首页> 外文期刊>European journal of clinical microbiology and infectious diseases: Official publication of the European Society of Clinical Microbiology >Ceftazidime- and imipenem-induced endotoxin release during treatment of gram-negative infections.
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Ceftazidime- and imipenem-induced endotoxin release during treatment of gram-negative infections.

机译:在治疗革兰氏阴性感染期间,头孢他啶和亚胺培南诱导的内毒素释放。

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摘要

To determine whether ceftazidime and imipenem, which target two different penicillin-binding proteins, result in different amounts of endotoxin and cytokine release in patients with gram-negative infection, plasma endotoxin, interleukin-6, and tumor necrosis factor alpha were measured during the first 24 h of antibiotic therapy in 27 patients with gram-negative infection who had been randomized to receive either ceftazidime 2 g t.i.d. (n=12) or imipenem/cilastatin 1 g t.i.d. (n=15). The source of infection was the digestive tract (n=13), the urinary tract (n=5), the respiratory tract (n=2), soft tissue (n=2), i.v. line (n=2), or other (n=3). After the first antibiotic injection, a significant increase in the median concentration of plasma interleukin-6 and plasma tumor necrosis factor alpha was noted, without significant differences related to the antibiotic administered. Antibiotic-induced endotoxemia was detectable in nine patients (including 7 with bacteremia). In conclusion, ceftazidime and imipenem had similar effects on endotoxin and cytokine release during the treatment of gram-negative infections.
机译:为了确定针对两种不同青霉素结合蛋白的头孢他啶和亚胺培南是否导致革兰氏阴性感染患者的内毒素和细胞因子释放量不同,在首次使用过程中测定了血浆内毒素,白介素-6和肿瘤坏死因子α随机分配接受头孢他啶2 g tid的27例革兰氏阴性感染患者的24小时抗生素治疗(n = 12)或亚胺培南/西司他丁1 g t.i.d. (n = 15)。感染源是消化道(n = 13),泌尿道(n = 5),呼吸道(n = 2),软组织(n = 2),静脉感染。行(n = 2)或其他(n = 3)。首次注射抗生素后,血浆白细胞介素6和血浆肿瘤坏死因子α的中位数浓度显着增加,而与所用抗生素无关。在9例患者(包括7例菌血症)中检测到了抗生素引起的内毒素血症。总之,在革兰氏阴性感染的治疗过程中,头孢他啶和亚胺培南对内毒素和细胞因子的释放具有相似的作用。

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