首页> 外文期刊>Clinical microbiology and infection: European Society of Clinical Microbiology and Infectious Diseases >Breakpoints for extended-spectrum beta-lactamase-producing Enterobacteriacae: pharmacokinetic/pharmacodynamic considerations.
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Breakpoints for extended-spectrum beta-lactamase-producing Enterobacteriacae: pharmacokinetic/pharmacodynamic considerations.

机译:产生广谱β-内酰胺酶的肠杆菌的转折点:药代动力学/药效学方面的考虑。

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摘要

An understanding of antibacterial pharmacokinetics and pharmacodynamics is central to setting clinical breakpoints. It is important to understand any impact that a resistance mechanism may have on these basic drug properties. With extended-spectrum beta-lactamase (ESBL)-producing strains of Enterobacteriacae, it is known that MIC, and hence T>MIC, for beta-lactams predicts outcome. Therefore, pharmacodynamic modelling can be used to set breakpoints for ESBL-producing bacteria with beta-lactams.
机译:对抗菌药物动力学和药效学的了解是设定临床断点的关键。重要的是要了解耐药机制可能对这些基本药物特性产生的影响。对于产肠杆菌的广谱β-内酰胺酶(ESBL)菌株,众所周知,β-内酰胺的MIC以及T> MIC可预测结果。因此,药效学建模可用于为带有β-内酰胺的ESBL产生细菌设置断点。

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