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氨基糖苷类药物对肾功能影响的临床研究——阿贝卡星的药代动力学及其血液透析和活性炭吸附清除作用

[Clinical study of aminoglycosides on renal dysfunction--pharmacokinetics of arbekacin and its elimination effects by hemodialysis and adsorption with charcoal].

作者信息

Arakawa S, Maeda H, Fujii A, Kamidono S, Hamada K, Miyazaki S, Hara S

机构信息

Department of Urology, Kobe University, School of Medicine.

出版信息

Hinyokika Kiyo. 1989 Apr;35(4):697-704.

PMID:2735273
Abstract

In vitro studies of elimination of arbekacin (HBK), a new aminoglycoside antibiotic, from blood by means of hemodialysis or adsorption with charcoal, and pharmacokinetic studies in patients with renal dysfunction were examined. HBK was well eliminated by hollow fiber type artificial kidney (HFAK) with a half-life of 0.13 hr. HBK was also well eliminated by an adsorption tube containing charcoal with even shorter half-life of 0.03 hr. As to pharmacokinetics of HBK in patients with renal dysfunction, blood levels became higher with a greater reduction in 24 hr endogenous creatinine clearance (Ccr). A decreasing tendency was also seen in urinary recovery rate. These results indicated that hemodialysis and adsorption with charcoal are useful for elimination of HBK from blood. It is recommendable in patients with renal dysfunction to take some measures such as prolongation of administration interval of HBK according to the extent of decrease in Ccr.

摘要

对新型氨基糖苷类抗生素阿贝卡星(HBK)通过血液透析或用活性炭吸附从血液中消除的体外研究,以及对肾功能不全患者的药代动力学研究进行了考察。中空纤维型人工肾(HFAK)能很好地消除HBK,半衰期为0.13小时。含活性炭的吸附管也能很好地消除HBK,半衰期更短,为0.03小时。至于HBK在肾功能不全患者中的药代动力学,随着24小时内生肌酐清除率(Ccr)更大程度的降低,血药浓度会升高。尿回收率也呈下降趋势。这些结果表明,血液透析和用活性炭吸附对从血液中消除HBK是有用的。对于肾功能不全患者,建议根据Ccr降低的程度采取一些措施,如延长HBK的给药间隔。

相似文献

1
[Clinical study of aminoglycosides on renal dysfunction--pharmacokinetics of arbekacin and its elimination effects by hemodialysis and adsorption with charcoal].氨基糖苷类药物对肾功能影响的临床研究——阿贝卡星的药代动力学及其血液透析和活性炭吸附清除作用
Hinyokika Kiyo. 1989 Apr;35(4):697-704.
2
[Pharmacokinetics of arbekacin in healthy volunteers and patients with renal insufficiency].
Jpn J Antibiot. 1989 Jan;42(1):200-7.
3
[Pharmacokinetics of arbekacin in dogs. I. Serum concentration and urinary excretion].阿贝卡星在犬体内的药代动力学。I. 血清浓度与尿排泄
Jpn J Antibiot. 1987 Feb;40(2):365-75.
4
[Pharmacokinetics of habekacin in patients with chronic renal insufficiency].[妥布霉素在慢性肾功能不全患者中的药代动力学]
Pathol Biol (Paris). 1987 Jun;35(5 Pt 2):739-41.
5
[Absorption, distribution, and excretion of arbekacin after intravenous and intramuscular administration in rats].
Jpn J Antibiot. 1987 Feb;40(2):357-64.
6
[Antibacterial activities of arbekacin, a new aminoglycoside antibiotic, against methicillin-cephem-resistant Staphylococcus aureus].
Jpn J Antibiot. 1987 Feb;40(2):349-56.
7
Antibacterial activity and ototoxicity in guinea pigs, and nephrotoxicity in rats of arbekacin.阿贝卡星对豚鼠的抗菌活性及耳毒性和对大鼠的肾毒性
Arzneimittelforschung. 1986 Oct;36(10):1511-7.
8
Pharmacokinetics of habekacin in patients with renal insufficiency.肾功能不全患者中阿贝卡星的药代动力学。
Antimicrob Agents Chemother. 1987 Apr;31(4):575-7. doi: 10.1128/AAC.31.4.575.
9
[Pharmacokinetics of arbekacin in dogs. II. The distribution of arbekacin in tissues].[阿贝卡星在犬体内的药代动力学。II. 阿贝卡星在组织中的分布]
Jpn J Antibiot. 1987 Feb;40(2):377-84.
10
[Comparative clinical trial of HBK and amikacin (AMK) in the treatment of respiratory infections].[HBK与阿米卡星(AMK)治疗呼吸道感染的比较临床试验]
Kansenshogaku Zasshi. 1987 Jan;61(1):22-53. doi: 10.11150/kansenshogakuzasshi1970.61.22.

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