Abstract
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a genetically determined myocardial disease predominantly affecting the right ventricle (RV). There is no single gold standard for the diagnosis of ARVC/D. New echocardiographic tools such as tissue deformation imaging allow quantitative regional wall motion analyses. This is especially important for early ARVC/D diagnosis where global RV dysfunction may be lacking. Several studies have shown incremental diagnostic value for tissue deformation imaging derived parameters in comparison to conventional echocardiography. 3D RV echocardiography is a new method to evaluate the RV and provides volumetric measurements in a broad spectrum of ARVC/D patients. Due to the frequent implantation of implantable cardioverter devices, echocardiography could play an important role in the follow-up of ARVC/D patients. Emerging new echocardiographic tools are currently changing the role of echocardiography in ARVC/D. In the future, MRI and echocardiography should be considered complementary to evaluate ARVC/D.
| Original language | English |
|---|---|
| Title of host publication | Cardiac MRI in the Diagnosis, Clinical Management, and Prognosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia |
| Editors | Aiden Abidov, Isabel B. Oliva , Frank I. Marcus |
| Publisher | Elsevier |
| Pages | 147-160 |
| Number of pages | 14 |
| ISBN (Print) | 9780128012833 |
| DOIs | |
| Publication status | Published - 10 Mar 2016 |
Keywords
- 3D echocardiography
- Arrhythmogenic right ventricular cardiomyopathy
- Diagnosis
- Echocardiography
- Prognosis
- Tissue deformation imaging
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