Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1979 Sep;42(3):316-25.
doi: 10.1136/hrt.42.3.316.

Relation of plasma aldosterone concentration to diuretic treatment in patients with severe heart disease

Relation of plasma aldosterone concentration to diuretic treatment in patients with severe heart disease

R K Knight et al. Br Heart J. 1979 Sep.

Abstract

To assess the relation of hyperaldosteronism and potassium depletion to the intensity of diuretic therapy we have measured plasma aldosterone by radioimmunoassay and total exchangeable potassium by radioisotope dilution in 24 patients when they were stable at the end of their preparation for cardiac operation. Some patients required intensive frusemide therapy to reach an optimal state for operation and many showed hyperaldosteronism. Plasma aldosterone was significantly related to daily dose of frusemide (r=0.77). Depletion of total exchangeable potassium expressed in terms of predicted weight was significantly related to plasma aldosterone (r= -0.64). The reduction in total exchangeable potassium is interpreted as chiefly related to loss of lean tissue mass from the wasting that leads to cardiac cachexia, but evidence is presented on the basis of measurements of extracellular fluid volume as sulphate space (20 patients) of entry of sodium into the cells which may indicate a true cellular potassium loss. Although plasma potassium is usually easily maintained with oral potassium supplements or aldosterone antagonists, we postulate that intensive diuretic therapy in severe heart disease may provoke hyperaldosteronism which accentuates potassium loss and may contribute to wasting and to intracellular potassium depletion in critical tissue, such as myocardium.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Clin Invest. 1946 May;25(3):389-400 - PubMed
    1. J Clin Endocrinol Metab. 1965 Feb;25:219-28 - PubMed
    1. Circulation. 1962 Jun;25:1015-23 - PubMed
    1. Lancet. 1961 Apr 1;1(7179):681-7 - PubMed
    1. Metabolism. 1958 Sep;7(5):651-67 - PubMed

LinkOut - more resources