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首页> 外文期刊>International Journal of Cardiology >Retrograde coaxial transarterial coil occlusion of congenital coronary arteriovenous fistula in a 22-month-old boy and a brief literature review.
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Retrograde coaxial transarterial coil occlusion of congenital coronary arteriovenous fistula in a 22-month-old boy and a brief literature review.

机译:在一个22个月大的男孩中,先天性冠状动静脉瘘逆行同轴经动脉线圈闭塞,并进行了简要的文献综述。

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摘要

Congenital coronary arteriovenous fistula (CAVF) to the right cardiac chamber or vessel is a rare anomaly that may cause severe morbidity and mortality . Surgical repair by means of either epicardial closure of the fistula or cardiopulmonary bypass and cardiotomy to close the site of drainage has been advised by many authors [2-4]. Recently, transcatheter coil occlusion has been advocated as a treatment of choice for congenital CAVF for its excellent results [5-14]. We report here successful retrograde coaxial transarterial coil occlusion of a fistula between the left anterior descending coronary artery and the right atrium (RA) in a 22-month-old boy. We make a brief review from the English literature of 26 reported pediatric patients with congenital CAVF treated by transcatheter coil occlusion.
机译:右心室或血管的先天性冠状动静脉瘘(CAVF)是一种罕见的异常,可能导致严重的发病率和死亡率。许多作者建议通过瘘管的心外膜闭合或心肺分流术以及心脏切开术来关闭引流部位的外科手术修复[2-4]。最近,经导管线圈闭塞因其出色的疗效而被提倡作为先天性CAVF的治疗选择[5-14]。我们在这里报告了在一个22个月大的男孩中,左冠状动脉前降支与右心房(RA)之间的瘘管逆行同轴逆行动脉闭塞成功。我们从英国文献中对26例经导管置入闭塞治疗的先天性CAVF患儿进行了简要回顾。

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