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Carotid Artery Stenting Using a Novel Self-Expanding Braided Nickel–Titanium Stent: Feasibility and Safety Porcine Trial

机译:新型自膨胀编织镍钛支架置入颈动脉支架的可行性和安全性

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摘要

We studied the deliverability and safety of a braided, self-expanding, closed-cell nickel–titanium (NiTi) stent (E-volution, Jotec GmbH, Hechingen, Germany) especially designed for the endovascular treatment of carotid artery bifurcation stenosis with special regard to in-stent stenosis and thrombosis compared with a laser-cut reference nitinol stent in a porcine model of percutaneous vascular interventions. We aimed to assess histopathologic response in minipig carotid and subclavian arteries. Eight minipigs received a total of 42 stents: 14 reference stents and 28 E-volution stents. Eleven of the E-volution stents were additionally coated with heparin. Control angiography was obtained immediately before and after vascular intervention as well as 4 weeks after the procedure. Primary endpoints were 28 days of angiographic analyses as well as histomorphometric analysis, including injury score, inflammation score, luminal diameter, vessel diameter, maximal neointimal thickness, and area of in-stent stenosis. Secondary end points were procedural success, 28-day mortality, and stent thrombosis. All stents could be delivered successfully without procedural complications, morbidity, or mortality during our observation time. As confirmed by histology, no in-stent thrombosis was observed. Compared with common carotid arteries, subclavian arteries are significantly more vulnerable to developing in-stent stenosis caused by neointima proliferation (p < 0.05). Compared with the use of 1 single stent/artery, serial application of two stents leads to a more excessive but not significantly different neointimal proliferation (p > 0.05). The E-volution stent, especially when heparin coated, is in line with the comparison to the laser-cut reference stent displaying similar results of angiographic, histologic, and histomorphometric analyses (p > 0.05). Compared with the reference laser-cut stent, the self-expanding nitinol stent (E-volution) with its advanced braiding technology is feasible and safe. In our opinion, the high radial resistive force and the advanced braided design with tight stent-strut interstices may be beneficial in terms of plaque stabilization. Further studies are necessary and warranted.
机译:我们研究了编织的,自膨胀的闭孔镍钛合金(NiTi)支架(E-volution,Jotec GmbH,Hechingen,德国)的可交付性和安全性,该支架特别设计用于血管内治疗颈动脉分叉狭窄在经皮血管介入治疗的猪模型中,与激光切割的镍钛合金支架相比,支架内狭窄和血栓形成的风险更高。我们旨在评估小型猪颈动脉和锁骨下动脉的组织病理学反应。八只小型猪共接受了42个支架:14个参考支架和28个E-volution支架。 E-volution支架中有11个另外涂有肝素。在进行血管介入之前和之后以及术后4周进行对照血管造影。主要终点是血管造影分析和组织形态计量分析的28天,包括损伤评分,炎症评分,管腔直径,血管直径,最大新内膜厚度和支架内狭窄区域。次要终点是手术成功,28天死亡率和支架血栓形成。在我们的观察时间内,所有支架均可成功交付,而无程序并发症,并发症或死亡。如组织学所证实,未观察到支架内血栓形成。与普通颈动脉相比,锁骨下动脉明显更易发生由新内膜增生引起的支架内狭窄(p <0.05)。与使用1个单一支架/动脉相比,连续使用两个支架导致新内膜增生更为过度但差异不显着(p> 0.05)。 E-volution支架,尤其是肝素涂层支架,与激光切割参考支架的比较相符,显示出相似的血管造影,组织学和组织形态学分析结果(p> 0.05)。与参考激光切割支架相比,采用先进的编织技术的自膨胀镍钛合金支架(E-volv)是可行和安全的。在我们看来,高的径向阻力和先进的编织设计以及紧密的支架-支柱间的空隙在牙菌斑稳定方面可能是有益的。进一步的研究是必要和必要的。

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