Ultrastructural study for vein regeneration after microvascular anastomosis in rabbit femoral vein.
- Author:
Hong Seop RHO
1
;
Chul Hwan KIM
;
Kyung Wook KIM
Author Information
1. Department of Oral and Maxillofacial Surgery, College of Dentistry, Dankook University, Korea. kkwoms@dku.edu
- Publication Type:Original Article
- Keywords:
Microvascular anastomosis;
Vein;
Regeneration
- MeSH:
Blood Cells;
Collagen;
Connective Tissue;
Endothelial Cells;
Femoral Vein*;
Fibrin;
Fibroblasts;
Free Tissue Flaps;
Giant Cells, Foreign-Body;
Granulation Tissue;
Heparin;
Microscopy, Electron, Scanning;
Muscle, Smooth;
Myocytes, Smooth Muscle;
Regeneration*;
Silk;
Spasm;
Sutures;
Thrombosis;
Vascular Patency;
Veins*
- From:Journal of the Korean Association of Oral and Maxillofacial Surgeons
2007;33(4):340-349
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Free flap transplantation with microvascular anastomosis has been successfully performed by development of surgical technique, materials and postoperative monitoring equipments of flap. But success rate of microvascular anastomosis is influenced by various factors, and failure rate is about 5-10%. The most influential factor for success rate is surgical technique and other factors that influence failure of microvascular anastomosis are ischemic time of free flap, thrombus formation of anastomosis region and vascular spasm. In this study, vascular patency and thrombus formation in experimental micro-venous anastomosis, and endothelial repair were observed with histologic analysis, scanning electron microscopy, transmission electron microscopic examination. The results were obtained as follows: 1. In vascular patency test in 30 minute and 7 days after micro-venous anastomosis with heparin irrigation, all of 12 anastomosis site were good vascular patency. 2. In thrombus formation in 2 weeks group(Experimental I), 2 site of 6 cases were observed thrombus, and in 4 weeks group(Experimental II), 1 site of 6 cases were observed thrombus. 3. In histologic examination, normal vein(Control Group) showed continued internal elastic lamina, well formed thick smooth muscle layer and connective tissue. The group of 2 weeks after microvenous anastomosis(Experimental I) showd locally recovered internal lamina, discontinued internal lamina, disorganized smooth muscle cells and granulation tissue around suture silk. In the group of 4 weeks after micro-venous anastomosis(Experimental II), anastomosis site showed almostly continued internal lamina, disorganized smooth muscle cells and cicartrized tissue around suture silk. 4. In scanning electron microscope examination in 2 weeks(Experimental I) after micro-venous anastomosis, mesh fibrin formation showed near to endothelial cells, and in 4 weeks after micro-venous anastomosis(EXperimental II), numerous blood cells and fibrin mesh formation was seen associated with irregular endothelial cell arrangement. 5. In transmission electron microscope examination in 2 weeks after micro-venous anastomosis(Experimental I), irregular arrangement of smooth muscle cells was seen adjacent to collagenized tissue around suture silk. In 4 weeks after micro-venous anastomosis(Experimental II), denuded venous wall composed of relatively well arranged smooth muscle cells was covered by endothelial cells, but fibroblast cells and foreign body giant cells near to suture silk was remained. From the results obtained in this study, results of good vascular patiency and anti-thrombotic effect of heparin were obtained as a local irrigation solution, and repair of venous endothelial cell was observed in 2 weeks after micro-venous anastomosis.
