儿童心脏病的冠状动脉:对年轻人管理的启示。

Fernando Baraona, Anne Marie Valente, Prashob Porayette, Francesca Romana Pluchinotta, Stephen P Sanders
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引用次数: 22

摘要

先天性心脏缺陷患者的生存率显著提高。许多人将在以后的生活中接受介入导管或外科手术。其他人会发展为动脉粥样硬化或术后冠心病。先天性心脏病患者的冠状动脉解剖结构与结构正常的心脏有很大的不同。这对诊断程序和干预措施都有影响。在某些缺陷中所见的独特心外膜路线可能影响冠状动脉造影的解释。介入手术,特别是在心脏底部,有可能损伤异常位置的冠状动脉,因此在手术前必须彻底勾画冠状动脉的解剖结构。在这篇综述中,我们将描述冠状动脉解剖的变异及其对介入和手术治疗的意义,以及在几类先天性心脏缺陷的后期随访中猝死的意义,这些先天性心脏缺陷包括:法洛四联症、动脉干、大动脉转位、双出口右心室、先天性纠正的大动脉转位和功能性单心室缺陷。我们还将讨论川崎病的冠状动脉异常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coronary Arteries in Childhood Heart Disease: Implications for Management of Young Adults.

Survival of patients with congenital heart defects has improved dramatically. Many will undergo interventional catheter or surgical procedures later in life. Others will develop atherosclerotic or post-surgical coronary heart disease. The coronary artery anatomy in patients with congenital heart disease differs substantially from that seen in the structurally normal heart. This has implications for diagnostic procedures as well as interventions. The unique epicardial course seen in some defects could impair interpretation of coronary angiograms. Interventional procedures, especially at the base of the heart, risk injuring unusually placed coronary arteries so that coronary artery anatomy must be delineated thoroughly prior to the procedure. In this review, we will describe the variants of coronary artery anatomy and their implications for interventional and surgical treatment and for sudden death during late follow-up in several types of congenital heart defects including: tetralogy of Fallot, truncus arteriosus, transposition of the great arteries, double outlet right ventricle, congenitally corrected transposition of the great arteries and defects with functionally one ventricle. We will also discuss the coronary abnormalities seen in Kawasaki disease.

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