Jones R N, Fuchs P C, Barry A L, Gavan T L, Sommers H M, Gerlach E H
Antimicrob Agents Chemother. 1980 Apr;17(4):743-9. doi: 10.1128/AAC.17.4.743.
The in vitro activity of cefoperazone (T-1551) against almost 9,000 recent clinical isolates at six institutions was tested and compared with that of cephalothin and gentamicin. The modal minimum inhibitory concentrations of cefoperazone were 16- and 4-fold less than those of cephalothin and gentamicin, respectively, against 5,503 strains of Enterobacteriaceae. Species normally resistant to cephalothin, such as indole-positive protease and enterobacters, were almost universally susceptible to cefoperazone. Cefoperazone demonstrated activity comparable to gentamicin against Pseudomonas aeruginosa and other pseudomonads.
对头孢哌酮(T - 1551)在六个机构针对近9000株近期临床分离菌株的体外活性进行了测试,并与头孢噻吩和庆大霉素的活性进行了比较。针对5503株肠杆菌科菌株,头孢哌酮的最低抑菌浓度中值分别比头孢噻吩和庆大霉素低16倍和4倍。通常对头孢噻吩耐药的菌种,如吲哚阳性变形杆菌和肠杆菌,几乎对头孢哌酮普遍敏感。头孢哌酮对铜绿假单胞菌和其他假单胞菌的活性与庆大霉素相当。