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首页> 外文期刊>Journal of the American Society of Echocardiography: official publication of the American Society of Echocardiography >Recommendations for Multimodality Assessment of Congenital Coronary Anomalies: A Guide from the American Society of Echocardiography Developed in Collaboration with the Society for Cardiovascular Angiography and Interventions, Japanese Society of Echocardiography, and Society for Cardiovascular Magnetic Resonance
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Recommendations for Multimodality Assessment of Congenital Coronary Anomalies: A Guide from the American Society of Echocardiography Developed in Collaboration with the Society for Cardiovascular Angiography and Interventions, Japanese Society of Echocardiography, and Society for Cardiovascular Magnetic Resonance

机译:先天性冠状动脉异常的多模评价的建议:与心血管血管造影和干预措施,日本超声心动图社会和心血管磁共振社会合作开发的美国超声心动图社会的指南

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摘要

Congenital coronary artery anomalies, both in isolation and associated with other forms of congenital heart disease, have been recognized as important lesions with significant potential morbidity and mortality, including sudden cardiac death in children and adolescents. Multimodality imaging techniques have demonstrated increasing utility in the characterization of most congenital coronary anomalies, both in children and adults, and may reduce the need for diagnostic catheterization in many cases. This document provides multimodality guidelines for optimization of imaging for congenital coronary anomalies, with a review of the benefits and limitations of the different imaging techniques (echocardiography, cardiac computed tomography, cardiac magnetic resonance imaging, nuclear myocardial perfusion imaging and angiography). Strategies for imaging congenital coronary anomalies when the coronary anomaly is in isolation (anomalous aortic origin of a coronary artery, anomalous left coronary from the pulmonary artery, and coronary artery fistulas) as well as coronary anomalies associated with other congenital heart disease (supravalvular aortic stenosis, transposition of the great arteries, tetralogy of Fallot, truncus arteriosus, pulmonary atresia with intact septum, and hypoplastic left heart syndrome) are described.
机译:先天性冠状动脉异常,既是分离和其他形式的先天性心脏病,都被认为是具有显着潜在发病率和死亡率的重要病变,包括儿童和青少年的突然心脏病死亡率。多模成像技术已经证明了儿童和成人中最先天性冠状体异常的表征增加的效用,并且在许多情况下可能会降低对诊断导管的需求。本文档提供了用于优化先天性冠状动脉异常的成像的多模式指南,审查了不同成像技术的益处和局限性(超声心动图,心脏计算断层扫描,心脏磁共振成像,核心肌灌注成像和血管造影)。当冠状动脉异常是分离(冠状动脉的异常主动脉源,来自肺动脉的异常左冠状动脉,以及冠状动脉瘘)以及与其他先天性心脏病相关的冠状动脉异常时(Supravalularbularbularic Stenosis相关,描述了大动脉的转子,Tetralogy的椎间盘,Truncus arteriosus,具有完整隔膜的肺部闭锁,以及软质左心综合征)。

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