Literature DB >> 31964657

Arrhythmic risk stratification in non-ischaemic dilated cardiomyopathy beyond ejection fraction.

Antonio Cannatà1,2, Giulia De Angelis1, Andrea Boscutti1, Camilla Normand3,4, Jessica Artico1, Piero Gentile1, Massimo Zecchin1, Stephane Heymans5,6,7, Marco Merlo8, Gianfranco Sinagra1.   

Abstract

Sudden cardiac death and arrhythmia-related events in patients with non-ischaemic dilated cardiomyopathy (NICM) have been significantly reduced over the last couple of decades as a result of evidence-based pharmacological and non-pharmacological therapeutic strategies. Nevertheless, the arrhythmic stratification in patients with NICM remains extremely challenging, and the simple indication based on left ventricular ejection fraction appears to be insufficient. Therefore, clinicians need to go beyond the current criteria for implantable cardioverter-defibrillator implantation in the direction of a multiparametric evaluation of arrhythmic risk. Several parameters for arrhythmic risk stratification, ranging from electrocardiographic, echocardiographic, imaging-derived and genetic markers, are crucial for proper arrhythmic risk stratification and a multiparametric evaluation of risk in patients with NICM. In particular, integration of cardiac magnetic resonance parameters (mostly late gadolinium enhancement) and specific genetic information (ie, presence of LMNA, PLN, FLNC mutations) appears fundamental for proper implementation of the current arrhythmic risk stratification. Finally, a novel approach focused on both arrhythmic risk and prediction of left ventricular reverse remodelling during follow-up might be useful for effective multiparametric and dynamic arrhythmic risk stratification in NICM. In the future, a complete and integrated evaluation might be mandatory to implement arrhythmic risk prediction in patients with NICM and to discriminate the competing risk between heart failure-related events and life-threatening arrhythmias. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  arrhythmic risk stratification; dilated cardiomyopathy; left ventricular reverse remodeling; multiparametric; sudden cardiac death

Mesh:

Year:  2020        PMID: 31964657     DOI: 10.1136/heartjnl-2019-315942

Source DB:  PubMed          Journal:  Heart        ISSN: 1355-6037            Impact factor:   5.994


  5 in total

1.  The clinical utility of pediatric cardiomyopathy genetic testing: From diagnosis to a precision medicine-based approach to care.

Authors:  Lauren E Parker; Andrew P Landstrom
Journal:  Prog Pediatr Cardiol       Date:  2021-07-01

Review 2.  Mildly symptomatic heart failure with reduced ejection fraction: diagnostic and therapeutic considerations.

Authors:  Alexandra Arvanitaki; Eleni Michou; Andreas Kalogeropoulos; Haralambos Karvounis; George Giannakoulas
Journal:  ESC Heart Fail       Date:  2020-05-05

3.  A clinical score for predicting left ventricular reverse remodelling in patients with dilated cardiomyopathy.

Authors:  Yuki Kimura; Takahiro Okumura; Ryota Morimoto; Shingo Kazama; Naoki Shibata; Hideo Oishi; Takashi Araki; Takashi Mizutani; Tasuku Kuwayama; Hiroaki Hiraiwa; Toru Kondo; Toyoaki Murohara
Journal:  ESC Heart Fail       Date:  2021-01-20

Review 4.  The Role of AI in Characterizing the DCM Phenotype.

Authors:  Clint Asher; Esther Puyol-Antón; Maleeha Rizvi; Bram Ruijsink; Amedeo Chiribiri; Reza Razavi; Gerry Carr-White
Journal:  Front Cardiovasc Med       Date:  2021-12-21

5.  A Novel Gene Signature to Predict Survival Time and Incident Ventricular Arrhythmias in Patients with Dilated Cardiomyopathy.

Authors:  Chenliang Ge; Yan He
Journal:  Dis Markers       Date:  2020-09-15       Impact factor: 3.434

  5 in total

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