Key result
Low BMI links to ~19-point lower rate of discharge SGLT2 inhibitor prescription in acute heart failure.
Why the study?
SGLT2 inhibitors are underutilized in patients with acute heart failure and low BMI, and their safety and outcomes in this population are uncertain.
Does SGLT2 inhibitor prescription at discharge improve outcomes or increase drug discontinuation rates in patients with acute heart failure and a low body mass index?
Cohort (n=621)
Does SGLT2 inhibitor prescription at discharge improve outcomes or increase drug discontinuation rates in patients with acute heart failure and a low body mass index?
Absolute Event Rate: 22.1% vs 41.5%
p-value: p=<0.001
SGLT2 inhibitors were underutilized in heart failure patients with low BMI, but their use was not associated with increased drug discontinuation or adverse outcomes, suggesting low BMI alone should not preclude SGLT2i prescription.
Low-BMI acute HF patients receive fewer SGLT2i prescriptions despite similar tolerability; leaves open outcome benefits in this subgroup.
for those ≥ 70 years. We assessed the clinical characteristics, SGLT2i prescription at discharge, discontinuation within 1 year, and clinical outcomes, including cardiovascular death, HF readmission, and all-cause mortality, were assessed. Time-to-event analyses and inverse probability of treatment weighting (IPTW) were performed.Of 621 patients (median age: 81 years), 29.0% had a low BMI and 35.6% received a SGLT2i at discharge. SGLT2is were prescribed significantly less frequently in patients with low BMI (22.1% versus 41.5%, P < 0.001). Kaplan-Meier analysis showed that the overall 1-year discontinuation-free rate was 0.880, with no significant difference between the BMI groups. In crude analyses, SGLT2i use was associated with lower cardiovascular event rates in the non-low BMI group and lower all-cause mortality in the low BMI group; however, after IPTW adjustment, the latter association was attenuated.SGLT2is were underutilized in patients with HF and low BMI, yet discontinuation and adverse outcomes were not increased. These findings suggest that low BMI alone should not be a reason to avoid or discontinue SGLT2is in patients with acute HF.
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Uemura et al. (2026) conducted a cohort in Acute heart failure (n=621). Low BMI vs. Non-low BMI was evaluated on SGLT2 inhibitor prescription at discharge (p=<0.001). Low BMI in patients with acute heart failure was associated with significantly less frequent prescription of SGLT2 inhibitors at discharge compared to non-low BMI (22.1% vs 41.5%, P<0.001).
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