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首页> 外文期刊>Journal of Clinical Microbiology >Use of Ancillary Carbapenemase Tests To Improve Specificity of Phenotypic Definitions for Carbapenemase-Producing Enterobacteriaceae
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Use of Ancillary Carbapenemase Tests To Improve Specificity of Phenotypic Definitions for Carbapenemase-Producing Enterobacteriaceae

机译:使用辅助碳青霉烯酶测试以提高生产碳青霉烯酶的肠杆菌科的表型定义的特异性

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Carbapenem-resistant Enterobacteriaceae (CRE), particularly those that are resistant due to carbapenemase production, are a significant threat to public health. Infections caused by CRE are associated with a high attributable mortality (1), and U.S. surveillance data have demonstrated a steady increase in the burden of disease caused by CRE since 2000 (2). The U.S. CRE epidemic is driven, in part, by Klebsiella pneumoniae isolates of sequence type (ST) 258 that express the K. pneumoniae carbapenemase (KPC) (3). Transfer of patients colonized or infected with this organism between health care institutions is thought to have led to the dissemination of ST 258 K. pneumoniae across the country. One particularly well documented outbreak described by the Centers for Disease Control and Prevention Epicenter Program demonstrated that patient transfers between 26 health care facilities across four counties lead to the spread of KPC-producing CRE to 40 patients over a 1-year period (4). Subsequent studies in this region documented that nearly 1 in 3 residents of long-term acute care facilities were colonized with KPC-producing CRE (5). CRE harboring other carbapenem-hydrolyzing enzymes, such as NDM, VIM, IMP, or the OXA-48 type, common in other areas of the world (6), are also spreading in the United States (7–9). The introduction of isolates expressing these carbapenemases to a single institution by a patient traveling from an area of endemicity can lead to rapid spread, as occurred in our own institution when an OXA-232-producing K. pneumoniae strain was introduced to our facility by a colonized patient, leading to transmission of CRE to 14 patients via reprocessed duodenoscopes (10). A similar outbreak, caused by an NDM-producing K. pneumoniae strain in the Chicago area, was also recently documented as associated with the use of reprocessed duodenoscopes (11). In both outbreaks, rapid recognition of an unusual CRE type led to the epidemiological investigations that ultimately identified the source of the outbreak.
机译:耐碳青霉烯的肠杆菌科(CRE),特别是那些因产生碳青霉烯酶而具有耐药性的肠杆菌,对公众健康构成重大威胁。由CRE引起的感染与高归因死亡率相关(1),美国监测数据表明自2000年以来由CRE引起的疾病负担稳步增加(2)。美国CRE流行病部分是由表达肺炎克雷伯菌碳青霉烯酶(KPC)的序列类型(ST)258的肺炎克雷伯菌分离株驱动的(3)。据认为,在医疗机构之间转移了定植或感染了这种生物的患者,这导致了ST 258肺炎克雷伯菌在全国的传播。疾病控制和预防中心震中中心计划描述的一个特别有据可查的暴发表明,在四个县的26个医疗机构之间进行患者转移,导致生产KPC的CRE在1年内扩散到40名患者(4)。随后在该地区进行的研究表明,长期护理机构中有近三分之一的居民被生产KPC的CRE所定植(5)。带有其他碳青霉烯水解酶的CRE在世界其他地区也很普遍(NDM,VIM,IMP或OXA-48型)(6),也在美国(7-9)扩散。从地方病地区来的患者将表达这些碳青霉烯酶的分离株引入单个机构会导致快速传播,就像在我们自己的机构中,当由OXA-232产生的肺炎克雷伯菌菌株引入我们的机构时一样。定植的患者,通过再处理十二指肠镜将CRE传播给14位患者(10)。最近也记录了由芝加哥地区NDM产生的肺炎克雷伯菌(K.pneumoniae)菌株引起的类似暴发,与使用再处理十二指肠镜有关(11)。在这两次暴发中,对一种异常CRE类型的快速识别导致了流行病学调查,最终确定了暴发源。

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