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[多种疾病老年患者中去乙酰头孢噻肟的消除]

[Elimination of desacetyl cefotaxime in geriatric patients with multiple diseases].

作者信息

Mühlberg W, Platt D

出版信息

Klin Wochenschr. 1982 Dec 15;60(24):1497-500. doi: 10.1007/BF01716101.

DOI:10.1007/BF01716101
PMID:6300510
Abstract

Plasma concentrations of cefotaxime and desacetyl cefotaxime were determined by HPLC in geriatric patients with multiple diseases. Comparison with a younger control group of healthy volunteers showed a prolongation of half-life of CTX and dCTX in the older patients. A significant correlation between pharmacokinetic parameters of dCTX and other clinical and chemical parameters was found. Half-life of dCTX was positively correlated with age of the geriatric patients (P less than 0.05). There was also a significant relationship between CHE in serum and plasma peak concentrations of dCTX. Time until reaching plasma peak concentrations correlated closely with total bilirubin (P less than 0.01), CHE (P less than 0.001), cholesterol (P less than 0.01), and urea (P less than 0.01). Accumulation of the pharmacologically active metabolite dCTX could not be excluded in one patient with kidney disease. In accordance with other investigators it is recommended to reduce the dose of cefotaxime in geriatric patients with kidney diseases.

摘要

采用高效液相色谱法测定患有多种疾病的老年患者血浆中头孢噻肟和去乙酰头孢噻肟的浓度。与较年轻的健康志愿者对照组相比,老年患者中头孢噻肟(CTX)和去乙酰头孢噻肟(dCTX)的半衰期延长。发现dCTX的药代动力学参数与其他临床和化学参数之间存在显著相关性。dCTX的半衰期与老年患者的年龄呈正相关(P<0.05)。血清中胆碱酯酶(CHE)与dCTX的血浆峰浓度之间也存在显著关系。达到血浆峰浓度的时间与总胆红素(P<0.01)、CHE(P<0.001)、胆固醇(P<0.01)和尿素(P<0.01)密切相关。在一名肾病患者中不能排除具有药理活性的代谢产物dCTX的蓄积。与其他研究者一致,建议在患有肾病的老年患者中减少头孢噻肟的剂量。

相似文献

1
[Elimination of desacetyl cefotaxime in geriatric patients with multiple diseases].[多种疾病老年患者中去乙酰头孢噻肟的消除]
Klin Wochenschr. 1982 Dec 15;60(24):1497-500. doi: 10.1007/BF01716101.
2
Comparative determination of cefotaxime and desacetyl cefotaxime in serum and bile by bioassay and high-performance liquid chromatography.
Arzneimittelforschung. 1981;31(2):362-5.
3
Pharmacokinetics of cefotaxime and its desacetyl metabolite in plasma and in cerebrospinal fluid.
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Cefotaxime and desacetylcefotaxime pharmacokinetics in very low birth weight neonates.极低出生体重儿中头孢噻肟和去乙酰头孢噻肟的药代动力学
J Pediatr. 1989 Mar;114(3):461-7. doi: 10.1016/s0022-3476(89)80573-6.
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Pharmacokinetics of cefotaxime and its active metabolite in children with renal dysfunction.头孢噻肟及其活性代谢产物在肾功能不全儿童中的药代动力学。
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Elimination kinetics of cefotaxime and desacetyl cefotaxime in patients with renal insufficiency and during hemodialysis.肾功能不全患者及血液透析期间头孢噻肟和去乙酰头孢噻肟的消除动力学
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9
Pharmacokinetics of cefotaxime and desacetyl-cefotaxime in cirrhosis of the liver.头孢噻肟和去乙酰头孢噻肟在肝硬化患者中的药代动力学
Chemotherapy. 1984;30(1):7-17. doi: 10.1159/000238238.
10
Pharmacokinetics of cefotaxime in preterm infants.头孢噻肟在早产儿中的药代动力学
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引用本文的文献

1
Pharmacokinetic modelling of cefotaxime and desacetylcefotaxime--a population study in 25 elderly patients.头孢噻肟和去乙酰头孢噻肟的药代动力学建模——25例老年患者的群体研究
Eur J Clin Pharmacol. 2004 Mar;60(1):11-6. doi: 10.1007/s00228-003-0725-9. Epub 2004 Feb 7.
2
Pharmacokinetics of antibiotics in the elderly.
Eur J Clin Microbiol. 1987 Jun;6(3):329-30. doi: 10.1007/BF02017633.

本文引用的文献

1
[Changes in pharmacokinetics in the aged and their practical consequences].[老年人药代动力学的变化及其实际影响]
Z Gerontol. 1981 Sep-Oct;14(5):382-7.
2
Drug metabolites in renal failure: pharmacokinetic and clinical implications.肾衰竭中的药物代谢产物:药代动力学及临床意义
Clin Pharmacokinet. 1981 Sep-Oct;6(5):329-45. doi: 10.2165/00003088-198106050-00001.
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[The dosage of important antibiotics and tuberculostatics in renal insufficiency].
Internist (Berl). 1981 Oct;22(10):601-6.
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[Cefotaxime. Pharmacokinetics in geriatric patients with multimorbidity].[头孢噻肟。老年多病患者的药代动力学]
Med Welt. 1982 Apr 16;33(15):551-60.
5
Comparative determination of cefotaxime and desacetyl cefotaxime in serum and bile by bioassay and high-performance liquid chromatography.
Arzneimittelforschung. 1981;31(2):362-5.
6
[Pharmacokinetics of cefotaxim in geriatric patients (author's transl)].头孢噻肟在老年患者中的药代动力学(作者译)
MMW Munch Med Wochenschr. 1980 Nov 14;122(46):1651-4.
7
The frequency of adverse drug reactions as dependent upon age, sex and duration of hospitalization.药物不良反应的发生率与年龄、性别及住院时长的关系。
Int J Clin Pharmacol Biopharm. 1976 Apr;13(3):187-95.