https://doi.org/10.55788/a66af138
The EMPULSE trial (NCT04157751) randomised 530 patients with stabilised acute HF to empagliflozin or placebo. Empagliflozin outperformed placebo concerning the primary endpoint of this study, a composite of all-cause death, HF events, and Kansas City Cardiomyopathy Questionnaire â Total Symptom Score (KCCQ-TSS) change from baseline [1]. The current analysis, presented by Prof. Piotr Ponikowski (Medical University of Wroclaw, Poland), assessed the decongestive effects of empagliflozin compared with placebo [2]. âThis analysis is important, as congestion presents the main reason for hospitalisation in patients with acute decompensated HF,â added Prof. Ponikowski [3]. Weight loss measured on day 15, 30, and 90 was the primary outcome to assess decongestion.
Prof. Ponikowski showed that the weight loss on day 15 (P<0.0001) and day 30 (P=0.0004) indeed correlated significantly with positive effects in the primary outcome of the EMPULSE trial. Weight loss was significantly larger on days 15, 30, and 90 in participants treated with empagliflozin than in participants who received placebo, with an adjusted mean differences of -1.97 kg (P<0.0001), -1.74 kg (P=0.0007), and -1.53 kg (P=0.0137), respectively. Correspondingly, change in body weight per mean daily dose of loop diuretic favoured the empagliflozin arm over the placebo arm on day 15 (adjusted mean difference 2.31 kg; P=0.002), day 30 (-2.79 kg; P=0.0152), and at day 90 (-3.18 kg; P=0.0319). Furthermore, the NT-proBNP levels of participants in the empagliflozin arm were significantly reduced compared with placebo users at all 3 timepoints.
âIn patients who were hospitalised for acute HF, empagliflozin therapy evoked an early and clinically meaningful decongestion that, importantly, was maintained until day 90,â summarised Prof. Ponikowski the results of the current analysis.
- Voors AA, et al. Nat Med. 2022;28(3):568â574.
- Biegus J, et al. EMPULSE â Empagliflozin in patients hospitalized with acute heart failure who have been stabilized. LBT Pharmacological treatment II, Heart Failure 2022, 21â24 May, Madrid, Spain.
- Chioncel O, et al. Eur J Heart Fail. 2017;19(10):1242â1254.
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Table of Contents: HFA 2022
Featured articles
Phase 3 and 4 Trials
GALACTIC-HF: Omecamtiv mecarbil as option for HFrEF patients with low SBP
HELIOS-A: Vutrisiran meets exploratory endpoints
Patiromer helps HFrEF patients to optimise RAAS inhibitors without hyperkalaemia
FIDELITY: Cardiorenal benefits of finerenone, regardless of LVH status
DAPA-VO2: Rapid effect of dapagliflozin on peak VO2 in stable HFrEF
Phase 1/2 Trials
Significant improvement in BP from istaroxime, a novel non-adrenergic agent
SERENADE: Macitentan fails in HFpEF plus PAH
Combination of filgrastim and dutogliptin appears safe in STEMI
Therapeutic Devices
Cardiac contractility modulation therapy promising for patients with HFpEF
REBALANCE-HF: Encouraging observations for splanchnic nerve ablation in HFpEF
Updates on SGLT2 Inhibitors
DAPA-HF: Dapagliflozin is safe and efficacious in frail patients
EMPEROR-Preserved: Empagliflozin stable across age groups
EMPULSE: Empagliflozin delivers rapid and clinically meaningful decongestion
Dapagliflozin performs consistently across LVEF in HF
Miscellaneous Topics
Cardiac wasting relevant for clinical outcomes in cancer
Urocortin-2 a potential treatment target for HFpEF
Should ATTR-CM be added to the differential diagnosis of patients with HF?
Delayed initiation of novel GDMTs associated with adverse outcomes in HF patients
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