舒巴坦钠
鲍曼不动杆菌
阿维巴坦
头孢他啶/阿维巴坦
微生物学
β-内酰胺酶抑制剂
琼脂稀释
氨苄西林
医学
药理学
化学
生物
头孢他啶
抗菌剂
抗生素
最小抑制浓度
铜绿假单胞菌
细菌
抗生素耐药性
亚胺培南
遗传学
作者
Carlos Hernán Rodríguez,Adriana Brune,Marcela Nastro,Carlos Vay,Àngela Famiglietti
摘要
Introduction. The therapeutic options to treat Acinetobacter baumannii infections are very limited. Aim. Our aim was to evaluate the activity of sulbactam combined directly with avibactam or the ampicillin-sulbactam/ceftazidime-avibactam combination against extensively drug-resistant A. baumannii isolates. Methodology. Extensively drug-resistant A. baumannii isolates ( n =127) collected at several South American hospitals were studied. Synergy with the sulbactam/avibactam combination was assessed in all isolates using the agar dilution method. Avibactam was used at a fixed concentration of 4 mg l −1 . A disc diffusion synergy test was also performed. Synergy by a time-kill experiment was performed in a selected isolate. Results. Synergy with sulbactam/avibactam was demonstrated in 124 isolates and it showed MIC values ≤4 mg l −1 . This synergy was not detected in the three New Delhi metallo-β-lactamase-harbouring isolates. Similar results were observed with the disc diffusion synergy test of ampicillin-sulbactam/ceftazidime-avibactam. In the time-kill experiments, sulbactam/avibactam showed a rapid synergistic and bactericidal activity in ampicillin-sulbactam-resistant isolates. Conclusions. This study demonstrated that the sulbactam/avibactam combination displayed synergistic activity against A. baumannii isolates. This synergy was observed when both inhibitors were also used as part of the commercially available combinations: ampicillin-sulbactam and ceftazidime-avibactam.
科研通智能强力驱动
Strongly Powered by AbleSci AI