Acta Clin Belg. 2001 Sep-Oct;56(5):307-15. doi: 10.1179/acb.2001.045.
The in vitro activity of isepamicin was compared to that of amikacin, gentamicin, cefepime, ciprofloxacin and meropenem against Gram-negative bacilli isolated from patients hospitalized in the intensive care unit (ICU) of 11 Belgian university or general hospitals between November 1998 and July 1999. The minimal inhibitory concentrations (MIC) for 1087 non-duplicate, consecutive aerobic Gram-negative isolates, including 798 Enterobacteriaceae and 289 non-fermenters, were determined by E-test for each antibiotic. Overall, isepamicin was active against 91% of all isolates and was found more active than ciprofloxacin (84% susceptibility), gentamicin (88% susceptibility), cefepime and amikacin (89% susceptibility each), but less active than meropenem (94% susceptibility). Enterobacter aerogenes isolates exhibited the highest resistance rate to ciprofloxacin (72%) while P. aeruginosa appeared the most resistant (frequently multi-resistant) pathogen. Compared to amikacin, MIC values for isepamicin were usually two- to fourfold lower for most inducible Enterobacteriacieae species and for Klebsiella spp., while they were identical for P. aeruginosa and other non-fermenters. Complete cross-susceptibility or cross-resistance between amikacin and isepamicin was observed in more than 95% of all tested isolates. On the other hand, 12% of all E. aerogenes isolates appeared resistant to amikacin and susceptible to isepamicin, while 6% of the P. aeruginosa were found to be resistant (or intermediate) to isepamicin and intermediate (or susceptible) to amikacin. No significant differences in pathogen distribution nor in resistance rates were observed between hospitals except for P. aeruginosa. Taking into account the species distribution and the prevalence of resistance to the different antibiotics tested, isepamicin appears as a suitable agent for empiric therapeutic use in severe ICU-acquired Gram-negative infections in Belgium.
1998年11月至1999年7月期间,在比利时11家大学医院或综合医院的重症监护病房(ICU),将异帕米星与阿米卡星、庆大霉素、头孢吡肟、环丙沙星和美罗培南对从住院患者中分离出的革兰氏阴性杆菌的体外活性进行了比较。采用E试验法测定了1087株非重复、连续的需氧革兰氏阴性分离菌(包括798株肠杆菌科细菌和289株非发酵菌)对每种抗生素的最低抑菌浓度(MIC)。总体而言,异帕米星对所有分离菌的活性为91%,发现其活性高于环丙沙星(敏感性84%)、庆大霉素(敏感性88%)、头孢吡肟和阿米卡星(各为89%敏感性),但低于美罗培南(敏感性94%)。产气肠杆菌分离株对环丙沙星的耐药率最高(72%),而铜绿假单胞菌似乎是耐药性最强(通常多重耐药)的病原体。与阿米卡星相比,异帕米星对大多数可诱导的肠杆菌科细菌和克雷伯菌属的MIC值通常低两至四倍,而对铜绿假单胞菌和其他非发酵菌则相同。在所有测试分离菌中,超过95%观察到阿米卡星和异帕米星之间完全交叉敏感或交叉耐药。另一方面,所有产气肠杆菌分离株中有12%对阿米卡星耐药而对异帕米星敏感,而6%的铜绿假单胞菌对异帕米星耐药(或中介)而对阿米卡星中介(或敏感)。除铜绿假单胞菌外,各医院之间在病原体分布和耐药率方面未观察到显著差异。考虑到菌种分布以及对所测试的不同抗生素的耐药流行情况,异帕米星似乎是比利时重症监护病房获得性严重革兰氏阴性感染经验性治疗的合适药物。