Minn K W, Serafin D, Mikat E, Klitzman B
Division of Plastic, Reconstructive, Maxillofacial, and Oral Surgery, Duke University Medical Center, Durham, N.C.
Plast Reconstr Surg. 1991 Mar;87(3):536-42. doi: 10.1097/00006534-199103000-00022.
Synthetic conduits have not been suitable for microvascular reconstruction owing primarily to their high thrombogenicity. Vein replacements are the most vulnerable to thrombosis because of their low shear rates and low pressure. Experimental replacement of microvenous segments with prosthetic segments has shown little success. Recent technological advances in biomaterials and control of thrombogenesis provide the potential for success in the development of venous prostheses. The purpose of this study was to assess the use of nonbiodegradable composite polyurethane microvascular prostheses for reconstruction of rat femoral veins. Rat femoral venous defects of 10 mm were reconstructed with autogenous vein (n = 12), unprocessed plain polyurethane (n = 5), and nonbiodegradable composite polyurethane (n = 31). Patency was evaluated by direct observation and proximal venous milking tests. The patency rate of composite grafts was not significantly different from that of isotopic vein (p = 0.5, Fisher's exact test), and both had higher patency than unprocessed polyurethane (p less than 0.01). Composite grafts were examined sequentially using light and scanning electron microscopy. Grafts were fully endothelialized between the first and third months. The neointimal, neomedial, and neoadventitial layers could be seen more distinctly over time. New opportunities in reconstructive microsurgery may be opened by microvascular prostheses that are complaint and thromboresistant.
合成导管一直不适合用于微血管重建,主要原因是其高血栓形成性。静脉替代物由于其低剪切速率和低压力,最容易发生血栓形成。用假体节段实验性替代微静脉节段的效果不佳。生物材料和血栓形成控制方面的最新技术进展为静脉假体的开发成功提供了可能。本研究的目的是评估不可生物降解的复合聚氨酯微血管假体在大鼠股静脉重建中的应用。用自体静脉(n = 12)、未处理的普通聚氨酯(n = 5)和不可生物降解的复合聚氨酯(n = 31)重建大鼠10毫米的股静脉缺损。通过直接观察和近端静脉挤压试验评估通畅情况。复合移植物的通畅率与同种异体静脉的通畅率无显著差异(p = 0.5,Fisher精确检验),两者的通畅率均高于未处理的聚氨酯(p < 0.01)。使用光学显微镜和扫描电子显微镜对复合移植物进行序贯检查。移植物在第一个月到第三个月之间完全内皮化。随着时间的推移,可以更清楚地看到新生内膜、新生中膜和新生外膜层。顺应性和抗血栓的微血管假体可能为重建显微外科带来新的机遇。