Key result
Early dapagliflozin fails to improve diuretic efficiency over usual care in acute heart failure.
Why the study?
Early dapagliflozin initiation during acute heart failure hospitalization may achieve both decongestion and guideline-directed medical therapy optimization, but its diuretic efficacy and safety were not established.
Does early dapagliflozin initiation improve diuretic efficiency in patients with hypervolemic acute heart failure?
RCT (n=240)
Open-label
Yes
Does early dapagliflozin initiation improve diuretic efficiency in patients with hypervolemic acute heart failure?
Odds Ratio: 0.65 (95% CI 0.41–1.02)
p-value: p=0.06
Early initiation of dapagliflozin in acute heart failure is safe and reduces loop diuretic requirements, despite not significantly improving the primary metric of weight-based diuretic efficiency.
BACKGROUND: The primary goals during acute heart failure (AHF) hospitalization are decongestion and guideline-directed medical therapy (GDMT) optimization. Unlike diuretics or other GDMT, early dapagliflozin initiation could achieve both AHF goals. OBJECTIVES: The authors aimed to assess the diuretic efficacy and safety of early dapagliflozin initiation in AHF. METHODS: In a multicenter, open-label study, 240 patients were randomized within 24 hours of hospital presentation for hypervolemic AHF to dapagliflozin 10 mg once daily or structured usual care with protocolized diuretic titration until day 5 or hospital discharge. The primary outcome, diuretic efficiency expressed as cumulative weight change per cumulative loop diuretic dose, was compared across treatment assignment using a proportional odds model adjusted for baseline weight. Secondary and safety outcomes were adjudicated by a blinded committee. RESULTS: For diuretic efficiency, there was no difference between dapagliflozin and usual care (OR: 0.65; 95% CI: 0.41-1.02; P = 0.06). Dapagliflozin was associated with reduced loop diuretic doses (560 mg [Q1-Q3: 260-1,150 mg] vs 800 mg [Q1-Q3: 380-1,715 mg]; P = 0.006) and fewer intravenous diuretic up-titrations (P ≤ 0.05) to achieve equivalent weight loss as usual care. Early dapagliflozin initiation did not increase diabetic, renal, or cardiovascular safety events. Dapagliflozin was associated with improved median 24-hour natriuresis (P = 0.03) and urine output (P = 0.005), expediting hospital discharge over the study period. CONCLUSIONS: Early dapagliflozin during AHF hospitalization is safe and fulfills a component of GDMT optimization. Dapagliflozin was not associated with a statistically significant reduction in weight-based diuretic efficiency but was associated with evidence for enhanced diuresis among patients with AHF. (Efficacy and Safety of Dapagliflozin in Acute Heart Failure [DICTATE-AHF]; NCT04298229).
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Cox et al. (2024) conducted an RCT in Acute Heart Failure (n=240). Dapagliflozin vs. Structured usual care with protocolized diuretic titration was evaluated on Diuretic efficiency expressed as cumulative weight change per cumulative loop diuretic dose (OR 0.65, 95% CI 0.41-1.02, p=0.06). Early dapagliflozin initiation in acute heart failure did not significantly improve weight-based diuretic efficiency compared to usual care (OR 0.65; 95% CI 0.41-1.02; P=0.06).
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