Fish Douglas N, Choi Michael K, Jung Rose
University of Colorado Health Sciences Center, Antimicrobial Research Laboratory, Department of Pharmacy Practice, 4200 E. 9th Ave, Box C238, Denver, CO 80262, USA.
J Antimicrob Chemother. 2002 Dec;50(6):1045-9. doi: 10.1093/jac/dkf211.
Owing to increasing resistance in Pseudomonas aeruginosa, empirical drug regimens may include agents to which some strains may be resistant. The purpose of this study was to evaluate the in vitro activities of different combinations of cephalosporin plus fluoroquinolone against P. aeruginosa isolates with varying susceptibility to the study drugs. Broth microdilution susceptibility testing was performed with 10 clinical isolates of P. aeruginosa. The bactericidal activity of cefepime or ceftazidime alone and in combination with ciprofloxacin, levofloxacin, gatifloxacin or moxifloxacin was evaluated using time-kill methods. Colony counts were determined at 0, 4, 8 and 24 h, using antimicrobial concentrations of 0.5 x MIC. All procedures were performed in duplicate. Synergy was defined as a >2-log decrease in cfu/mL at 24 h compared with the single most active agent. The MICs for tested strains were: ceftazidime 0.75-32, cefepime 0.125-8, ciprofloxacin 0.0078-8, levofloxacin 0.023-16, gatifloxacin 0.023-16 and moxifloxacin 0.0521-32 mg/L. Four strains were susceptible to all drugs, two strains were cephalosporin susceptible and fluoroquinolone resistant, and two strains were cephalosporin resistant and fluoroquinolone susceptible. Two strains were resistant or intermediately susceptible to all drugs. Various cephalosporin and fluoroquinolone combinations were synergic against P. aeruginosa, including strains resistant to one or both agents in combination. No synergy was observed in two strains susceptible to all drugs. There were no differences noted between different cephalosporin and fluoroquinolone combinations. Concentrations used in this study are clinically achievable with recommended regimens in most cases.
由于铜绿假单胞菌的耐药性不断增加,经验性用药方案可能包括一些菌株可能耐药的药物。本研究的目的是评估头孢菌素加氟喹诺酮不同组合对研究药物敏感性不同的铜绿假单胞菌分离株的体外活性。对10株铜绿假单胞菌临床分离株进行了肉汤微量稀释药敏试验。采用时间杀菌法评估头孢吡肟或头孢他啶单独及与环丙沙星、左氧氟沙星、加替沙星或莫西沙星联合使用时的杀菌活性。使用0.5×MIC的抗菌药物浓度,在0、4、8和24小时测定菌落计数。所有程序均重复进行。协同作用定义为与单一活性最强的药物相比,24小时时cfu/mL下降>2个对数。受试菌株的MIC分别为:头孢他啶0.75 - 32、头孢吡肟0.125 - 8、环丙沙星0.0078 - 8、左氧氟沙星0.023 - 16、加替沙星0.023 - 16和莫西沙星0.0521 - 32mg/L。4株菌株对所有药物敏感,2株菌株对头孢菌素敏感但对氟喹诺酮耐药,2株菌株对头孢菌素耐药但对氟喹诺酮敏感。2株菌株对所有药物耐药或中介敏感。各种头孢菌素和氟喹诺酮组合对铜绿假单胞菌具有协同作用,包括对一种或两种联合药物耐药的菌株。在对所有药物敏感的2株菌株中未观察到协同作用。不同的头孢菌素和氟喹诺酮组合之间未发现差异。本研究中使用的浓度在大多数情况下通过推荐方案在临床上是可以达到的。