Key result
Empagliflozin was well tolerated over 2 years in a hemodialysis patient with HFrEF, improving fluid status, heart failure symptoms, and preserving residual kidney function.
Why the study?
Evidence on cardiovascular and renal benefits of SGLT2 inhibitors in patients receiving maintenance hemodialysis is limited due to their exclusion from major randomized trials.
Does empagliflozin improve volume status, heart failure symptoms, and preserve residual kidney function in non-diabetic patients with HFrEF undergoing maintenance hemodialysis?
Case Report (n=1)
Does empagliflozin improve volume status, heart failure symptoms, and preserve residual kidney function in non-diabetic patients with HFrEF undergoing maintenance hemodialysis?
Initiation of empagliflozin in a non-diabetic hemodialysis patient with HFrEF and residual kidney function appears feasible and is associated with clinical improvements in volume management, heart failure symptoms, and preserved diuresis.
May support feasibility in selected cases but should not change practice; hypothesis-generating for cardiorenal benefits in hemodialysis patients with HFrEF.
Sodium–glucose cotransporter-2 (SGLT2) inhibitors provide established cardiovascular and renal protection in patients with heart failure and chronic kidney disease, irrespective of diabetes status, but evidence in individuals receiving maintenance hemodialysis remains limited because this population has been excluded from major randomized trials. We report the case of a 76-year-old non-diabetic patient with heart failure with reduced ejection fraction (HFrEF) and end-stage kidney disease undergoing thrice-weekly hemodialysis in whom empagliflozin was initiated 12 months after dialysis initiation. Over two years of follow-up, treatment was well tolerated and associated with improvements in volume status, blood pressure control, and heart failure–related symptoms and overall quality of life, as reflected by a substantial increase in Kansas City Cardiomyopathy Questionnaire scores. Residual kidney function remained preserved, with sustained urine output and measurable residual glomerular filtration rate. Bioimpedance spectroscopy demonstrated reduced overhydration and improved fluid management, accompanied by lower loop diuretic requirements. No major adverse events were observed, apart from a single low urinary tract infection. This case highlights the potential feasibility and cardiorenal benefits of SGLT2 inhibitor initiation in selected hemodialysis patients with HFrEF and residual diuresis. Further randomized controlled studies are needed to clarify safety, mechanisms, and clinical efficacy in this high-risk population.
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Laura Gîrdan (2026) conducted a case report in End-stage kidney disease with HFrEF (n=1). Empagliflozin was evaluated. Empagliflozin was well tolerated over 2 years in a hemodialysis patient with HFrEF, improving fluid status, heart failure symptoms, and preserving residual kidney function.
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