Carbonell A M, Matthews B D, Dréau D, Foster M, Austin C E, Kercher K W, Sing R F, Heniford B T
Department of General Surgery, Carolinas Medical Center, 1000 Blythe Boulevard, MEB #601, Charlotte, NC 28203, USA.
Surg Endosc. 2005 Mar;19(3):430-5. doi: 10.1007/s00464-004-8810-4. Epub 2004 Dec 9.
Despite the use of a sterile technique and the administration of prophylactic antibiotics during surgical procedures, mesh infection continues to complicate the use of biomaterials. The purpose of this study was to compare the susceptibility to infection of prosthetic biomaterials in a live-animal model.
The following seven prosthetic mesh biomaterials were used in this study. Expanded polytetrafluoroethylene (ePTFE) with silver/chlorhexidine (DM+), ePTFE (DM), porcine intestinal submucosa (S), polypropylene (M), ePTFE/polypropylene (X), hyaluronate/carboxymethylcellulose/polypropylene (SM), and human acellular dermal matrix (A). Lewis rats (n = 108) underwent creation of a single ventral hernia; 105 of them were repaired with a different mesh (2-cm2 piece). Twelve pieces of each mesh were inoculated at the time of hernia repair with 10(8) Staphylococcus aureus (n = 84). Three pieces of each mesh were placed without bacterial inoculation (n = 21). In three animals, no mesh was placed; instead, the peritoneum of the hernia defect was inoculated (n = 3). After 5 days, the animals were killed and the mesh was explanted (peritoneum for the nonmesh control). The mesh was vortex-washed and incubated in tryptic soy broth. Bacterial counts were determined using serial dilutions and spot plates and quantified in colony-forming units (CFU) per square centimeter of mesh present in the vortex wash fluid (wash count) and the soy broth (broth count). Data are presented as the mean log(10), with analysis of variance (ANOVA) and Tukey's test used to determine significance (p < 0.05).
The DM+ material had no detectable live bacteria in the wash or broth counts in 10 of 12 tested samples (p = 0.05). Of the samples that showed bacterial growth, the peritoneum control group had a lower wash count than A (p = 0.05) and the lowest broth count of all the materials except for DM+ (p = 0.05). In addition, SM had a significantly lower wash count than A (p = 0.05), with no broth count difference. In regard to wash and broth counts, DM, M, X, SM, S, and A were no different (p = NS).
The DM+ material was the least susceptible to infection. Impregnation with silver/chlorhexidine killed the inoculated bacteria, preventing their proliferation on the mesh surface. Other than DM+, native peritoneal tissue appears to be the least susceptible to infection. Silver/chlorhexidine appears to be an effective bactericidal agent for use with mesh biomaterials.
尽管在外科手术过程中采用了无菌技术并使用了预防性抗生素,但网片感染仍然是生物材料使用中的一个复杂问题。本研究的目的是在活体动物模型中比较人工生物材料对感染的易感性。
本研究使用了以下七种人工网片生物材料。含银/氯己定的膨体聚四氟乙烯(ePTFE)(DM+)、ePTFE(DM)、猪小肠黏膜下层(S)、聚丙烯(M)、ePTFE/聚丙烯(X)、透明质酸盐/羧甲基纤维素/聚丙烯(SM)和人脱细胞真皮基质(A)。108只Lewis大鼠接受了单个腹疝造模;其中105只用不同的网片(2平方厘米大小)进行修复。在疝修补时,每种网片的12片接种10⁸金黄色葡萄球菌(n = 84)。每种网片的3片不接种细菌(n = 21)。在三只动物中,不放置网片,而是对疝缺损的腹膜进行接种(n = 3)。5天后,处死动物并取出网片(未放置网片的对照组取腹膜)。将网片进行涡旋冲洗并在胰蛋白胨大豆肉汤中孵育。使用系列稀释和平板计数法测定细菌数量,并以每平方厘米网片在涡旋冲洗液(冲洗计数)和大豆肉汤(肉汤计数)中的菌落形成单位(CFU)进行量化。数据以平均log(10)表示,采用方差分析(ANOVA)和Tukey检验确定显著性(p < 0.05)。
在12个测试样本中的10个样本中,DM+材料在冲洗计数或肉汤计数中未检测到活菌(p = 0.05)。在显示细菌生长的样本中,腹膜对照组的冲洗计数低于A组(p = 0.05),且在除DM+之外的所有材料中肉汤计数最低(p = 0.05)。此外,SM的冲洗计数显著低于A组(p = 0.05),肉汤计数无差异。关于冲洗计数和肉汤计数,DM、M、X、SM、S和A之间无差异(p =无显著性差异)。
DM+材料对感染的易感性最低。用银/氯己定浸渍可杀死接种的细菌,防止其在网片表面增殖。除DM+外,天然腹膜组织似乎对感染的易感性最低。银/氯己定似乎是一种用于网片生物材料的有效杀菌剂。