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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