Furosemide kinetics and dynamics in patients with cirrhosis
- PMID: 3720175
- DOI: 10.1038/clpt.1986.132
Furosemide kinetics and dynamics in patients with cirrhosis
Abstract
Factors that influence intersubject variability in response to furosemide have been investigated in normal subjects and patients with cirrhosis. Furosemide pharmacokinetics and pharmacodynamics were measured in eight normal subjects and 14 patients with cirrhosis, eight of whom were resistant to diuretic therapy. Furosemide renal clearance decreased in proportion to creatinine clearance, whereas nonrenal clearance and volume of distribution were unchanged. These pharmacokinetic changes were, however, minimal and resulted in an only marginal alteration in the plasma concentration-time curve. The maximal rate of urinary sodium excretion decreased with reductions in creatinine clearance (r = 0.77). However, the extent of reduction in urinary excretion of sodium was proportionally greater than the reduction in creatinine clearance, whereas the rate of urinary furosemide excretion required to achieve 50% of maximal response did not change. Furosemide's pharmacokinetics were not, therefore, appreciably altered by cirrhosis. However, cirrhosis was associated with a reduction in pharmacodynamic response to this diuretic.
Similar articles
-
Influence of hepatic cirrhosis and end-stage renal disease on pharmacokinetics and pharmacodynamics of furosemide.Eur J Clin Pharmacol. 1981;20(1):27-33. doi: 10.1007/BF00554663. Eur J Clin Pharmacol. 1981. PMID: 7308269
-
Furosemide kinetics in patients with hepatic cirrhosis with ascites.Clin Pharmacol Ther. 1981 Oct;30(4):461-7. doi: 10.1038/clpt.1981.189. Clin Pharmacol Ther. 1981. PMID: 7285480
-
Pharmacokinetics and pharmacodynamic effects of furosemide in patients with liver cirrhosis.Int J Clin Pharmacol Ther Toxicol. 1985 Mar;23(3):129-33. Int J Clin Pharmacol Ther Toxicol. 1985. PMID: 3997298
-
Clinical consequences of the biphasic elimination kinetics for the diuretic effect of furosemide and its acyl glucuronide in humans.J Pharm Pharmacol. 1999 Mar;51(3):239-48. doi: 10.1211/0022357991772402. J Pharm Pharmacol. 1999. PMID: 10344623 Review.
-
Disposition and response to bumetanide and furosemide.Am J Cardiol. 1986 Jan 24;57(2):20A-25A. doi: 10.1016/0002-9149(86)91002-7. Am J Cardiol. 1986. PMID: 3511654 Review.
Cited by
-
Urinary excretion and diuretic action of furosemide in rats: increased response to the urinary excretion rate of furosemide in rats with acute renal failure.Pharm Res. 1988 Nov;5(11):699-703. doi: 10.1023/a:1015951710204. Pharm Res. 1988. PMID: 3247273
-
Simultaneously Predicting the Pharmacokinetics of CES1-Metabolized Drugs and Their Metabolites Using Physiologically Based Pharmacokinetic Model in Cirrhosis Subjects.Pharmaceutics. 2024 Feb 5;16(2):234. doi: 10.3390/pharmaceutics16020234. Pharmaceutics. 2024. PMID: 38399287 Free PMC article.
-
Human albumin infusion for treating oedema in people with nephrotic syndrome.Cochrane Database Syst Rev. 2019 Jul 12;7(7):CD009692. doi: 10.1002/14651858.CD009692.pub2. Cochrane Database Syst Rev. 2019. PMID: 31425606 Free PMC article. Review.
-
The changes in renal function after a single dose of intravenous furosemide in patients with compensated liver cirrhosis.BMC Gastroenterol. 2006 Nov 29;6:39. doi: 10.1186/1471-230X-6-39. BMC Gastroenterol. 2006. PMID: 17134488 Free PMC article. Clinical Trial.
-
Clinical pharmacokinetic considerations in the treatment of increased intracranial pressure.Clin Pharmacokinet. 1987 Jul;13(1):1-25. doi: 10.2165/00003088-198713010-00001. Clin Pharmacokinet. 1987. PMID: 3304768 Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical