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Sodium Glucose Co-Transporter 2 Inhibitors in Patients With Heart Failure and Transcatheter Aortic Valve Replacement
Farah Yasmin1, Mohammad Hamza2, Muhammad Ahmed Ali Fahim1
1Dow University of Health Sciences, Karachi, Pakistan.
Insights
Sodium glucose co-transporter 2 (SGLT2) inhibitors did not significantly reduce the primary composite cardiovascular outcome in patients with congestive heart failure (CHF) undergoing transcatheter aortic valve replacement (TAVR). However, SGLT2 inhibitors showed benefits in reducing hospitalizations.
Area of Science:
- Cardiology
- Pharmacology
- Medical Informatics
Background:
- Patients undergoing transcatheter aortic valve replacement (TAVR) often have congestive heart failure (CHF), increasing their risk of adverse cardiovascular events.
- Sodium glucose co-transporter 2 (SGLT2) inhibitors have shown promise in managing CHF patients.
Purpose of the Study:
- To investigate the cardiovascular outcomes of SGLT2 inhibitors compared to standard care in CHF patients undergoing TAVR.
- Utilize a large research network database for observational cohort analysis.
Main Methods:
- Retrospective cohort analysis of deidentified patient data from the TriNETX research network.
- Included CHF patients (≥18 years) who underwent TAVR and received either SGLT2 inhibitors or standard care.
- Propensity score matching was used, with outcomes assessed at 6-month and 1-year follow-up.
Main Results:
- The primary composite outcome (acute myocardial infarction, stroke, all-cause mortality, acute CHF) was not significantly different between groups at 6 months or 1 year.
- SGLT2 inhibitors were associated with a significantly lower risk of acute myocardial infarction and all-cause hospitalizations/emergency room visits at 6 months.
- At 1 year, all-cause hospitalizations remained significantly lower in the SGLT2 inhibitor group.
Conclusions:
- SGLT2 inhibitor use in CHF patients undergoing TAVR was not associated with a reduced risk of the primary composite cardiovascular outcome.
- SGLT2 inhibitors may offer benefits in reducing hospitalizations for CHF patients undergoing TAVR.
Background:
Patients undergoing transcatheter aortic valve replacement (TAVR) have a high risk of adverse cardiovascular outcomes due to comorbid conditions such as congestive heart failure (CHF). Recent trials show promising results of sodium glucose co-transporter 2 inhibitors in CHF patients.
Objectives:
In this observational cohort study, we aim to explore the cardiovascular outcomes of SGLT2 inhibitors vs standard care in CHF patients undergoing TAVR using a large research network database.
Methods:
A retrospective cohort analysis of deidentified, aggregate patient data from the TriNETX research network was conducted. Subjects with CHF who underwent a TAVR procedure, were ≥18 years old, and received either SGLT2 inhibitors or standard of care were included in the analysis. After propensity score matching, outcomes were reported at 6-month and 1-year follow-up. The primary outcome was a composite of acute myocardial infarction, stroke, all-cause mortality, and acute CHF.
Results:
A total of 21,828 CHF patients undergoing TAVR were identified, of whom 2,464 were on SGLT2 inhibitors therapy. Following propensity score matching, 2,039 patients were included in each group. The primary composite outcome was not statistically different at 6 months among patients receiving SGLT2 inhibitors compared to those receiving standard care (HR: 0.79; P = 0.067). SGLT2 inhibitors use was associated with a significantly lower risk of acute myocardial infarction (HR: 0.69; P = 0.043) and all-cause hospitalization/emergency room visits (HR: 0.69; P < 0.001). At 1 year, no significant differences were observed for the primary and individual endpoints except for all-cause hospitalizations (HR: 0.73; P < 0.001) and urinary tract infections (HR: 0.77; P = 0.009).
Conclusions:
Among CHF patients undergoing TAVR, SGLT2i use was not associated with a reduced risk of the primary composite outcome at 6-months and 1-year intervals.
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