Gentles T L, Lock J E, Perry S B
Department of Cardiology, Children's Hospital, Boston, Massachusetts 02115.
J Am Coll Cardiol. 1993 Sep;22(3):867-72. doi: 10.1016/0735-1097(93)90205-f.
The aim of this study was to evaluate the efficacy and safety of high pressure balloons (17 to 20 atm, Blue Max, Meditech) to dilate branch pulmonary artery stenosis.
The low success rate (50% to 60%) for angioplasty of branch pulmonary artery stenosis using low pressure balloons is due primarily to the inability to eliminate the balloon waist. Hence, higher inflation pressures may improve results.
Hemodynamic and angiographic data from 52 patients (0.3 to 34.8 years old) who underwent high pressure balloon dilation of branch pulmonary artery stenosis between October 1990 and February 1992 were reviewed retrospectively, as were data from previous low pressure dilations in these patients. Common diagnoses included tetralogy of Fallot (n = 9), tetralogy of Fallot with pulmonary atresia (n = 23), single ventricle (n = 8) and isolated congenital pulmonary stenosis (n = 7). The 52 patients had 72 vessels dilated. Criteria for success were a > or = 50% increase in vessel diameter or a > 20% decrease in right ventricular to aortic pressure ratio.
Of 36 vessels with previously unsuccessful low pressure balloon dilation, 23 (63%) were successfully dilated with high pressure balloons. Of the 36 remaining vessels, 29 (81%) were successfully dilated with high pressure balloons. Factors associated with success were stenosis at a surgical anastomosis and disappearance of the balloon waist with dilation. Aneurysms developed in three vessels. Complications occurred in seven patients (13%); in two patients the distal pulmonary artery was perforated by a stiff guide wire, causing death in one.
Dilation of stenotic peripheral pulmonary arteries with high pressure balloons improves the success rate of angioplasty both in patients who have had unsuccessful dilation with a low pressure balloon and in those without previous attempted dilation.
本研究旨在评估高压球囊(17至20个大气压,Blue Max,美迪泰克公司)扩张肺动脉分支狭窄的疗效和安全性。
使用低压球囊进行肺动脉分支狭窄血管成形术的成功率较低(50%至60%),主要原因是无法消除球囊腰部。因此,更高的充盈压力可能会改善治疗效果。
回顾性分析了1990年10月至1992年2月期间接受高压球囊扩张肺动脉分支狭窄的52例患者(年龄0.3至34.8岁)的血流动力学和血管造影数据,以及这些患者之前低压扩张的数据。常见诊断包括法洛四联症(9例)、法洛四联症合并肺动脉闭锁(23例)、单心室(8例)和孤立性先天性肺动脉狭窄(7例)。这52例患者共扩张了72支血管。成功标准为血管直径增加≥50%或右心室与主动脉压力比值降低>20%。
在之前低压球囊扩张未成功的36支血管中,23支(63%)通过高压球囊成功扩张。在其余36支血管中,29支(81%)通过高压球囊成功扩张。与成功相关的因素包括手术吻合处狭窄以及扩张时球囊腰部消失。3支血管出现动脉瘤。7例患者(13%)发生并发症;2例患者的远端肺动脉被硬导丝穿孔,其中1例死亡。
对于低压球囊扩张失败的患者以及之前未尝试过扩张的患者,使用高压球囊扩张狭窄的外周肺动脉可提高血管成形术的成功率。