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首页> 外文期刊>Journal of endovascular therapy: an official journal of the International Society of Endovascular Specialists >Percutaneous transluminal angioplasty with drug-eluting balloons for salvage of infrainguinal bypass grafts
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Percutaneous transluminal angioplasty with drug-eluting balloons for salvage of infrainguinal bypass grafts

机译:带药物洗脱球囊的经皮腔内血管成形术可挽救膀胱下旁路移植物

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Purpose: To evaluate the safety and feasibility of using drug-eluting balloons (DEBs) in the treatment of infrainguinal bypass graft stenoses. Methods: A nonrandomized prospective study evaluated the feasibility of DEB treatment for intragraft/anastomotic stenoses arising >1 month after infrainguinal bypass grafting; stenoses due to graft/technical problems (e.g., vein torsion) were excluded, as were failed grafts that could not be successfully recanalized with catheter-directed thrombolysis. Between February 2010 and February 2012, 41 patients (35 men; mean age 71 years, range 46-87) were treated with DEBs for 63 anastomotic/intragraft stenoses in vein or prosthetic grafts. Follow-up was performed with duplex ultrasonography. The primary endpoint at 12 months was graft occlusion or >50% restenosis at the DEB treatment site. Results: DEB treatment was technically successful in 61 (96.8%) of the 63 lesions with no complications other than one instance of vasospasm; one totally occluded segment and one restenosis were treated surgically. The mean follow-up was 16.7 months (range 3-24). The estimated cumulative target site primary and secondary patency rates at 6 months were 91% and 96%, respectively, and 70% and 90%, respectively, at both 12 and 18 months (no restenoses after 12 months). The estimated mean durations of primary and secondary treatment site patency were 20.3 and 22.7 months, respectively (p=0.033). At 6 and 12/18 months, the cumulative rates were 96% and 90%, respectively, for graft patency and 98% and 93% for freedom from amputation. Conclusion: DEBs proved to be a feasible, safe, and effective treatment for vein and prosthetic bypass graft stenoses, with excellent technical success and acceptable short and midterm patency.
机译:目的:评估使用药物洗脱球囊(DEB)治疗下尿道旁路移植术狭窄的安全性和可行性。方法:一项非随机的前瞻性研究评估了DEB治疗行宫腔旁路移植术后> 1个月出现的移植内/吻合口狭窄的可行性;排除由于移植物/技术问题(例如,静脉扭曲)引起的狭窄,以及无法通过导管定向溶栓术成功修复的失败的移植物。在2010年2月至2012年2月之间,对DEB进行了41例患者(35名男性,平均年龄71岁,范围46-87)进行了静脉或人工移植物的63例吻合口/移植内狭窄治疗。随访采用双工超声检查。 12个月时的主要终点是DEB治疗部位的移植物闭塞或> 50%的再狭窄。结果:在63例病变中有61例(96.8%)获得了DEB治疗,除一种血管痉挛外,没有其他并发症。一例完全闭塞,一例再狭窄经手术治疗。平均随访时间为16.7个月(范围3-24)。在12个月和18个月时(6个月时),估计的累积目标部位第一和第二次通畅率分别为91%和96%,分别为70%和90%(12个月后无再狭窄)。初级和次级治疗部位通畅的估计平均持续时间分别为20.3和22.7个月(p = 0.033)。在6和12/18个月时,移植物通畅的累积率分别为96%和90%,无截肢的累积率分别为98%和93%。结论:DEBs被证明是一种可行,安全,有效的静脉和人工旁路移植物狭窄治疗方法,具有出色的技术成功性和可接受的短期和中期通畅性。

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