| Literature DB >> 31504368 |
Erwan Donal1,2, Victoria Delgado3, Chiara Bucciarelli-Ducci4, Elena Galli1,2, Kristina H Haugaa5, Philippe Charron6,7, Jens-Uwe Voigt8, Nuno Cardim9, P G Masci10, Maurizio Galderisi11, Oliver Gaemperli10, Alessia Gimelli12, Yigal M Pinto13, Patrizio Lancellotti14, Gilbert Habib15,16, Perry Elliott17,18, Thor Edvardsen5, Bernard Cosyns19, Bogdan A Popescu20.
Abstract
Dilated cardiomyopathy (DCM) is defined by the presence of left ventricular or biventricular dilatation and systolic dysfunction in the absence of abnormal loading conditions or coronary artery disease sufficient to explain these changes. This is a heterogeneous disease frequently having a genetic background. Imaging is important for the diagnosis, the prognostic assessment and for guiding therapy. A multimodality imaging approach provides a comprehensive evaluation of all the issues related to this disease. The present document aims to provide recommendations for the use of multimodality imaging according to the clinical question. Selection of one or another imaging technique should be based on the clinical condition and context. Techniques are presented with the aim to underscore what is 'clinically relevant' and what are the tools that 'can be used'. There remain some gaps in evidence on the impact of multimodality imaging on the management and the treatment of DCM patients where ongoing research is important. Published on behalf of the European Society of Cardiology. All rights reserved.Entities:
Keywords: cardiac magnetic resonance; dilated cardiomyopathy; echocardiography; nuclear imaging; prognosis; treatment
Mesh:
Year: 2019 PMID: 31504368 DOI: 10.1093/ehjci/jez178
Source DB: PubMed Journal: Eur Heart J Cardiovasc Imaging ISSN: 2047-2404 Impact factor: 6.875