4.7 Article

Recommendations for cardiovascular magnetic resonance in adults with congenital heart disease from the respective working groups of the European Society of Cardiology

Journal

EUROPEAN HEART JOURNAL
Volume 31, Issue 7, Pages 794-805

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/eurheartj/ehp586

Keywords

Adult congenital heart disease; Cardiovascular magnetic resonance; Imaging; Tetralogy of Fallot; Transposition of the great arteries; Atrial septal defect; Ventricular septal defect; Aortic coarctation

Funding

  1. British Heart Foundation
  2. CMR
  3. GUCH Working Groups of the European Society of Cardiology

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This paper aims to provide information and explanations regarding the clinically relevant options, strengths, and limitations of cardiovascular magnetic resonance (CMR) in relation to adults with congenital heart disease (CHD). Cardiovascular magnetic resonance can provide assessments of anatomical connections, biventricular function, myocardial viability, measurements of flow, angiography, and more, without ionizing radiation. It should be regarded as a necessary facility in a centre specializing in the care of adults with CHD. Also, those using CMR to investigate acquired heart disease should be able to recognize and evaluate previously unsuspected CHD such as septal defects, anomalously connected pulmonary veins, or double-chambered right ventricle. To realize its full potential and to avoid pitfalls, however, CMR of CHD requires training and experience. Appropriate pathophysiological understanding is needed to evaluate cardiovascular function after surgery for tetralogy of Fallot, transposition of the great arteries, and after Fontan operations. For these and other complex CHD, CMR should be undertaken by specialists committed to long-term collaboration with the clinicians and surgeons managing the patients. We provide a table of CMR acquisition protocols in relation to CHD categories as a guide towards appropriate use of this uniquely versatile imaging modality.

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