Sader Helio S, Fey Paul D, Limaye Ajit P, Madinger Nancy, Pankey George, Rahal James, Rybak Michael J, Snydman David R, Steed Lisa L, Waites Ken, Jones Ronald N
JMI Laboratories, North Liberty, IA 52317, USA.
Antimicrob Agents Chemother. 2009 Oct;53(10):4127-32. doi: 10.1128/AAC.00616-09. Epub 2009 Jul 27.
Vancomycin MIC creep has been reported by some institutions but not confirmed in large surveillance studies. We evaluated the possible occurrence of MIC creep when testing vancomycin and daptomycin against methicillin (oxacillin)-resistant Staphylococcus aureus (MRSA) by using precise incremental reference MIC methods. Nine hospitals (one in each U.S. census region) randomly selected bloodstream MRSA strains (target, 40/year) from 2002 to 2006. MICs were determined by the reference broth microdilution method using incremental dilutions (eight for each log(2) dilution step). Isolates for which vancomycin MICs were >1 microg/ml were typed by pulsed-field gel electrophoresis (PFGE). The vancomycin MIC mode was either 0.625 microg/ml (for eight hospitals) or 0.813 microg/ml (for one hospital), and vancomycin MIC results for 72.9% of strains were between 0.563 and 0.688 microg/ml. No yearly variation in the central tendency of vancomycin MICs for the wild-type population in any medical center was observed; however, when data were analyzed by the geometric mean statistic, vancomycin MIC increases (at three sites) and declines (at three sites) were observed. The daptomycin MIC mode varied from 0.156 microg/ml (2003 to 2005) to 0.219 microg/ml (2002 and 2006), and MIC results for 83.5% (80.3 to 89.2% in each of the centers) of isolates fell between these values. Among PFGE-typed strains, 43 of 55 (78%; from seven hospitals) showed a pattern consistent with that of the USA100 clone, which was represented by all strains from two hospitals and 64 to 88% of strains from five other medical centers; only one strain (2%) was USA300. In conclusion, the perception of MIC creep may vary according to the methods used to analyze the data. Geometric mean MIC data revealed a possible, very-low-level MIC creep at three of nine sites over the 5-year period, which was not evident using modal MICs or the data from all nine hospitals (+0.02 mug/ml). The occurrence of isolates for which the vancomycin MIC was >1 microg/ml was very unusual, with no increased trend, but these organisms were usually clonal (USA100).
一些机构报告了万古霉素最低抑菌浓度(MIC)漂移现象,但大型监测研究未证实这一点。我们通过使用精确的递增参考MIC方法,评估了对耐甲氧西林(苯唑西林)金黄色葡萄球菌(MRSA)检测万古霉素和达托霉素时MIC漂移的可能发生情况。2002年至2006年期间,九家医院(美国每个普查区域各一家)随机选取血流感染的MRSA菌株(目标为每年40株)。采用递增稀释法(每个对数(2)稀释步骤有八个稀释度)通过参考肉汤微量稀释法测定MIC。万古霉素MIC>1μg/ml的分离株通过脉冲场凝胶电泳(PFGE)进行分型。万古霉素MIC模式在八家医院为0.625μg/ml,在一家医院为0.813μg/ml,72.9%的菌株万古霉素MIC结果在0.563至0.688μg/ml之间。在任何医疗中心,野生型群体的万古霉素MIC中心趋势均未观察到年度变化;然而,当通过几何平均统计分析数据时,观察到万古霉素MIC在三个地点升高,在三个地点下降。达托霉素MIC模式从2003年至2005年的0.156μg/ml变化至2002年和2006年的0.219μg/ml,83.5%(每个中心为80.3%至89.2%)的分离株MIC结果落在这些值之间。在PFGE分型的菌株中,55株中的43株(78%;来自七家医院)显示出与USA100克隆一致的模式,两家医院的所有菌株以及其他五家医疗中心64%至88%的菌株代表了该克隆;只有一株(2%)是USA300。总之,根据用于分析数据的方法,对MIC漂移的认识可能会有所不同。几何平均MIC数据显示,在5年期间,九个地点中的三个地点可能存在非常低水平的MIC漂移,使用模式MIC或来自所有九家医院的数据(+0.02μg/ml)时并不明显。万古霉素MIC>1μg/ml的分离株的出现非常罕见,没有增加的趋势,但这些菌株通常是克隆性的(USA100)。