Kirch W, Ohnhaus E E, Dylewicz P, Pabst J, Storstein L
Am Heart J. 1986 Feb;111(2):325-9. doi: 10.1016/0002-8703(86)90148-1.
Following administration of digitoxin, 1 mg intravenously, the pharmacokinetics of this glycoside were studied in eight healthy volunteers and in eight patients with hepatorenal insufficiency (mean creatinine clearance 19.6 +/- 2.9 ml/min; antipyrine clearance 25.6 +/- 3.2 ml/min; means +/- SEM). Liver cirrhosis of the patients was confirmed by liver biopsy. Plasma protein binding of digitoxin (means +/- SEM) was 95.1 +/- 0.7% in the patients and 95.6 +/- 1.2% in the volunteers (NS). Total body clearance of digitoxin was 0.0530 +/- 0.0040 ml/min/kg of body weight in the patients and 0.0547 +/- 0.0043 ml/min/kg of body weight in the healthy subjects (NS). When elimination half-lives of the patients and the volunteers were compared, there was also no significant difference (7.0 +/- 0.77 days in the patient group and 7.8 +/- 0.8 days in the volunteers). Our data concerning digitoxin kinetics in patients with hepatorenal insufficiency do not indicate an accumulation of the drug in these patients.
静脉注射1毫克洋地黄毒苷后,在8名健康志愿者和8名肝肾不全患者(平均肌酐清除率19.6±2.9毫升/分钟;安替比林清除率25.6±3.2毫升/分钟;均值±标准误)中研究了这种糖苷的药代动力学。患者的肝硬化通过肝活检得以证实。洋地黄毒苷的血浆蛋白结合率(均值±标准误)在患者中为95.1±0.7%,在志愿者中为95.6±1.2%(无显著性差异)。洋地黄毒苷的总体清除率在患者中为0.0530±0.0040毫升/分钟/千克体重,在健康受试者中为0.0547±0.0043毫升/分钟/千克体重(无显著性差异)。比较患者和志愿者的消除半衰期时,也没有显著差异(患者组为7.0±0.77天,志愿者组为7.8±0.8天)。我们关于肝肾不全患者洋地黄毒苷动力学的数据并未表明该药物在这些患者中会蓄积。