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头孢曲松和头孢噻肟在肝硬化腹水患者中的药代动力学。

The pharmacokinetics of ceftriaxone and cefotaxime in cirrhotic patients with ascites.

作者信息

Hary L, Andrejak M, Leleu S, Orfila J, Capron J P

机构信息

Unité de Pharmacologie Clinique, Laboratoire de Bactériologie, Université de Picardie, France.

出版信息

Eur J Clin Pharmacol. 1989;36(6):613-6. doi: 10.1007/BF00637745.

Abstract

We have compared in two separate studies the kinetics of ceftriaxone and cefotaxime in 8 cirrhotic patients with ascites and 8 control subjects after a single 20 min intravenous infusion of 1 g of each drug. The apparent volumes of distribution (Vz) were found to be significantly higher in cirrhotics than in control subjects (0.87, versus 0.49, l.kg-1, for cefotaxime and 0.23 versus 0.13 for ceftriaxone). The elimination kinetics of ceftriaxone were similar in the two groups. In contrast, the total and non-renal clearances of cefotaxime were reduced in cirrhotic patients. The two drugs rapidly entered the ascitic fluid. Peritoneal concentrations of ceftriaxone were higher than 7 micrograms.ml-1 from the second hour after the infusion and were 8.9 micrograms.ml-1 at 24 h. Peritoneal concentrations of cefotaxime were higher than 4 micrograms.ml-1 from 0.5 to 8 h after the infusion.

摘要

我们在两项独立研究中比较了8例肝硬化腹水患者和8例对照受试者单次静脉输注1克头孢曲松和头孢噻肟20分钟后这两种药物的动力学。发现肝硬化患者的表观分布容积(Vz)显著高于对照受试者(头孢噻肟分别为0.87和0.49升/千克,头孢曲松分别为0.23和0.13)。两组中头孢曲松的消除动力学相似。相比之下,肝硬化患者中头孢噻肟的总清除率和非肾清除率降低。这两种药物迅速进入腹水。输注后第二小时起,头孢曲松的腹腔浓度高于7微克/毫升,24小时时为8.9微克/毫升。输注后0.5至8小时,头孢噻肟的腹腔浓度高于4微克/毫升。

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