Qadri S M, Ueno Y, Ellis M E
King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Chemotherapy. 1991;37(1):15-22. doi: 10.1159/000238827.
In vitro antibacterial activity of the new penem FCE 22101 was tested against blood culture isolates from 1,374 consecutive patients in a major tertiary care referral center in Saudi Arabia. Many of the isolates were significantly more resistant to commonly used beta lactams. Of the 809 members of Enterobacteriaceae tested all but 14 isolates of Enterobacter were susceptible to FCE 22101 with an MIC range of 0.12-8.0 micrograms/ml. It inhibited all the 183 isolates of Staphylococcus aureus, both methicillin-sensitive and methicillin-resistant. Ninety percent of coagulase-negative staphylococci and enterococci were susceptible to this new penem. All isolates of Acinetobacter, CDC group VE-2 and Brucella melitensis from blood were inhibited by FCE 22101. However, it was ineffective against pseudomonads. Of the nine other beta lactam drugs tested for comparison, only imipenem was found to be more inhibitory, at lower MIC values, than FCE 22101.
新型青霉烯类药物FCE 22101的体外抗菌活性,在沙特阿拉伯一家大型三级医疗转诊中心,针对1374例连续患者的血培养分离株进行了测试。许多分离株对常用的β-内酰胺类药物耐药性显著更高。在测试的809株肠杆菌科细菌中,除14株阴沟肠杆菌分离株外,其余所有菌株对FCE 22101均敏感,其MIC范围为0.12 - 8.0微克/毫升。它抑制了所有183株金黄色葡萄球菌,包括甲氧西林敏感株和甲氧西林耐药株。90%的凝固酶阴性葡萄球菌和肠球菌对这种新型青霉烯类药物敏感。血液中的所有不动杆菌属、CDC组VE - 2和羊布鲁氏菌分离株均被FCE 22101抑制。然而,它对假单胞菌无效。在测试比较的其他9种β-内酰胺类药物中,只有亚胺培南在较低的MIC值下比FCE 22101具有更强的抑制作用。