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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Assessment of the Potential for Inducing Resistance in Multidrug-Resistant Organisms from Exposure to Minocycline, Rifampin, and Chlorhexidine Used To Treat Intravascular Devices
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Assessment of the Potential for Inducing Resistance in Multidrug-Resistant Organisms from Exposure to Minocycline, Rifampin, and Chlorhexidine Used To Treat Intravascular Devices

机译:评估从暴露于米诺环素,利福平和氯己定治疗血管内器件的多药物抗性生物体抗性抗性的可能性

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摘要

To assess the potential for the induction of antimicrobial resistance following repeated subinhibitory exposures to the combination minocycline (MIN), rifampin (RIF), and chlorhexidine (CHX), a total of 29 clinical microbial pathogenic isolates were repeatedly exposed to subinhibitory concentrations of MIN, RIF, and CHX for 20 passages. MICs of the MIN, RIF, and CHX combination were assessed at each passage to evaluate the potential for resistance to have been induced. The combination of MIN, RIF, and CHX showed significant antimicrobial efficacy and synergy against organisms resistant to all 3 individual components (MIC of >= 16 mu g/ml for MIN or MIC of >= 4 mu g/ml for RIF or CHX). Among the organisms originally resistant to 2 or more individual components and the organisms originally susceptible to 2 or more individual components, there was no evidence that organisms became resistant following 20 repeated subinhibitory exposure cycles to the triple combination. The risk of resistance developing to the triple combination is extremely low because microbes are inhibited or killed before resistance can simultaneously emerge to all three agents. Surveillance studies monitoring the development of resistance should be conducted in a clinical setting.
机译:为了评估对多碳碱(Min),利福平(RIF)和氯己定(CHX)进行重复的水性抑制后诱导抗微生物抗性的潜力,共29例临床微生物致病性分离物反复暴露于水下浓度的min, RIF,和20个段落的CHX。在每个通道中评估Min,RIF和CHX组合的MIC,以评估抗性的潜力。 Min,RIF和CHX的组合显示出显着的抗微生物功效和抗生物体的抗菌效力和协同作用对所有3个单独的组分(MIC> =16μg/ mIM的MIC或MIC的MIC> =4μg/ ml的RIF或CHX) 。在最初耐2个或更多个单个组分和最初易受2个或更多个个体成分的生物体的生物体中,没有证据表明有机体在20重复的水下速度暴露于三重组合后变得抗性。抗性发展到三重组合的风险极低,因为在抗性之前抑制或杀死微生物可以同时出现所有三种试剂。监测监测监测抗性的发展应在临床环境中进行。

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