Effects of a 7-day treatment with midodrine in non-azotemic cirrhotic patients with and without ascites
- PMID: 17156883
- DOI: 10.1016/j.jhep.2006.09.012
Effects of a 7-day treatment with midodrine in non-azotemic cirrhotic patients with and without ascites
Abstract
Background/aims: Splanchnic arterial vasodilatation has been causally related with hyperdynamic circulation and impaired natriuresis in advanced cirrhosis and has also been suggested to be responsible for the subtle sodium retention in pre-ascitic cirrhosis. This study evaluated the effects of a 7-day treatment with the alpha1-adrenergic agonist midodrine in non-azotemic cirrhotic patients with and without ascites.
Methods: Thirty-nine cirrhotic patients were studied at baseline and 7 days after administration of oral midodrine 10mg, t.i.d. (11 without and 12 with ascites) or placebo (8 without and 8 with ascites).
Results: A significant increase in urine sodium excretion was noted after midodrine administration in patients without and with ascites, in line with significant increases in mean arterial pressure and systemic vascular resistance, and significant decreases in cardiac output and heart rate. Significant increases in glomerular filtration rate, filtration fraction, and urine volume and significant decreases in plasma renin activity and aldosterone were observed in patients with ascites. Placebo had no effect in any study group.
Conclusions: The administration of midodrine for 7 days improves systemic haemodynamics and sodium excretion in non-azotemic cirrhotic patients without or with ascites. In patients with ascites, but not in those without ascites, these effects are associated with a suppression of the activity of the renin-angiotensin-aldosterone system, suggesting that the increase in natriuresis is related to the improvement in the effective arterial blood volume.
Similar articles
-
Acute effects of the oral administration of midodrine, an alpha-adrenergic agonist, on renal hemodynamics and renal function in cirrhotic patients with ascites.Hepatology. 1998 Oct;28(4):937-43. doi: 10.1002/hep.510280407. Hepatology. 1998. PMID: 9755229
-
The effects of chronic treatment with octreotide versus octreotide plus midodrine on systemic hemodynamics and renal hemodynamics and function in nonazotemic cirrhotic patients with ascites.Am J Gastroenterol. 2005 Apr;100(4):879-85. doi: 10.1111/j.1572-0241.2005.40899.x. Am J Gastroenterol. 2005. PMID: 15784036 Clinical Trial.
-
Midodrine in patients with cirrhosis and refractory or recurrent ascites: a randomized pilot study.J Hepatol. 2012 Feb;56(2):348-54. doi: 10.1016/j.jhep.2011.04.027. Epub 2011 Jul 13. J Hepatol. 2012. PMID: 21749847 Clinical Trial.
-
Sodium retention in heart failure and cirrhosis: potential role of natriuretic doses of mineralocorticoid antagonist?Circ Heart Fail. 2009 Jul;2(4):370-6. doi: 10.1161/CIRCHEARTFAILURE.108.821199. Circ Heart Fail. 2009. PMID: 19808361 Review.
-
Midodrine and octreotide in treatment of cirrhosis-related hemodynamic complications.Ann Pharmacother. 2009 Apr;43(4):692-9. doi: 10.1345/aph.1L373. Epub 2009 Mar 18. Ann Pharmacother. 2009. PMID: 19299324 Review.
Cited by
-
Management of Ascites in Patients with Cirrhosis: An Update.J Clin Med. 2021 Nov 10;10(22):5226. doi: 10.3390/jcm10225226. J Clin Med. 2021. PMID: 34830508 Free PMC article. Review.
-
Guidelines on the management of ascites in cirrhosis.Gut. 2021 Jan;70(1):9-29. doi: 10.1136/gutjnl-2020-321790. Epub 2020 Oct 16. Gut. 2021. PMID: 33067334 Free PMC article.
-
Systemic hemodynamic and renal effects of midodrine and octreotide in cirrhotic patients with ascites.J Res Med Sci. 2011 Dec;16(12):1636-7. J Res Med Sci. 2011. PMID: 22973377 Free PMC article. No abstract available.
-
What is the Role of Midodrine in Patients with Decompensated Cirrhosis?Gastroenterol Hepatol (N Y). 2011 Feb;7(2):134-6. Gastroenterol Hepatol (N Y). 2011. PMID: 21475424 Free PMC article. No abstract available.
-
Asia-Pacific association for study of liver guidelines on management of ascites in liver disease.Hepatol Int. 2023 Aug;17(4):792-826. doi: 10.1007/s12072-023-10536-7. Epub 2023 May 26. Hepatol Int. 2023. PMID: 37237088 No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical