Effects of empagliflozin in patients at risk of heart failure: the empire prevent metabolic trial - Scorecard - MDSpire

Effects of empagliflozin in patients at risk of heart failure: the empire prevent metabolic trial

  • By

  • Camilla Fuchs Andersen

  • Julie Hempel Larsen

  • Massar Omar

  • Nina Nouhravesh

  • Caroline Michaela Kistorp

  • Christian Tuxen

  • Filip K Knop

  • Per Lav Madsen

  • Julie Lyng Forman

  • Filip Søskov Davidovski

  • Lars Køber

  • Morten Schou

  • Jacob Eifer Møller

  • Jesper Jensen

  • January 8, 2026

  • 0 min

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Clinical Scorecard: Impact of Empagliflozin on Heart Failure Risk in Overweight Patients: Findings from the Empire Prevent Metabolic Study

At a Glance

CategoryDetail
ConditionHeart failure risk in overweight or obese non-diabetic patients
Key MechanismsReduction of estimated extracellular volume (eECV) and evaluation of epicardial adipose tissue (EAT) mass
Target PopulationNon-diabetic patients aged 60–84 years with BMI > 28 kg/m2 and additional heart failure risk factors
Care SettingOutpatient cardiology clinics in hospital settings

Key Highlights

  • Empagliflozin significantly reduced estimated extracellular volume (eECV) compared to placebo after 180 days.
  • Empagliflozin did not significantly affect epicardial adipose tissue (EAT) mass in the study population.
  • Empagliflozin was safe and well tolerated with few reported side effects in non-diabetic overweight or obese patients.

Guideline-Based Recommendations

Diagnosis

  • Identify patients aged 60–84 years with BMI > 28 kg/m2 and at least one additional heart failure risk factor (hypertension, ischemic heart disease, previous stroke/TIA, or CKD with eGFR 30–45 mL/min/1.73 m2).
  • Exclude patients with known type 2 diabetes or established heart failure.

Management

  • Consider empagliflozin 10 mg once daily for 180 days to reduce extracellular fluid volume in high-risk overweight or obese non-diabetic patients.
  • Monitor for potential benefits in heart failure prevention through reduction of hypervolemia.

Monitoring & Follow-up

  • Assess changes in estimated extracellular volume (eECV) as a surrogate marker for fluid status.
  • Monitor epicardial adipose tissue (EAT) mass, although no significant change is expected with empagliflozin in this population.
  • Observe for adverse effects and overall safety during treatment.

Risks

  • Empagliflozin was generally safe with few side effects reported in the trial population.
  • No specific risks identified related to empagliflozin use in non-diabetic overweight or obese patients in this study.

Patient & Prescribing Data

Non-diabetic adults aged 60–84 years with overweight or obesity and additional heart failure risk factors.

Empagliflozin 10 mg daily for 6 months reduces extracellular fluid volume, potentially lowering heart failure risk, without affecting cardiac fat mass.

Clinical Best Practices

  • Screen overweight or obese patients without diabetes for heart failure risk factors before initiating empagliflozin.
  • Use empagliflozin to target fluid overload as a preventive strategy for heart failure in high-risk populations.
  • Monitor patient response through surrogate markers such as eECV and clinical assessment.
  • Educate patients on the safety profile and expected outcomes of empagliflozin treatment.

References

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