Echocardiographic Applications in the Diagnosis and Management of Patients with ARVC

Thomas P. Mast*, Arco J. Teske, Pieter A. Doevendans, Maarten J. Cramer

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapterAcademicpeer-review

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 languageEnglish
Title of host publicationCardiac MRI in the Diagnosis, Clinical Management, and Prognosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia
EditorsAiden Abidov, Isabel B. Oliva , Frank I. Marcus
PublisherElsevier
Pages147-160
Number of pages14
ISBN (Print)9780128012833
DOIs
Publication statusPublished - 10 Mar 2016

Keywords

  • 3D echocardiography
  • Arrhythmogenic right ventricular cardiomyopathy
  • Diagnosis
  • Echocardiography
  • Prognosis
  • Tissue deformation imaging

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