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从美国医疗中心分离出的革兰氏阳性菌的抗菌药敏性:达托霉素监测项目(2007 - 2008年)的结果

Antimicrobial susceptibility of Gram-positive bacteria isolated from US medical centers: results of the Daptomycin Surveillance Program (2007-2008).

作者信息

Sader Helio S, Jones Ronald N

机构信息

JMI Laboratories, North Liberty, IA 52317, USA.

出版信息

Diagn Microbiol Infect Dis. 2009 Oct;65(2):158-62. doi: 10.1016/j.diagmicrobio.2009.06.016.

Abstract

Gram-positive bacterial strains (12 443) consecutively collected during 2007 to 2008 in hospitals located in the United States were tested by reference broth microdilution methods against daptomycin and comparison agents. Methicillin (oxacillin) resistance rates were 55.9% and 74.0% for Staphylococcus aureus and coagulase-negative staphylococci, respectively, and the vancomycin resistance rate among Enterococcus faecalis and Enterococcus faecium were 5.4% and 75.4%, respectively. Daptomycin was very active against all Gram-positive species with MIC(90) values of 0.5, 0.25, 0.5, and 2 microg/mL for staphylococci, beta-hemolytic streptococci, viridans group streptococci, and enterococci, respectively. Overall, 99.9% of S. aureus, 100.0% of E. faecalis, and 99.5% of E. faecium were susceptible to daptomycin. In addition, daptomycin MIC distributions for S. aureus and enterococci from 2007 to 2008 were very similar to those from 2002 to 2003. In summary, high rates of methicillin-resistant staphylococci and vancomycin-resistant enterococci were observed in US hospitals, but daptomycin remains active against these clinically important Gram-positive organisms with no evidence of potency loss since its approval for clinical use in late 2003.

摘要

2007年至2008年期间在美国各医院连续收集的12443株革兰氏阳性菌,采用参考肉汤微量稀释法对达托霉素及对照药物进行了检测。金黄色葡萄球菌和凝固酶阴性葡萄球菌的耐甲氧西林(苯唑西林)率分别为55.9%和74.0%,粪肠球菌和屎肠球菌的耐万古霉素率分别为5.4%和75.4%。达托霉素对所有革兰氏阳性菌均具有很高活性,对葡萄球菌、β溶血性链球菌、草绿色链球菌和肠球菌的MIC(90)值分别为0.5、0.25、0.5和2μg/mL。总体而言,99.9%的金黄色葡萄球菌、100.0%的粪肠球菌和99.5%的屎肠球菌对达托霉素敏感。此外,2007年至2008年期间金黄色葡萄球菌和肠球菌的达托霉素MIC分布与2002年至2003年期间非常相似。总之,在美国医院中观察到耐甲氧西林葡萄球菌和耐万古霉素肠球菌的比例很高,但达托霉素对这些临床上重要的革兰氏阳性菌仍然具有活性,自2003年末批准临床使用以来,没有效力丧失的迹象。

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