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肾功能不全患者胸腔积液中头孢西丁的水平。

Pleural fluid levels of cefoxitin in patients with renal impairment.

作者信息

Barrueco M, Otero M J, Garcia M J, Lanao J M, Dominguez-Gil A

出版信息

Int J Clin Pharmacol Ther Toxicol. 1986 Sep;24(9):485-9.

PMID:3781682
Abstract

The pharmacokinetics of cefoxitin was studied in 14 patients with a pleural effusion, 8 of which had normal renal function and the other 6 varying degrees of renal impairment. All patients received a single dose of 30 mg/kg i.v. bolus of the antibiotic. The serum and pleural fluid concentrations of cefoxitin were determined microbiologically. The serum elimination half-life of the antibiotic in the group of patients with normal renal function had a mean value of 1.35 +/- 0.56 h while that of the second group ranged between 2.00 h and 40.79 h, according to the deterioration in renal function. The disappearance half-life of cefoxitin from pleural fluid increased parallel to the degree of renal impairment, reaching a value of 30.09 h for a creatinine clearance (Ccr) of 5.8 ml/min. From the data obtained, dosage regimens were programmed according to the degree of renal function with the aim of achieving safe and efficient cefoxitin levels in both biological fluids.

摘要

对14例胸腔积液患者的头孢西丁药代动力学进行了研究,其中8例肾功能正常,另外6例有不同程度的肾功能损害。所有患者均静脉推注单剂量30mg/kg的该抗生素。采用微生物学方法测定头孢西丁的血清和胸腔积液浓度。肾功能正常患者组中该抗生素的血清消除半衰期平均值为1.35±0.56小时,而第二组根据肾功能损害程度,其半衰期在2.00小时至40.79小时之间。头孢西丁在胸腔积液中的消除半衰期随肾功能损害程度平行增加,当肌酐清除率(Ccr)为5.8ml/min时达到30.09小时。根据获得的数据,根据肾功能程度制定给药方案,目的是在两种生物体液中达到安全有效的头孢西丁水平。

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