Key result
SGLT2 inhibitors linked to ~32% lower mortality and less cardioversion in AF patients.
Why the study?
Although SGLT2 inhibitors offer various cardiovascular benefits, data examining their effects on clinical outcomes associated with AF remain limited.
Does SGLT2 inhibitor use reduce ischemic stroke, ACS, cardioversion, and all-cause mortality in patients with atrial fibrillation?
Observational (n=52,538)
Yes
Does SGLT2 inhibitor use reduce ischemic stroke, ACS, cardioversion, and all-cause mortality in patients with atrial fibrillation?
In patients with atrial fibrillation, SGLT2 inhibitors were associated with reduced all-cause mortality and cardioversion, but an increased risk of ischemic stroke.
SGLT2 inhibitors were associated with lower AF mortality and cardioversion; hypothesis-generating and requires RCTs before practice change.
BACKGROUND: Sodium glucose cotransporter 2 (SGLT2) inhibitors have been associated with various cardiovascular benefits. There is limited data examining the effect of these medications on atrial fibrillation (AF) associated clinical outcomes. We compared ischemic stroke, acute coronary syndrome (ACS), cardioversion, and all-cause mortality outcomes in AF patients on SGLT2 inhibitors to propensity matched controls. MATERIALS AND METHODS: We conducted a retrospective study with a global medical research network database. AF patients were identified via ICD codes that must have been present for at least one month. Patients on SGLT2 inhibitors were identified as those on dapagliflozin, empagliflozin, or canagliflozin for at least one month. AF patients on SGLT2 inhibitors were propensity matched to those not on SGLT2 inhibitors based on age, race, ethnicity, cardiovascular comorbidities, valvular disease, pulmonary disease, urinary diseases, cardiovascular procedures, cardiovascular medications, and anticoagulants. We examined incidence of ischemic stroke, at least one ACS episode, cardioversion, and all-cause mortality. RESULTS: In 26,269 AF patients, SGLT2 inhibitors were associated with lower risk of cardioversion (HR 0.921, 95% CI 0.841 - 0.999, p = 0.0245) and all-cause mortality (HR 0.676, 95% CI 0.635 - 0.721, p < 0.0001). However, there was an association with increased risk for ischemic stroke (HR 1.081, 95% CI 1.012 - 1.154, p 0.0201). There was no clear association with ACS events. CONCLUSIONS: In patients with AF, use of SGLT2 inhibitors was associated with a lower risk of cardioversion and all-cause mortality and higher probability of survival based on Kaplan-Meier analysis.
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Justin Haloot (2021) conducted an observational in Atrial Fibrillation (n=52,538). SGLT2 inhibitors (empagliflozin, dapagliflozin, or canagliflozin) vs. No SGLT2 inhibitors was evaluated on All-cause mortality (HR 0.676, 95% CI 0.635 - 0.721, p=< 0.0001). In patients with atrial fibrillation, the use of SGLT2 inhibitors was associated with a significantly lower risk of all-cause mortality (HR 0.676) and cardioversion compared to matched controls.
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