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获得性和先天性冠状动脉异常。

Acquired and congenital coronary artery abnormalities.

作者信息

Young Ming-Lon, McLeary Michael, Chan Kak-Chen

机构信息

1Heart Institute,Joe DiMaggio Children's Hospital,Hollywood,Florida,United States of America.

2Department of Radiology,Joe DiMaggio Children's Hospital,Hollywood,Florida,United States of America.

出版信息

Cardiol Young. 2017 Jan;27(S1):S31-S35. doi: 10.1017/S1047951116002201.

Abstract

Sudden unexpected cardiac deaths in approximately 20% of young athletes are due to acquired or congenital coronary artery abnormalities. Kawasaki disease is the leading cause for acquired coronary artery abnormalities, which can cause late coronary artery sequelae including aneurysms, stenosis, and thrombosis, leading to myocardial ischaemia and ventricular fibrillation. Patients with anomalous left coronary artery from the pulmonary artery can develop adequate collateral circulation from the right coronary artery in the newborn period, which remains asymptomatic only to manifest in adulthood with myocardial ischaemia, ventricular arrhythmias, and sudden death. Anomalous origin of coronary artery from the opposite sinus occurs in 0.7% of the young general population aged between 11 and 15 years. If the anomalous coronary artery courses between the pulmonary artery and the aorta, sudden cardiac death may occur during or shortly after vigorous exercise, especially in patients where the anomalous left coronary artery originates from the right sinus of Valsalva. Symptomatic patients with evidence of ischaemia should have surgical correction. No treatment is needed for asymptomatic patients with an anomalous right coronary artery from the left sinus of Valsalva. At present, there is no consensus regarding how to manage asymptomatic patients with anomalous left coronary artery from the right sinus of Valsalva and interarterial course. Myocardial bridging is commonly observed in cardiac catheterisation and it rarely causes exercise-induced coronary syndrome or cardiac death. In symptomatic patients, refractory or β-blocker treatment and surgical un-bridging may be considered.

摘要

约20%的年轻运动员猝死是由获得性或先天性冠状动脉异常所致。川崎病是获得性冠状动脉异常的主要原因,可导致包括动脉瘤、狭窄和血栓形成等晚期冠状动脉后遗症,进而引起心肌缺血和心室颤动。肺动脉起源的左冠状动脉异常患者在新生儿期可从右冠状动脉形成足够的侧支循环,起初无症状,到成年期才表现为心肌缺血、室性心律失常和猝死。冠状动脉起源于对侧窦在11至15岁的年轻普通人群中的发生率为0.7%。如果异常冠状动脉走行于肺动脉和主动脉之间,剧烈运动期间或运动后不久可能发生心脏猝死,尤其是异常左冠状动脉起源于瓦尔萨尔瓦右窦的患者。有缺血证据的有症状患者应接受手术矫正。瓦尔萨尔瓦左窦起源的右冠状动脉异常的无症状患者无需治疗。目前,对于如何处理瓦尔萨尔瓦右窦起源的左冠状动脉异常且走行于动脉间的无症状患者尚无共识。心肌桥在心脏导管检查中很常见,很少引起运动诱发的冠状动脉综合征或心脏猝死。对于有症状的患者,可考虑使用难治性药物或β受体阻滞剂治疗以及手术解除心肌桥。

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