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Published on: June 10, 2025
Indirect comparison of SGLT2 inhibitors in patients with established heart failure: evidence based on Bayesian
Hai-Bin Chen1, Yao-Lin Yang1, Rong-Sen Meng1
1Department of Cardiology, Guangdong Second Provincial General Hospital, Guangzhou, Guangdong, China, 510317.
Aims:
Head-to-head comparisons among SGLT2 inhibitors treatments in established heart failure remain absent. We conducted a systematic review of dedicated heart failure trials to assess indirectly the composite outcomes and individual clinical endpoints among SGLT2 inhibitor treatments.
Methods And Results:
We systematically reviewed randomized controlled trials comparing SGLT2 inhibitors versus placebo in patients with established heart failure. A Bayesian approach to network meta-analysis was applied. Five trials including four treatment strategies were included in this study. The composite of cardiovascular death or hospitalization for heart failure showed no significant difference in the comparison between dapagliflozin and empagliflozin (OR 1.00, 95% CI 0.66-1.55), dapagliflozin and sotagliflozin (OR 1.54, 95% CI 0.91-2.65), and empagliflozin and sotagliflozin (OR 1.53, 95% CI 0.90-2.69). All-cause mortality showed no significant difference in the comparison between dapagliflozin and empagliflozin (OR 0.92, 95% CI 0.711-1.18), dapagliflozin and sotagliflozin (OR 1.05, 95% CI 0.68-1.59), and empagliflozin and sotagliflozin (OR 1.14, 95% CI 0.74-1.73). Cardiovascular death showed no significant difference in the comparison between dapagliflozin and empagliflozin (OR 0.94, 95% CI 0.71-1.23), dapagliflozin and sotagliflozin (OR 0.96, 95% CI 0.61-1.55), and empagliflozin and sotagliflozin (OR 1.03, 95% CI 0.64-1.66). Hospitalization for heart failure showed no significant difference in the comparison between dapagliflozin and empagliflozin (OR 1.13, 95% CI 0.64-1.97), dapagliflozin and sotagliflozin (OR 1.56, 95% CI 0.74-3.15), and empagliflozin and sotagliflozin (OR 1.39, 95% CI 0.68-2.78).
Conclusions:
In patients with established heart failure, there was no significant difference of the major efficacy outcomes among SGLT2 inhibitor treatments; however, sotagliflozin may be associated with the lowest risk of the composite of cardiovascular death or hospitalization for heart failure, and dapagliflozin may be associated with the lowest risk of all-cause and cardiovascular mortality.
Insights
This study found no significant differences in major outcomes among SGLT2 inhibitors for heart failure patients. However, sotagliflozin showed a trend towards lower composite events, while dapagliflozin suggested reduced mortality risks.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Direct head-to-head comparisons of SGLT2 inhibitors in heart failure are lacking.
- This study provides an indirect comparison of SGLT2 inhibitor treatments in established heart failure.
Approach:
- A systematic review and Bayesian network meta-analysis of randomized controlled trials comparing SGLT2 inhibitors versus placebo in heart failure patients.
- Included five trials encompassing four treatment strategies.
Key Points:
- No significant differences were observed for the composite of cardiovascular death or hospitalization for heart failure (HF) among dapagliflozin, empagliflozin, and sotagliflozin.
- All-cause mortality, cardiovascular death, and hospitalization for HF also showed no significant differences between these SGLT2 inhibitors.
- Sotagliflozin showed a trend towards the lowest risk for the composite outcome, while dapagliflozin suggested the lowest risk for all-cause and cardiovascular mortality.
Conclusions:
- Among patients with established heart failure, SGLT2 inhibitor treatments demonstrated comparable efficacy for major clinical outcomes.
- Individual SGLT2 inhibitors may offer differential benefits, with sotagliflozin potentially reducing composite events and dapagliflozin potentially reducing mortality.
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