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因压力监测设备受污染导致重症监护病房爆发液化沙雷氏菌感染。

Critical care unit outbreak of Serratia liquefaciens from contaminated pressure monitoring equipment.

作者信息

Harnett S J, Allen K D, Macmillan R R

机构信息

Departments of Microbiology, St Helens and Knowsley NHS Trust, Whiston Hospital, Prescot, Merseyside L35 5DR, UK.

出版信息

J Hosp Infect. 2001 Apr;47(4):301-7. doi: 10.1053/jhin.2001.0941.

Abstract

Between October and December 1999, Serratia liquefaciens was isolated from 11 patients in an adult critical care unit. One patient was infected on two separate occasions. In total, there were 10 positive blood cultures and five positive intravascular catheter tips. Eight cases were clinically infected, three were possibly infected and one was not. All patients with clinical isolates received appropriate empirical antibiotic treatment and responded well. Environmental investigation revealed S. liquefaciens in syringes and connector tubing used to calibrate the intravascular line pressure monitoring equipment of eight patients. Three of these patients also had clinical isolates of S. liquefaciens. Analysis by pulsed-field gel electrophoresis found clinical and environmental isolates to be of the same strain. The most likely mode of transmission was a non-sterile sphygmomanometer tip used daily for calibration. Inadequate microbiological sampling methods may have limited detection of S. liquefaciens. Several other examples of poor infection control techniques were identified during the outbreak, notably lapses in hand hygiene during intravascular pressure monitoring. It was also observed that unlabelled multidose heparin and insulin vials were shared between patients and personal hand creams were used by staff. However, these were not directly implicated in the outbreak. The outbreak ended when poor infection control practices were corrected. Calibration syringes and connector tubing were discarded after a single use. The sphygmomanometer was replaced by a pneumatic pressure transducer tester with connector tube and the frequency of calibration reduced to a single test following line insertion only. The non-disposable tube was disinfected with alcohol wipes between patients.

摘要

1999年10月至12月期间,在一家成人重症监护病房中,从11名患者身上分离出了液化沙雷氏菌。有一名患者在两个不同的时间点受到感染。总共进行了10次血培养呈阳性,5次血管内导管尖端培养呈阳性。8例为临床感染,3例可能感染,1例未感染。所有临床分离出该菌的患者均接受了适当的经验性抗生素治疗,且反应良好。环境调查发现,在用于校准8名患者血管内压力监测设备的注射器和连接管中存在液化沙雷氏菌。其中3名患者的临床分离株也为液化沙雷氏菌。脉冲场凝胶电泳分析发现,临床分离株和环境分离株属于同一菌株。最可能的传播途径是每天用于校准的血压计探头未消毒。微生物采样方法不当可能限制了对液化沙雷氏菌的检测。在此次疫情期间还发现了其他一些感染控制技术不佳的例子,尤其是在进行血管内压力监测时手部卫生的疏忽。还观察到患者之间共用未贴标签的多剂量肝素和胰岛素瓶,工作人员使用个人护手霜。然而,这些与疫情没有直接关联。当纠正了不良的感染控制措施后,疫情结束。校准注射器和连接管一次性使用后即丢弃。血压计被带有连接管的气动压力传感器测试仪取代,校准频率降低至仅在血管导管插入后进行一次测试。在不同患者之间使用酒精擦拭对非一次性管道进行消毒。

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