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新型袢利尿剂托拉塞米在肝硬化腹水患者中优于呋塞米的优势。一项随机、双盲交叉试验。

Advantages of the new loop diuretic torasemide over furosemide in patients with cirrhosis and ascites. A randomized, double blind cross-over trial.

作者信息

Gerbes A L, Bertheau-Reitha U, Falkner C, Jüngst D, Paumgartner G

机构信息

Department of Medicine II, Klinikum Grosshadern, University of Munich, Germany.

出版信息

J Hepatol. 1993 Mar;17(3):353-8. doi: 10.1016/s0168-8278(05)80217-x.

Abstract

Torasemide is a new loop diuretic with a longer half-life and longer action than furosemide in healthy subjects. In order to evaluate the pharmacodynamic effects, single oral doses of furosemide (80 mg) and torasemide (20 mg), which were equipotent in healthy subjects, were given to 14 patients with cirrhosis and ascites. Before the study patients underwent an equilibration period of 4 days without diuretics. The drugs were alternated following a randomized double-blind cross-over design after a wash-out period of at least 2 days. Urine was collected at defined intervals for 24 h after drug administration and blood samples were taken before, 6 h and 24 h after medication. Torasemide induced greater cumulative 24 h diuresis (2863 +/- 343 vs. 2111 +/- 184 ml, p < 0.01) than furosemide. Torasemide did not differ from furosemide for cumulative 0-6 h sodium excretion (96 +/- 17 vs. 92 +/- 23 mmol sodium) but caused a more pronounced cumulative 6-24 h natriuresis (38 +/- 11 vs. 17 +/- 4 mmol, p < 0.05). Five patients exhibited a weak response to furosemide (0-36 mmol sodium/24 h, median 24 mmol; 690-1460 ml urinary volume/24 h, median 1325 ml). These patients showed significantly higher natriuresis and diuresis following torasemide (26-136 mmol sodium/24 h, median 78 mmol, p < 0.05; 1670-3610 ml urinary volume/24 h, median 2200 ml, p < 0.05). Twenty-four hours after administration of both drugs there were no significant changes in hemodynamic, renal or hormonal parameters. No adverse effects were noted with either treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

托拉塞米是一种新型袢利尿剂,在健康受试者中半衰期和作用时间均长于呋塞米。为评估其药效学效应,对14例肝硬化腹水患者给予单剂量口服呋塞米(80毫克)和托拉塞米(20毫克),这两种药物在健康受试者中效力相当。研究前患者经历4天无利尿剂的平衡期。在至少2天的洗脱期后,按照随机双盲交叉设计交替给药。给药后24小时内按规定间隔收集尿液,给药前、给药后6小时和24小时采集血样。托拉塞米诱导的24小时累积尿量(2863±343对2111±184毫升,p<0.01)高于呋塞米。托拉塞米与呋塞米在0至6小时累积钠排泄量方面无差异(96±17对92±23毫摩尔钠),但在6至24小时累积利钠作用更明显(38±11对17±4毫摩尔,p<0.05)。5例患者对呋塞米反应较弱(0至36毫摩尔钠/24小时,中位数24毫摩尔;690至1460毫升尿量/24小时,中位数1325毫升)。这些患者使用托拉塞米后利钠和利尿作用显著增强(26至136毫摩尔钠/24小时,中位数78毫摩尔,p<0.05;1670至3610毫升尿量/24小时,中位数2200毫升,p<0.05)。两种药物给药24小时后,血流动力学、肾脏或激素参数均无显著变化。两种治疗均未观察到不良反应。(摘要截断于250字)

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