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In Vitro Activities of Combinations of Rifampin with Other Antimicrobials against Multidrug-Resistant Acinetobacter baumannii

机译:利福平与其他抗多重耐药鲍曼不动杆菌的抗菌药物的体外活性

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摘要

The antimicrobial treatment of multidrug-resistant (MDR) Acinetobacter baumannii infections has become a great challenge for medical staff all over the world. Increasing numbers of MDR A. baumannii infections have been identified and reported, but effective clinical treatments for them are decreasing. The objective of this study was to investigate the in vitro activities of combinations of rifampin (an established antimicrobial) and other antimicrobials, including biapenem, colistin, and tigecycline, against 73 clinical isolates of MDR A. baumannii. In total, 73 clinical isolates of MDR A. baumannii were collected from two A-level general hospitals in Beijing, and the MICs of rifampin, biapenem, colistin, and tigecycline were determined. The checker-board method was used to determine the fractional inhibitory concentration indices (FICIs), that is, whether the combinations acted synergistically against these isolates. The MIC50, MIC90, and MICrange of rifampin combined with biapenem, colistin, and tigecycline against the isolates were clearly lower than those for four antimicrobials (rifampin, biapenem, colistin, and tigecycline) that were used alone. Combinations of rifampin with biapenem, colistin, and tigecycline individually demonstrated the following interactions: synergistic interactions (FICI <= 0.5) for 31.51%, 34.25%, and 31.51% of the isolates, partially synergistic interactions (0.5 < FICI < 1) for 49.31%, 43.83%, and 47.94% of the isolates, and additive interactions (FICI = 1) for 19.18%, 21.92%, and 20.55% of the isolates, respectively. There were no indifferent (1 < FICI < 4) or antagonistic (FICI >= 4) interactions. Therefore, combinations of rifampin with biapenem, colistin, or tigecycline may be future therapeutic alternatives for the treatment of MDR A. baumannii infections.
机译:多重耐药性鲍曼不动杆菌感染的抗菌治疗已成为全球医务人员的巨大挑战。已经发现并报道了越来越多的MDR鲍曼不动杆菌感染,但是针对它们的有效临床治疗正在减少。这项研究的目的是研究利福平(一种已建立的抗菌药物)和其他抗菌药物(包括比阿培南,粘菌素和替加环素)的组合对73种MDR鲍曼不动杆菌临床分离株的体外活性。总共从北京的两家A级综合医院收集了73株MDR鲍曼不动杆菌临床分离株,并测定了利福平,比阿培南,大肠菌素和替加环素的MIC。棋盘格方法用于确定分数抑制浓度指数(FICI),即组合是否对这些分离株具有协同作用。利福平与比阿培南,大肠菌素和替加环素组合使用的利福平的MIC50,MIC90和MICrange明显低于单独使用的四种抗微生物药(利福平,比阿培南,粘菌素和替加环素)的分离物。利福平与比安培南,大肠菌素和替加环素的组合分别显示以下相互作用:分离株的协同相互作用(FICI <= 0.5)分别为31.51%,34.25%和31.51%,部分协同相互作用(0.5 = 4)相互作用。因此,利福平与比阿培南,大肠菌素或替加环素的组合可能是治疗MDR鲍曼不动杆菌感染的未来治疗选择。

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