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Association of SGLT2 Inhibitor Use with All-Cause Mortality Following CIED Implantation for Conduction Disease in
Hidayet Ozan Arabaci1, Fatih Ozkan2, Zafer Guven2
1Department of Cardiology, Yuksekova State Hospital, 30300 Hakkari, Turkey.
Insights
Sodium-glucose cotransporter-2 (SGLT2) inhibitor use was linked to reduced mortality in patients receiving cardiac implantable electronic devices (CIEDs) for conduction disease. This suggests SGLT2 inhibitors may improve survival in this specific patient group.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Patients with cardiac implantable electronic devices (CIEDs) for conduction disease face long-term mortality risks, even with preserved systolic function.
- The impact of sodium-glucose cotransporter-2 (SGLT2) inhibitors on mortality in this population is not well understood.
Purpose of the Study:
- To investigate the association between early SGLT2 inhibitor use and all-cause mortality in patients with preserved left ventricular ejection fraction (LVEF) undergoing CIED implantation for conduction disease.
Main Methods:
- Retrospective cohort study of 540 patients with LVEF ≥ 50% undergoing CIED implantation for conduction disease.
- SGLT2 inhibitor exposure defined as use within 3 months post-implantation.
- All-cause mortality assessed using multivariable Cox regression and Kaplan-Meier analysis over a median follow-up of 64.2 months.
Main Results:
- 206 patients (38.1%) had documented SGLT2 inhibitor exposure.
- SGLT2 inhibitor use was associated with a significantly lower adjusted hazard of death (HR, 0.48; p < 0.001).
- Improved survival observed in SGLT2 inhibitor users in the overall cohort and in subgroups without heart failure or diabetes.
Conclusions:
- Early SGLT2 inhibitor use is independently associated with reduced all-cause mortality in patients with preserved LVEF receiving CIEDs for conduction disease.
- These findings are hypothesis-generating and highlight the potential benefit of SGLT2 inhibitors in this population.
- Prospective studies are warranted to confirm these observational results.
Abstract:
Background/Objectives: Patients receiving a cardiac implantable electronic device (CIED) for conduction disease may remain at substantial long-term risk despite preserved systolic function at implantation. The prognostic association of sodium-glucose cotransporter-2 (SGLT2) inhibitor use in this population is uncertain. We therefore examined the relationship between early documented SGLT2 inhibitor use and subsequent all-cause mortality in patients with preserved left ventricular ejection fraction (LVEF) undergoing CIED implantation for conduction disease. Methods: In this retrospective single-center cohort study, we screened consecutive adults who underwent CIED implantation for conduction disease between January 2018 and June 2024. Patients with LVEF ≥ 50% and complete clinical, laboratory, electrocardiographic, and echocardiographic data were included. SGLT2 inhibitor exposure was defined as documented initiation or active use within 3 months after implantation. The primary endpoint was all-cause mortality. Associations were evaluated using multivariable Cox proportional-hazards regression and Kaplan-Meier analyses. Results: Among 2176 screened patients, 540 fulfilled the eligibility criteria, of whom 206 (38.1%) had documented SGLT2 inhibitor exposure. During a median observation period of 64.2 months (range, 7-90 months), 185 deaths occurred. SGLT2 inhibitor exposure was associated with a lower adjusted hazard of death (HR, 0.48; 95% CI, 0.38-0.69; p < 0.001). Survival also differed between exposure groups in the overall cohort (log-rank p = 0.006) and in patients without either heart failure or diabetes mellitus (log-rank p = 0.020). Conclusions: In patients with preserved LVEF undergoing CIED implantation for conduction disease, documented SGLT2 inhibitor use was independently associated with lower all-cause mortality. These observational findings are hypothesis-generating and warrant confirmation in prospective studies.
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