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Pharmacological Study of Cefoxitin as an Alternative Antibiotic Therapy to Carbapenems in Treatment of Urinary Tract Infections Due to Extended-Spectrum-β-Lactamase-Producing Escherichia coli

机译:头孢西丁作为碳青霉烯类药物替代抗生素的药理学研究用于治疗因产广谱β-内酰胺酶的大肠埃希氏菌引起的尿路感染

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摘要

Cefoxitin could be an alternative to carbapenems in extended-spectrum-beta-lactamase-producing Escherichia coli (ESBL-EC) infections. However, pharmacological and clinical data regarding cefoxitin are limited. Using a recent pharmacological model and the MICs of ESBL-EC collected from pyelonephritis, we determined the probabilities to reach four pharmacological targets: free cefoxitin concentrations above the MIC during 50% and 100% of the administration interval (T>MIC = 50% and T>MIC = 100%, respectively) and free cefoxitin concentrations above 4× MIC during 50% and 100% of the administration interval (T>4MIC = 50% and T>4MIC = 100%, respectively). Cefoxitin could be used to treat ESBL-EC pyelonephritis, but administration modalities should be optimized according to MICs in order to reach pharmacological targets.
机译:头孢西丁可能是产生广谱β-内酰胺酶的大肠杆菌(ESBL-EC)感染中碳青霉烯类药物的替代品。但是,有关头孢西丁的药理和临床数据有限。使用最新的药理模型和从肾盂肾炎收集的ESBL-EC的MIC,我们确定了达到四个药理目标的可能性:在给药间隔的50%和100%期间,MIC上方的游离头孢西丁浓度(T> MIC = 50%和在施用间隔的50%和100%(分别为T> 4MIC = 50%和T> 4MIC = 100%)期间,T> MIC = 100%)和4x MIC以上的游离头孢西丁浓度。头孢西丁可用于治疗ESBL-EC肾盂肾炎,但应根据MIC优化给药方式,以达到药理学目标。

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