Philippon A, Paul G, Nevot P
C.H.U. Cochin, Service de Bactériologie 75674-Paris Cedex 14, France.
J Antimicrob Chemother. 1981 Sep;8 Suppl B:119-22. doi: 10.1093/jac/8.suppl_b.119.
The in-vitro antibacterial activity of ceftazidime was compared with that of cefsulodin and ticarcillin against 140 strains of Pseudomonas aeruginosa. Against 123 clinical isolates, geometric mean MICs were 1499mg/l for ticarcillin, 15 mg/l for cefsulodin and 2.1 mg/l for ceftazidime. Against constitutive beta-lactamase producers (93 strains), and according to the type of enzyme (TEM-1, carbenicillinases, oxacillinases), ceftazidime had similar activity but MICs of cefsulodin were particularly affected by highly ticarcillin-resistant (carbenicillinase pIs 53, 5.7 and 575) strains. Against ticarcillin-resistant (constitutive beta-lactamase non-producers) and ticarcillin-susceptible strains, the MICs of ceftazidime were slightly lower than those of cefsulodin.
将头孢他啶与头孢磺啶和替卡西林对140株铜绿假单胞菌的体外抗菌活性进行了比较。对于123株临床分离株,替卡西林的几何平均最低抑菌浓度(MIC)为1499mg/l,头孢磺啶为15mg/l,头孢他啶为2.1mg/l。对于组成型β-内酰胺酶产生菌(93株),根据酶的类型(TEM-1、羧苄青霉素酶、苯唑西林酶),头孢他啶具有相似的活性,但头孢磺啶的MICs受高度耐替卡西林(羧苄青霉素酶pIs 53、5.7和575)菌株的影响尤为明显。对于耐替卡西林(非组成型β-内酰胺酶产生菌)和对替卡西林敏感的菌株,头孢他啶的MICs略低于头孢磺啶。