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首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Vancomycin MIC creep in non-vancomycin-intermediate Staphylococcus aureus (VISA), vancomycin-susceptible clinical methicillin-resistant S. aureus (MRSA) blood isolates from 2001-05.
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Vancomycin MIC creep in non-vancomycin-intermediate Staphylococcus aureus (VISA), vancomycin-susceptible clinical methicillin-resistant S. aureus (MRSA) blood isolates from 2001-05.

机译:万古霉素MIC在非万古霉素中间金黄色葡萄球菌(VISA)中分离,这是从2001-05开始对万古霉素敏感的耐甲氧西林金黄色葡萄球菌(MRSA)临床分离株。

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OBJECTIVES: To assess whether methicillin-resistant Staphylococcus aureus (MRSA) vancomycin MIC shifts (MIC creep) at a tertiary care institution occurred that may have gone undetected using traditional susceptibility markers (percentage susceptible, MIC(50), MIC(90)) over a 5 year period. Additionally, MIC trends were evaluated for oxacillin, linezolid and daptomycin. METHODS: Etest MICs were performed on MRSA blood culture isolates (January 2001-December 2005). Only one isolate per patient was studied. The reported Etest MIC result was used and not rounded upward. MIC(50), MIC(90), median and geometric mean MIC, percentage susceptible and percentage resistant were calculated for each drug in each year. Non-parametric methods (linear correlation and Mantel-Haenszel chi(2)) were used to assess MIC trends over time and the association of vancomycin, linezolid and daptomycin MICs with oxacillin MICs. RESULTS: All isolates were susceptible to vancomycin, linezolid and daptomycin and resistant to oxacillin. MICs increased for vancomycin, linezolid and oxacillin (P < 0.0001); however, daptomycin MICs decreased slightly (P = 0.0386). For vancomycin, linezolid and oxacillin, there were significant increases (P < 0.0001) in the percentage of isolates with MICs that were higher than the respective 2001 median MIC, but not for daptomycin (P = 0.1361). Oxacillin MICs were associated with MICs of linezolid (r = 0.364, P < 0.0001), vancomycin (r = 0.353, P < 0.0001) and daptomycin (r = 0.106, P = 0.0063). CONCLUSIONS: Oxacillin, vancomycin and linezolid MICs increased over time. For vancomycin and linezolid, these MIC increases were not reliably detected by percentage susceptibility as they occurred below the susceptibility breakpoint. Although the MICs of all agents appeared to be associated with increasing oxacillin MICs, the strongest associations were noted for vancomycin and linezolid.
机译:目的:评估在三级医疗机构中是否发生了耐甲氧西林金黄色葡萄球菌(MRSA)万古霉素MIC转变(MIC蠕变),而使用传统的敏感性标记(易感百分比,MIC(50),MIC(90))超过5年期限。此外,评估了奥沙西林,利奈唑胺和达托霉素的MIC趋势。方法:对MRSA血液培养分离株(2001年1月至2005年12月)进行MIC测试。每位患者仅研究了一种分离株。报告的Etest MIC结果已使用,未向上舍入。每年计算每种药物的MIC(50),MIC(90),中位数和几何平均MIC,易感性百分比和耐药百分比。非参数方法(线性相关和Mantel-Haenszel chi(2))用于评估MIC随时间的变化趋势以及万古霉素,利奈唑胺和达托霉素MIC与奥沙西林MIC的关联。结果:所有分离株均对万古霉素,利奈唑胺和达托霉素敏感,对奥沙西林耐药。万古霉素,利奈唑胺和奥沙西林的MICs增加(P <0.0001);然而,达托霉素的MICs略有下降(P = 0.0386)。对于万古霉素,利奈唑胺和奥沙西林,带有MIC的分离株百分比显着增加(P <0.0001),高于各自的2001年中值MIC,但达托霉素则没有(P = 0.1361)。奥沙西林MIC与利奈唑胺(r = 0.364,P <0.0001),万古霉素(r = 0.353,P <0.0001)和达托霉素(r = 0.106,P = 0.0063)的MIC相关。结论:奥沙西林,万古霉素和利奈唑胺的MICs随时间增加。对于万古霉素和利奈唑胺,这些MIC的增加不能通过敏感性百分比可靠地检测到,因为它们发生在敏感性临界点以下。尽管所有药物的MIC似乎都与奥沙西林MIC的增加有关,但万古霉素和利奈唑胺的相关性最强。

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