Key result
SGLT2 inhibitors fail to significantly reduce readmission or death across frailty levels.
Why the study?
Evidence regarding the effectiveness of SGLT2 inhibitors according to frailty status in elderly patients with acute heart failure remains limited.
Do SGLT2 inhibitors reduce hospital readmission and mortality in elderly polypathological patients with acute heart failure, and does functional frailty modify this effectiveness?
Observational (n=794)
Do SGLT2 inhibitors reduce hospital readmission and mortality in elderly polypathological patients with acute heart failure, and does functional frailty modify this effectiveness?
Functional frailty does not appear to significantly modify the clinical effectiveness of SGLT2 inhibitors in elderly patients with acute heart failure, supporting their broad use across frailty phenotypes.
Benefits appear consistent across frailty levels in elderly acute HF; hypothesis-generating and requires randomized confirmation.
Background/Objectives: Acute heart failure (AHF) is the leading cause of hospitalization among patients over 65 years and is frequently associated with frailty. Sodium-glucose cotransporter type 2 inhibitors (SGLT2i) currently represent the only drug class recommended across the entire ejection fraction spectrum, although evidence regarding their effectiveness according to frailty status remains limited. Aims: To determine whether functional frailty, measured by the Short Physical Performance Battery (SPPB) test, influences the effectiveness of SGLT2i in reducing hospital readmission and mortality in elderly patients with AHF. Methods: Observational study of 794 polypathological patients admitted to Internal Medicine with AHF. An interaction analysis assessed whether SPPB, as a continuous variable, modified the association between SGLT2i and the composite outcome (hospital readmission or death), using a Cox model. The sample was further divided by SPPB test score (below 4 (N = 477) or ≥4 (N = 317)) for exploratory analyses. Descriptive and comparative analyses were performed according to SGLT2i administration, using the chi-squared test for qualitative variables and Student’s t-test for quantitative ones (Fisher’s and Mann–Whitney U test as appropriate). Survival analysis was done using Kaplan–Meier curves and Cox regression, with multivariable adjustment for confounders. Results: No significant interaction was found between SPPB score and SGLT2i (p = 0.506). When SPPB was dichotomised, SGLT2i treatment was associated with significantly lower all-cause mortality (3.7% vs. 12.0%; p = 0.018) and readmission (30.3% vs. 45.2%; p = 0.021) in SPPB ≥ 4, with mortality and readmission also numerically lower, without reaching statistical significance, in SPPB < 4 (mortality 12.9% vs. 16.9%, p = 0.410; readmission 34.5% vs. 42.0%, p = 0.220). After adjustment, SGLT2i treatment in the SPPB ≥ 4 group remained associated with a numerically lower hazard for the composite outcome (HR 0.652; 95% CI 0.418–1.018; p = 0.060). Conclusions: No evidence was found that functional frailty modifies the effectiveness of SGLT2i in elderly polypathological patients with AHF. An exploratory analysis suggested a possible gradient of greater association with SPPB ≥ 4, although this should be interpreted as hypothesis-generating.
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Guzmán-Carreras et al. (2026) conducted an observational in Acute heart failure (n=794). SGLT2 inhibitors vs. No SGLT2 inhibitor therapy was evaluated on Composite outcome of hospital readmission or death (adjusted hazard in SPPB ≥ 4 group) (HR 0.652, 95% CI 0.418-1.018, p=0.060). SGLT2 inhibitors were associated with a numerically lower hazard for readmission or death in patients with SPPB ≥ 4 (HR 0.652; 95% CI 0.418-1.018), with no significant interaction by frailty status (p=0.506).
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