Hoban D J, Jones R N, Harrell L J, Knudson M, Sewell D
University of Manitoba, Winnipeg, Canada.
Diagn Microbiol Infect Dis. 1993 Aug-Sep;17(2):157-61. doi: 10.1016/0732-8893(93)90027-5.
Common lots of reference MIC (minimum inhibitory concentration) method reagents were used to monitor ofloxacin, a newer fluoroquinolone, and 13 other drugs against 3200 recent clinical isolates in February-April 1992. Five medical centers in the United States and Canada contributed 640 strains per facility as follows: Escherichia coli, Staphylococcus aureus, coagulase-negative staphylococci, Klebsiella spp., and Pseudomonas aeruginosa (100 strains each); Streptococcus pneumoniae (40 strains); and Enterobacter cloacae, Serratia marcescens, Salmonella spp., Haemophilus influenzae, and Moraxella catarrhalis (20 strains each). Quality-control strains were processed concurrently, MICs recorded, and data processed at a common location. Selected ofloxacin-resistant isolates were retested at a reference laboratory to confirm resistances and determine cross-resistant patterns. Results indicate the following (a) fluoroquinolones were superior in usable spectrum of activity to other orally administered drugs (for example, cefaclor, cefixime, ampicillin, amoxicillin-clavulanate, minocycline, oxacillin, and trimethoprim-sulfamethoxazole); (b) ofloxacin and ciprofloxacin were generally equal to gentamicin and cefotaxime against commonly isolated Gram-negative pathogens; (c) fluoroquinolone resistance was rare among enteric bacilli, pneumococci (ciprofloxacin > ofloxacin), H. influenzae, and M. catarrhalis, but more common among oxacillin-resistant staphylococci and P. aeruginosa; (d) cross resistance was generally observed between ofloxacin and ciprofloxacin but was species or genus dependent; and (e) a new fluoroquinolone, levofloxacin, demonstrated promising activity against contemporary pathogens.
1992年2月至4月期间,使用常见批次的参考MIC(最低抑菌浓度)方法试剂,对一种新型氟喹诺酮类药物氧氟沙星以及其他13种药物针对3200株近期临床分离菌株进行了监测。美国和加拿大的五个医疗中心每个机构提供了640株菌株,具体如下:大肠杆菌、金黄色葡萄球菌、凝固酶阴性葡萄球菌、克雷伯菌属和铜绿假单胞菌(各100株);肺炎链球菌(40株);阴沟肠杆菌、粘质沙雷氏菌、沙门氏菌属、流感嗜血杆菌和卡他莫拉菌(各20株)。同时对质量控制菌株进行处理,记录MIC,并在一个共同地点处理数据。对选定的耐氧氟沙星分离株在参考实验室进行重新检测,以确认耐药性并确定交叉耐药模式。结果表明:(a)氟喹诺酮类药物在可用活性谱方面优于其他口服药物(例如头孢克洛、头孢克肟、氨苄西林、阿莫西林 - 克拉维酸、米诺环素、苯唑西林和甲氧苄啶 - 磺胺甲恶唑);(b)氧氟沙星和环丙沙星对常见分离的革兰氏阴性病原体的抗菌活性通常与庆大霉素和头孢噻肟相当;(c)氟喹诺酮耐药性在肠道杆菌、肺炎球菌(环丙沙星>氧氟沙星)、流感嗜血杆菌和卡他莫拉菌中很少见,但在耐苯唑西林葡萄球菌和铜绿假单胞菌中更常见;(d)氧氟沙星和环丙沙星之间通常观察到交叉耐药,但具有种属依赖性;(e)一种新型氟喹诺酮类药物左氧氟沙星对当代病原体显示出有前景的活性。