Assessing Peri-Implant Tissue Infection Prevention in a Percutaneous Model

被引:14
作者
Perry, Emily L. [1 ,2 ]
Beck, J. Peter [1 ,3 ]
Williams, Dustin L. [1 ,2 ,4 ]
Bloebaum, Roy D. [1 ,2 ,3 ]
机构
[1] Vet Affairs Hlth Care Syst, Bone & Joint Res Lab, Salt Lake City, UT USA
[2] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
[3] Univ Utah, Dept Orthopaed, Salt Lake City, UT 84112 USA
[4] ARUP Inst Clin & Expt Pathol, ARUP Labs, Salt Lake City, UT USA
关键词
osseointegration; percutaneous; infection; antimicrobial; Ceragenins (TM); STEROID ANTIBIOTICS; PROSTHESES; PEPTIDE; REHABILITATION; EXPERIENCE; AMPUTATION;
D O I
10.1002/jbm.b.31528
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Background: Infection remains the main challenge to percutaneous, intramedullary osseointegrated implant technology. The purpose of this investigation was to determine if a broad spectrum antimicrobial, Ceragenin (TM) (CSA-13) could prevent pin track infections in a percutaneous tibial pin site in a sheep model. Methods: In 20 sheep, a smooth titanium alloy pin/implant was inserted percutaneously through the medial skin and both cortices of the proximal tibia. In 10 sheep, the pin/skin interface was treated with a CSA-13-embedded foam pad. Ten sheep served as controls receiving an untreated pad. At the end of 24 weeks, or if they presented with clinical signs of infection, the animals were euthanized. Histological stains were processed from soft tissue and bone, and bacterial cultures were taken from tissue, bone, and blood. In addition to clinical signs, sheep were considered infected if at least one tissue culture and/or histologically stained sample was positive. Results: Compared with the controls, CSA-13 did not prevent pin track infection (p = 0.88). Large gaps around the pin indicated a lack of skin-pin adhesion. Conclusions: In this application, CSA-13 was not effective in preventing pin track infections. This study suggests that maintaining skin attachment, at the implant surface of osseointegrated implants, is essential as a primary barrier to infection. Local antimicrobial treatments should be considered a secondary barrier to bacterial invasion of the pin/skin interface and deeper tissues. (C) 2009 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 92B: 397-408, 2010
引用
收藏
页码:397 / 408
页数:12
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