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Peer-reviewed veterinary case report

Spironolactone effects on survival in Dobermans with heart failure

By Laskary, A et al.·Published in Journal of veterinary cardiology : the official journal of the European Society of Veterinary Cardiology·2022·Department of Clinical Studies, Canada·View original on PubMed

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Original publication title: Prospective clinical trial evaluating spironolactone in Doberman pinschers with congestive heart failure due to dilated cardiomyopathy.

Species:
dog

Plain-English summary

A group of 67 Doberman pinschers with congestive heart failure (CHF) caused by dilated cardiomyopathy (DCM) were given either spironolactone, a medication that helps manage heart conditions, or a placebo alongside their usual treatment. While the average time until cardiac death was similar between the two groups, the dogs receiving spironolactone had fewer cases of atrial fibrillation, a common heart rhythm problem. This suggests that spironolactone may help improve heart health in these dogs, even if it didn't significantly extend their lifespan.

People also search for: Doberman pinscher heart failure treatment · spironolactone for dogs · congestive heart failure in dogs symptoms

Abstract

INTRODUCTION/OBJECTIVES: Whether the aldosterone antagonist spironolactone has beneficial survival effects in dogs with dilated cardiomyopathy (DCM) is not known. The primary objective of the study was to evaluate the effect of spironolactone, when added to conventional therapy, on survival time in Doberman pinschers with congestive heart failure (CHF) due to DCM. ANIMALS: Sixty-seven client-owned Doberman pinschers with CHF due to DCM. MATERIALS AND METHODS: The trial design was prospective, randomized, blinded, and placebo controlled. Dogs were randomized to receive 50-75 mg of spironolactone twice daily (n = 34) or a placebo (n = 33), in addition to standard CHF therapy. Follow-up visits were targeted every one-six weeks until endpoint. Quality-of-life questionnaire and physical examination were performed at every visit, while renal biochemistry, ECG, echocardiography, and thoracic radiography were reassessed as needed. The primary endpoint was time to cardiac death, defined as death or euthanasia from CHF or sudden death. RESULTS: Median time to primary endpoint in the spironolactone group (183 days) was not statistically significantly different than that for the placebo group (124 days) (P = 0.254). The development of atrial fibrillation (AF) was significantly less frequent in the spironolactone group (n = 7) than the placebo group (n = 15, P = 0.037). CONCLUSIONS: While median time to cardiac death in the spironolactone group was not statistically significantly different than that in the placebo group, adding spironolactone to conventional therapy resulted in reduced occurrence of AF.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/34315691/