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Arterial stenting with self-expandable and balloon-expandable endoprostheses

机译:自扩张式和球囊扩张式内支架的动脉支架

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摘要

textabstractCoronary angioplasty is complicated by acute occlusion (within 24 hours) and late restenosis (within 6 months) in 2-5% and 20-40% of the cases, respectively. Vascular endoprostheses (stents) may provide the cardiologist with a solution to some of these complications. Several stent-devices are now available for experimental and clinical evaluation. In this study we describe our experience with two metallic stents in normal arteries of swine. Self-expandable, stainless steel stents (3.5 mm diameter) were implanted in 17 peripheral arteries, eight of which were deendothelialized by prior balloon angioplasty. Following implantation, the animals received antithrombotic therapy with acenocoumarol and aspirin (8 stents), or aspirin alone (9 stents). After 1 week repeat angiography was performed, which showed patency of all stented arteries. Microscopy showed complete covering by neointima, 80 μm in thickness. This self-expandable stent (SES) and a balloon-expandable stent (BES), constructed of tantalum, were implanted in normal coronary arteries. SES (3.0 and 3.5 mm) receiving animals were treated with coumadines (10 stents) or received no antithrombotic treatment (16 stents) after implantation. BES receiving animals were also not treated (10 stents). Three untreated animals with SES died suddenly within 48 hours. Postmortem examination showed partial or complete thrombosis of all six stents in these animals, resulting in a patency rate of 62% after 1 week. All animals with SES, which were treated with coumadines, and all animals with BES (untreated) had patent stents after one week. It is concluded that SES implanted in normal coronary arteries of pigs, which do not receive additional antithrombotic treatment, show a 38% occlusion rate within 48 hours, but show 100% patency after 1 week, when the animals are treated with coumadines. BES implanted in normal coronary arteries of pigs, which do not receive antithrombotic drugs, are 100% patent after 1 week.
机译:急性血管闭塞症(24小时内)和晚期再狭窄(6个月内)分别在2%至5%和20%至40%的病例中并发。血管内假体(支架)可以为心脏病专家解决其中一些并发症。现在有几种支架设备可用于实验和临床评估。在这项研究中,我们描述了在猪的正常动脉中使用两个金属支架的经验。自扩张式不锈钢支架(直径3.5 mm)被植入17个外周动脉中,其中8个通过先前的球囊血管成形术进行了去内皮化。植入后,动物接受乙酰香豆酚和阿司匹林(8个支架)或单独使用阿司匹林(9个支架)的抗血栓治疗。 1周后进行重复血管造影,显示所有带支架的动脉通畅。显微镜显示厚度为80μm的新内膜完全覆盖。将这种由钽制成的自扩张支架(SES)和球囊扩张支架(BES)植入正常冠状动脉中。植入SES(3.0和3.5 mm)的动物接受香豆素(10个支架)治疗或未接受抗血栓治疗(16个支架)。接受BES的动物也未接受治疗(10个支架)。三只未经治疗的SES动物在48小时内突然死亡。死后检查显示这些动物中所有六个支架的部分或全部血栓形成,导致1周后通畅率为62%。一周后,所有用香豆素处理过的SES动物和所有BES(未处理过)动物都在一个星期后有了专利支架。结论是,在未接受额外抗血栓治疗的情况下,植入正常猪冠状动脉的SES在48小时内显示38%的闭塞率,但在用香豆素处理动物1周后显示100%的通畅。植入正常猪的冠状动脉的BES在未使用抗血栓药物的情况下,在1周后获得了100%的专利。

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