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钆增强心脏磁共振成像对肥厚型心肌病不良事件风险分层的心肌组织特征分析。

Myocardial tissue characterization by gadolinium-enhanced cardiac magnetic resonance imaging for risk stratification of adverse events in hypertrophic cardiomyopathy.

机构信息

Division of Hospital Medicine, Northwestern University Feinberg School of Medicine, 211 E Ontario St, Chicago, IL, 60611, USA.

Division of Cardiology, The Bluhm Cardiovascular Institute, Northwestern University Feinberg School of Medicine, 676 N St Clair, Suite 600, Chicago, IL, 60611, USA.

出版信息

Int J Cardiovasc Imaging. 2020 Jun;36(6):1147-1156. doi: 10.1007/s10554-020-01808-6. Epub 2020 Mar 12.

Abstract

Hypertrophic cardiomyopathy (HCM) is a genetic cardiomyopathy with a wide spectrum of clinical manifestations. Patients can be asymptomatic or suffer major adverse events including sudden cardiac death, ventricular arrhythmias, and heart failure. Identification of individuals with HCM who are at risk for these complications remains challenging. While echocardiography remains the mainstay of diagnostic evaluation, cardiac magnetic resonance imaging (CMR) is an important adjunctive diagnostic modality with emerging applications for risk-stratification of adverse events in the HCM population. Although not included in current guidelines for HCM management, there is increasing evidence to support the use of CMR for routine prognostic assessment of HCM patients. In this review we discuss the use of CMR techniques, including late gadolinium enhancement, T1 mapping, and quantification of extracellular volume fraction, for the risk stratification of three major adverse events in HCM: sudden cardiac death, ventricular arrhythmias, and congestive heart failure.

摘要

肥厚型心肌病(HCM)是一种具有广泛临床表现的遗传性心肌病。患者可能无症状,也可能发生重大不良事件,包括心源性猝死、室性心律失常和心力衰竭。识别有发生这些并发症风险的 HCM 患者仍然具有挑战性。虽然超声心动图仍然是诊断评估的主要方法,但心脏磁共振成像(CMR)是一种重要的辅助诊断方式,在 HCM 人群中对不良事件的风险分层具有新兴的应用。尽管 CMR 目前并未被纳入 HCM 管理指南,但越来越多的证据支持 CMR 用于 HCM 患者的常规预后评估。在这篇综述中,我们讨论了 CMR 技术的应用,包括晚期钆增强、T1 映射和细胞外容积分数的定量,用于 HCM 三种主要不良事件的风险分层:心源性猝死、室性心律失常和充血性心力衰竭。

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