Early initiation of SGLT2 inhibitors within 6 weeks after first HFrEF hospitalization reduced 1-year all-cause mortality by 25% (HR 0.75) and hospitalizations by 14% (HR 0.86).
Does the initiation of SGLT2 inhibitors within 6 weeks following first heart failure hospitalization reduce 1-year mortality and hospitalizations in patients with newly diagnosed HFrEF?
70,042 patients with newly diagnosed heart failure with reduced ejection fraction (HFrEF) who experienced their first HF hospitalization between September 2021 and December 2023. The propensity-matched cohort included 14,670 matched pairs (mean age 64 ± 17 years; 41.6% female; 20% Black).
Initiation of SGLT2 inhibitors within 6 weeks following first heart failure hospitalization
Non-users of SGLT2 inhibitors within 6 weeks following first heart failure hospitalization (propensity score matched to baseline characteristics)
1-year all-cause mortalityhard clinical
Early initiation of SGLT2 inhibitors within 6 weeks of a first heart failure hospitalization in newly diagnosed HFrEF patients is associated with significantly reduced 1-year all-cause mortality and hospitalizations in real-world practice.
Abstract Aims Sodium-glucose cotransporter-2 inhibitors (SGLT2is) improve outcomes in patients with heart failure (HF), and are recommended to be initiated in the 6 weeks following an HF hospitalization. We aimed to explore prescription rates and clinical benefits of SGLT2is among patients with newly diagnosed HF and reduced ejection fraction (HFrEF) in real-world practice. Methods We conducted a retrospective analysis using the TriNetX Global Collaborative research network. Patients with HFrEF who experienced their first HF hospitalization between September 2021 and December 2023 were identified and were categorized into 2 groups based on the initiation of SGLT2is within 6 weeks following HF hospitalization. After using propensity score matching to baseline characteristics, Cox hazard ratios (HRs) were calculated to compare outcomes over a1-year period. Results Among the identified 70,042 patients with HFrEF, 21.3% were initiated on SGLT2is within 6 weeks following their first HF hospitalization. SGLT2i users were younger, more likely to be male and had a higher prevalence of diabetes, compared with SGLT2i non-users. After matching, 14,670 matched pairs were created (mean age 64 ± 17 years; 41.6% female; 20% Black). SGLT2i users vs. non-users had a lower risk of 1-year all-cause mortality (HR, 95%CI=0.75, 0.69 to 0.83), all-cause hospitalizations (HR, 95%CI=0.86, 0.83 to 0.91), and emergency department visits (HR, 95%CI=0.91, 0.86 to 0.96). Conclusion In this large multinational real-world data of patients with HFrEF, the prescription rate for SGLT2is within 6 weeks after the first HF hospitalization remained low. However, SGLT2i initiation was associated with improved outcomes, underscoring the importance of guideline-recommended early use.
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Takashi Kohno
Luca Monzo
Guillaume Baudry
ESC Heart Failure
Centre de Recherche en Automatique de Nancy
Tokyo Medical University Hospital
Custodix (Belgium)
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Kohno et al. (Sat,) reported a other. Early initiation of SGLT2 inhibitors within 6 weeks after first HFrEF hospitalization reduced 1-year all-cause mortality by 25% (HR 0.75) and hospitalizations by 14% (HR 0.86).
www.synapsesocial.com/papers/6996a887ecb39a600b3ef5f7 — DOI: https://doi.org/10.1093/eschf/xvag008