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Targeted Molecular Detection of Nosocomial Carbapenemase-Producing Gram-Negative Bacteria—On Near- and Distant-Patient Surfaces

机译:针对近距离患者表面的医院碳碱酶产生革兰氏阴性细菌的靶向分子检测

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摘要

Background: Here, we describe an integrative method to detect carbapenemase-producing Gram-negative bacteria (gn-Cp) on surfaces/fomites in the patient environment. We examined environmental samples from 28 patient rooms occupied with patients who were proven to be colonised with gn-Cp by rectal screening. Methods: We took samples after 24 h, 72 h and one week. For sampling, we divided the patient environment into four parts and took samples from near- and extended patient areas. To obtain a representative bacterial swab from a larger surface, such as the patient cabinet, we used Polywipes. Bacterial DNA was isolated. Carbapenemase was detected with specific qPCR primers. Results: With this culture- and molecular-based approach, we could control the effectiveness of cleaning and disinfection in everyday clinical practice. Therefore, we could track the spread of gn-Cp within the patient room. The number of positive detections fluctuated between 30.5% (mean value positive results after 72 h) and 35.2% (after 24 h and one week). Conclusion: The method used to detect multidrug-resistant bacteria in the environment of patients by using PolywipesTM is reliable and can therefore be used as an effective, new tool in hygiene and infection control.
机译:背景:在此,我们描述了一种在患者环境中探测碳碱酶产生克毒素的克毒革兰阴性细菌(GN-CP)的一致性方法。我们通过直肠筛选将被证明与GN-CP的患者占用的患者占用的28名患者的环境样本进行了检查。方法:我们在24小时,72小时和一周后进行了样品。对于抽样,我们将患者环境划分为四个部分,并从附近和延伸的患者区域采用样品。为了获得来自较大表面的代表性细菌拭子,例如患者柜,我们使用了Polywipes。分离细菌DNA。用特异性QPCR引物检测碳碱酶。结果:通过这种文化和基于分子的方法,我们可以控制日常临床实践中的清洁和消毒的有效性。因此,我们可以跟踪患者室内GN-CP的传播。阳性检测的数量波动在30.5%(平均值阳性结果后72小时后)和35.2%(24小时后)。结论:用于检测患者环境中的多药抗性细菌的方法可靠,因此可以用作卫生和感染控制的有效新工具。

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