Bladder Symptoms Provoked by Short, Rapid-Acting Loop Diuretics: A Frequent but Often Overlooked Problem.

Jeffrey Testani, Negiin Pourafshar, Salim Shah, Christopher S Wilcox, Milton Packer, Patrick Rossignol, Bertram Pitt, Faiez Zannad, Karina Han, Suzanne Shah, Rachael D Sussman

Journal: American journal of hypertension 2025;38(2):100-103

PMID: 39485998

Abstract

BACKGROUND

Bladder dysfunction entails overactive bladder (OAB) defined as symptoms of urinary urgency, frequency, and/or nocturia with or without incontinence if there is no obvious pathology or infection or lower urinary tract symptoms that includes recognized causes of bladder dysfunction.

METHODS

Literature search.

RESULTS

Symptoms of OAB are reported in about 15% of the adult US population. This is increased 2- to 3-fold in patients with congestive heart failure (CHF), hypertension, cardiovascular disease (CVD), chronic kidney disease (CKD), or the elderly where it often accompanies prescription for short, rapid-acting loop diuretics. However, less than 2% of patients seeking care for OAB receive treatment. The fear of urinary incontinence from short, rapid-acting loop diuretics may contribute to medication nonadherence and less well-controlled, apparently resistant hypertension. The bladder contracts to rapid stretch. Thus, less rapid-acting diuretics such as thiazides or extended-release formulations of loop diuretics may be preferable for those with bladder dysfunction. Alternatively, the use of a mineralocorticosteroid receptor antagonist, angiotensin receptor antagonist/neprilysin inhibitor, or sodium glucose-linked transport type 2 inhibitor may allow a reduction in the dose of a short, rapid-acting loop diuretic for those with bladder dysfunction.

CONCLUSIONS

A worsening of symptoms from bladder dysfunction by short, rapid-acting loop diuretics occurs frequently in patients with CVD, CHF, hypertension, and CKD where it can contribute to impaired quality of life and poor adherence and thereby to worsening outcomes.

© The Author(s) 2024. Published by Oxford University Press on behalf of American Journal of Hypertension, Ltd. All rights reserved. For commercial re-use, please contact [email protected] for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact [email protected].

Address: Hypertension Center and Division of Nephrology and Hypertension, Georgetown University, Washington, District of Columbia, USA.; Department of Urology, Georgetown University, Washington, District of Columbia, USA.; Department of Cardiovascular Medicine, Yale University, New Haven, Connecticut, USA.; Baylor Heart and Vascular Institute, Dallas, Texas, USA.; Department of Cardiovascular Disease, Université de Lorraine and CHRU Nancy, CIC-P and FCRIN INI-CRCT, France.; Medical Specialties and Nephrology Departments, Princess Grace Hospital, and Monaco Private Hemodialysis Centre, Monaco, Monaco.; Department of Cardiovascular Disease, Université de Lorraine and CHRU Nancy, CIC-P and FCRIN INI-CRCT, France.; Department of Cardiology, University of Michigan, Ann Arbor, Michigan, USA.; Sarfez Inc, Vienna, Virginia, USA.
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