Takeuchi repair of anomalous left coronary artery from the pulmonary artery

被引:9
|
作者
Cramer, Jonathan W. [1 ]
Cinquegrani, Michael [2 ]
Cohen, Scott B. [1 ,2 ]
机构
[1] Med Coll Wisconsin, Childrens Hosp Wisconsin, Dept Pediat, Div Cardiol, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Internal Med, Div Adult Cardiovasc Med, Milwaukee, WI 53226 USA
关键词
Takeuchi repair; Congenital heart disease; Cardiovascular CT; Anomalous left coronary artery from the pulmonary artery;
D O I
10.1016/j.jcct.2015.02.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare form of congenital heart disease that has been successfully palliated for decades. Prior to coronary reimplantation, the Takeuchi repair was the most common operative palliation. The Takeuchi repair is still seen today at less experienced congenital centers or when reimplantation is not possible. Patients who have had the Takeuchi repair are at risk of having subsequent complications related to this repair. Unfortunately, due to the surgical rarity, the post surgical anatomy is often poorly understood by cardiologists leading to inadequate risk factor assessment and compromised patient care. Coronary computed tomography angiography is a useful imaging modality to follow patients who have had the Takeuchi repair. (C) 2015 Society of Cardiovascular Computed Tomography. All rights reserved.
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收藏
页码:457 / 458
页数:2
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