Kogel H, Vollmar J F, Cyba-Altunbay S, Mohr W, Frösch D, Amselgruber W
Department of Vascular and Thoracic Surgery, University Hospital, Ulm, FRG.
Thorac Cardiovasc Surg. 1989 Apr;37(2):119-24. doi: 10.1055/s-2007-1020302.
Based on the experimental experiences in more than 180 implantations of different materials as venous substitutes segments of the inferior vena cava have been replaced in 34 dogs by Polyurethane (low microporosity) and modified e-PTFE prostheses (increased microporosity of 60 microns and 90 microns fibril length). The 12 months patency rate didn't differ between both tested optimized materials and ranged from 43 to 50%. After a follow-up of 12 months the grafts were taken out and analysed by light, immunofluorescence microscopy, scanning and transmission electron microscopy. In addition a new technique of microcorrosion casts was used for SEM-analyses. As a result a transmural microvessel system in the microporous meshwork of the prostheses with multiple orifices at the inner surface of the grafts could be demonstrated. Complete endothelialization was only observed in e-PTFE prostheses of high microporosity (greater than 60 microns fiber length). There is strong evidence that a full tissue incorporation of microporous artificial grafts mainly depends on a sufficient primary intramural deposit of blood components (fibrin, platelets, leucocytes), which initiates cell invasion from the surrounding tissue, accompanied by a highly developed microvessel network. A multifocal endothelialization takes place from the numerous microvascular orifices on the inner surface of the prostheses. Other sources such as pannus invasion or adhesion of multipotent cells from the blood stream play probably a very limited role.
基于180多次不同材料植入的实验经验,在34只狗身上,用聚氨酯(低微孔率)和改性e-PTFE假体(增加微孔率至60微米和90微米纤维长度)替换了下腔静脉的静脉替代段。两种测试的优化材料的12个月通畅率没有差异,范围在43%至50%之间。随访12个月后,取出移植物,通过光学显微镜、免疫荧光显微镜、扫描和透射电子显微镜进行分析。此外,一种新的微腐蚀铸型技术用于扫描电子显微镜分析。结果表明,在假体的微孔网络中存在一个透壁微血管系统,在移植物内表面有多个小孔。仅在高微孔率(纤维长度大于60微米)的e-PTFE假体中观察到完全内皮化。有强有力的证据表明,微孔人工移植物的完全组织整合主要取决于血液成分(纤维蛋白、血小板、白细胞)在壁内的充分初始沉积,这引发了周围组织的细胞侵入,并伴有高度发达的微血管网络。多灶性内皮化从假体内表面的众多微血管孔发生。其他来源,如血管翳侵入或来自血流的多能细胞粘附,可能起的作用非常有限。