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Article

Role of arrhythmic phenotype in prognostic stratification and management of dilated cardiomyopathy.

European journal of heart failure - 1 Mar 2024

Setti Martina, Merlo Marco, Gigli Marta, Munaretto Laura, Paldino Alessia, Stolfo Davide, Pio Loco Carola, Medo Kristen, Gregorio Caterina, De Luca Antonio, Graw Sharon, Castrichini Matteo, Cannatà Antonio, Ribichini Flavio Luciano, Dal Ferro Matteo, Taylor Matthew, Sinagra Gianfranco, Mestroni Luisa

Abstract excerpt

AIMS: Dilated cardiomyopathy (DCM) with arrhythmic phenotype combines phenotypical aspects of DCM and predisposition to ventricular arrhythmias, typical of arrhythmogenic cardiomyopathy. The definition of DCM with arrhythmic phenotype is not universally accepted, leading to uncertainty in the identification of high-risk patients. This study aimed to assess the prognostic impact of arrhythmic phenotype in risk...

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Share to Arrhythmias, Cardiac
Share to Cardiomyopathy, Dilated

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Death, Sudden, Cardiac

Share to Genetic Testing

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Share to Stroke Volume

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Share to Tachycardia, Ventricular

Source

Identifiers

PMID: 38404225
DOI: 10.1002/ejhf.3168

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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