In Vitro Activity of Imipenem-Relebactam Alone or in Combination with Amikacin or Colistin against Pseudomonas aeruginosa

被引:23
作者
Asempa, Tomefa E. [1 ]
Nicolau, David P. [1 ,2 ]
Kuti, Joseph L. [1 ]
机构
[1] Hartford Hosp, Ctr Antiinfect Res & Dev, Hartford, CT 06115 USA
[2] Hartford Hosp, Div Infect Dis, Hartford, CT 06115 USA
关键词
beta-lactamase; beta-lactamase inhibitor; multidrug; synergy; time-kill; INFECTIOUS-DISEASES SOCIETY; BETA-LACTAMASE INHIBITOR; CRITICALLY-ILL; RESISTANCE; THERAPY; SYNERGY; RISK; PHARMACOKINETICS; ANTIBIOTICS; PNEUMONIA;
D O I
10.1128/AAC.00997-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Relebactam is a novel class A/C beta-lactamase inhibitor that restores imipenem in vitro activity against multidrug-resistant and carbapenem-nonsusceptible Pseudomonas aeruginosa. Time-kill analyses were performed to evaluate the potential role of imipenem-relebactam in combination with amikacin or colistin against P. aeruginosa. Ten clinical P. aeruginosa isolates (9 imipenem nonsusceptible) with imipenem-relebactam MICs ranging from 1/4 to 8/4 mu g/ml were included. The isolates had varied susceptibilities to imipenem (1 to 32 mu g/ml), amikacin (4 to 128 mu g/ml), and colistin (0.5 to 1 mu g/ml). Duplicate 24-h time-kill studies were conducted using the average steady-state concentrations (Css(avg)) observed after the administration of imipenemrelebactam at 500 mg/250mg every 6 hours (q6h) alone and in combination with the Css(avg) of 25 mg/kg of body weight/day amikacin and 360 mg/day colistin in humans. Imipenem-relebactam alone resulted in 24-h bacterial densities of -2.93 +/- 0.38, -1.67 +/- 0.29, +0.38 +/- 0.96, and +0.15 +/- 0.65 log(10) CFU/ml at imipenem-relebactam MICs of 1/4, 2/4, 4/4, and 8/4 mu g/ml, respectively. No synergy was demonstrated against the single imipenem-susceptible isolate. Against the imipenem-nonsusceptible isolates (n = 9), imipenem-relebactam combined with amikacin resulted in synergy (-2.61 +/- 1.50 log(10) CFU/ml) against all amikacin-susceptible isolates and in two of three amikacin-intermediate (i. e., MIC, 32 mu g/ml) isolates (-2.06 +/- 0.19 log(10) CFU/ml). Synergy with amikacin was not observed when the amikacin MIC was >32 mu g/ml. Imipenem-relebactam combined with colistin demonstrated synergy in eight out of the nine imipenem-resistant isolates (-3.17 +/- 1.00 log(10) CFU/ml). Against these 10 P. aeruginosa isolates, imipenem-relebactam combined with either amikacin or colistin resulted in synergistic activity against the majority of strains. Further studies evaluating combination therapy with imipenem-relebactam are warranted.
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页数:9
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