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.
Background:
we sought to review the evolution in the diagnosis and treatment of Arrhythmogenic Cardiomyopathy (ACM), a clinically multifaceted entity beyond the observation of ventricular arrhythmias, and the outcome of therapies aiming at sudden death prevention in a single center experience.
Methods:
retrospective analysis of the data of consecutive patients with an implanted cardioverter-defibrillator (ICD) and a confirmed diagnosis of ACM according to the proposed Padua Criteria, who were referred to our center from January 1992 to October 2021.
Results:
we enrolled 72 patients (66% males, mean age at implant 46 16 years), 63.9% implanted for primary prevention. At the time of ICD implant, 29 (40.3%) patients had a right ventricular involvement, 24 (33.3%) had a dominant LV involvement and 19 (26.4%) had a biventricular involvement. After a median follow-up of 6,1 years [IQR: 2.5-9.9], 34 patients (47.2%) had 919 sustained episodes of ventricular arrhythmias (VA). 27 patients (37.5%) had 314 episodes of life-threatening arrhythmias (LT-VA), defined as sustained ventricular tachycardia 200 beats/min. Considering only the patients with an ICD capable of delivering ATP, 80.4% of VA and 65% of LT-VA were successfully terminated with ATP. 16 (22.2%) patients had an inappropriate ICD activation, mostly caused by atrial fibrillation, while in 9 patients (12.5%) there was a complication needing reintervention (in 3 cases there was a loss of ventricular sensing dictating lead revision). During the follow-up 11 (15.3%) patients died, most of them due to heart failure, and 8 (11.1%) underwent heart transplantation.
Conclusions:
ACM is increasingly diagnosed owing to heightened suspicion at ECG examination and to improved imaging technology and availability, though the diagnostic workflow is particularly challenging in the earliest disease stages. ICD therapy is the cornerstone of sudden death prevention, albeit its efficacy is not based on controlled studies, and VT ablation/medical therapy are complementary to this strategy. The high burden of ATP-terminated VA makes shock-only devices debatable. The progressive nature of ACM leads to severe biventricular enlargement and refractory heart failure, which pose significant treatment issues when a predominant RV dysfunction occurs owing to the reduced possibility for mechanical circulatory assistance.
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