Pozet N, Brazier J L, Aïssa A H, Khenfer D, Faucon G, Apoil E, Traeger J
Eur J Clin Pharmacol. 1983;24(5):635-8. doi: 10.1007/BF00542213.
The acute effects of a single dose of diltiazem (Tildiem), a calcium antagonist, were studied in 9 patients with severely impaired renal function (GFR between 0.03 and 0.87 ml/s/1.73 m2). Control measurements were made of inulin and PAH clearance, creatinine, blood pressure, heart rate and ECG. Following administration of diltiazem 120 mg, 7 blood samples were collected in the first 12 h and after 24 h, 32 h, 48 h; urine was collected for the first 12 h, 12-24 h and 24-48 h, and blood pressure, heart rate and ECG were recorded after 6 h. Diltiazem and its main metabolite, desacetyldiltiazem, had a pharmacokinetic profile similar to that in patients with normal renal function (peak plasma concentration, half-life and urinary excretion). Diltiazem is normally eliminated in the urine to a small extent, because it is metabolized, and this also applies to desacetyldiltiazem, which is probably further metabolized.
对9例肾功能严重受损(肾小球滤过率在0.03至0.87 ml/s/1.73 m²之间)的患者研究了单剂量钙拮抗剂地尔硫䓬(恬尔心)的急性效应。对菊粉和对氨基马尿酸清除率、肌酐、血压、心率及心电图进行了对照测量。给予120 mg地尔硫䓬后,在最初12小时内采集7份血样,在24小时、32小时、48小时后各采集1份;收集最初12小时、12至24小时以及24至48小时的尿液,并在6小时后记录血压、心率及心电图。地尔硫䓬及其主要代谢产物去乙酰地尔硫䓬的药代动力学特征与肾功能正常患者相似(血浆峰浓度、半衰期及尿排泄)。地尔硫䓬通常经尿液少量排泄,因为它会被代谢,去乙酰地尔硫䓬也是如此,它可能会进一步代谢。