SGLT2 inhibitors reduce sudden cardiac death risk in heart failure: Meta‐analysis of randomized clinical trials

• Published in: Journal of cardiovascular electrophysiology 2023-05, Vol.34 (5), p.1277-1285
• Main Authors: Oates, Connor P., Santos‐Gallego, Carlos G., Smith, Alex, Basyal, Binaya, Moss, Noah, Kawamura, Iwanari, Musikantow, Daniel R., Turagam, Mohit K., Miller, Marc A., Whang, William, Dukkipati, Srinivas R., Reddy, Vivek Y., Koruth, Jacob S.
• Format: Article
• Language: English
• Subjects: Atrial Fibrillation - complications; Cardiac arrhythmia; Clinical trials; Congestive heart failure; Death; Death, Sudden, Cardiac - epidemiology; Death, Sudden, Cardiac - etiology; Death, Sudden, Cardiac - prevention & control; Diabetes Mellitus, Type 2; Heart failure; Heart Failure - complications; Heart Failure - diagnosis; Heart Failure - drug therapy; Humans; Meta-analysis; Na+/glucose cotransporter; Patients; Placebos; Prospective Studies; Randomized Controlled Trials as Topic; SGLT2 inhibitor; Sodium-Glucose Transporter 2 Inhibitors - adverse effects; sudden cardiac death; Ventricle
• ISSN: 1045-3873; 1540-8167
• DOI: 10.1111/jce.15894

Introduction Multiple randomized controlled trials have demonstrated sodium‐glucose cotransporter‐2 inhibitors (SGLT2i) decrease the composite endpoint of cardiovascular death or heart failure hospitalizations in all heart failure patients. It is uncertain whether SGLT2i impacts the risk of sudden cardiac death in patients with heart failure. Methods A comprehensive search was performed to identify relevant data published before August 28, 2022. Trials were included if: (1) all patients had clinical heart failure (2) SGLT2i and placebo were compared (3) all patients received conventional medical therapy and (4) reported outcomes of interest (sudden cardiac death [SCD], ventricular arrhythmias, atrial arrhythmias). Results SCD was reported in seven of the eleven trials meeting selection criteria: 10 796 patients received SGLT2i and 10 796 received placebo. SGLT2i therapy was associated with a significant reduction in the risk of SCD (risk ratios [RR]: 0.68; 95% confidence intervals [CI]: 0.48−0.95; p = .03; I2 = 0%). Absent dedicated rhythm monitoring, there were no significant differences in the incidence of sustained ventricular arrhythmias not associated with SCD (RR: 1.03; 95% CI: 0.83−1.29; p = .77; I2 = 0%) or atrial arrhythmias (RR: 0.91; 95% CI: 0.77–1.09; p = .31; I2 = 29%) between patients receiving an SGLT2i versus placebo. Conclusion SGLT2i therapy is associated with a reduced risk of SCD in patients with heart failure receiving contemporary medical therapy. Prospective trials are needed to determine the long‐term impact of SGLT2i therapy on atrial and ventricular arrhythmias.