Bert F, Bruneau B, Lambert-Zechovsky N, Branger C
Service de Microbiologie, Hôpital Beaujon, Clichy, France.
Chemotherapy. 1994 May-Jun;40(3):183-7. doi: 10.1159/000239190.
The in vitro activity of piperacillin, cefoperazone, cefsulodin, ceftazidime, aztreonam and imipenem was studied against 44 isolates of Pseudomonas aeruginosa with 'intrinsic' resistance to ticarcillin in comparison with 20 ticarcillin-susceptible strains, by MIC determination and the disk diffusion test. The activity of the antibiotics, imipenem excepted, against the resistant strains was reduced when compared to the susceptible strains. The most significant reduction was found for aztreonam and the least significant for ceftazidime. When considering the breakpoints, all strains were intermediate with aztreonam and cefoperazone, but most of them remained susceptible to ceftazidime, piperacillin and cefsulodin.
通过最小抑菌浓度(MIC)测定和纸片扩散试验,研究了哌拉西林、头孢哌酮、头孢磺啶、头孢他啶、氨曲南和亚胺培南对44株对替卡西林具有“固有”耐药性的铜绿假单胞菌的体外活性,并与20株对替卡西林敏感的菌株进行了比较。与敏感菌株相比,除亚胺培南外,其他抗生素对耐药菌株的活性均有所降低。氨曲南的活性降低最为显著,头孢他啶的活性降低最不显著。考虑到断点时,所有菌株对氨曲南和头孢哌酮均为中介,但大多数菌株对头孢他啶、哌拉西林和头孢磺啶仍敏感。