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美罗培南等碳青霉烯类药物对重症监护病房分离的重要临床细菌的体外活性:来自 SMART 计划的全国范围数据。

In vitro activities of doripenem and other carbapenems against clinically important bacteria isolated in intensive care units: nationwide data from the SMART Programme.

机构信息

Department of Intensive Care Units, Min-Sheng General Hospital, Taoyuan County, Taiwan.

出版信息

Eur J Clin Microbiol Infect Dis. 2010 Apr;29(4):471-5. doi: 10.1007/s10096-009-0866-6. Epub 2010 Jan 27.

DOI:10.1007/s10096-009-0866-6
PMID:20108018
Abstract

This nationwide surveillance of clinically important bacteria from the intensive care units (ICUs) of major teaching hospitals throughout Taiwan investigated the susceptibilities to doripenem and other comparator carbapenems from September through November 2005. Minimum inhibitory concentrations (MICs) were determined for 1,311 clinical isolates using the broth microdilution method according to Clinical and Laboratory Standards Institute (CLSI) 2005 guidelines. Doripenem showed similar (within four-fold difference of MICs) in vitro activity to meropenem for Enterobacteriaceae and probably comparable activity to meropenem against important nosocomial non-fermentative Gram-negative bacilli (NFGNBs), including Pseudomonas aeruginosa, Acinetobacter baumannii and Burkholderia cepacia. Among the four carbapenems analysed, doripenem and meropenem exhibited better in vitro activity than imipenem or ertapenem against extended-spectrum beta-lactamase (ESBL)-producing Klebsiella pneumoniae and Escherichia coli isolates. However, the meropenem MIC(90) against ESBL-producing K. pneumoniae isolates was 2 microg/ml. Besides, doripenem with the MIC(90) of 0.5 microg/ml to Streptococcus pneumoniae possibly suggested its potential therapeutic effect regarding community-acquired pneumonia. Because of the heavy resistance burden in Taiwan, closely monitoring the evolutionary trend of carbapenem susceptibilities against clinically important pathogens is crucial in the future.

摘要

本项全国性监测研究调查了 2005 年 9 月至 11 月期间台湾主要教学医院重症监护病房(ICU)中临床重要细菌对多利培南和其他比较碳青霉烯类药物的敏感性。采用肉汤微量稀释法,根据临床和实验室标准协会(CLSI)2005 年指南,对 1311 株临床分离株进行了最低抑菌浓度(MIC)测定。对于肠杆菌科细菌,多利培南与美罗培南的体外活性相似(MIC 相差不超过 4 倍),可能与美罗培南对重要医院获得性非发酵革兰阴性杆菌(NFGNB)的活性相当,包括铜绿假单胞菌、鲍曼不动杆菌和洋葱伯克霍尔德菌。在分析的 4 种碳青霉烯类药物中,多利培南和美罗培南对产超广谱β-内酰胺酶(ESBL)的肺炎克雷伯菌和大肠埃希菌的体外活性优于亚胺培南或厄他培南。然而,产 ESBL 的肺炎克雷伯菌对美罗培南的 MIC90 为 2μg/ml。此外,多利培南对肺炎链球菌的 MIC90 为 0.5μg/ml,这可能表明其对社区获得性肺炎具有潜在的治疗效果。由于台湾的耐药负担较重,因此密切监测碳青霉烯类药物对临床重要病原体敏感性的演变趋势至关重要。

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