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不同程度肾功能损害受试者静脉注射单剂量噻托溴铵的药代动力学

Pharmacokinetics of intravenous, single-dose tiotropium in subjects with different degrees of renal impairment.

作者信息

Türck Dietrich, Weber Werner, Sigmund Ralf, Budde Klemens, Neumayer Hans-H, Fritsche Lutz, Rominger Karl-Ludwig, Feifel Ulrich, Slowinski Torsten

机构信息

Drug Metabolism and Pharmacokinetics Department, Boehringer Ingelheim Pharma GmbH & Co KG, Birkendorfer Strasse 65, 88397 Biberach an der Riss, Germany.

出版信息

J Clin Pharmacol. 2004 Feb;44(2):163-72. doi: 10.1177/0091270003261315.

Abstract

Tiotropium, a new potent anticholinergic bronchodilator, is excreted mainly by the kidney. To investigate the pharmacokinetics of tiotropium in renal impairment, the authors evaluated the pharmacokinetics and safety after administration of a single dose of intravenous tiotropium 4.8 microg, given as an infusion over 15 minutes in subjects with normal renal function and a wide range of renal impairment based on measured creatinine clearance (normal: > 80 mL/min, n = 6; mild impairment: > 50-80 mL/min, n = 5; moderate impairment: 30-50 mL/min, n = 7; severe impairment: < 30 mL/min, n =6). As expected for a drug excreted predominantly in unchanged form by the kidneys, tiotropium plasma concentrations increased as renal impairment worsened, with mean values of 55.5 (16.2 percent geometric coefficient of variation [%gCV]), 77.1 (20.1 %gCV), 101 (29.8 %gCV), and 108 (27.3 %gCV) pgh/mL for AUC(0-4h) in the normal renal function and the mild, moderate, and severe renal impairment groups, respectively. The percentage of tiotropium dose excreted unchanged in the urine decreased from 60.1% of dose (17.7 %gCV) to 59.3% (14.4 %gCV), 39.9% (34.5 %gCV), and 37.4% (10.2 %gCV) in the normal renal function and the mild, moderate, and severe renal impairment groups, respectively. Plasma protein binding of tiotropium did not significantly change in the renal-impaired subjects. Two subjects with normal renal function experienced headache 10 hours after the infusion, which was mild and transient. No adverse events occurred in subjects with renal impairment. There were no clinically relevant changes in blood pressure, pulse rate, 12-lead ECG, physical examination, hematology, or clinical chemistry, compared with baseline values, in any subject after intravenous administration of tiotropium. Tiotropium should only be used in patients with moderate to severe renal insufficiency if the potential benefit outweighs the potential risks.

摘要

噻托溴铵是一种新型强效抗胆碱能支气管扩张剂,主要经肾脏排泄。为研究噻托溴铵在肾功能损害患者中的药代动力学,作者评估了在肾功能正常及基于实测肌酐清除率存在广泛肾功能损害的受试者(正常:>80 mL/分钟,n = 6;轻度损害:>50 - 80 mL/分钟,n = 5;中度损害:30 - 50 mL/分钟,n = 7;重度损害:<30 mL/分钟,n = 6)中,静脉输注4.8微克单剂量噻托溴铵(输注时间15分钟)后的药代动力学及安全性。正如预期的那样,对于主要以原形经肾脏排泄的药物,随着肾功能损害加重,噻托溴铵血浆浓度升高,在肾功能正常、轻度、中度和重度肾功能损害组中,AUC(0 - 4h)的平均值分别为55.5(几何变异系数[%gCV]为16.2%)、77.1(20.1%gCV)、101(29.8%gCV)和108(27.3%gCV)皮克/毫升。噻托溴铵以原形经尿液排泄的剂量百分比在肾功能正常组为剂量的60.1%(17.7%gCV),在轻度、中度和重度肾功能损害组中分别降至59.3%(14.4%gCV)、39.9%(34.5%gCV)和37.4%(10.2%gCV)。肾功能损害受试者中噻托溴铵的血浆蛋白结合率无显著变化。两名肾功能正常的受试者在输注后10小时出现头痛,症状轻微且短暂。肾功能损害受试者未发生不良事件。静脉注射噻托溴铵后,与基线值相比,任何受试者的血压、脉搏率、12导联心电图、体格检查、血液学或临床化学检查均无临床相关变化。仅当潜在获益大于潜在风险时,噻托溴铵才可用于中度至重度肾功能不全患者中。

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