Verbist L, Verhaegen J
Department of Microbiology, University Hospital St. Rafaël, Leuven, Belgium.
Eur J Clin Microbiol Infect Dis. 1996 Aug;15(8):683-5. doi: 10.1007/BF01691160.
The comparative in vitro activity of trovafloxacin (CP 99,219), a new fluoroquinolone, was evaluated against 511 clinical isolates. MICs of trovafloxacin were fourfold higher than those of ciprofloxacin for 184 Enterobacteriaceae and 110 non-fermentative gram-negative bacilli. However, trovafloxacin was 16-fold more active than ciprofloxacin against 162 gram-positive staphylococci, pneumococci, streptococci, and enterococci, and two- to fourfold more active against Haemophilus influenzae and Moraxella catarrhalis. MICs of trovafloxacin were correspondingly higher for strains with acquired resistance to ciprofloxacin.
对新型氟喹诺酮曲伐沙星(CP 99,219)的体外活性进行了评估,以检测其对511株临床分离菌的作用。对于184株肠杆菌科细菌和110株非发酵革兰氏阴性杆菌,曲伐沙星的最低抑菌浓度(MIC)比环丙沙星高4倍。然而,曲伐沙星对162株革兰氏阳性葡萄球菌、肺炎球菌、链球菌和肠球菌的活性比环丙沙星高16倍,对流感嗜血杆菌和卡他莫拉菌的活性高2至4倍。对于对环丙沙星获得性耐药的菌株,曲伐沙星的MIC相应更高。