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奎奴普丁/达福普汀与对照抗菌药物对全球临床试验及其他实验室分离株的体外活性评估。

Evaluation of in vitro activity of quinupristin/dalfopristin and comparator antimicrobial agents against worldwide clinical trial and other laboratory isolates.

作者信息

Dowzicky M, Nadler H L, Feger C, Talbot G, Bompart F, Pease M

机构信息

Rhône-Poulenc Rorer Pharmaceuticals, Collegeville, Pennsylvania 19426, USA.

出版信息

Am J Med. 1998 May 29;104(5A):34S-42S. doi: 10.1016/s0002-9343(98)00153-3.

DOI:10.1016/s0002-9343(98)00153-3
PMID:9684656
Abstract

This report summarizes the activities of quinupristin/dalfopristin (Q/D) and appropriate comparator antibiotics, including ciprofloxacin, erythromycin, gentamicin, rifampin, teicoplanin, and vancomycin, against selected gram-positive pathogens, including Enterococcus faecium, Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, Streptococcus agalactiae, and Streptococcus pyogenes. The study pathogens were obtained from 2 sources: (1) clinical isolates taken from patients participating in Q/D worldwide Phase III comparative and noncomparative (emergency-use program) clinical trials; and (2) other isolates collected from the laboratories of 45 geographically distinct medical centers around the world. Q/D was highly active, with minimum inhibitory concentrations (MICs) < or = 1.0 microg/mL against most isolates, including those known to be resistant to methicillin, vancomycin, or erythromycin. Q/D was active (MICs < or = 1 microg/mL) against 95% of the vancomycin-resistant E. faecium strains, for example, whereas ciprofloxacin was active against 6%. Q/D was equally active against methicillin-susceptible or -resistant S. aureus strains (MIC90=1 microg/mL), as was vancomycin (MIC90=2 microg/mL), whereas ciprofloxacin was much less active against methicillin-resistant strains than against methicillin-susceptible strains (MIC90=32 vs 1 microg/mL). Given its spectrum of activity, Q/D may provide a viable option for the treatment of severe respiratory and skin and skin-structure infections caused by gram-positive bacteria, especially when strains with known or suspected resistance to other commonly used antibiotics are present.

摘要

本报告总结了奎奴普丁/达福普汀(Q/D)及适当的对照抗生素(包括环丙沙星、红霉素、庆大霉素、利福平、替考拉宁和万古霉素)对选定革兰氏阳性病原体的活性,这些病原体包括粪肠球菌、金黄色葡萄球菌、表皮葡萄球菌、肺炎链球菌、无乳链球菌和化脓性链球菌。研究病原体来自两个来源:(1)从参与Q/D全球III期比较性和非比较性(紧急使用计划)临床试验的患者中分离得到的临床菌株;(2)从全球45个地理位置不同的医学中心实验室收集的其他菌株。Q/D具有高度活性,对大多数菌株的最低抑菌浓度(MIC)≤1.0μg/mL,包括那些已知对甲氧西林、万古霉素或红霉素耐药的菌株。例如,Q/D对95%的耐万古霉素粪肠球菌菌株有活性(MIC≤1μg/mL),而环丙沙星对6%的此类菌株有活性。Q/D对甲氧西林敏感或耐药的金黄色葡萄球菌菌株活性相同(MIC90=1μg/mL),万古霉素也是如此(MIC90=2μg/mL),而环丙沙星对耐甲氧西林菌株的活性比对甲氧西林敏感菌株低得多(MIC90=32 vs 1μg/mL)。鉴于其活性谱,Q/D可能为治疗由革兰氏阳性菌引起的严重呼吸道感染以及皮肤和皮肤结构感染提供一个可行的选择,尤其是当存在对其他常用抗生素已知或疑似耐药的菌株时。

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引用本文的文献

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J Microbiol. 2008 Feb;46(1):108-11. doi: 10.1007/s12275-007-0217-1.
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Newer treatment options for skin and soft tissue infections.皮肤和软组织感染的新型治疗选择。
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Combination of quinupristin-dalfopristin (Synercid) and rifampin is highly synergistic in experimental Staphylococcus aureus joint prosthesis infection.
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Treatment options for vancomycin-resistant enterococcal infections.耐万古霉素肠球菌感染的治疗选择。
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Quinupristin-Dalfopristin.奎奴普丁-达福普汀
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