Chow A W, Wong J, Bartlett K H
Department of Medicine, University of British Columbia, Vancouver, Canada.
Diagn Microbiol Infect Dis. 1988 Apr;9(4):213-7. doi: 10.1016/0732-8893(88)90111-3.
The susceptibility of 54 clinical isolates of Acinetobacter calcoaceticus ss. anitratus to 16 antimicrobial agents was determined in vitro with inoculum of 10(4) and 10(6) cfu by a standard agar dilution method. The most active agents were imipenem, SCH 34343, ciprofloxacin, difloxacin (A-56619), and A-56620. Only imipenem and Abbott quinolones (A-56619 and A-56620) remained active when tested with the heavier inoculum. Except for ticarcillin and ceftazidime, which showed only moderate activity, the extended-spectrum penicillins and cephalosporins, as well as aztreonam and aminoglycosides, were inactive against these highly resistant strains. Nine isolates were selected for combination studies of ciprofloxacin with seven beta-lactams and three aminoglycosides using a checkerboard agar dilution technique. Synergistic or additive interactions at clinically achievable concentrations were more common with amikacin (eight isolates), tobramycin (seven), ceftazidime (six), cefoperazone (six), and aztreonam (six), than with other agents, including mezlocillin (four), piperacillin (three), gentamicin (two), and cefsulodin (two). Antagonism was rare, only occurring with mezlocillin in a single strain. These data suggest that combinations of ciprofloxacin with these agents may be useful for some nosocomial multidrug resistant A. calcoaceticus ss. anitratus infections.
采用标准琼脂稀释法,以10⁴和10⁶ cfu的接种量,对54株醋酸钙不动杆菌鲍曼不动杆菌临床分离株对16种抗菌药物的敏感性进行了体外测定。活性最强的药物是亚胺培南、SCH 34343、环丙沙星、双氟沙星(A - 56619)和A - 56620。用较大接种量测试时,只有亚胺培南和雅培喹诺酮类药物(A - 56619和A - 56620)仍有活性。除替卡西林和头孢他啶仅表现出中等活性外,广谱青霉素和头孢菌素以及氨曲南和氨基糖苷类药物对这些高度耐药菌株均无活性。选择9株分离株,采用棋盘琼脂稀释技术,对环丙沙星与7种β-内酰胺类药物和3种氨基糖苷类药物进行联合研究。在临床可达到的浓度下,与阿米卡星(8株)、妥布霉素(7株)、头孢他啶(6株)、头孢哌酮(6株)和氨曲南(6株)的协同或相加相互作用比与其他药物更常见,包括美洛西林(4株)、哌拉西林(3株)、庆大霉素(2株)和头孢磺啶(2株)。拮抗作用罕见,仅在1株菌株中与美洛西林发生。这些数据表明,环丙沙星与这些药物联合使用可能对某些医院获得性多重耐药鲍曼不动杆菌感染有用。