Key result
In patients with cardiac implantable electronic devices, SGLT2i use was associated with a reduced risk of atrial tachy-arrhythmias (HR 0.78; 95% CI 0.70-0.87; p<0.001).
Why the study?
SGLT2 inhibitors were associated with reduced atrial fibrillation hospitalizations, prompting evaluation of their effects on atrial tachy-arrhythmias in CIED patients.
Does SGLT2 inhibitor use reduce atrial tachy-arrhythmia burden in patients with cardiac implantable electronic devices?
Cohort (n=13,888)
Blinded event adjudication
Yes
Does SGLT2 inhibitor use reduce atrial tachy-arrhythmia burden in patients with cardiac implantable electronic devices?
In patients with CIEDs, particularly those with heart failure, SGLT2 inhibitor use is associated with a significant reduction in atrial tachy-arrhythmia burden and all-cause mortality.
Answers are grounded in this paper and cite their sources.
May support arrhythmia reduction with SGLT2i in CIED patients; hypothesis-generating and requires randomized confirmation.
INTRODUCTION: Use of sodium glucose cotransporter 2 inhibitors (SGLT2i) was associated with a reduction in atrial fibrillation hospitalizations. Therefore, we aim to evaluate the effects of SGLT2i on atrial tachy-arrhythmias (ATA) in patients with cardiac implantable electronic devices (CIEDs). METHODS: All 13 888 consecutive patients implanted with a CIED in two tertiary medical centers were enrolled. Treatment with SGLT2i was assessed as a time dependent variable. The primary endpoint was the total number of ATA. Secondary endpoints included total number of ventricular tachy-arrhythmias (VTA), ATA and VTA, and death. All events were independently adjudicated blinded to the treatment. Multivariable propensity score modeling was performed. RESULTS: During a total follow-up of 24 442 patient years there were 62 725 ATA and 10 324 VTA events. Use of SGLT2i (N = 696) was independently associated with a significant 22% reduction in the risk of ATA (hazard ratio [HR] = 0.78 [95% confidence interval {CI} = 0.70-0.87]; p < .001); 22% reduction in the risk of ATA/VTA (HR = 0.78 [95% CI = 0.71-0.85]; p < .001); and with a 35% reduction in the risk of all-cause mortality (HR = 0.65 [95% CI = 0.45-0.92]; p = .015), but was not significantly associated with VTA risk (HR = 0.92 [95% CI = 0.80-1.06]; p = .26). SGLT2i were associated with a lower ATA burden in heart failure (HF) patients but not among diabetes patients (HF: HR = 0.68, 95% CI = 0.58-0.80, p < .001 vs. Diabetes: HR = 0.95, 95% CI = 0.86-1.05, p = .29; p < .001 for interaction between SGLT2i indication and ATA burden). CONCLUSION: Our real world findings suggest that in CIED HF patients, those with SGLT2i had a pronounced reduction in ATA burden and all-cause mortality when compared with those not on SGLT2i.
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Younis et al. (2023) conducted a cohort in Cardiac implantable electronic devices (CIEDs) (n=13,888). Sodium glucose cotransporter 2 inhibitors (SGLT2i) vs. No SGLT2i was evaluated on Total number of atrial tachy-arrhythmias (ATA) (HR 0.78, 95% CI 0.70-0.87, p=<.001). In patients with cardiac implantable electronic devices, SGLT2i use was associated with a reduced risk of atrial tachy-arrhythmias (HR 0.78; 95% CI 0.70-0.87; p<0.001).
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