Evolving concepts in dilated cardiomyopathy.

Abstract:

:Dilated cardiomyopathy (DCM) represents a particular aetiology of systolic heart failure that frequently has a genetic background and usually affects young patients with few co-morbidities. The prognosis of DCM has improved substantially during the last decades due to more accurate aetiological characterization, the red-flag integrated approach to the disease, early diagnosis through systematic familial screening, and the concept of DCM as a dynamic disease requiring constant optimization of medical and non-pharmacological evidence-based treatments. However, some important issues in clinical management remain unresolved, including the role of cardiac magnetic resonance for diagnosis and risk categorization and the interaction between genotype and clinical phenotype, and arrhythmic risk stratification. This review offers a comprehensive survey of these and other emerging issues in the clinical management of DCM, providing where possible practical recommendations.

journal_name

Eur J Heart Fail

authors

Merlo M,Cannatà A,Gobbo M,Stolfo D,Elliott PM,Sinagra G

doi

10.1002/ejhf.1103

subject

Has Abstract

pub_date

2018-02-01 00:00:00

pages

228-239

issue

2

eissn

1388-9842

issn

1879-0844

journal_volume

20

pub_type

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