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beta-Lactams without a suicide inhibitor.

机译:β-内酰胺没有自杀抑制剂。

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摘要

Existing clinical studies concerning the impact of therapy with third-generation cephalosporins or cefepime on infections caused by extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae are retrospective, non-randomised, and have been carried out with a small number of patients and low-dosage schedules that lack PK-PD correlations with clinical efficacy. Rates of clinical failure and mortality are higher than those in studies with non-ESBL- producing Enterobacteriaceae. Therefore, in settings with a high prevalence of ESBL-producing Enterobacteriaceae, empirical therapy with advanced cephalosporins should be avoided. Temocillin, an old beta-lactam that is stable in the presence of both ESBLs and AmpC beta-lactamases, seems to deserve revival, although clinical data are limited.
机译:关于治疗对第三代头孢菌素或头脑对延长光谱β-内酰胺酶(ESBL)引起的感染的影响的现有临床研究 - 发回肠杆菌痤疮症引起的感染是回顾性的,非随机化,并且已经用少数患者进行 低剂量调度缺乏与临床疗效的PK-PD相关性。 临床失败和死亡率的速率高于非ESBL-产生的肠杆菌的研究。 因此,在产生ESBL产生高患病率的环境中,应避免使用先进的头孢菌素的经验治疗。 Temocillin,在ESBLS和AMPCβ-内酰胺酶存在下稳定的旧β-内酰胺似乎值得复兴,但临床数据有限。

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