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Long-term efficacy of SGLT2 inhibitors for elderly patients with acute decompensated heart failure: The OASIS-HF
Michitaka Amioka1,2, Hiroki Kinoshita3, Yuto Fuji2
1Deparment of Cardiovascular Medicine, Shininokuchi Medical Clinic, Hiroshima, Japan.
Insights
Sodium-glucose cotransporter 2 inhibitors (SGLT2i) significantly reduce heart failure (HF) rehospitalization and cardiovascular death in elderly patients. SGLT2i also protect kidney function and decrease long-term repeated HF hospitalizations.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Sodium-glucose cotransporter 2 inhibitors (SGLT2i) are established cardioprotective agents, reducing cardiovascular death and heart failure (HF) hospitalizations.
- Limited data exist on the impact of SGLT2i on preventing rehospitalization after an initial HF event.
Purpose of the Study:
- To investigate the effect of SGLT2i on rehospitalization rates and cardiovascular death in elderly patients hospitalized for acute decompensated HF.
- To assess the impact of SGLT2i on renal function, specifically the estimated glomerular filtration rate (eGFR) slope.
Main Methods:
- A multicentre, prospective observational cohort study (OASIS-HF) enrolled 361 patients aged ≥75 years hospitalized for acute decompensated HF.
- Patients were divided into two groups: conventional medical therapy and SGLT2i.
- Outcomes evaluated included composite events of HF rehospitalization or cardiovascular death, annual rehospitalization rates, and the change in eGFR slope at 1 year.
Main Results:
- Over a mean follow-up of 24.9 months, SGLT2i use was associated with a lower incidence of composite events (35.4% vs. 22.1%, P=0.016).
- The average annual HF rehospitalization rate was significantly lower in the SGLT2i group (0.14 vs. 0.22, P=0.019).
- The decline in eGFR over 1 year was significantly slower in the SGLT2i group (-3.55 mL/min/1.73 m² vs. -1.42 mL/min/1.73 m², P=0.025).
Conclusions:
- SGLT2 inhibitors reduce the composite risk of HF rehospitalization or cardiovascular death in elderly patients.
- SGLT2i treatment is associated with a significant decrease in long-term repeated HF hospitalizations.
- SGLT2 inhibitors also demonstrate a protective effect against worsening renal function in this patient population.
Aims:
Sodium-glucose cotransporter 2 inhibitors (SGLT2i) have been widely demonstrated to reduce the risk of cardiovascular death and heart failure (HF) hospitalization, regardless of left ventricular ejection fraction (LVEF). However, data on the extent to which rehospitalization is suppressed following HF hospitalization are limited. This study investigated the effects of SGLT2i on rehospitalization and cardiovascular death.
Methods And Results:
The OASIS-HF study, a multicentre, prospective observational cohort study, enrolled 361 patients aged ≥75 years hospitalized for acute decompensated HF. The impact on composite events of HF rehospitalization or cardiovascular death and the number of annual rehospitalizations were evaluated between the conventional medical therapy and SGLT2i groups. The change in eGFR slope at the 1-year mark after the initiation of treatment in both groups was also assessed. Over an average follow-up period of 24.9 months, composite events occurred in 70 (35.4%) of the conventional therapy group and 36 (22.1%) of the SGLT2i group (log-rank: P = 0.016). The average number of rehospitalizations for HF per year was 0.22 ± 0.13 vs. 0.14 ± 0.08, respectively (P = 0.019). The change in eGFR over 1 year was significantly slower in the SGLT2i group compared with the conventional group (-3.55 ± 8.46 vs. -1.42 ± 7.28 mL/min/1.73 m2, P = 0.025).
Conclusions:
The SGLT2i are not only associated with the reduction of the composite events of HF rehospitalization or cardiovascular death and protect against worsening renal function but also with a decrease in long-term repeated HF rehospitalizations.
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