Key result
Adding SGLT2 inhibitors to optimal medical therapy in HFrEF patients significantly improved right ventricular free wall strain (+91% vs. +28%, p=0.039) at 3 months compared to OMT alone.
Why the study?
The impact of SGLT2 inhibitors added to optimal medical therapy on right ventricular systolic function using advanced echocardiographic analysis in outpatients with HFrEF has been poorly investigated.
Does adding an SGLT2 inhibitor to optimal medical therapy improve right ventricular systolic function in outpatients with HFrEF?
RCT (n=36)
Single-blind
randomized
No
Does adding an SGLT2 inhibitor to optimal medical therapy improve right ventricular systolic function in outpatients with HFrEF?
Absolute Event Rate: 91% vs 28%
p-value: p=0.039
Adding an SGLT2 inhibitor to optimal medical therapy significantly improves right ventricular systolic function parameters at 3 months in outpatients with HFrEF.
SGLT2i addition may improve RV systolic function in HFrEF; leaves open need for larger trials before practice change.
Background: The impact of sodium-glucose cotransporter-2 inhibitors (SGLT2is) in addition to optimal medical therapy (OMT) on the right ventricular (RV) systolic function using advanced echocardiographic analysis among outpatients with heart failure and a reduced ejection fraction (HFrEF) has thus far been poorly investigated. Methods: This was a single-center, prospective, single-blinded study in which an echocardiographic expert was blinded to the allocation of the treatment. A total of 36 outpatients with HFrEF were randomized to either OMT or OMT+SGLT2i. Both groups underwent an echocardiographic examination of the RV systolic function at the baseline and at the 3-month follow-up (3mFU). Results: The patients in both groups did not significantly differ with respect to the relevant baseline comorbidities, therapy, and clinical characteristics. The patients receiving OMT+SGLT2i showed a significant improvement from the baseline to the 3mFU in all the measured RV echocardiographic parameters, while for the OMT group, a significant improvement after the 3mFU was observed for TAPSE and s’. The mean percent change from the baseline to the 3mFU was significant when comparing OMT+SGLT2i to the OMT group concerning RV FWS (+91% vs. +28%, p = 0.039), TR maxPG (−27% vs. +19%, p = 0.005), and TR Vmax (−17% vs. +13%, p = 0.008), respectively. Conclusions: Adding SGLT2i to OMT in patients with HFrEF resulted in a greater improvement in the RV systolic function from the baseline to the 3mFU compared to the OMT alone.
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Mustapić et al. (2022) conducted an RCT in Heart failure with reduced ejection fraction (HFrEF) (n=36). SGLT2 inhibitors (SGLT2i) + optimal medical therapy (OMT) vs. Optimal medical therapy (OMT) alone was evaluated on Mean percent change in right ventricular free wall strain (RV FWS) from baseline to 3 months (p=0.039). Adding SGLT2 inhibitors to optimal medical therapy in HFrEF patients significantly improved right ventricular free wall strain (+91% vs. +28%, p=0.039) at 3 months compared to OMT alone.
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