Download Arrythmogenic Right Ventricular Cardiomyopathy (ARVC, Boxer

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Transcript
Arrythmogenic Right
Ventricular Cardiomyopathy
Arrythmogenic right ventricular cardiomyopathy (ARVC) is an adult-onset inherited disease, with
the presenting age, and range of clinical symptoms in the offspring of affected parents being
quite variable. It also known as “Boxer Cardiomyopathy” and is characterized by irregular and rapid
ventricular arrhythmias.
The disease may take one of three forms:
1) asymptomatic with premature ventricular beats (PVCs)
2) symptomatic with PVCs resulting in collapse/fainting
3) heart failure due to a reduction in cardiac contractility
The prognosis of a patient with AVRC is very difficult to predict. Antiarrythmic medications are
frequently used to combat arrhythmias, frequency of collapse events, and sudden death.
Since a normal ECG does not rule out the presence of AVRC, a 24-hour holter monitor is
considered standard for diagnosis.
Below is an ECG (EKG) showing several premature ventricular beats (PVCs) which are the high
spiked waves. At the end of the example there are three PVCs in a row that represent a triplet, three
in a row. Many PVCs together are more likely to cause symptoms.
The prognosis of a patient with AVRC is very difficult to predict. Antiarrythmic medications are
frequently used to combat arrhythmias, frequency of collapse events, and sudden death.
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