【经皮治疗多发性心脏缺损】。

M Ledesma, F D Gómez, C Alva Espinosa
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引用次数: 0

摘要

我们报告6例经皮介入治疗多发性先天性心脏缺损的经验。年龄2.3 ~ 10岁(平均6.1岁),随访1 ~ 84个月(平均28.8个月)。2例有主动脉缩窄(AC)和持续性动脉导管(PDA)。2例合并肺动脉瓣狭窄(PVS)和PDA, 1例合并主动脉瓣狭窄(AE)和PDA, 1例合并AC、二尖瓣狭窄和主动脉下瓣狭窄(Shone综合征)。所有使用Gianturco线圈或Rashkind闭塞器的患者动脉导管均闭塞。AC患者球囊后瓣膜梯度从46降至9 mmHg, PVS从110降至10 mmHg, AE从40降至14 mmHg。在一例患有肖尼综合征的8岁男孩中,我们使用Inoue导管进行主动脉缩窄血管成形术和二尖瓣成形术。他被转到主动脉下修复狭窄的手术。随访时均无症状。结论;经皮介入治疗对于多发性先天性心脏缺陷患者是可行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Percutaneous treatment of multiple heart defects].

We describe our experience in 6 cases with multiple congenital heart defects treated by percutaneous intervention. Their age ranged from 2.3 to 10 years (mean 6.1), with follow-up from 1 to 84 months (mean 28.8). Two cases had coarctation of the aorta (AC) and persistent ductus arteriosus (PDA). Two patients had pulmonary valve stenosis (PVS) and PDA, one case with aortic stenosis (AE) and PDA and one case with AC, mitral stenosis and subaortic stenosis (Shone's Syndrome). Ductus arteriosus was occluded in all patients with Gianturco coils or Rashkind occluder. The valvular gradient post balloon decreased in cases with AC from 46 to 9 mmHg, with PVS from 110 to 10 mmHg and with AE from 40 to 14 mmHg. In a 8 year old boy with Shone's syndrome, we performed angioplasty of aortic coarctation, mitral valvuloplasty with Inoue catheter. He was referred to surgery for subaortic repair stenosis. All are asymptomatic at follow-up. In conclusion; percutaneous intervention is possible in patients with multiple congenital heart defects.

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