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氨曲南联合阿洛西林或哌拉西林对铜绿假单胞菌的作用

Effect of aztreonam in combination with azlocillin or piperacillin on Pseudomonas aeruginosa.

作者信息

Wu D H, Baltch A L, Smith R P, Conley P E

出版信息

Antimicrob Agents Chemother. 1984 Oct;26(4):519-21. doi: 10.1128/AAC.26.4.519.

Abstract

Aztreonam, a synthetic monobactam antimicrobial agent specifically active against aerobic, gram-negative microorganisms, was studied in combination with the extended-spectrum penicillins azlocillin and piperacillin against 46 strains of Pseudomonas aeruginosa. Of these strains, 4.3% were synergistically inhibited, and 19.7% showed evidence for an additive effect of the antibiotics. All other strains showed indifference. The addition of cefoxitin to these combinations increased the MICs of azlocillin and piperacillin by two to three tubes, whereas zero- to one-tube increases were noted for aztreonam MICs. Attempts to block cefoxitin-induced beta-lactamase production by using clindamycin were unsuccessful even at high clindamycin concentrations.

摘要

氨曲南是一种合成的单环β-内酰胺类抗菌剂,对需氧革兰氏阴性微生物具有特异性活性。本研究将其与广谱青霉素阿洛西林和哌拉西林联合,用于对抗46株铜绿假单胞菌。在这些菌株中,4.3%受到协同抑制,19.7%显示出抗生素的相加作用。所有其他菌株无反应。在这些联合用药中加入头孢西丁,可使阿洛西林和哌拉西林的最低抑菌浓度(MIC)升高两到三个稀释度管,而氨曲南的MIC仅升高零到一个稀释度管。即使使用高浓度的克林霉素,试图通过它来阻断头孢西丁诱导的β-内酰胺酶产生也未成功。

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