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A Prospective, Randomized Comparison of Duodenoscope Reprocessing Surveillance Methods

机译:一种预热监测方法的预期,随机比较

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Duodenoscope use in healthcare facilities has been associated with transmission of multidrug resistant pathogens between patients. To assist healthcare facilities in monitoring the quality of their duodenoscope reprocessing procedures and limit patient risk of infection, the Centers for Disease Control and Prevention (CDC) deployed voluntary interim duodenoscope sampling and culturing surveillance protocols in 2015. Though the interim methods were widely adopted, alternative surveillance protocols were developed and implemented at individual institutions. Here, we compared two sampling methods—the 2015 CDC interim protocol and an alternative protocol developed by the University of Wisconsin Hospitals and Clinics (UWHC). We hypothesized that the UWHC protocol would detect a higher incidence of bacterial contamination from reprocessed duodenoscopes. A total of 248 sampling events were performed at UWHC. The CDC protocol (n?=?129 sampling events) required culturing samples collected from each duodenoscope after brushing its terminal end and flushing its lumen with sterile water. The UWHC protocol (n?=?119 sampling events) required culturing samples collected from each duodenoscope after swabbing its elevator, immersing its terminal end into broth and flushing its lumen with saline. With the CDC method, 8.53% (n?=?11) of the duodenoscopes sampled were positive for bacterial growth with 15 isolates recovered. Using the UWHC method, 15.13% (n?=?18) of cultures were positive for bacterial growth with 20 isolates recovered. The relative risk of identifying a contaminated duodenoscope using the CDC interim method, however, was not different than when using the UWHC protocol. Mean processing time (27.35 and 5.11 minutes, p0.001) and total cost per sample event ($17.87 and $15.04) were lower using the UWHC method. As the UWHC protocol provides similar detection rates as the CDC protocol, the UWHC method is useful, provided the shorter processing time and lower cost to perform.
机译:DuodenoScope在医疗保健设施中使用与患者之间的多药抗性病原体的传输有关。协助医疗保健设施监测他们的多剂量检验的质量,并限制患者感染风险,疾病控制和预防中心(CDC)在2015年部署了自愿临时非翻译镜抽样和培养监测议定书。虽然临时方法被广泛采用,替代监督议定书在个人机构开发和实施。在这里,我们比较了两种采样方法 - 2015年CDC临时协议和由威斯康星大学医院和诊所(UWHC)开发的替代方案。我们假设UWHC协议将检测从再加工的十二指肠镜检查的细菌污染的较高发病率。在UWHC中共进行了248个采样事件。 CDC协议(N?= 129采样事件)在刷涂其终端并用无菌水冲洗其内腔并冲洗其内腔后,从每种剂量腔腔腔腔中收集的培养样品。 UWHC协议(n?= 119采样事件)在擦拭其电梯后,从每种剂型镜中收集的培养样品,将其末端浸入肉汤中并用盐水冲洗其内腔。随着CDC方法,取样的8.53%(n?=β11)对细菌生长有阳性,其中15分离物回收。使用UWHC方法,15.13%(N?= 18)培养物对于细菌生长阳性,其中20分离株回收。然而,使用CDC临时方法识别受污染的非引入镜的相对风险与使用UWHC协议时不差异。使用UWHC方法,平均处理时间(27.35和5.11分钟,P <0.001)和每种样品事件的总成本(17.87美元和15.04美元)。由于UWHC协议提供类似的检测速率作为CDC协议,因此UWHC方法是有用的,提供了更短的处理时间和更低的成本。

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