterogeneous group of structural, mechanical, and electrical heart muscle disorders which often correlate with life-threatening arrhythmias and progressive heart failure accounting for significant cardiovascular morbidity and mortality. Currently, cardiomyopathies still repre...
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Gespeichert in:

Autor*in:	Hamza El Hadi [verfasserIn] Anne Freund [verfasserIn] Steffen Desch [verfasserIn] Holger Thiele [verfasserIn] Nicolas Majunke [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2023

Schlagwörter:	hypertrophic cardiomyopathy dilated cardiomyopathy arrhythmogenic cardiomyopathy heart failure sudden cardiac death

Übergeordnetes Werk:	In: Biomedicines - MDPI AG, 2014, 11(2023), 2, p 524
Übergeordnetes Werk:	volume:11 ; year:2023 ; number:2, p 524

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.3390/biomedicines11020524

Katalog-ID:	DOAJ081002947

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language	English
source	In Biomedicines 11(2023), 2, p 524 volume:11 year:2023 number:2, p 524
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authorswithroles_txt_mv	Hamza El Hadi @@aut@@ Anne Freund @@aut@@ Steffen Desch @@aut@@ Holger Thiele @@aut@@ Nicolas Majunke @@aut@@
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author	Hamza El Hadi
spellingShingle	Hamza El Hadi misc QH301-705.5 misc hypertrophic cardiomyopathy misc dilated cardiomyopathy misc arrhythmogenic cardiomyopathy misc heart failure misc sudden cardiac death misc Biology (General) Hypertrophic, Dilated, and Arrhythmogenic Cardiomyopathy: Where Are We?
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topic_title	QH301-705.5 Hypertrophic, Dilated, and Arrhythmogenic Cardiomyopathy: Where Are We? hypertrophic cardiomyopathy dilated cardiomyopathy arrhythmogenic cardiomyopathy heart failure sudden cardiac death
topic	misc QH301-705.5 misc hypertrophic cardiomyopathy misc dilated cardiomyopathy misc arrhythmogenic cardiomyopathy misc heart failure misc sudden cardiac death misc Biology (General)
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title	Hypertrophic, Dilated, and Arrhythmogenic Cardiomyopathy: Where Are We?
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title_sort	hypertrophic, dilated, and arrhythmogenic cardiomyopathy: where are we?
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title_auth	Hypertrophic, Dilated, and Arrhythmogenic Cardiomyopathy: Where Are We?
abstract	Cardiomyopathies are a heterogeneous group of structural, mechanical, and electrical heart muscle disorders which often correlate with life-threatening arrhythmias and progressive heart failure accounting for significant cardiovascular morbidity and mortality. Currently, cardiomyopathies still represent a leading reason for heart transplantation worldwide. The last years have brought remarkable advances in the field of cardiomyopathies especially in terms of understanding the molecular basis as well as the diagnostic evaluation and management. Although most cardiomyopathy treatments had long focused on symptom management, much of the current research efforts aim to identify and act on the disease-driving mechanisms. Regarding risk assessment and primary prevention of sudden cardiac death, additional data are still pending in order to pave the way for a more refined and early patient selection for defibrillator implantation. This review summarizes the current knowledge of hypertrophic, dilated and arrhythmogenic cardiomyopathy with a particular emphasis on their pathophysiology, clinical features, and diagnostic approach. Furthermore, the relevant ongoing studies investigating novel management approaches and main gaps in knowledge are highlighted.
abstractGer	Cardiomyopathies are a heterogeneous group of structural, mechanical, and electrical heart muscle disorders which often correlate with life-threatening arrhythmias and progressive heart failure accounting for significant cardiovascular morbidity and mortality. Currently, cardiomyopathies still represent a leading reason for heart transplantation worldwide. The last years have brought remarkable advances in the field of cardiomyopathies especially in terms of understanding the molecular basis as well as the diagnostic evaluation and management. Although most cardiomyopathy treatments had long focused on symptom management, much of the current research efforts aim to identify and act on the disease-driving mechanisms. Regarding risk assessment and primary prevention of sudden cardiac death, additional data are still pending in order to pave the way for a more refined and early patient selection for defibrillator implantation. This review summarizes the current knowledge of hypertrophic, dilated and arrhythmogenic cardiomyopathy with a particular emphasis on their pathophysiology, clinical features, and diagnostic approach. Furthermore, the relevant ongoing studies investigating novel management approaches and main gaps in knowledge are highlighted.
abstract_unstemmed	Cardiomyopathies are a heterogeneous group of structural, mechanical, and electrical heart muscle disorders which often correlate with life-threatening arrhythmias and progressive heart failure accounting for significant cardiovascular morbidity and mortality. Currently, cardiomyopathies still represent a leading reason for heart transplantation worldwide. The last years have brought remarkable advances in the field of cardiomyopathies especially in terms of understanding the molecular basis as well as the diagnostic evaluation and management. Although most cardiomyopathy treatments had long focused on symptom management, much of the current research efforts aim to identify and act on the disease-driving mechanisms. Regarding risk assessment and primary prevention of sudden cardiac death, additional data are still pending in order to pave the way for a more refined and early patient selection for defibrillator implantation. This review summarizes the current knowledge of hypertrophic, dilated and arrhythmogenic cardiomyopathy with a particular emphasis on their pathophysiology, clinical features, and diagnostic approach. Furthermore, the relevant ongoing studies investigating novel management approaches and main gaps in knowledge are highlighted.
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title_short	Hypertrophic, Dilated, and Arrhythmogenic Cardiomyopathy: Where Are We?
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