Department of Orthopaedics, University of Utah, Salt Lake City, Utah.
Division of Infectious Diseases, Department of Internal Medicine, University of Utah, Salt Lake City, Utah.
J Arthroplasty. 2018 Jan;33(1):211-215. doi: 10.1016/j.arth.2017.08.017. Epub 2017 Aug 24.
Despite recommendations against the use of splash basins, due to the potential of bacterial contamination, our observation has been that they continue to be used in operating theaters. In hopes of decontaminating the splash basin, we sought to determine if the addition of chlorhexidine gluconate (CHG) would eliminate aerobic bacterial growth within the splash basin.
After Institutional Review Board approval, we began enrollment in a randomized controlled trial comparing 2 splash basin solutions. Splash basins (n = 111) were randomized to either the standard of care (control) solution of sterile water or the experimental solution containing 0.05% CHG. One 20 mL aliquot was taken from the basin at the end of the surgical case and delivered to an independent laboratory. Samples were plated on tryptic soy agar (medium) and incubated at 30°C-35°C to encourage growth. After 48-72 hours, the agar plates were examined for growth and a standard plate count of aerobic cultures was performed.
The sterile water group was found to have bacterial growth in 9% of samples compared to no growth in the CHG group (P = .045). The organisms included Micrococcus luteus, Staphylococcus hominis, Gram-variable coccobacilli, and unidentifiable Gram-positive rods.
Given the safety and efficacy of a concentration of 0.05% CHG in reducing the bacterial contamination in the operative splash basin, it would seem that if the practice of using a splash basin in the operating theater is to be continued, the addition of an antiseptic solution such as that studied here should be considered.
尽管有建议反对使用溅水盘,因为存在细菌污染的潜在风险,但我们观察到溅水盘仍在手术室中使用。为了消毒溅水盘,我们试图确定添加葡萄糖酸氯己定(CHG)是否会消除溅水盘中的需氧细菌生长。
在机构审查委员会批准后,我们开始进行一项随机对照试验,比较两种溅水盘溶液。将溅水盘(n=111)随机分为标准护理(对照)溶液的无菌水或含有 0.05%CHG 的实验溶液。在手术结束时从盆中取出 20 毫升等分试样,并送到独立实验室。将样品接种于胰蛋白酶大豆琼脂(培养基)上,并在 30°C-35°C 下孵育以促进生长。48-72 小时后,检查琼脂平板是否有生长,并进行需氧培养的标准平板计数。
与 CHG 组无生长相比,无菌水组发现 9%的样本中有细菌生长(P=0.045)。分离出的微生物包括藤黄微球菌、人葡萄球菌、革兰氏可变球菌和无法识别的革兰氏阳性杆菌。
鉴于 0.05%CHG 浓度在减少手术溅水盘中细菌污染方面的安全性和有效性,如果要继续在手术室中使用溅水盘,则应考虑添加抗菌溶液,如本研究中所研究的溶液。