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控制产碳青霉烯酶革兰氏阴性菌的传播:治疗方法和感染控制。

Controlling the spread of carbapenemase-producing Gram-negatives: therapeutic approach and infection control.

机构信息

Division of Epidemiology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

出版信息

Clin Microbiol Infect. 2010 Feb;16(2):102-11. doi: 10.1111/j.1469-0691.2009.03115.x.

Abstract

Although the rapid spread of carbapenemase-producing Gram-negatives (CPGNs) is providing the scientific community with a great deal of information about the molecular epidemiology of these enzymes and their genetic background, data on how to treat multidrug-resistant or extended drug-resistant carbapenemase-producing Enterobacteriaceae and how to contain their spread are still surprisingly limited, in spite of the rapidly increasing prevalence of these organisms and of their isolation from patients suffering from life-threatening infections. Limited clinical experience and several in vitro synergy studies seem to support the view that antibiotic combinations should be preferred to monotherapies. But, in light of the data available to date, it is currently impossible to quantify the real advantage of drug combinations in the treatment of these infections. Comprehensive clinical studies of the main therapeutic options, broken down by pathogen, enzyme and clinical syndrome, are definitely lacking and, as carbapenemases keep spreading, are urgently needed. This spread is unveiling the substantial unpreparedness of European public health structures to face this worrisome emergency, although experiences from different countries-chiefly Greece and Israel-have shown that CPGN transmission and cross-infection can cause a substantial threat to the healthcare system. This unpreparedness also affects the treatment of individual patients and infection control policies, with dramatic scarcities of both therapeutic options and infection control measures. Although correct implementation of such measures is presumably cumbersome and expensive, the huge clinical and public health problems related to CPGN transmission, alongside the current scarcity of therapeutic options, seem to fully justify this choice.

摘要

尽管产碳青霉烯酶的革兰氏阴性菌(CPGNs)的快速传播为科学界提供了大量有关这些酶的分子流行病学及其遗传背景的信息,但关于如何治疗多药耐药或广泛耐药的产碳青霉烯酶肠杆菌科以及如何控制其传播的数据仍然令人惊讶地有限,尽管这些生物体的流行率和从患有危及生命的感染的患者中分离出来的速度都在迅速增加。有限的临床经验和几项体外协同研究似乎支持这样一种观点,即抗生素联合应用应该优于单药治疗。但是,鉴于迄今为止可用的数据,目前无法量化这些感染的联合用药治疗的实际优势。按病原体、酶和临床综合征对主要治疗选择进行全面的临床研究,目前显然缺乏这种研究,而且随着碳青霉烯酶的不断传播,这种研究非常紧迫。这种传播揭示了欧洲公共卫生结构在应对这种令人担忧的紧急情况方面的实质性准备不足,尽管来自不同国家(主要是希腊和以色列)的经验表明,CPGN 的传播和交叉感染可能对医疗保健系统造成重大威胁。这种准备不足还影响了个体患者的治疗和感染控制政策,治疗选择和感染控制措施都严重短缺。尽管此类措施的正确实施可能很麻烦且昂贵,但与 CPGN 传播相关的巨大临床和公共卫生问题以及目前治疗选择的匮乏似乎完全证明了这一选择的合理性。

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