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Effect of Dapagliflozin in Patients with Heart Failure: A Systematic Review and Meta-Analysis
Ahmed E Ali1,2, Muhammad Sabry Mazroua2,3, Mariam ElSaban2,4
1Mansoura Specialized Hospital, Mansoura, Egypt.
Insights
Dapagliflozin significantly reduces mortality and hospitalizations in heart failure patients. This sodium-glucose cotransporter-2 inhibitor offers promising cardiovascular benefits.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Heart failure (HF) is a leading cause of global mortality and hospital admissions.
- Sodium-glucose cotransporter-2 (SGLT2) inhibitors, like dapagliflozin, are emerging as treatments with cardiovascular benefits.
- This study systematically reviews dapagliflozin's impact on heart failure outcomes.
Approach:
- A systematic review and meta-analysis of randomized controlled trials.
- Searched major databases (PubMed, Scopus, ScienceDirect) for studies from January 2017 to September 2022.
- Included 9 eligible studies with 14,032 patients, analyzing all-cause mortality, HF hospitalization, and cardiovascular death.
Key Points:
- Dapagliflozin significantly reduced all-cause mortality (RR = 0.89, P = 0.006).
- Hospitalization due to heart failure was significantly decreased (RR = 0.76, P < 0.00001).
- Cardiovascular death risk was also lowered (RR = 0.87, P = 0.01), with no significant heterogeneity observed.
Conclusions:
- Dapagliflozin demonstrates efficacy in reducing mortality and heart failure hospitalizations.
- The drug benefits a broad spectrum of heart failure patients.
- SGLT2 inhibitors represent a valuable therapeutic option for managing heart failure.
Background:
Heart failure (HF) is a major cause of recurrent hospitalization and death worldwide. Sodium-glucose cotransporter-2 inhibitors including dapagliflozin are anti-diabetic drugs with promising cardiovascular (CV) effects. We performed systematic review and meta-analysis of randomized controlled trials investigating the effects of dapagliflozin in heart failure patients.
Methods:
We searched PubMed, Scopus and ScienceDirect databases. A total of 1,567 studies from January 2017 to September 10, 2022, were screened. After applying exclusion criteria, 22 studies were retrieved for full-text screening, and nine of them were eligible for this meta-analysis. Effect estimates for dichotomous variables were expressed as risk ratio (RR) and 95% CI. The primary outcomes were the incidence of all-cause mortality, hospitalization due to HF, and CV death. This review was registered on PROSPERO with ID CRD42022347793.
Results:
A total of 14,032 patients were included. The overall risk ratio of all-cause mortality favored the dapagliflozin group over the placebo/standard therapy group (RR = 0.89, 95% CI: 0.82-0.97, P = 0.006) and the pooled studies were not heterogenous (I2 = 0%). Additionally, dapagliflozin significantly reduced the hospitalization due to heart failure (RR = 0.76, 95% CI: 0.70-0.84, P > 0.00001, I2 = 0%), cardiovascular death (RR = 0.87, 95% CI: 0.78-0.97, P = 0.01, I2 = 0%) and their composite outcomes.
Conclusion:
Dapagliflozin reduces the risk of all-cause mortality, heart failure hospitalizations and cardiovascular death in a wide range of heart failure patients.
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