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首页> 外文期刊>Catheterization and cardiovascular interventions: Official journal of the Society for Cardiac Angiography & Interventions >Initial clinical experience with distal protection using the FilterWire in patients undergoing coronary artery and saphenous vein graft percutaneous intervention.
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Initial clinical experience with distal protection using the FilterWire in patients undergoing coronary artery and saphenous vein graft percutaneous intervention.

机译:在接受冠状动脉动脉和隐静脉移植经皮干预的患者中,使用过滤器的远端保护经验的最初临床经验。

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摘要

Percutaneous coronary intervention (PCI) of saphenous vein grafts (SVG) and native coronary arteries may be associated with embolization of particulate debris into the distal microcirculation. The FilterWire uses a polyurethane filter bag contained on a radiopaque loop to trap embolic debris during native vessel and SVG intervention. The objectives of this study were to assess the feasibility and safety of the FilterWire during PCI and to examine the size and content of the particulate debris captured during SVG and native vessel intervention. Early angiographic, in-hospital, and 30-day clinical outcomes were reviewed in 35 patients with 36 lesions treated with the FilterWire during PCI. Lesions were located in 22 (61%) native coronary arteries and in 14 (39%) SVGs. Multivessel coronary artery disease was present in 75% of patients. Lesions were complex (ACC/AHA complexity B2 or C) in 81% of cases. The FilterWire was successfully delivered and deployed distal to the site of coronary intervention in 92% of lesions, including 95% of native vessels and 82% of SVG lesions. Embolic debris was entrapped in 82% of these cases. The average particulate debris had a mean major axis of 490 microm (range, 45-3,302 microm) and minor axis of 226 microm (range, 33-1,677 microm). Although reduced flow was common (36.1%) when the FilterWire was in place, there were no sustained episodes of abrupt closure and only one (2.8%) patient developed sustained no-reflow after FilterWire removal. Distal branch vessel embolization was found in four (11.1%) cases. Major adverse cardiac events occurred in 5 (14%) of 35 patients treated with the device, although 2 of these patients were evolving an acute myocardial infarction at the time of the procedure; in patients meeting the prospectively defined inclusion criteria, the major adverse cardiac event was 6%. These results suggest that the FilterWire is a feasible and safe method of collecting particulate debris released during SVG and native vessel coronary intervention. Its benefit over conventional therapy and other distal protection devices is currently under study.
机译:隐静脉移植物(SVG)和天然冠状动脉的经皮冠状动脉干预(PCI)可能与颗粒碎屑栓塞到远端微循环中有关。 FilterWire使用在Radiopaque环上包含的聚氨酯过滤袋,以在天然血管和SVG干预期间捕获栓塞碎片。这项研究的目标是评估PCI期间过滤器的可行性和安全性,并检查在SVG和天然血管干预期间捕获的颗粒物碎片的大小和含量。在PCI期间,审查了35例36例病变患者的早期血管造影,院内和30天的临床结果。病变位于22(61%)天然冠状动脉中,在14(39%)SVG中。 75%的患者中存在多人冠状动脉疾病。在81%的病例中,病变是复杂的(ACC/AHA复杂性B2或C)。在92%的病变中,该过滤器已成功交付并部署到冠状动脉干预部位的远端,其中包括95%的天然血管和82%的SVG病变。栓塞碎片被捕获到其中82%的情况下。平均颗粒碎片的平均主要轴为490 microM(范围为45-3,302 microm)和226 microm(范围为33-1,677 microm)。尽管流量降低是常见的(36.1%),但在过滤器上到位时,没有持续的突然闭合发作,只有一名(2.8%)患者在去除过滤器WIRE后出现了持续的无流量。在四个(11.1%)病例中发现了远端分支血管栓塞。在接受该装置治疗的35例患者中,有5例(14%)发生了重大的不良心脏事件,尽管其中2例在手术时正在进化出急性心肌梗死。在符合前瞻性定义的纳入标准的患者中,主要的不良心脏事件为6%。这些结果表明,过滤器是一种可行且安全的方法,可以收集在SVG和天然血管冠状动脉干预期间释放的颗粒物碎片。目前正在研究其比常规疗法和其他远端保护设备的好处。

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