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雷贝拉唑:稳定期终末期肾衰竭患者的药代动力学与耐受性

Rabeprazole: pharmacokinetics and tolerability in patients with stable, end-stage renal failure.

作者信息

Keane W F, Swan S K, Grimes I, Humphries T J

机构信息

Total Renal Research, Inc., Minneapolis, Minnesota, USA.

出版信息

J Clin Pharmacol. 1999 Sep;39(9):927-33. doi: 10.1177/00912709922008542.

Abstract

The authors compare the pharmacokinetic profiles, safety, and tolerability of rabeprazole, a new proton pump inhibitor (PPI), in healthy volunteers and in subjects with stable, end-stage renal failure. This single-center, open-label trial included two groups of subjects: 10 healthy males with 24-hour creatinine clearance > or = 90 mL/min/m2 and 10 males with renal failure (24-hour creatinine clearance < or = 5 mL/min/m2) receiving hemodialytic therapy. Normal subjects received a single, oral 20 mg rabeprazole dose. Those with renal failure received a 20 mg dose of rabeprazole on the day after hemodialysis and a second dose after a 2-week washout period during dialysis. Blood samples were drawn before and up to 24 hours after rabeprazole administration for determination of plasma rabeprazole concentrations by high-performance liquid chromatography. Safety and tolerability of rabeprazole were determined by reporting adverse events and comparing vital signs, ECG, physical examinations, and clinical laboratory tests before and during treatment. Comparison of pharmacokinetic results from healthy volunteers with those from subjects with renal failure indicated no clinically significant differences between groups. In addition, there were no statistically significant differences between any pharmacokinetic parameters recorded during or after hemodialysis. Rabeprazole was well tolerated by both groups. Only two drug-related adverse events were reported, and there were no significant treatment-emergent changes in vital signs or ECG. Treatment-emergent changes in hematologic and clinical chemistry parameters were observed for a few subjects in each group and generally represented only slight deviations from the normal range. These results indicate that no dosage adjustment of rabeprazole is required in patients with renal dysfunction. These findings and the well-documented clinical efficacy of this new PPI in patients with gastric ulcers, duodenal ulcers, or gastroesophageal reflux disease support rabeprazole's use in the treatment of patients with acid peptic disorders.

摘要

作者比较了新型质子泵抑制剂(PPI)雷贝拉唑在健康志愿者和稳定的终末期肾衰竭患者中的药代动力学特征、安全性和耐受性。这项单中心、开放标签试验包括两组受试者:10名健康男性,其24小时肌酐清除率≥90 mL/min/m²,以及10名接受血液透析治疗的肾衰竭男性(24小时肌酐清除率≤5 mL/min/m²)。正常受试者口服单剂20 mg雷贝拉唑。肾衰竭患者在血液透析后的第二天接受20 mg雷贝拉唑剂量,并在透析期间为期2周的洗脱期后接受第二剂。在雷贝拉唑给药前及给药后长达24小时采集血样,通过高效液相色谱法测定血浆雷贝拉唑浓度。通过报告不良事件并比较治疗前后的生命体征、心电图、体格检查和临床实验室检查来确定雷贝拉唑的安全性和耐受性。健康志愿者与肾衰竭受试者的药代动力学结果比较表明,两组之间无临床显著差异。此外,血液透析期间或之后记录的任何药代动力学参数之间也无统计学显著差异。两组对雷贝拉唑的耐受性均良好。仅报告了两例与药物相关的不良事件,生命体征或心电图无显著的治疗期出现的变化。每组有少数受试者观察到血液学和临床化学参数的治疗期出现的变化,一般仅代表与正常范围的轻微偏差。这些结果表明,肾功能不全患者无需调整雷贝拉唑的剂量。这些发现以及这种新型PPI在胃溃疡、十二指肠溃疡或胃食管反流病患者中充分记录的临床疗效支持雷贝拉唑用于治疗酸相关性疾病患者。

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