Peer-reviewed veterinary case report
Comparison of the effects of dual, triple, and quadruple medical therapy on cardiac death in a retrospective cohort of dogs with myxomatous mitral valve disease at American College of Veterinary Internal Medicine stage C: is more necessarily better?
- Journal:
- Journal of the American Veterinary Medical Association
- Year:
- 2025
- Authors:
- Romito, Giovanni et al.
- Affiliation:
- University of Bologna · Italy
- Species:
- dog
Abstract
OBJECTIVE: To compare selected cardiac effects of dual therapy (DT; furosemide and pimobendan), triple therapy (TT; furosemide, pimobendan, and benazepril), and quadruple therapy (QT; furosemide, pimobendan, benazepril, and spironolactone) in dogs with myxomatous mitral valve disease at American College of Veterinary Internal Medicine (ACVIM) stage C. METHODS: This was a multicenter retrospective study involving dogs with ACVIM stage C myxomatous mitral valve disease treated with DT, TT, or QT. Statistical analysis was aimed at comparing the effects of treatment protocols on a primary outcome (cardiac death) and selected cardiovascular intermediate events (progression from ACVIM stage C to D and development of clinically relevant pulmonary hypertension and arrhythmias). RESULTS: 211 dogs were included (DT group, 65; TT group, 105; QT group, 41). No statistically significant differences were found when comparing the rate of cardiac death between the DT and TT groups (P = .29), DT and QT groups (P = .32), and TT and QT groups (P = .94). No statistically significant differences were observed among the DT, TT, and QT Kaplan-Meier cardiac death survival curves in either the unadjusted (P = .32) or adjusted (P = .37) analyses. CONCLUSIONS: In this study sample, QT and TT did not provide a higher clinically evident cardiac protective effect compared to DT. CLINICAL RELEVANCE: DT was not inferior to TT and QT in terms of cardiac death in dogs with ACVIM stage C myxomatous mitral valve disease included in this study.
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Search related cases →Original publication: https://pubmed.ncbi.nlm.nih.gov/40840525/