首页> 外文期刊>Journal of endovascular therapy: an official journal of the International Society of Endovascular Specialists >Goltz, J.P.a , Ritter, C.O.a , Kellersmann, R.b , Klein, D.a , Hahn, D.a , Kickuth, R.a Endovascular treatment of popliteal artery segments P1 and P2 in patients with critical limb ischemia: Initial experience using a helical nitinol stent with increased radial force
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Goltz, J.P.a , Ritter, C.O.a , Kellersmann, R.b , Klein, D.a , Hahn, D.a , Kickuth, R.a Endovascular treatment of popliteal artery segments P1 and P2 in patients with critical limb ischemia: Initial experience using a helical nitinol stent with increased radial force

机译:Goltz,J.P.a,Ritter,C.O.a,Kellersmann,R.b,Klein,D.a,Hahn,D.a,Kickuth,R.a严重肢体缺血患者的pop动脉段P1和P2的血管内治疗:使用螺旋镍钛合金支架并增加径向力的初步经验

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Purpose: To evaluate efficacy, safety, and midterm patency of a helical, self-expanding nitinol stent after failed percutaneous transluminal angioplasty (PTA) of popliteal artery segments P1 and P2 in patients with chronic critical limb ischemia (CLI) or lifestyle-limiting claudication. Methods: Between February 2009 and March 2011, 40 patients (23 men; mean age 77±10 years) classified as Rutherford category 3 (n=10) or 4/5 (n=30) underwent PTA of the proximal and mid popliteal artery followed by implantation of a SUPERA stent for elastic recoil, residual stenosis, or flow-limiting dissection. All patients had an elevated operative risk. Before and after the procedure and during the 12-month follow-up, a clinical investigation, ankle-brachial-index (ABI) measurement, and color-coded duplex sonography and/or digital subtraction angiography were performed. Primary endpoints were limb salvage and anatomical patency at 12 months. Results: Stent implantation was successful in all patients. The major complication rate was 7.5% (an access-site pseudoaneurysm, 2 retroperitoneal hematomas, and 1 death from retroperitoneal bleeding). Mean follow-up was 15.9 months (range 0.5-27.9). The mean baseline ABI of 0.37 significantly increased to 0.91 at 12 months (p<0.01). Three (7.5%) patients underwent bypass surgery owing to lack of clinical improvement (<0.10 improvement in ABI). Primary and secondary patency rates at 12 months in the 34 patients eligible for follow-up were 68.4% and 79.8%, respectively. The major amputation rate was 5% at 1 year. Five (12.5%) in-stent stenoses and 1 of 2 (5.0%) in-stent occlusions were successfully recanalized (the second occlusion was asymptomatic). Conclusion: Implantation of this helical stent into segments of the popliteal artery at the knee joint in CLI patients is a safe and clinically effective bailout method with acceptable intermediate patency.
机译:目的:评估慢性critical肢缺血(CLI)或生活方式受限c行患者pop动脉P1和P2经皮腔内血管成形术(PTA)失败后,螺旋自扩张镍钛合金螺旋支架自扩张的疗效,安全性和中期通畅。方法:2009年2月至2011年3月,对40例(卢瑟福3级(n = 10)或4/5(n = 30))患者进行(骨近端和mid中动脉PTA手术(23名男性;平均年龄77±10岁)然后植入SUPERA支架进行弹性后坐,残余狭窄或限流性解剖。所有患者的手术风险均较高。在手术前后,以及在12个月的随访期间,进行了临床研究,踝臂指数(ABI)测量以及彩色编码的双工超声检查和/或数字减影血管造影。主要终点为12个月时肢体抢救和解剖通畅。结果:所有患者均成功植入支架。主要并发症发生率为7.5%(有假位动脉瘤,2例腹膜后血肿和1例腹膜后出血死亡)。平均随访15.9个月(范围0.5-27.9)。平均基线ABI为0.37,在12个月时显着增加至0.91(p <0.01)。由于缺乏临床改善(ABI改善<0.10),三名(7.5%)患者接受了搭桥手术。符合随访条件的34例患者在12个月时的初次和二次通畅率分别为68.4%和79.8%。 1年时的主要截肢率为5%。 5例(12.5%)支架内狭窄和2例(5.0%)支架内闭塞中的1例成功再通(第二次无症状)。结论:在CLI患者中,将这种螺旋支架植入into关节的is动脉段是一种安全且临床有效的救治方法,中间通畅程度可接受。

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