Sofianou D, Tsoulfa S, Kontodimou L, Polydorou F, Malaka E
Department of Medical Microbiology, Aristotelian University of Thessaloniki, Greece.
J Chemother. 1997 Oct;9(5):341-6. doi: 10.1179/joc.1997.9.5.341.
Cefepime, a new parenteral cephalosporin, was evaluated for its in vitro antibacterial activity in comparison with other broad-spectrum antibiotics against a total of 445 recently isolated microorganisms of nosocomial origin. Cefepime was highly active against all species of Enterobacteriaceae with minimum inhibitory concentrations (MIC90S) ranging from 0.25-8 micrograms/ml. Cefepime showed moderate activity against Acinetobacter spp (MIC50 and MIC90, 16 micrograms/ml) but its activity was superior to that of any drug tested, except imipenem. Against Pseudomonas aeruginosa its activity was comparable to that of ceftazidime and was greater than that of cefotaxime, aztreonam, ciprofloxacin and aminoglycosides. Of all the agents tested, imipenem was the most active compound. Cefepime was active against Staphylococcus aureus and coagulase-negative methicillin-susceptible staphylococci but it had no activity against methicillin-resistant staphylococci and enterococci.
头孢吡肟是一种新型肠外头孢菌素,我们将其与其他广谱抗生素进行比较,评估了它对总共445株近期分离出的医院源性微生物的体外抗菌活性。头孢吡肟对所有肠杆菌科细菌均具有高度活性,其最低抑菌浓度(MIC90)范围为0.25 - 8微克/毫升。头孢吡肟对不动杆菌属表现出中度活性(MIC50和MIC90为16微克/毫升),但其活性优于除亚胺培南外的任何受试药物。对于铜绿假单胞菌,其活性与头孢他啶相当,且大于头孢噻肟、氨曲南、环丙沙星和氨基糖苷类药物。在所有受试药物中,亚胺培南是活性最强的化合物。头孢吡肟对金黄色葡萄球菌和凝固酶阴性的甲氧西林敏感葡萄球菌有活性,但对耐甲氧西林葡萄球菌和肠球菌无活性。