Arrhythmogenic right ventricular cardiomyopathy resident survival guide

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Steven Bellm, M.D. [2]

Arrhythmogenic right ventricular cardiomyopathy resident survival guide Microchapters
Overview
Classification
Causes
Diagnosis
Treatment
Do's
Dont's

Overview

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetic disease characterized by myocyte loss and fibro-fatty tissue replacement of the right ventricular myocardium. This puts patients into risk of life-threatening ventricular arrhythmias and slowly progressive ventricular dysfunction. The diagnostic is challenging. Diagnosis of ARVC relays on a scoring system, with major or minor criteria on the Revised Task Force Criteria. Pharmacologic treatment of arrhythmias, catheter ablation of ventricular tachycardia, and ICD are main goals of the treatment.

Classification

Stages of disease

• Concealed phase: Subclinical asymptomatic phase
• Overt electrical disorder: Palpitations, syncope and typically with symptomatic ventricular arrhythmias of RV
• RV failure: Progressive loss of RV myocardium due to fibro-fatty replacement impairs RV function, pump failure
• Biventricular failure: Involvement of the interventricular septum and LV causing congestive heart failure (HF)

Patterns of expression

• Classic ARVC:Increased RV to LV volume ratio, more severe involvement of the RV, negative anterior T waves and ventricular arrhythmias with LBBB morphology
• Left-dominant arrhythmogenic cardiomyopathy (LDAC):Predominantly involves the LV, LV wall motion abnormalities, chamber dilation, systolic impairment, and late gadolinium enhancement (LGE), ventricular arrhythmias of right bundle branch block (RBBB) morphology, (infero)-lateral T-wave inversion
• Biventricular arrhythmogenic:Early and parallel involvement of the RV and LV, biventricular dilation and systolic impairment, ventricular arrhythmias of both RBBB and LBBB configuration may occur, ratio of RV to LV volume remains close to 1

Causes

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetic disease.

Complete Diagnostic Approach

A complete diagnostic approach should be carried out after a focused initial rapid evaluation is conducted and following initiation of any urgent intervention.

History and symptoms: ❑  Hints for etiology (family history) ❑  Duration and onset of illness/ symptoms ❑  Severity and triggers of dyspnea/ orthopnea and fatigue/ weakness, presence of chest pain, exercise capacity, physical activity, sexual activity (NYHA?) ❑  Palpitations/ (pre)syncope/ ventricular tachycardias/ cardiac arrest or fibrillation ❑  Weight loss/weight gain (cachexia/ volume overload?) ❑  Symptoms of transient ischemic attack or thromboembolism (anticoagulation necessary?) ❑  Presence of peripheral edema, ascites or anasarca (volume overload?) ❑  Problems with breathing at night/ sleep ❑  Medical history ❑  Prior hospitalizations ❑  Medication ❑  Diet (restriction of sodium and fluid intake?)

Physical examination: ❑  Vital signs: ❑  Pulse (strength and regularity) ❑  Blood pressure ❑  Respiratory rate ❑  General appearance: ❑  BMI(weight loss/weight gain) ❑  Peripheral edema ❑  JVD ❑  Heart: ❑  Heart sounds, murmur, Carotid and peripheral pulses ❑  Lungs: ❑  Rales? ❑  Pleural effusion? ❑  Hepatomegaly, pulsatile liver and/or ascites (volume overload) ❑  Extremities: ❑  Temperature of lower extremities

Laboratory findings: ❑  Complete blood count ❑  Chemistry: ❑  Troponin, BNP or NT-proBNP ❑  Serum electrolytes (including calcium and magnesium) ❑  Blood urea nitrogen ❑  Serum creatinine ❑  Glucose ❑  Fasting lipid profile ❑  Liver function tests ❑  Thyroid-stimulating hormone

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Treatment

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References