Toma E, Barriault D
Hôtel-Dieu de Montréal and University of Montreal, Québec, Canada.
J Clin Microbiol. 1995 Jul;33(7):1712-5. doi: 10.1128/jcm.33.7.1712-1715.1995.
The in vitro activity of fusidic acid was assessed and was compared with those of cloxacillin, cefamandole, vancomycin, teicoplanin, ofloxacin, ciprofloxacin, pefloxacin, and fleroxacin against 500 gram-positive cocci: 151 Staphylococcus aureus, 197 coagulase-negative staphylococci, and 152 Enterococcus faecalis strains. All clinical isolates were concomitantly tested by disk diffusion and agar dilution procedures as outlined by the National Committee for Clinical Laboratory Standards. The results with fusidic acid were further analyzed by regression line and error rate-bounded methods. With control American Type Culture Collection organisms, the values were within the limits of the National Committee for Clinical Laboratory Standards or published limits. The incidence of resistance to fusidic acid was 0.7% for S. aureus, 2.5% for coagulase-negative staphylococci, and 99.3% for E. faecalis. The correlation coefficient between the results of disk diffusion and agar dilution tests with fusidic acid was 0.90. Current interpretive criteria for susceptibility to fusidic acid (i.e., MIC of < 2 micrograms/ml and inhibitory zone of 20 mm) gave 1% false susceptibility (all strains being E. faecalis). This error rate is practically eliminated if a zone diameter of 21 mm is considered the breakpoint for susceptibility.
评估了夫西地酸的体外活性,并将其与氯唑西林、头孢孟多、万古霉素、替考拉宁、氧氟沙星、环丙沙星、培氟沙星和氟罗沙星对500株革兰氏阳性球菌的活性进行了比较,这些球菌包括151株金黄色葡萄球菌、197株凝固酶阴性葡萄球菌和152株粪肠球菌。所有临床分离株均按照美国国家临床实验室标准委员会概述的纸片扩散法和琼脂稀释法同时进行检测。用回归线和误差率限定法对夫西地酸的结果进行了进一步分析。对于对照美国典型培养物保藏中心的菌株,其数值在国家临床实验室标准委员会的限度范围内或已公布的限度内。金黄色葡萄球菌对夫西地酸的耐药率为0.7%,凝固酶阴性葡萄球菌为2.5%,粪肠球菌为99.3%。夫西地酸纸片扩散试验和琼脂稀释试验结果之间的相关系数为0.90。目前夫西地酸敏感性的解释标准(即最低抑菌浓度<2微克/毫升且抑菌圈直径为20毫米)产生了1%的假敏感率(所有菌株均为粪肠球菌)。如果将抑菌圈直径21毫米视为敏感性断点,则该误差率实际上可消除。