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March 14, 2026Clinical Drug Investigation0 citationsOpen Access

Determinants and Prognostic Impact of In-Hospital Sodium-Glucose Cotransporter-2 Inhibitor Initiation in Patients with Heart Failure

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TOTakuya OkamotoKMKoichiro MatsumuraSHShohei Hakozaki

Key Points

  • This study evaluates the initiation rate of SGLT2 inhibitors in hospitalized heart failure patients and its prognostic impact.
  • Retrospective observational analysis of a prospective registry
  • Included 781 patients hospitalised for heart failure
  • Assessment of clinical factors associated with SGLT2i non-initiation using multivariable logistic regression
  • Evaluation of long-term outcomes through Cox proportional hazards analysis
  • SGLT2i initiation rate during hospitalization was 37.3%
  • Treatment discontinuation post-initiation occurred in 8.6%
  • Higher incidence of composite endpoint at 1 year in non-initiation group (37.5% vs 21.3%)
  • Cognitive dysfunction and malnutrition were linked to non-initiation
  • Not prescribed SGLT2i at discharge correlated with worse long-term outcomes (hazard ratio 1.70)

Abstract

Initiation of sodium-glucose cotransporter-2 inhibitors (SGLT2i) in patients hospitalised for heart failure (HF) is crucial for improving long-term outcomes. However, in real-world practice, a considerable proportion of patients are discharged without initiation. This study aimed to evaluate the initiation rate of SGLT2i, identify clinical factors associated with non-initiation, and examine the impact on long-term prognosis in patients hospitalised for HF. This single-centre, retrospective, observational analysis of a prospective registry included 781 consecutive patients who were hospitalised for HF between 2021 and 2024. The primary endpoint was the in-hospital initiation rate of SGLT2i. Secondary endpoints included clinical factors associated with non-initiation, assessed using multivariable logistic regression, and the incidence of the composite endpoint of all-cause mortality or HF rehospitalisation at 1 year according to SGLT2i prescription status at discharge, evaluated by log-rank test and Cox proportional hazards analysis. A total of 467 patients (median age 81 74–87 years, 50.3% male) were included in the final analysis. The initiation rate of SGLT2i during hospitalisation was 37.3% (174/467), and treatment discontinuation after initiation occurred in 8.6% (15/174). Multivariable analysis revealed that older age, non-diabetes, impaired renal function, higher left ventricular ejection fraction, malnutrition, impaired mobility, and cognitive dysfunction were independently associated with non-initiation. Among 346 patients with available follow-up data, the incidence of the composite endpoint at 1 year was significantly higher in the non-initiation group than in the initiation group (37.5% vs 21.3%, log-rank p = 0.001). In multivariable Cox analysis, not prescribed SGLT2i at discharge remained independently associated with worse long-term outcomes (hazard ratio 1.70, 95% confidence interval 1.07–2.69, p = 0.02). Both conventional clinical factors (e.g., diabetes, left ventricular ejection fraction) and aging-related factors (e.g., nutritional status, mobility, cognitive function) were independently associated with non-initiation of SGLT2i in hospitalised patients with HF. Importantly, non-initiation at discharge was significantly associated with worse long-term outcomes, underscoring the need to promote active initiation of SGLT2i in this population.

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Cite This Study

Okamoto et al. (2026) studied this question.

synapsesocial.com/papers/69b4ba1818185d8a39802b76https://doi.org/10.1007/s40261-026-01539-x
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