Key result
Dapagliflozin cuts new loop diuretic initiation by ~32% with consistent benefits across subgroups.
Why the study?
Although dapagliflozin reduces worsening heart failure or cardiovascular death in heart failure with mildly reduced or preserved ejection fraction, its safety and efficacy according to background diuretic therapy and its influence on longitudinal diuretic use required evaluation.
Does dapagliflozin reduce worsening heart failure or cardiovascular death and reduce longitudinal diuretic utilization across different background diuretic regimens in patients with heart failure with mildly reduced or preserved ejection fraction?
RCT (n=6,263)
Randomized
Does dapagliflozin reduce worsening heart failure or cardiovascular death and reduce longitudinal diuretic utilization across different background diuretic regimens in patients with heart failure with mildly reduced or preserved ejection fraction?
In patients with HFmrEF or HFpEF, dapagliflozin provides consistent clinical benefits and safety across all baseline diuretic regimens while significantly reducing the need for new loop diuretic initiation and dose escalation over time.
Supports dapagliflozin initiation across all diuretic regimens in HFmrEF/HFpEF; extends evidence to reduced longitudinal diuretic needs.
AIMS: Dapagliflozin reduced the combined risk of worsening heart failure or cardiovascular death among patients with heart failure with mildly reduced or preserved ejection fraction. In this study, the safety and efficacy of dapagliflozin according to background diuretic therapy and the influence of dapagliflozin on longitudinal diuretic use were evaluated. METHODS AND RESULTS: In this pre-specified analysis of the Dapagliflozin Evaluation to Improve the LIVEs of Patients With Preserved Ejection Fraction Heart Failure (DELIVER) trial, the effects of dapagliflozin vs. placebo were assessed in the following subgroups: no diuretic, non-loop diuretic, and loop diuretic furosemide equivalent doses of <40, 40, and >40 mg, respectively. Of the 6263 randomized patients, 683 (10.9%) were on no diuretic, 769 (12.3%) were on a non-loop diuretic, and 4811 (76.8%) were on a loop diuretic at baseline. Treatment benefits of dapagliflozin on the primary composite outcome were consistent by diuretic use categories (Pinteraction = 0.64) or loop diuretic dose (Pinteraction = 0.57). Serious adverse events were similar between dapagliflozin and placebo arms, irrespective of diuretic use or dosing. Dapagliflozin reduced new initiation of loop diuretics by 32% [hazard ratio (HR) 0.68; 95% confidence interval (CI): 0.55-0.84, P < 0.001] but did not influence discontinuations/disruptions (HR 0.98; 95% CI: 0.86-1.13, P = 0.83) in follow-up. First sustained loop diuretic dose increases were less frequent, and sustained dose decreases were more frequent in patients treated with dapagliflozin: net difference of -6.5% (95% CI: -9.4 to -3.6; P < 0.001). The mean dose of loop diuretic increased over time in the placebo arm, a longitudinal increase that was significantly attenuated with treatment with dapagliflozin (placebo-corrected treatment effect of -2.5 mg/year; 95% CI: -1.5, -3.7, P < 0.001). CONCLUSION: In patients with heart failure with mildly reduced or preserved ejection fraction, the clinical benefits of dapagliflozin relative to placebo were consistent across a wide range of diuretic categories and doses with a similar safety profile. Treatment with dapagliflozin significantly reduced new loop diuretic requirement over time.
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Chatur et al. (2023) conducted an RCT in Heart failure with mildly reduced or preserved ejection fraction (n=6,263). Dapagliflozin vs. Placebo was evaluated on New initiation of loop diuretics (and consistency of primary composite outcome of worsening heart failure or cardiovascular death across diuretic subgroups) (HR 0.68, 95% CI 0.55-0.84, p=<0.001). Dapagliflozin reduced new loop diuretic initiation by 32% (HR 0.68; 95% CI 0.55-0.84; P<0.001) and showed consistent clinical benefits across baseline diuretic subgroups (Pinteraction=0.64).
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