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抗感染血管假体的研发。

Development of an infection-resistant vascular prosthesis.

作者信息

Moore W S, Chvapil M, Seiffert G, Keown K

出版信息

Arch Surg. 1981 Nov;116(11):1403-7. doi: 10.1001/archsurg.1981.01380230027004.

Abstract

To develop an infection-resistant arterial prosthesis, amikacin was bonded to 6-mm, uncrimped, filamentous velour prostheses using a collagen-release system. Infrarenal abdominal aortas were resected in 26 mongrel dogs. Thirteen dogs had their aortas replaced with the antibiotic-bonded grafts and 13 dogs had their aortas replaced with a graft containing collagen without antibiotics. Following closure of the abdominal incision, each dog received an intravenous infusion of 10(8) organisms of Staphylococcus aureus administered over a 30-minute interval. Three weeks after recovery from operation, the grafts were removed under aseptic conditions; all 13 (100%) of the control grafts were infected, but only one of 12 experimental grafts (8%) was infected. There were no adverse healing effects; to the contrary, there appeared to be accelerated development of a cellular neointima and fibroblastic infiltration to the interstices. Antibiotic bonding with a collagen-release system is a promising method for imparting infection resistance to a vascular prosthesis.

摘要

为开发一种抗感染的动脉假体,使用胶原蛋白释放系统将阿米卡星结合到6毫米、未卷曲的丝状绒面假体上。在26只杂种犬中切除肾下腹主动脉。13只犬的主动脉被抗生素结合移植物替代,13只犬的主动脉被含胶原蛋白但不含抗生素的移植物替代。腹部切口闭合后,每只犬在30分钟内静脉输注10⁸个金黄色葡萄球菌。术后恢复三周后,在无菌条件下取出移植物;所有13个(100%)对照移植物均被感染,但12个实验移植物中只有1个(8%)被感染。没有不良愈合影响;相反,似乎有细胞性新生内膜加速形成和成纤维细胞向间隙浸润。用胶原蛋白释放系统进行抗生素结合是赋予血管假体抗感染能力的一种有前景的方法。

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