Moazami N, Bessler M, Argenziano M, Choudhri A F, Cabreriza S E, Allendorf J D, Rose E A, Oz M C
Department of Surgery, Columbia-Presbyterian Medical Center, New York, New York 10032, USA.
ASAIO J. 1996 Sep-Oct;42(5):M381-5.
Percutaneous stents are used in vascular applications in conjunction with angioplasty and in combination with graft material for repair of abdominal aneurysms. The authors have designed a collapsible bioprosthetic aortic valve for placement by a transluminal catheter technique. This trileaflet stent valve is composed of stainless steel and bovine pericardium. Stent valves, 23 and 29 mm, were tested in a pulse duplicator system with rigid rings from 21 to 31 mm in 2 mm increments. At a mean flow of 3.1 L/min (+/-0.7), normal systemic aortic pressure was generated with a transvalvular gradient of 14.9 +/- 7 mmHg (mean +/- SD). Regurgitation fraction ranged from 10 to 18% (mean 13.8 +/- 3%) in the best ring size. Valves with the best hemodynamic profile were used for implantation in three 70 kg pigs in an open chest model. The valve was collapsed in a 24 Fr catheter designed to allow slow, controlled release. After resection of the native leaflets, the new valve was placed in the subcoronary position. No additional sutures were used for securing the valve. Two animals were successfully weaned from cardiopulmonary bypass and maintained systemic pressures of 100/45 (+/-10) and 116/70 (+/-15) mmHg, respectively. Intraoperative color echocardiography revealed minimal regurgitation, central flow, full apposition of all leaflets, and no interference with coronary blood flow. Both animals were sacrificed after being off bypass for 2 hr. Postmortem examination revealed the valves to be securely anchored. The third animal was weaned from cardiopulmonary bypass but developed refractory ventricular fibrillation because of valve dislodgment due to structural failure. Although long term survival data are needed, development of a hemodynamically acceptable prosthetic aortic valve for transluminal placement is feasible.
经皮支架用于血管介入手术,与血管成形术联合使用,并与移植材料结合用于修复腹主动脉瘤。作者设计了一种可折叠的生物人工主动脉瓣,通过腔内导管技术进行植入。这种三叶式支架瓣膜由不锈钢和牛心包组成。分别为23毫米和29毫米的支架瓣膜在脉冲复制系统中进行测试,使用内径从21毫米到31毫米、间隔为2毫米的刚性环。在平均流量为3.1升/分钟(±0.7)时,可产生正常的体循环主动脉压力,跨瓣压差为14.9±7毫米汞柱(平均值±标准差)。在最佳环尺寸下,反流分数范围为10%至18%(平均13.8±3%)。具有最佳血流动力学特征的瓣膜被用于在开胸模型的三只70千克猪体内植入。瓣膜被折叠在一个24F导管中,该导管设计用于实现缓慢、可控的释放。切除天然瓣膜叶后,将新瓣膜置于冠状动脉下位置。未使用额外的缝线来固定瓣膜。两只动物成功脱离体外循环,分别维持体循环压力为100/45(±10)和116/70(±15)毫米汞柱。术中彩色超声心动图显示反流极小、血流中心、所有瓣膜叶完全贴合,且未干扰冠状动脉血流。两只动物在脱离体外循环2小时后被处死。尸检显示瓣膜固定牢固。第三只动物脱离体外循环,但由于瓣膜因结构故障移位而出现难治性心室颤动。尽管需要长期生存数据,但开发一种血流动力学可接受的用于腔内植入的人工主动脉瓣是可行的。