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首页> 外文期刊>Journal of vascular and interventional radiology: JVIR >Heparin-bonded, expanded polytetrafluoroethylene-lined stent graft in the treatment of femoropopliteal artery disease: 1-year results of the VIPER (Viabahn Endoprosthesis with Heparin Bioactive Surface in the Treatment of Superficial Femoral Artery Obstructive Disease) trial
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Heparin-bonded, expanded polytetrafluoroethylene-lined stent graft in the treatment of femoropopliteal artery disease: 1-year results of the VIPER (Viabahn Endoprosthesis with Heparin Bioactive Surface in the Treatment of Superficial Femoral Artery Obstructive Disease) trial

机译:肝素结合的,扩大的聚四氟乙烯内衬支架移植物治疗股pop动脉疾病:VIPER(Viabahn内支架术与肝素生物活性表面在治疗股浅动脉阻塞性疾病中)的1年结果

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Purpose: To evaluate the performance of a heparin-bonded, expanded polytetrafluoroethylene (ePTFE)-lined nitinol endoprosthesis in the treatment of long-segment occlusive disease of the femoropopliteal artery (FPA) and to identify factors associated with loss of patency. Materials and Methods: In a single-arm, prospective, 11-center study (VIPER [Gore Viabahn Endoprosthesis with Heparin Bioactive Surface in the Treatment of Superficial Femoral Artery Obstructive Disease] trial), 119 limbs (113 patients; 69 men; mean age, 67 y), including 88 with Rutherford category 3-5 disease and 72 with Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II) C or D lesions of the FPA, underwent stent graft implantation. The mean lesion length was 19 cm; 56% of lesions were occlusions. Follow-up evaluations included color duplex ultrasonography in all patients, with patency defined as a peak systolic velocity ratio< 2.5. Results: At 12 months, Rutherford category and ankle-brachial index (ABI) were significantly improved (mean category improvement, 2.4; ABI increased from 0.6??0.2 to 0.9??0.19; P<.0001). Primary and secondary patency rates were 73% and 92%. The primary patency for devices oversized<20% at the proximal landing zone was 88%, whereas the primary patency for devices oversized by>20% was 70% (P =.047). Primary patency was not significantly affected by device diameter (5 vs 6 vs 7 mm) or lesion length (??20 cm vs>20 cm). The 30-day major adverse event rate was 0.8%. Conclusions: The heparin-bonded, ePTFEitinol stent graft provided clinical improvement and a primary patency rate of 73% at 1 year in the treatment of long-segment FPA disease. Careful sizing of the device relative to vessel landing zones is essential for achieving optimal outcomes. ? 2013 SIR.
机译:目的:评估肝素键合,扩展的聚四氟乙烯(ePTFE)衬里的镍钛合金内修复物在治疗股pop动脉长节闭塞性疾病(FPA)中的性能,并确定与通畅性丧失相关的因素。材料和方法:在单臂,前瞻性,11个中心的研究中(VIPER [Gore Viabahn内支架术结合肝素生物活性表面治疗股浅动脉阻塞性疾病]试验),共有119条肢体(113例患者; 69名男性;平均年龄) ,67岁),其中88例患有卢瑟福3-5类疾病,72例患有跨界动脉疾病(TASC II)FPA C或D病变的社会间共识,进行了支架植入术。平均病变长度为19厘米; 56%的病变是阻塞。随访评估包括所有患者的彩色双工超声检查,通畅定义为收缩压峰值速度比<2.5。结果:在第12个月时,卢瑟福类别和踝肱指数(ABI)显着改善(平均类别改善2.4; ABI从0.6 ?? 0.2升高至0.9 ?? 0.19; P <.0001)。初次和二次通畅率分别为73%和92%。在近端着陆区,尺寸超大<20%的器械的主要通畅率为88%,而尺寸大于20%的器械的主要通畅率为70%(P = .047)。器械直径(5 vs. 6 vs. 7 mm)或病变长度(?20 cm vs> 20 cm)对原发通畅性没有显着影响。 30天的主要不良事件发生率为0.8%。结论:肝素键合的ePTFE /镍钛合金支架移植物在治疗长段FPA疾病方面提供了临床改善,并且在1年时初次通畅率为73%。相对于船只着陆区仔细确定设备的尺寸对于实现最佳结果至关重要。 ? 2013年SIR。

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