替加环素
舒巴坦钠
鲍曼不动杆菌
头孢哌酮
棋盘
肉汤微量稀释
微生物学
抗菌剂
抗生素
多重耐药
药理学
医学
最小抑制浓度
生物
抗生素耐药性
细菌
亚胺培南
铜绿假单胞菌
遗传学
作者
Bin Liu,Yan Bai,You-ning Liu,Xiuzhen Di,Xin Zhang,Rui Wang,Jin Wang
标识
DOI:10.1179/1973947814y.0000000203
摘要
Over the last decade, multidrug-resistant Acinetobacter baumannii (MDRAB) has emerged as one of the most problematic nosocomial pathogens. Empirical combination therapy has become a common practice to treat patients infected with MDRAB. In vitro interactions of tigecycline with cefoperazone-sulbactam were assessed in 72 MDRAB isolates. Minimum inhibitory concentrations (MICs) were determined by broth microdilution method. Antibiotic interactions were determined by chequerboard and time-kill assays. Chequerboard analysis showed 29·2% synergy and no antagonistic interactions. Time-kill assays confirmed the synergistic interaction between two agents for three of four selected extensively drug-resistant A. baumannii (XDRAB) isolates. No antagonism was revealed by time-kill assays. Moreover, tigecycline in combination with cefoperazone-sulbactam appeared to be more effective than tigecycline in combination with sulbactam against XDRAB. In conclusion, in vitro synergistic activities of tigecycline in combination with cefoperazone-sulbactam against MDRAB were demonstrated, suggesting a superior treatment option against MDRAB.
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