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首页> 外文期刊>The New England journal of medicine >Pseudomonas aeruginosa and Serratia marcescens contamination associated with a manufacturing defect in bronchoscopes.
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Pseudomonas aeruginosa and Serratia marcescens contamination associated with a manufacturing defect in bronchoscopes.

机译:铜绿假单胞菌和粘质沙雷氏菌污染与支气管镜制造缺陷有关。

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BACKGROUND: Several outbreaks and pseudo-outbreaks of Pseudomonas aeruginosa and Serratia marcescens infections associated with bronchoscopy have been reported. We conducted an investigation of P. aeruginosa and S. marcescens isolates related to bronchoscopy at a community hospital. METHODS: We reviewed the records of all bronchoscopic procedures at the community hospital from July to October 2001. Environmental samples were obtained. Pulsed-field gel electrophoresis (PFGE) was performed on isolates of P. aeruginosa. RESULTS: From July 1 to October 31, 2001, 66 bronchoscopic procedures were performed in 60 patients, and 43 specimens were obtained for bacterial culture; 20 of the specimens (47 percent) were positive for P. aeruginosa. Six (30 percent) of the specimens that were positive for P. aeruginosa also yielded S. marcescens. All 20 P. aeruginosa isolates were associated with procedures performed with three of four new bronchoscopes from the same manufacturer. Contrary to manufacturing specifications, the biopsy-port caps on all four bronchoscopes were easily removable, and P. aeruginosa was cultured from the biopsy ports of the three implicated bronchoscopes. The PFGE patterns of P. aeruginosa isolates from the bronchoscopes, patients, and two environmental samples were indistinguishable. One patient was hospitalized with P. aeruginosa pneumonia 11 days after bronchoscopy. The manufacturer reported a design change instituted in 1997, and production problems may have resulted in the distribution of bronchoscopes that did not meet specifications. CONCLUSIONS: We documented contamination of bronchoscopes with P. aeruginosa and S. marcescens and possible infection of patients at a community hospital as a result of the inadequate disinfection of bronchoscopes because of a manufacturing defect.
机译:背景:已经报道了与支气管镜检查相关的铜绿假单胞菌和粘质沙雷氏菌感染的几次暴发和假暴发。我们在社区医院对与支气管镜检查有关的铜绿假单胞菌和marcescens分离株进行了调查。方法:我们回顾了2001年7月至2001年10月社区医院所有支气管镜检查程序的记录。获得了环境样本。对铜绿假单胞菌的分离物进行脉冲场凝胶电泳(PFGE)。结果:2001年7月1日至10月31日,对60例患者进行了66次支气管镜检查,并采集了43个标本进行细菌培养。标本中有20个(占47%)为铜绿假单胞菌阳性。铜绿假单胞菌阳性的标本中有六个(30%)也产生了粘菌链球菌。所有20株铜绿假单胞菌的分离株均与同一制造商的4台新支气管镜中的3台进行了相关操作。与制造规格相反,所有四个支气管镜上的活检口盖都可以轻松拆卸,并且从三个牵连的支气管镜的活检口培养铜绿假单胞菌。从支气管镜,患者和两个环境样品中分离出的铜绿假单胞菌的PFGE模式无法区分。支气管镜检查后11天,一名患者因铜绿假单胞菌肺炎住院。制造商报告了1997年进行的设计更改,并且生产问题可能导致分销不符合规格的支气管镜。结论:我们记录了由于制造缺陷导致支气管镜消毒不足,铜绿假单胞菌和粘液链球菌污染了支气管镜,并且在社区医院感染了患者。

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