Arrhythmogenic right ventricular cardiomyopathy resident survival guide: Difference between revisions

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==Classification==
==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===


==Causes==
==Causes==

Revision as of 15:13, 10 March 2015

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
FIRE
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.[1]

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

Causes

Life Threatening Causes

Common Causes

FIRE: Focused Initial Rapid Evaluation

A Focused Initial Rapid Evaluation (FIRE) should be performed to identify patients in need of immediate intervention.

 
 
 
 
 
 
 
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Complete Diagnostic Approach

 
 
 
 
 
 
 
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Treatment

shown

hidden

Do's

Dont's

References

  1. Pinamonti B, Brun F, Mestroni L, Sinagra G (2014). "Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges". World J Cardiol. 6 (12): 1234–44. doi:10.4330/wjc.v6.i12.1234. PMC 4278158. PMID 25548613.