von Kodolitsch Y, Franzen O, Lund G K, Koschyk D H, Ito W D, Meinertz T
Clinic of Internal Medicine III, University Hospital Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany.
Z Kardiol. 2005 Jan;94(1):1-13. doi: 10.1007/s00392-005-0153-1.
Congenital anomalies of the coronary arteries occur in 0.2-1.2% of the general population; they cause 12% of sports-related sudden cardiac deaths and 1.2% of non-sports-related deaths. We review some of the substantial advances that have been made both, in the understanding of the embryonic development of the coronary arteries and in the clinical diagnosis and management of their anomalies. In this second part of our review we elucidate recent approaches to defining coronary anomalies and provide information on their incidence and prognosis. In addition, we discuss the options for screening large populations for potentially lethal coronary malformations and elucidate the role of invasive diagnostic modalities such as intravascular ultrasound, flow wire and pressure wire. The clinical relevance of coronary anomalies is discussed particularly for the ill-defined group of anomalies that only occasionally cause severe clinical events comprising anomalous origination of a coronary artery from the opposite sinus (ACAOS), coronary artery fistulae and myocardial bridging. Finally, we provide an update on current diagnostic and therapeutic recommendations.
先天性冠状动脉异常在普通人群中的发生率为0.2%-1.2%;它们导致12%的与运动相关的心源性猝死和1.2%的非运动相关死亡。我们回顾了在冠状动脉胚胎发育的理解以及其异常的临床诊断和管理方面取得的一些重大进展。在本综述的第二部分中,我们阐明了定义冠状动脉异常的最新方法,并提供了有关其发病率和预后的信息。此外,我们讨论了对大量人群进行潜在致命性冠状动脉畸形筛查的选项,并阐明了血管内超声、血流导丝和压力导丝等侵入性诊断方法的作用。特别针对一组定义不明确的异常情况讨论了冠状动脉异常的临床相关性,这些异常情况仅偶尔导致严重临床事件,包括冠状动脉起源于对侧窦(ACAOS)、冠状动脉瘘和心肌桥接。最后,我们提供了当前诊断和治疗建议的最新情况。