Ronco E, Vacheron F, Orabona A
Pathol Biol (Paris). 1987 May;35(5):558-62.
The in vitro activity of 18 antibiotic (beta-lactam agents, quinolones and aminoglycoside has been evaluated against 192 clinical isolates of Pseudomonas aeruginosa. Minimal inhibitor concentrations (MICs) were determined by the agar dilution technique. The 50% and 90% MICs were respectively: ticarcillin (32/greater than 1 024), azlocillin (16/512), piperacillin (8/512), cefsulodin (4/128), ceftazidime (2/8), aztreonam (4/16), imipenem (2/4), nalidixic acid (128/256), pefloxacin (1/8), norfloxacin (1/8), ofloxacin (2/8), ciprofloxacin (0.25/2), gentamicin (8/256), sisomicin (4/256), tobramycin (2/128) dibekacin (4/256), netilmicin (16/256), amikacin (8/16). The sensitivity to beta-lactam agents and to quinolones was usual. Resistance to aminoglycosides was frequently observed (59%): 35.7% of the resistant isolates were resistant to gentamicin-sisomicin-tobramycin-dibekacin-netilmicin, 30% to netilmicin alone, 17.8% to gentamicin-sisomicin-tobramycin-dibekacin-netilmicin-amikacin, 7% to gentamicin-netilmicin, 5.3% to gentamicin-sisomicin-tobramycin-dibekacin; we did not find any P. aeruginosa resistant only to gentamicin or gentamicin-sisomicin.
已对18种抗生素(β-内酰胺类药物、喹诺酮类药物和氨基糖苷类药物)针对192株铜绿假单胞菌临床分离株的体外活性进行了评估。采用琼脂稀释技术测定最低抑菌浓度(MICs)。50%和90%的MICs分别为:替卡西林(32/大于1024)、阿洛西林(16/512)、哌拉西林(8/512)、头孢磺啶(4/128)、头孢他啶(2/8)、氨曲南(4/16)、亚胺培南(2/4)、萘啶酸(128/256)、培氟沙星(1/8)、诺氟沙星(1/8)、氧氟沙星(2/8)、环丙沙星(0.25/2)、庆大霉素(8/256)、西索米星(4/256)、妥布霉素(2/128)、地贝卡星(4/256)、奈替米星(16/256)、阿米卡星(8/16)。对β-内酰胺类药物和喹诺酮类药物的敏感性常见。经常观察到对氨基糖苷类药物耐药(59%):35.7%的耐药分离株对庆大霉素-西索米星-妥布霉素-地贝卡星-奈替米星耐药,30%仅对奈替米星耐药,17.8%对庆大霉素-西索米星-妥布霉素-地贝卡星-奈替米星-阿米卡星耐药,7%对庆大霉素-奈替米星耐药,5.3%对庆大霉素-西索米星-妥布霉素-地贝卡星耐药;我们未发现仅对庆大霉素或庆大霉素-西索米星耐药的铜绿假单胞菌。