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Multimodality imaging in the diagnosis, risk stratification, and management of patients with dilated cardiomyopathies: an expert consensus document from the European Association of Cardiovascular Imaging

机译:扩张心肌病患者诊断,风险分层和管理中的多模成像:来自欧洲心血管成像协会的专家共识文件

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摘要

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.
机译:扩张的心肌病(DCM)由左心室或前肢扩张的存在而定义,没有足以解释这些变化的异常负载条件或冠状动脉疾病的情况下的收缩功能障碍。这是一种经常具有遗传背景的异质疾病。成像对于诊断,预后评估和指导治疗是重要的。多模成像方法提供了对与该疾病相关的所有问题的综合评估。本文件旨在根据临床问题提供用于使用多模态成像的建议。选择一个或另一个成像技术应基于临床状况和背景。展示技术的目的是强调什么是“临床相关”,以及可以使用的工具'。关于多层态成像对管理和持续研究的DCM患者的影响的影响,存在一些差距。

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