TY - JOUR
T1 - Dapagliflozin in Patients Hospitalized for Heart Failure
T2 - Primary Results of the DAPA ACT HF-TIMI 68 Randomized Clinical Trial and Meta-Analysis of Sodium-Glucose Cotransporter-2 Inhibitors in Patients Hospitalized for Heart Failure
AU - Berg, David D.
AU - Patel, Siddharth M.
AU - Haller, Paul M.
AU - Cange, Abby L.
AU - Palazzolo, Michael G.
AU - Bellavia, Andrea
AU - Kuder, Julia F.
AU - Desai, Akshay S.
AU - Inzucchi, Silvio E.
AU - McMurray, John J.V.
AU - O’Meara, Eileen
AU - Verma, Subodh
AU - Bělohlávek, Jan
AU - Drożdż, Jarosław
AU - Merkely, Béla
AU - Ogunniyi, Modele O.
AU - Drasnar, Tomáš
AU - Izzo, Joseph L.
AU - Sarman, Balazs
AU - McGinty, John E.
AU - Ramanathan, Krishnan
AU - Mulkay, Angel J.
AU - Przybylski, Andrzej
AU - Ruff, Christian T.
AU - O’Donoghue, Michelle L.
AU - Murphy, Sabina A.
AU - Sabatine, Marc S.
AU - Wiviott, Stephen D.
N1 - Publisher Copyright:
© (2025), (Lippincott Williams and Wilkins). All rights reserved.
PY - 2025/1
Y1 - 2025/1
N2 - BACKGROUND: – SGLT2 (sodium-glucose cotransporter-2) inhibitors reduce the risk of cardiovascular death or worsening heart failure (HF) in outpatients with HF. Data on initiation in patients hospitalized for HF are limited. METHODS: – We conducted a randomized, double-blind, placebo-controlled trial evaluating the efficacy and safety of in-hospital initiation of dapagliflozin (10 mg daily) in patients hospitalized for HF. The primary efficacy outcome was a composite of time to cardiovascular death or worsening HF through 2 months. Key safety outcomes included symptomatic hypotension and worsening kidney function. A prespecified meta-analysis of randomized trials evaluating initiation of SGLT2 inhibitors in patients hospitalized for HF was performed. RESULTS: – Of 2401 patients (median age, 69 [Q1–Q3, 58–77] years, 815 [33.9%] women, 448 [18.7%] Black race, 1717 [71.5%] left ventricular ejection fraction ≤40%, 1074 [44.7%] newly diagnosed HF) randomized between September 2020 and March 2025, 1218 were assigned to dapagliflozin and 1183 to placebo. The primary outcome occurred in 133 patients (10.9%) in the dapagliflozin group and 150 (12.7%) in the placebo group (hazard ratio [HR], 0.86 [95% CI, 0.68–1.08]; P=0.20). A worsening HF event occurred in 115 (9.4%) and 122 (10.3%) patients in the dapagliflozin and placebo groups, respectively (HR, 0.91 [95% CI, 0.71–1.18]). Cardiovascular death occurred in 30 (2.5%) and 37 (3.1%) patients (HR, 0.78 [95% CI, 0.48–1.27]), and death from any cause occurred in 36 (3.0%) and 53 (4.5%) patients in the dapagliflozin and placebo groups, respectively (HR, 0.66 [95% CI, 0.43–1.00]). The rates of symptomatic hypotension were 3.6% and 2.2%, and the rates of worsening kidney function were 5.9% and 4.7% with dapagliflozin and placebo, respectively. In a meta-analysis of patients hospitalized for HF, SGLT2 inhibitors reduced the early risk of cardiovascular death or worsening HF (HR, 0.71 [95% CI, 0.54–0.93] P=0.012) and of all-cause death (HR, 0.57 [95% CI, 0.41–0.80]; P=0.001). CONCLUSIONS: – In this trial, in-hospital initiation of dapagliflozin did not significantly reduce the risk of cardiovascular death or worsening HF through 2 months in hospitalized HF patients. However, the totality of randomized clinical trial data suggests that in-hospital initiation of SGLT2 inhibitors may reduce the early risk of cardiovascular death or worsening HF and of all-cause mortality. REGISTRATION: – URL: https://www.clinicaltrials.gov; Unique identifier: NCT04363697.
AB - BACKGROUND: – SGLT2 (sodium-glucose cotransporter-2) inhibitors reduce the risk of cardiovascular death or worsening heart failure (HF) in outpatients with HF. Data on initiation in patients hospitalized for HF are limited. METHODS: – We conducted a randomized, double-blind, placebo-controlled trial evaluating the efficacy and safety of in-hospital initiation of dapagliflozin (10 mg daily) in patients hospitalized for HF. The primary efficacy outcome was a composite of time to cardiovascular death or worsening HF through 2 months. Key safety outcomes included symptomatic hypotension and worsening kidney function. A prespecified meta-analysis of randomized trials evaluating initiation of SGLT2 inhibitors in patients hospitalized for HF was performed. RESULTS: – Of 2401 patients (median age, 69 [Q1–Q3, 58–77] years, 815 [33.9%] women, 448 [18.7%] Black race, 1717 [71.5%] left ventricular ejection fraction ≤40%, 1074 [44.7%] newly diagnosed HF) randomized between September 2020 and March 2025, 1218 were assigned to dapagliflozin and 1183 to placebo. The primary outcome occurred in 133 patients (10.9%) in the dapagliflozin group and 150 (12.7%) in the placebo group (hazard ratio [HR], 0.86 [95% CI, 0.68–1.08]; P=0.20). A worsening HF event occurred in 115 (9.4%) and 122 (10.3%) patients in the dapagliflozin and placebo groups, respectively (HR, 0.91 [95% CI, 0.71–1.18]). Cardiovascular death occurred in 30 (2.5%) and 37 (3.1%) patients (HR, 0.78 [95% CI, 0.48–1.27]), and death from any cause occurred in 36 (3.0%) and 53 (4.5%) patients in the dapagliflozin and placebo groups, respectively (HR, 0.66 [95% CI, 0.43–1.00]). The rates of symptomatic hypotension were 3.6% and 2.2%, and the rates of worsening kidney function were 5.9% and 4.7% with dapagliflozin and placebo, respectively. In a meta-analysis of patients hospitalized for HF, SGLT2 inhibitors reduced the early risk of cardiovascular death or worsening HF (HR, 0.71 [95% CI, 0.54–0.93] P=0.012) and of all-cause death (HR, 0.57 [95% CI, 0.41–0.80]; P=0.001). CONCLUSIONS: – In this trial, in-hospital initiation of dapagliflozin did not significantly reduce the risk of cardiovascular death or worsening HF through 2 months in hospitalized HF patients. However, the totality of randomized clinical trial data suggests that in-hospital initiation of SGLT2 inhibitors may reduce the early risk of cardiovascular death or worsening HF and of all-cause mortality. REGISTRATION: – URL: https://www.clinicaltrials.gov; Unique identifier: NCT04363697.
KW - hospitalization
KW - randomized clinical trial
KW - sodium-glucose cotransporter 2 inhibitors
KW - worsening heart failure.
UR - https://www.scopus.com/pages/publications/105022258098
U2 - 10.1161/CIRCULATIONAHA.125.076575
DO - 10.1161/CIRCULATIONAHA.125.076575
M3 - Article
C2 - 40884036
AN - SCOPUS:105022258098
SN - 0009-7322
VL - 152
SP - 1411
EP - 1422
JO - Circulation
JF - Circulation
ER -