Fekete T, McGowen J, Cundy K R
Antimicrob Agents Chemother. 1987 Feb;31(2):321-2. doi: 10.1128/AAC.31.2.321.
One hundred clinical isolates of the Bacteroides fragilis group of bacteria were tested by agar dilution for susceptibility to cefazolin alone or in combination with clavulanic acid or sulbactam. For cefazolin, the MIC for 50% of the isolates (MIC50) was 32 micrograms/ml, the breakpoint for susceptibility. With the addition of 0.5 micrograms of clavulanic acid per ml, the MIC for 90% of the isolates (MIC90) was 8 micrograms/ml, well within the achievable range of concentrations in serum or tissue. Similarly, with the addition of 0.5 micrograms of sulbactam per ml, the MIC90 was 16 micrograms/ml. The addition of a higher concentration (4.0 micrograms/ml) of clavulanic acid or sulbactam resulted in MIC90S which were fourfold lower than those with 0.5 micrograms/ml. A fixed ratio of cefazolin-beta-lactamase inhibitor of 4:1 resulted in an MIC50 and MIC90 which were intermediate between the 0.5- and 4.0-micrograms/ml fixed concentration of beta-lactamase inhibitor.
采用琼脂稀释法对100株脆弱拟杆菌群细菌临床分离株进行了测试,以检测它们对单独使用头孢唑林或与克拉维酸或舒巴坦联合使用时的敏感性。对于头孢唑林,50%分离株的最低抑菌浓度(MIC50)为32微克/毫升,此为敏感性的折点。每毫升添加0.5微克克拉维酸后,90%分离株的最低抑菌浓度(MIC90)为8微克/毫升,完全在血清或组织可达到的浓度范围内。同样,每毫升添加0.5微克舒巴坦后,MIC90为16微克/毫升。添加更高浓度(4.0微克/毫升)的克拉维酸或舒巴坦后,MIC90比添加0.5微克/毫升时低四倍。头孢唑林与β-内酰胺酶抑制剂4:1的固定比例所产生的MIC50和MIC90介于β-内酰胺酶抑制剂0.5微克/毫升和4.0微克/毫升固定浓度之间。