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全球扩展型碳青霉烯酶肺炎克雷伯菌的临床流行病学。

Clinical epidemiology of the global expansion of Klebsiella pneumoniae carbapenemases.

机构信息

Department of Medicine, Department of Public Health Sciences, University of Miami Miller School of Medicine, Miami, FL 33136, USA.

出版信息

Lancet Infect Dis. 2013 Sep;13(9):785-96. doi: 10.1016/S1473-3099(13)70190-7.

Abstract

Klebsiella pneumoniae carbapenemases (KPCs) were originally identified in the USA in 1996. Since then, these versatile β-lactamases have spread internationally among Gram-negative bacteria, especially K pneumoniae, although their precise epidemiology is diverse across countries and regions. The mortality described among patients infected with organisms positive for KPC is high, perhaps as a result of the limited antibiotic options remaining (often colistin, tigecycline, or aminoglycosides). Triple drug combinations using colistin, tigecycline, and imipenem have recently been associated with improved survival among patients with bacteraemia. In this Review, we summarise the epidemiology of KPCs across continents, and discuss issues around detection, present antibiotic options and those in development, treatment outcome and mortality, and infection control. In view of the limitations of present treatments and the paucity of new drugs in the pipeline, infection control must be our primary defence for now.

摘要

产碳青霉烯酶肺炎克雷伯菌(KPCs)于 1996 年最初在美国被发现。自此,这些多功能β-内酰胺酶在国际范围内在革兰氏阴性菌中传播,尤其是肺炎克雷伯菌,尽管它们在不同国家和地区的确切流行情况有所不同。感染产 KPC 生物体的患者的死亡率很高,这可能是由于剩余的抗生素选择有限(通常是粘菌素、替加环素或氨基糖苷类)。最近,使用粘菌素、替加环素和亚胺培南的三联药物组合与血培养阳性患者的生存率提高有关。在这篇综述中,我们总结了跨大陆的 KPC 流行病学,并讨论了检测、现有抗生素选择和正在开发的抗生素选择、治疗结果和死亡率以及感染控制方面的问题。鉴于目前治疗方法的局限性和新药物的匮乏,感染控制必须是我们目前的首要防御措施。

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