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肾功能不全或甲状腺功能亢进患者的地西泮动力学

Diazepam kinetics in patients with renal insufficiency or hyperthyroidism.

作者信息

Ochs H R, Greenblatt D J, Kaschell H J, Klehr U, Divoll M, Abernethy D R

出版信息

Br J Clin Pharmacol. 1981 Dec;12(6):829-32. doi: 10.1111/j.1365-2125.1981.tb01315.x.

DOI:10.1111/j.1365-2125.1981.tb01315.x
PMID:7340884
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1401920/
Abstract

1 Eight patients with end-stage renal insufficiency on maintenance haemodialysis, and seven patients with newly diagnosed hyperthyroidism, received a single intravenous dose of diazepam, followed by blood sampling over the next 7 days. Fifteen healthy volunteer controls, matched with patients for age and sex, were similarly studied. 2 Diazepam half-life in renal failure patients (mean 37 h) was greatly reduced compared to controls (mean 92 h, P less than 0.05) and clearance of total (free plus bound) diazepam correspondingly increased (0.94 v 0.34 ml min-1 kg-1, P less than 0.01). 3 However, differences were largely related to disease-related changes in drug binding and distribution. Mean unbound fraction of diazepam in plasma of renal patients (7.0%) was greatly increased over controls (1.4%, P less than 0.01) and Vd of unbound diazepam greatly reduced (57 v 157 l/kg, P less than 0.01). 4 Clearance of pharmacologically active unbound diazepam (intrinsic clearance) was not significantly different between renal patients and controls (23 vs 30 ml min-1 kg-1). 5 None of the kinetic variables for total or unbound diazepam in thyrotoxic patients differed significantly from those in controls matched for age and sex. 6 End-stage renal failure (or its associated drug therapy) alters diazepam protein binding and distribution, but does not significantly change clearance of unbound drug. Thyrotoxicosis does not influence diazepam kinetics.

摘要
  1. 8例维持性血液透析的终末期肾功能不全患者和7例新诊断的甲状腺功能亢进患者接受了单次静脉注射地西泮,随后在接下来的7天内进行血样采集。选取了15名年龄和性别与患者相匹配的健康志愿者作为对照,进行了类似的研究。2. 肾衰竭患者地西泮的半衰期(平均37小时)与对照组(平均92小时,P<0.05)相比大幅缩短,总地西泮(游离加结合)的清除率相应增加(0.94对0.34毫升/分钟·千克,P<0.01)。3. 然而,差异主要与疾病相关的药物结合和分布变化有关。肾衰竭患者血浆中地西泮的平均游离分数(7.0%)较对照组(1.4%,P<0.01)大幅增加,游离地西泮的分布容积大幅降低(57对157升/千克,P<0.01)。4. 肾衰竭患者和对照组之间具有药理活性的游离地西泮的清除率(内在清除率)无显著差异(23对30毫升/分钟·千克)。5. 甲状腺毒症患者总地西泮或游离地西泮的动力学变量与年龄和性别相匹配的对照组相比均无显著差异。6. 终末期肾衰竭(或其相关的药物治疗)会改变地西泮的蛋白结合和分布,但不会显著改变游离药物的清除率。甲状腺毒症不会影响地西泮的动力学。

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1
Diazepam kinetics in patients with renal insufficiency or hyperthyroidism.肾功能不全或甲状腺功能亢进患者的地西泮动力学
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本文引用的文献

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Diazepam disposition determinants.地西泮处置的决定因素。
Clin Pharmacol Ther. 1980 Mar;27(3):301-12. doi: 10.1038/clpt.1980.40.
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Alterations in drug distribution and clearance due to obesity.
J Pharmacol Exp Ther. 1981 Jun;217(3):681-5.
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Protein binding of diphenylhydantoin and desmethylimipramine in plasma from patients with poor renal function.肾功能不全患者血浆中苯妥英钠和去甲丙咪嗪的蛋白结合情况。
N Engl J Med. 1971 Jul 29;285(5):264-7. doi: 10.1056/NEJM197107292850506.
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Pharmacokinetics of drugs in patients with the nephrotic syndrome.肾病综合征患者的药物药代动力学
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Binding of drugs to serum albumin (first of two parts).药物与血清白蛋白的结合(两部分中的第一部分)
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Inter- and intrasubject variation in diazepam free fraction.地西泮游离分数的个体间和个体内变异。
Clin Pharmacol Ther. 1979 Aug;26(2):247-55. doi: 10.1002/cpt1979262247.