Sigwart U
Department for Invasive Cardiology, National Heart and Lung Hospitals, London, England.
Herz. 1990 Oct;15(5):319-28.
Even before the introduction of transluminal balloon dilatation of coronary arteries, Dotter had conceived intravascular endoprostheses and, in 1969, published a report of his observations after implantation of a spiral-shaped support of surgical steel and nickel-titanium ligation in peripheral arteries of the dog. Interest in intravascular supports developed especially in consideration of frequent unsatisfactory long-term results after coronary angioplasty. Coronary artery occlusion is observed in about 5% of balloon dilatations due to dissection, thrombosis, spasm or a combination of these phenomena. The rate of recurrent stenosis after uncomplicated balloon dilatation is about 30%, that of recanalization of chronic occlusion or dilatation of stenosed bypass grafts about 50%. Stent technology: In order to provide a meaningful solution to unresolved problems of balloon dilatation, the ideal endoprosthesis must be rapidly and reliably implantable as well as sufficiently flexible to conform to vascular curvatures. It should have a low profile, must be biocompatible and not thrombogenic; it should be rapidly endothelialized with no excessive proliferatory stimulus. Rigid stents are limited in length; elastic stents display a better transition to normal coronary arteries. Negatively-charged metallic surfaces appear less thrombogenic than those positively charged, the former, however, are usually not free of corrosion. The generally positive charge of stainless steel, the most commonly used material, is tempered with a special surface treatment. Currently, materials under investigation are nickel-titanium, tantalum and biodegradable plastic. Of importance for endothelialization are the wall thickness of the stent and the relationship of material to pore size. Filaments of stainless steel measuring 0.09 mm in diameter are completely covered by neoendothelium within three weeks. In laboratory animals, within minutes after implantation, all three stents currently in clinical use are covered with a thin layer of thrombocytes and fibrin; after one day, endothelial-like and pseudoendothelial cells develop along the metal structures. After one week, there is a flow-oriented behaviour of the surface cell formation embedding the stent between neoendothelial and lamina elastica interna, a process which is complete in three months. The thickness of the neointimal proliferation may be dependent on the stent geometry and may vary between 0.09 and 0.4 mm.(ABSTRACT TRUNCATED AT 400 WORDS)
甚至在冠状动脉腔内球囊扩张术引入之前,多特就已构想了血管内假体,并于1969年发表了一篇报告,介绍了他在狗的外周动脉植入手术用钢和镍钛合金结扎的螺旋形支撑物后的观察结果。鉴于冠状动脉成形术后频繁出现不尽人意的长期效果,人们对血管内支撑物的兴趣日益浓厚。由于夹层、血栓形成、痉挛或这些现象的综合作用,约5%的球囊扩张术中会观察到冠状动脉闭塞。单纯球囊扩张术后再狭窄率约为30%,慢性闭塞再通或狭窄旁路移植血管扩张的再通率约为50%。支架技术:为了有效解决球囊扩张未解决的问题,理想的血管内假体必须能够快速、可靠地植入,并且具有足够的柔韧性以适应血管弯曲。它应该外形小巧,必须具有生物相容性且不具有血栓形成性;它应该能迅速内皮化,且不会产生过度的增殖刺激。刚性支架长度有限;弹性支架向正常冠状动脉的过渡更好。带负电荷的金属表面似乎比带正电荷的表面血栓形成性更低,然而,前者通常并非无腐蚀问题。最常用的材料不锈钢通常带正电荷,通过特殊的表面处理可使其电荷得到缓和。目前正在研究的材料有镍钛合金、钽和可生物降解塑料。对于内皮化而言,支架的壁厚以及材料与孔径的关系很重要。直径0.09毫米的不锈钢细丝在三周内会被新生内膜完全覆盖。在实验动物中,植入后几分钟内,目前临床使用的所有三种支架都会被一层薄薄的血小板和纤维蛋白覆盖;一天后,内皮样细胞和假内皮细胞沿金属结构生长。一周后,表面细胞形成呈现出以血流为导向的行为,将支架嵌入新生内膜和内弹力膜之间,这个过程在三个月内完成。新生内膜增殖的厚度可能取决于支架的几何形状,范围在0.09至0.4毫米之间。(摘要截选至400字)