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经皮肺动脉分支狭窄球囊扩张血管成形术

Percutaneous balloon dilation angioplasty of pulmonary artery branch stenosis.

作者信息

Bass J L

出版信息

Cardiovasc Intervent Radiol. 1986;9(5-6):299-302. doi: 10.1007/BF02577960.

Abstract

Congenital or acquired branch pulmonary artery stenosis can produce significant right ventricular hypertension and complicate the management of patients with tetralogy of Fallot. Repair is difficult using conventional surgical techniques. Balloon dilation angioplasty may be beneficial to some patients with these lesions. The technique currently used at the University of Minnesota is described. Results indicate that half of attempted dilations are successful with increased diameter of the narrowed areas, decreased pressure gradient, and improved pulmonary blood flow to the involved lung. Failure may be caused by technical limitations (28%) or lesions that are not dilatable with current equipment (22%). Undilatable lesions are more common in children over 2 years of age, in isolated pulmonary artery stenosis, and with associated surgical shunts. Complications are uncommon.

摘要

先天性或后天性分支肺动脉狭窄可导致显著的右心室高压,并使法洛四联症患者的治疗复杂化。使用传统手术技术进行修复很困难。球囊扩张血管成形术可能对一些患有这些病变的患者有益。本文描述了明尼苏达大学目前使用的技术。结果表明,一半的扩张尝试是成功的,狭窄区域直径增加,压力梯度降低,受累肺的肺血流量增加。失败可能是由技术限制(28%)或当前设备无法扩张的病变(22%)引起的。不可扩张的病变在2岁以上儿童、孤立性肺动脉狭窄以及伴有外科分流的患者中更为常见。并发症并不常见。

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