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首页> 外文期刊>The Journal of Cardiovascular Surgery: Official Journal of the International Society for Cardiovascular Surgery >Non-randomized, prospective, multi-centre evaluation of the ABSOLUTE .035 peripheral self-expanding stent system for occluded or stenotic superficial femoral or proximal popliteal arteries (ASSESS Trial): acute and 30-day results.
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Non-randomized, prospective, multi-centre evaluation of the ABSOLUTE .035 peripheral self-expanding stent system for occluded or stenotic superficial femoral or proximal popliteal arteries (ASSESS Trial): acute and 30-day results.

机译:非闭合性,前瞻性,多中心评估的ABSOLUTE .035外周自扩张支架系统用于股浅或近端or动脉狭窄或狭窄(ASSESS试验):急性和30天结果。

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摘要

AIM: The aim of the paper was to investigate the performance of the ABSOLUTE .035 Peripheral Self-Expanding Stent System in preventing restenosis of superficial femoral or proximal popliteal arteries. Due to a lack of large controlled trials proving its long-term durability femoropopliteal artery stenting is still a matter of debate. In this paper we report the study design, the acute and short-term results of a prospective European registry on the treatment of TASC B and C femoropopliteal lesions with the use of the ABSOLUTE stent. METHODS: This prospective, non-randomized, multi-centre study enrolled 122 patients with symptomatic peripheral occlusive disease at 14 sites in Europe. Patients were included with obstructed femoropopliteal arteries. Key inclusion criteria were de novo lesions =/>4.0 mm and =/<7.0 mm in diameter, and =/>40 mm and =/<200 mm in length. Single target vessel treatment had to be performed with a maximum of three stents. RESULTS: Mean target lesion length was 108+/-44 mm (range 22.2 to 200 mm) and mean reference vessel diameter 4.6+/-0.8 mm by quantitative angiography; 71% of the lesions analyzable by quantitative angiography (QA) had total occlusions. A total of 227 stents were implanted, 224 of which were deployed successfully (98.7%). Mean percentage of diameter stenosis was reduced from 90.9+/-15.5 % (range 41.3 to 100) to 19.0+/-8.4% (range 2.3 to 41.5). Device and procedural success were 83.6% each whereas technical success reached 100%. Sixteen lesions had a =/>30% residual stenosis post-procedure, 6 of them (37.5%) rated as being calcified. Eleven patients experienced major complications (9.1%) and 6 patients experienced minor complications (5%) within 30 days. Duplex ultrasound based 1-month restenosis rate was 9.3%. Target lesion revascularization (TLR) and target vessel revascularization (TVR) rates were 0.8% and 1.7%, respectively and amputation rate was 0.8%. Mean ankle-brachial index (ABI) at rest and after exercise increased significantly from baseline to 30 days follow-up by 0.63+/- 0.20 to 0.94+/-0.17 and from 0.44+/-0.23 to 0.85+/-0.21, respectively (P<0.001 each). CONCLUSION: The treatment of TASC B and C femoro-popliteal lesions with use of the ABSOLUTE stent is safe and feasible. Short-term follow-up documents persistent improvement of hemodynamics. The 6- and 12-month data have to be awaited for further CONCLUSIONS:
机译:目的:本文的目的是研究ABSOLUTE .035外周自扩张支架系统在预防股浅或pop小动脉再狭窄方面的性能。由于缺乏大型对照试验证明其长期耐用性,股fe动脉支架置入术尚有争议。在本文中,我们报告了使用ABSOLUTE支架治疗TASC B和C股pop骨病变的前瞻性欧洲注册研究的研究设计,急性和短期结果。方法:这项前瞻性,非随机,多中心研究在欧洲的14个地点招募了122例有症状的周围性闭塞性疾病患者。患者被纳入股fe动脉阻塞。纳入的主要标准是新生病变直径= /> 4.0 mm和= / <7.0 mm,长度= /> 40 mm和= / <200 mm。单靶血管治疗最多只能使用三个支架。结果:通过定量血管造影,平均目标病变长度为108 +/- 44 mm(范围为22.2至200 mm),平均参考血管直径为4.6 +/- 0.8 mm。通过定量血管造影(QA)可以分析的病变中有71%完全闭塞。总共植入了227个支架,其中224个已成功部署(98.7%)。直径狭窄的平均百分比从90.9 +/- 15.5%(范围从41.3降低到100)降低到19.0 +/- 8.4%(范围从2.3降低到41.5)。设备和程序成功率分别为83.6%,而技术成功率则达到100%。十六个病变在手术后残留狭窄率为30%,其中有六个(37.5%)被定为钙化。 30天内有11例患者出现了严重并发症(9.1%),6例患者出现了轻微并发症(5%)。基于双工超声的1个月再狭窄率为9.3%。目标病变血运重建率(TLR)和目标血管血运重建率(TVR)分别为0.8%和1.7%,截肢率为0.8%。从基线到30天随访,静止和运动后的平均踝肱指数(ABI)分别显着增加0.63 +/- 0.20至0.94 +/- 0.17和0.44 +/- 0.23至0.85 +/- 0.21 (每个P <0.001)。结论:使用ABSOLUTE支架治疗TASC B和C股mor骨病变是安全可行的。短期随访记录了血流动力学的持续改善。必须等待6个月和12个月的数据才能得出进一步的结论:

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