The Challenges of Diagnosis and Treatment of Arrhythmogenic Cardiomyopathy: Are We there yet?

Alberto Spadotto1,2, Domenico Morabito1,2, Alessandro Carecci1,2

  • 1IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.

Insights

Arrhythmogenic Cardiomyopathy (ACM) diagnosis and treatment have evolved. Implantable cardioverter-defibrillator (ICD) therapy is crucial for preventing sudden death, with ATP effectively managing arrhythmias.

Area of Science:

  • Cardiology
  • Genetics
  • Electrophysiology

Background:

  • Arrhythmogenic Cardiomyopathy (ACM) is a complex heart muscle disease.
  • Diagnosis and treatment have advanced, focusing on sudden cardiac death prevention.

Purpose of the Study:

  • To review the evolution of ACM diagnosis and treatment.
  • To evaluate the outcomes of therapies for sudden death prevention in ACM patients.

Main Methods:

  • Retrospective analysis of 72 ACM patients with implanted cardioverter-defibrillators (ICDs).
  • Patients diagnosed using Padua Criteria from 1992 to 2021.
  • Median follow-up of 6.1 years.

Main Results:

  • 47.2% experienced ventricular arrhythmias (VA), 37.5% had life-threatening VA.
  • ATP successfully terminated 80.4% of VA and 65% of life-threatening VA.
  • 15.3% died, primarily from heart failure; 11.1% underwent heart transplantation.

Conclusions:

  • ACM diagnosis is improving with advanced imaging and ECG suspicion.
  • ICD therapy is key for sudden death prevention, complemented by VT ablation/medical therapy.
  • Progressive ACM can lead to heart failure, complicating management, especially with RV dysfunction.
Abstract

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