Why the study?
SGLT2 inhibitors are recommended in heart failure regardless of ejection fraction, but their role in reducing post-TAVR cardiovascular complications remains underexplored.
Does SGLT2i use reduce major adverse cardiovascular events in diabetic patients following transcatheter aortic valve replacement?
Cohort (n=9,930)
Yes
Does SGLT2i use reduce major adverse cardiovascular events in diabetic patients following transcatheter aortic valve replacement?
SGLT2i use in diabetic patients following TAVR is associated with significantly reduced cardiovascular morbidity and mortality up to 1 year.
Background Transcatheter aortic valve replacement (TAVR), a standard therapy for aortic stenosis, is preferred for older or high-risk patients. Various complications, including heart failure (HF), resulting in increased mortality, have been reported in the literature. Sodium-glucose cotransporter-2 inhibitors (SGLT2i) are recommended in HF, irrespective of ejection fraction; however, their role in reducing post-TAVR cardiovascular complications remains underexplored. We conducted a retrospective study to evaluate cardiovascular outcomes associated with the use of SGLT2i in post-TAVR patients. Methods This retrospective cohort was based on a global database of electronic health records of more than 160 million patients. After propensity-score matching, the study population included 9930 post-TAVR diabetic patients divided into 2 cohorts based on their exposure to SGLT2i. Exposure to SGLT2i was defined as exposure after 1 day of TAVR. Results In this study of 9930 post-TAVR diabetic patients, the primary outcome of major adverse cardiovascular events and secondary outcomes, ie, cardiovascular mortality, ischemic stroke, and HF exacerbation, were significantly reduced in SGLT2i-exposed post-TAVR patients at the 1-month and 1-year follow-up. Hemorrhagic stroke was comparable at the 1-month follow-up; however, it was significantly lower in SGLT2i-exposed cohorts at the 1-year follow-up. The risk of new-onset myocardial infarction was significantly reduced at 1 month; however, it was comparable between the 2 cohorts at the 1-year follow-up. Our study also demonstrated a significant reduction in the risk of end-stage renal disease in the SGLT2i-exposed cohort at the 1-year follow-up. The periprocedural risk of acute kidney injury (within 7 days of TAVR) as well as at the 1-month and 1-year follow-up was significantly lower in the SGLT2i-exposed cohort. Conclusions In this study, post-TAVR SGLT2i use in diabetic patients was associated with reduced cardiovascular morbidity and mortality for up to 1 year.
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Hanif et al. (2026) conducted a cohort in Diabetes and post-Transcatheter Aortic Valve Replacement (TAVR) (n=9,930). Sodium-glucose cotransporter-2 inhibitors (SGLT2i) vs. No SGLT2i exposure was evaluated on Major adverse cardiovascular events.
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