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首页> 外文期刊>BMC Infectious Diseases >In vitro antimicrobial effects of aztreonam, colistin, and the 3-drug combination of aztreonam, ceftazidime and amikacin on metallo-β-lactamase-producing Pseudomonas aeruginosa
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In vitro antimicrobial effects of aztreonam, colistin, and the 3-drug combination of aztreonam, ceftazidime and amikacin on metallo-β-lactamase-producing Pseudomonas aeruginosa

机译:氨曲南,大肠菌素以及氨曲南,头孢他啶和丁胺卡那霉素的3种药物组合对产生金属β-内酰胺酶的铜绿假单胞菌的体外抗菌作用

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Background There are limited choice of antimicrobial agents to treat infection with metallo-β-lactamase-producing Pseudomonas aeruginosa. We evaluate the antimicrobial effects of aztreonam alone, colistin alone and the 3-drug combination of aztreonam, ceftazidime and amikacin on 23 strains of metallo-β-lactamase-producing P. aeruginosa by time-killing tests. Methods Strains used were from different hospitals in Japan and had different pulse-field gel electrophoresis patterns by restriction with SpeI. The minimum inhibitory concentrations of 11 antimicrobial agents (piperacillin, piperacillin/tazobactam, imipenem, meropenem, aztreonam, ceftazidime, amikacin, tobramycin, arbekacin, ciprofloxacin and colistin) were determined using the agar dilution test. The effects of aztreonam, colistin and the combination of aztreonam, ceftazidime and amikacin were determined by time-killing studies. Results Bacteriostatic effects after 6 hours of drug exposure were observed in 12 strains (52.2%) of 23 strains of metallo-β-lactamase-producing P. aeruginosa with 48 mg/l aztreonam, in 19 strains (82.6%) with the 3-drug combination of 16 mg/l aztreonam, 16 mg/l ceftazidime, and 4 mg/l amikacin, and in 23 strains (100%) with 2 mg/l colistin. Bactericidal effects after 6 h drug exposure were observed in 1 strain (4.3%) with 48 mg/l aztreonam, in 8 strains (30.4%) with the 3-drug combination and in all 23 strains (100%) with 2 mg/l colistin. Conclusion Evaluation of in vitro antimicrobial effects on metallo-β-lactamase-producing P. aeruginosa revealed relatively good effects of the 3-drug combination of aztreonam, ceftazidime and amikacin and marked effects of colistin.
机译:背景技术用于治疗产生金属β-内酰胺酶的铜绿假单胞菌(Pseudomonas aeruginosa)的感染的抗菌剂选择有限。我们通过时间杀灭试验评估了单独的氨曲南,单独的粘菌素和氨曲南,头孢他啶和丁胺卡那霉素的3种药物组合对23种金属β-内酰胺酶生产铜绿假单胞菌菌株的抗菌作用。方法使用的菌株来自日本不同的医院,并受SpeI限制,具有不同的脉冲场凝胶电泳图谱。使用琼脂稀释试验确定11种抗菌剂(哌拉西林,哌拉西林/他唑巴坦,亚胺培南,美罗培南,氨曲南,头孢他啶,阿米卡星,妥布霉素,阿贝卡星,环丙沙星和粘菌素的最低抑菌浓度)。通过消灭时间的研究确定了氨曲南,粘菌素的作用以及氨曲南,头孢他啶和丁胺卡那霉素的组合。结果暴露于药物6小时后,在23株产生金属β-内酰胺酶的铜绿假单胞菌中,有48毫克/升氨曲南的12株(52.2%)中有19株(82.6%)观察到了抑菌作用,其中3- 16毫克/升氨曲南,16毫克/升头孢他啶和4毫克/升丁胺卡那霉素的药物组合,以及23株(100%)含2毫克/升粘菌素的药物组合。药物暴露6 h后,在1株(4.3%)的氨曲南中,8株(30.4%)的3药组合中以及23株(100%)的2 mg / l中观察到了杀菌作用。大肠菌素。结论评价对产生金属-β-内酰胺酶的铜绿假单胞菌的体外抗菌作用表明,氨曲南,头孢他啶和丁胺卡那霉素的3种药物组合具有相对较好的效果,而粘菌素的效果则显着。

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