Efficacy and Safety of Dapagliflozin in Patients with Heart Failure and Mildly Reduced or Preserved Ejection Fractions: A Systematic Review and Meta-Analysis
Year: 2026
Type: review
Study designs: Systematic Review, Meta-Analysis
Abstract: Introduction: Dapagliflozin, an SGLT2 inhibitor, has shown benefits in heart failure. This meta-analysis evaluates its efficacy and safety in patients with heart failure with mildly reduced or preserved ejection fraction (HFmrEF or HFpEF). Methods: PubMed, Cochrane, and Web of Science were searched for studies published between 2019 and 2024. Six randomized trials involving 8,651 patients with ejection fraction >40% were included. Primary outcomes were heart failure hospitalization and mortality. Safety outcomes included adverse events. Pooled risk ratios (RR) with 95% confidence intervals (CI) were calculated. The review is registered with PROSPERO (CRD420261307461). Results: Dapagliflozin reduced heart failure hospitalizations by 21% (RR0.79, 95% CI 0.69–0.89, p=0.0002). Reductions in all-cause mortality (RR 0.95, 95% CI 0.86–1.06, p=0.35) and cardiovascular death (RR0.94, 95% CI 0.81–1.10, p=0.48) were not significant; moderate heterogeneity was observed for cardiovascular death (I²=66%). Dapagliflozin was not associated with significant increases in serious adverse events (RR0.96, 95% CI 0.91–1.01), volume depletion (RR1.36, 95% CI 0.91–2.02), acute kidney injury (RR0.94, 95% CI 0.82–1.08), or hypoglycaemia (RR0.98, 95% CI 0.35–2.74). Conclusion: Dapagliflozin reduces heart failure hospitalizations in HFpEF and HFmrEF patients without significant adverse effects. Careful monitoring for volume depletion is advised. Further studies are needed on mortality.
Authors: Binod Duwadi, Dibin Kumar Bista, Sujata Nagarkoti, Bimal Duwadi, Milan Malla, Mohammed Imran
Institutions: Cairo University, Queen Elizabeth Hospital, Mayo Clinic in Florida
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: diamond
OpenAlex ID: W7147416939
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