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Postantibiotic effects and postantibiotic sub-MIC effects of roxithromycin, clarithromycin, and azithromycin on respiratory tract pathogens.

机译:罗红霉素,克拉霉素和阿奇霉素对呼吸道病原体的抗生素后作用和抗生素后亚MIC作用。

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摘要

Pharmacodynamic parameters have become increasingly important for the determination of the optimal dosing schedules of antibiotics. In this study, the postantibiotic effects (PAEs), the postantibiotic sub-MIC effects (PA SMEs), and the sub-MIC effects (SMEs) of roxithromycin, clarithromycin, and azithromycin on reference strains of Streptococcus pyogenes group A, Streptococcus pneumoniae, and Haemophilus influenzae were investigated. The PAE was induced by 2x MICs (S. pneumoniae) or 10x MICs of the different drugs for 2 h, and the antibiotics were eliminated by washing and dilution. The PA SMEs were studied by addition of 0.1, 0.2, and 0.3x MICs during the postantibiotic phase of the bacteria, and the SMEs were studied by exposition of the bacteria to the drugs at the sub-MICs only. Growth curves were followed by viable counts for 24 h. The SMEs were generally very short. A PAE of 2.9 to 8 h was noted for all antibiotics against all strains. Clarithromycin induced a statistically significantly shorter PAE on S. pneumoniae than did roxithromycin and azithromycin and did so also against H. influenzae in comparison with azithromycin. The PA SMEs were long and varied at 0.3x MIC between 6.4 19.6 h. This pronounced suppression of regrowth of bacteria which are first treated with a suprainhibitory concentration of antibiotics and then reexposed to sub-MIC levels indicates that long dosing intervals for macrolides and azalides can be allowed.
机译:对于确定抗生素的最佳给药方案,药效参数变得越来越重要。在这项研究中,罗红霉素,克拉霉素和阿奇霉素对A型化脓性链球菌参考菌株,肺炎链球菌的抗生素后效应(PAE),抗生素后亚MIC效应(PA SMEs)和亚MIC效应(SMEs)。和流感嗜血杆菌进行了调查。通过2x MIC(肺炎链球菌)或10x不同药物的MIC诱导PAE 2小时,并通过洗涤和稀释消除抗生素。通过在细菌的抗生素后阶段添加0.1、0.2和0.3x MIC来研究PA SME,并且仅通过将细菌暴露于亚MIC的药物中来研究SME。生长曲线之后是24小时的可行计数。中小企业通常很短。对于所有菌株,所有抗生素的PAE为2.9至8小时。与罗奇霉素和阿奇霉素相比,克拉霉素在肺炎链球菌上引起的PAE在统计学上明显更短,并且与阿奇霉素相比,对流感嗜血杆菌也是如此。 PA中小企业很长,在6.4 19.6小时之间的MIC为0.3x时变化很大。首先用超抑制浓度的抗生素处理然后再暴露于亚MIC水平的这种明显的细菌再生抑制作用表明,可以延长大环内酯类和氮杂内酯类药物的给药间隔。

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