Arrhythmogenic Right Ventricular Cardiomyopathy

Article Author:
Sandy Shah
Article Editor:
Steve Bhimji
10/27/2018 12:31:23 PM
PubMed Link:
Arrhythmogenic Right Ventricular Cardiomyopathy


Arrhythmogenic right ventricular cardiomyopathy (ARVC), also known as arrhythmogenic right ventricular dysplasia (ARVD), is a genetic disorder of the myocardium. ARVC/D is fatty infiltration of the right ventricular free wall.


ARVC is typically inherited in an autosomal dominant pattern with variable penetrance and incomplete expression. Approximately 40% to 50% of ARVC/D patients have a mutation in genes encoding a desmosome protein. There is an autosomal recessive trait variant associated with palmoplantar keratosis and wooly hair named Naxos disease.


In the general population, the prevalence of ARVC/D is 1:2500 to 1:5000. The prevalence is increased in Italy (Padua, Venice) and Greece (Island of Naxos). This disorder accounts for 5% to 10% of unexplained sudden death in individuals less than 65 years of age. It occurs in young adults with a male to female ratio of 2.7:1.


ARVC/D pathogenesis is unknown. Apoptosis seems to play a role in pathogenesis. The disease process starts in the subepicardial region, extends to the endocardial surface, and leads to transmural involvement. 

Aneurysmal dilatation is present in 50% of the cases. An aneurysm occurs in the diaphragm, apical area, and infundibulum, known as the triangle of dysplasia. The left ventricle is involved in 50% to 67% of cases. Involvement of the left ventricle suggests a poor prognosis.

The two pathology patterns seen with ARVC/D are fatty infiltration and fibro-fatty infiltration.


Microscopic features of the right ventricle show several changes of which the dominant feature is the presence of fibrofatty or fat replacement of the myocardial muscle. The muscles may show a moth-eaten appearance, mild inflammation, and scarring. Very rarely does one see frank myocyte necrosis. Some researchers are using immunohistochemistry to reveal the diffuse loss of desmosomal proteins, which is suggestive of an arrhythmogenic right ventricle.

History and Physical

ARVC/D presentation varies from the asymptomatic state to palpitations, fatigue, syncope, or even cardiac arrest during exercise. ARVC/D is a progressive disease. The right ventricle becomes more involved over time, leading to right ventricular failure. By the time the individual develops right ventricular failure, the left ventricle may develop histologic changes. Eventually, the left ventricle failure develops, leading to biventricular failure. The disease further progresses to congestive heart failure, atrial fibrillation, and thromboembolic events.


Diagnosis of ARVC/D is challenging. No one test can make the diagnosis, and multiple tools are utilized to make the diagnosis including history, ECG, Echo, MRI, and endomyocardial biopsy.

  1. ECG - The most common ECG abnormality seen in ARVC/D is T wave inversion in the precordial leads V1 to V3. The epsilon wave is found in 50% of cases of ARVC/D. Ventricular ectopy of left bundle branch block morphology with QRS axis -90 to +100 degree is from fatty degeneration of right ventricle (RV apex, RV inflow tract, RV outflow tract).
  2. Echocardiography - Echocardiography may reveal an enlarged right ventricle (RV), hypokinetic RV, and paper thin RV free wall.
  3. Cardiac MRI - Cardiac MRI is an excellent tool for visualizing the right ventricle. It may reveal a transmural diffuse bright signal in the RV free wall due to myocardial atrophy with fatty replacement.
  4. Endomyocardial biopsy - Transvenous biopsy of the right ventricle can be highly specific for ARVC/D, but it has low sensitivity.

The diagnosis of ARVC/D is based on a combination of major and minor criteria. Diagnosis of ARVC/D requires two major criteria or 1 major and two minor criteria or 4 minor criteria.

Major Criteria

  1. Right ventricular dysfunction

    a. Severe dilatation and reduction of RV ejection fraction with little or no LV impairment

    b. Localized RV aneurysms

    c. Severe segmental dilatation of the RV

  2. Tissue characterization

    a. Fibrofatty replacement of myocardium on endomyocardial biopsy

  3. Conduction abnormalities

    a. Epsilon waves in V1 - V3

    b. Localized prolongation (> 110 ms) of QRS in V1-V3

  4. Family history

    a. Familial disease confirmed on autopsy or surgery

Minor Criteria

  1. Right ventricular dysfunction

   a. Mild global RV dilatation and / or reduced ejection fraction with normal LV

   b. Mild segmental dilatation of the RV

   c. Regional RV hypokinesis

  2. Tissue characterization

  3. Conduction abnormalities

   a. Inverted T waves in V2 and V3 in an individual over 12 years old, in the absence of right bundle branch block

   b. Late potentials on signal-averaged ECG

   c. Ventricular tachycardia with left bundle branch block morphology

   d. Frequent PVCs (> 1000 PVCs/ 24 hours)

  4. Family history

   a. Family history of sudden cardiac death before age 35

   b. Family history of ARVC/D

Treatment / Management

The goal of ARVC/D is to prevent or decrease sudden cardiac death.

Management of ARVC/D includes pharmacologic, surgical, catheter ablation, and placement of implantable cardiac defibrillator.

1. Pharmacologic treatment involves arrhythmia suppression and prevention of thrombus formation.

  a. Sotalol is a beta blocker and class III antiarrhythmic agent. It is the most effective antiarrhythmic agent in ARVC/D.

  b. Warfarin is an anticoagulant. With decreased right ventricular ejection fraction and dyskinesis, anticoagulation may help prevent thrombus formation and further complications such as pulmonary embolism.

2. Radiofrequency catheter ablation may be used to treat refractory or incessant ventricular tachycardia. It is 60-90% successful. Recurrence rate is 60% due to the progression of the disease.

3. The implantable cardiac defibrillator is the most effective against sudden cardiac death. Indications for ICD in ARVC/D are:

  a. Cardiac arrest due to ventricular tachycardia or ventricular fibrillation

  b. Symptomatic ventricular tachycardia that is not inducible during programmed stimulation

  c. Failed programmed stimulation-guided drug therapy

  d. Severe right ventricular involvement with poor tolerance of ventricular tachycardia

  e. Sudden death of immediate family member

4. Cardiac transplant surgery is performed in ARVC/D if there is uncontrolled arrhythmia or failure to manage right ventricular or biventricular failure with pharmacologic therapy. 

Differential Diagnosis

At autopsy, one has to differentiate between normal fat deposition in the right ventricle and the presence of scars in the subepicardium due to ischemia. In most hearts, some amount of adipose tissue is found in the right ventricle, but there are usually no myocyte changes or presence of fibrosis.


In the past the prognosis was poor, but with the availability of cardiac MRI and CT tomography, the diagnosis is made much earlier. The screening of young athletes also has saved lives. Today, the long-term prognosis is favorable, especially in family members who are screened for the disorder.

Pearls and Other Issues

All first-degree family members should be screened for ARVC/D. Screening including ECG, echocardiogram, signal-averaged ECG, Holter monitor, Cardiac MRI, and exercise stress test should begin during the teenage years.