Cardiomyopathies: Current Treatment and Future Options: The Second Edition

A special issue of Journal of Clinical Medicine (ISSN 2077-0383). This special issue belongs to the section "Cardiology".

Deadline for manuscript submissions: 15 March 2025 | Viewed by 29

Special Issue Editor


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Guest Editor
Chair Internal Medicine – Cardiology, Osterstr. 110, 26506 Norden, Germany
Interests: arrhythmogenic cardiomyopathy: current treatment and future options (Entresto, MR inhibitors); hypertrophic cardiomyopathy: current treatment (betablocker, verapamil, disopyramid) and future options (mavacamten, surgical options, gene therapy); dilated cardiomyopathy: the role of standard treatment and future options; amyloid cardiomyopathy; takotsubo cardiomyopathy; phospholamban cardiomyopathy; RBM20 cardiomyopathy; Lamin A/C cardiomyopathy
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Special Issue Information

Dear Colleagues,

This is the second edition of “Cardiomyopathy: Current Treatment and Future Options” (https://www.mdpi.com/journal/jcm/special_issues/Cardiomyopathies_Treatment_Future_Options).

According to the newest ESC guidelines (from 2023), recognized cardiomyopathies include hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy, arrhythmogenic right-ventricular cardiomyopathy, and non-dilated left-ventricular cardiomyopathy. Takotsubo cardiomyopathy and non-compaction cardiomyopathy should not be counted as cardiomyopathies.

We will discuss current key topics in hypertrophic, dilated, and restrictive cardiomyopathy.

The term “arrhythmogenic cardiomyopathy” has been withdrawn from use. It is no longer appropriate to use the terms “right-dominant arrhythmogenic cardiomyopathy”, “biventricular arrhythmogenic cardiomyopathy”, or “left-dominant arrhythmogenic cardiomyopathy”. These conditions should be discussed in broader terms.

Genetic counseling will be carried out in all patients, with different cardiomyopathies, and we will discuss the use of the names “desmoplakin cardiomyopathy”, “phospholamban cardiomyopathy”, “TMEM43 cardiomyopathy”, and so on to describe different features of a known genetic disease.

Prof. Dr. Stefan Peters
Guest Editor

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Keywords

  • hypertrophic cardiomyopathy
  • dilated cardiomyopathy
  • restrictive cardiomyopathy
  • amyloid cardiomyopathy
  • arrhythmogenic right ventricular cardiomyopathy
  • non-dilated left ventricular cardiomyopathy

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