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首页> 外文期刊>Journal of endovascular therapy: an official journal of the International Society of Endovascular Specialists >A novel cautery instrument for on-site fenestration of aortic stent-grafts: A feasibility study of 18 patients
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A novel cautery instrument for on-site fenestration of aortic stent-grafts: A feasibility study of 18 patients

机译:一种用于主动脉支架移植现场开窗的新型烧灼工具:对18例患者的可行性研究

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The article by Stephen and colleagues1 shows a novel cautery instrument for on-site fenes-tration of Dacron endografts, but we believe that fenestration techniques may be applied to polytetrafluoroethylene (PTFE) endografts as well. Our group has developed a new technique using a physician-customized fen-estrated C3 Excluder (W.L Gore & Associates, Flagstaff, AZ, USA) to treat aortic aneurysms with unsuitable necks. On a back table, the bifurcated Excluder is released until the contralateral leg is entirely liberated (Figure, A). Five-millimeter fenestrations are constructed with a circular object cutter (punch). The edges of the fenestrations are reinforced with a radiopaque wire from a snare (Covi-dien, Mansfield, MA, USA); the wire is anchored to the graft with CV6 PTFE suture (W.L. Gore & Associates). Next, the fenestrations are pre-cannulated with 0.018-inch guidewires. After that, the opened main body and contralateral leg of the endograft are manually constricted and re-sheathed into a 22-F tube segment detached from a 22-F Dryseal introducer flow valve (Figure, B and C). This tube segment containing the re-sheathed endoprosthesis is inserted in a 22-F Dryseal sheath. Once delivered to the target site, the Dryseal is partially retracted using a "pin and pull" mechanism until the main body is completely exposed outside the sheath, positioning the fenestration at the level of the visceral vessels. Next, the target visceral arteries are selectively cannulated and balloon-expandable covered stents (Advanta V12; Atrium Medical Corporation, Hudson, NH, USA) are deployed (Figure, D and E).
机译:Stephen及其同事的文章[1]显示了一种用于现场固定Dacron移植物的新型烧灼工具,但我们相信开窗技术也可以应用于聚四氟乙烯(PTFE)移植物。我们的小组已开发出一种新技术,该技术使用了医生定制的,按fen评估的C3 Excluder(W.L Gore&Associates,美国亚利桑那州弗拉格斯塔夫)来治疗颈部不合适的主动脉瘤。在后面的桌子上,松开分叉的Excluder,直到完全释放对侧腿(图A)。五毫米的窗是用圆形物体切割器(打孔器)制成的。开孔的边缘用网罗的不透射线增强(美国马萨诸塞州曼斯菲尔德的科维迪安);用CV6 PTFE缝线(W.L. Gore&Associates)将金属丝锚固到移植物上。接下来,用0.018英寸的导丝预开窗。此后,将人工打开的内窥镜的主体和对侧腿收缩,并将其重新护套成与22F Dryseal导引器流量阀分离的22F管段(图B和C)。将该包含重新护套的内假体的管段插入22-F Dryseal护套中。到达目标部位后,干密封件使用“销钉拉动”机制部分缩回,直到主体完全暴露在护套外部,将开窗孔定位在内脏血管的水平。接下来,选择性地插管目标内脏动脉,并展开球囊扩张的覆膜支架(Advanta V12; Atrium Medical Corporation,美国新罕布什尔州哈德森)(图D和E)。

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