Venditti M, Brandimarte C, Santini C, Valente B, Martino P, Serra P
Chemioterapia. 1984 Aug;3(4):258-61.
Aztreonam, ceftriaxone, moxalactam, cefotaxime, cefsulodin, cefoperazone, piperacillin, azlocillin, carbenicillin, amikacin, gentamicin, tobramycin, sisomicin and dibekacin were tested by broth dilution against 161 isolates of Pseudomonas aeruginosa. Seventy-one of these strains were selected for their resistance to carbenicillin and aminoglycosides and classified as "multiply resistant" strains. Over all, aztreonam showed the greatest antipseudomonal activity by far, followed by ceftriaxone, moxalactam, cefotaxime and amikacin. Piperacillin, azlocillin, cefsulodin, and cefoperazone were highly active against carbenicillin and/or aminoglycoside-susceptible P. aeruginosa strains, but were also poorly inhibitory against multiply resistant isolates.
采用肉汤稀释法对氨曲南、头孢曲松、拉氧头孢、头孢噻肟、磺苄西林、头孢哌酮、哌拉西林、阿洛西林、羧苄西林、阿米卡星、庆大霉素、妥布霉素、西索米星和地贝卡星进行了测试,以检测其对161株铜绿假单胞菌的抗菌活性。其中71株菌株因对羧苄西林和氨基糖苷类耐药而被选为“多重耐药”菌株。总体而言,氨曲南的抗铜绿假单胞菌活性最强,其次是头孢曲松、拉氧头孢、头孢噻肟和阿米卡星。哌拉西林、阿洛西林、磺苄西林和头孢哌酮对羧苄西林和/或氨基糖苷类敏感的铜绿假单胞菌菌株具有高活性,但对多重耐药菌株的抑制作用较差。