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Management of Heart Failure Patient with CKD
Debasish Banerjee1,2, Giuseppe Rosano2, Charles A Herzog3
1Renal and Transplantation Unit, St George's University Hospitals National Health Service Foundation Trust, London, United Kingdom.
Insights
Patients with chronic kidney disease (CKD) and heart failure (HF) often do not benefit from standard HF therapies. Evidence supports using certain drugs and devices, even in advanced CKD, to improve outcomes for these complex patients.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Chronic kidney disease (CKD) is highly prevalent in heart failure (HF) patients, significantly increasing mortality and morbidity, especially in those on dialysis.
- Despite advancements in HF treatment, patients with CKD have not consistently benefited from evidence-based therapies.
- This review examines the current evidence for kidney replacement, device, and drug therapies for HF in the context of CKD.
Purpose of the Study:
- To review the prevalence of CKD in HF patients.
- To evaluate the evidence for various therapeutic interventions in HF patients with CKD.
- To highlight challenges and potential solutions for implementing evidence-based HF therapies in CKD patients.
Main Methods:
- Literature review of studies on HF treatments in patients with varying stages of CKD, including those on dialysis.
- Analysis of evidence for beta-blockers, renin-angiotensin-aldosterone system inhibitors, sodium-glucose cotransporter inhibitors, diuretics, iron therapy, cardiac resynchronization therapy, and dialysis.
- Examination of treatment guidelines and clinical trial data for efficacy and safety in CKD populations.
Main Results:
- Beta-blockers show benefit across all CKD stages, including dialysis. Angiotensin receptor neprilysin inhibitors are effective down to eGFR 20 ml/min/1.73 m².
- Sodium-glucose cotransporter inhibitors improve outcomes in CKD stages 3-4. Intravenous iron and cardiac resynchronization therapy demonstrate benefits in specific CKD populations.
- Diuretic therapy, while complex, can be managed successfully. Peritoneal dialysis aids symptomatic fluid overload in dialysis patients.
Conclusions:
- Evidence supports the use of specific drug and device therapies for heart failure with reduced ejection fraction (HFrEF) in patients with CKD, even in advanced stages.
- Barriers to treatment, such as fear of adverse effects, limit uptake. Multidisciplinary approaches, including combined cardiology-nephrology clinics, are crucial for optimal management.
- Implementing evidence-based therapies requires a coordinated, multidisciplinary strategy to improve outcomes for HF patients with CKD.
Abstract:
CKD is common in patients with heart failure, associated with high mortality and morbidity, which is even higher in people undergoing long-term dialysis. Despite increasing use of evidence-based drug and device therapy in patients with heart failure in the general population, patients with CKD have not benefitted. This review discusses prevalence and evidence of kidney replacement, device, and drug therapies for heart failure in CKD. Evidence for treatment with β-blockers, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, angiotensin receptor neprilysin inhibitors, and sodium-glucose cotransporter inhibitors in mild-to-moderate CKD has emerged from general population studies in patients with heart failure with reduced ejection fraction (HFrEF). β-Blockers have been shown to improve outcomes in patients with HFrEF in all stages of CKD, including patients on dialysis. However, studies of HFrEF selected patients with creatinine <2.5 mg/dl for ACE inhibitors, <3.0 mg/dl for angiotensin-receptor blockers, and <2.5 mg/dl for mineralocorticoid receptor antagonists, excluding patients with severe CKD. Angiotensin receptor neprilysin inhibitor therapy was successfully used in randomized trials in patients with eGFR as low as 20 ml/min per 1.73 m2 Hence, the benefits of renin-angiotensin-aldosterone axis inhibitor therapy in patients with mild-to-moderate CKD have been demonstrated, yet such therapy is not used in all suitable patients because of fear of hyperkalemia and worsening kidney function. Sodium-glucose cotransporter inhibitor therapy improved mortality and hospitalization in patients with HFrEF and CKD stages 3 and 4 (eGFR>20 ml/min per 1.73 m2). High-dose and combination diuretic therapy, often necessary, may be complicated with worsening kidney function and electrolyte imbalances, but has been used successfully in patients with CKD stages 3 and 4. Intravenous iron improved symptoms in patients with heart failure and CKD stage 3; and high-dose iron reduced heart failure hospitalizations by 44% in patients on dialysis. Cardiac resynchronization therapy reduced death and hospitalizations in patients with heart failure and CKD stage 3. Peritoneal dialysis in patients with symptomatic fluid overload improved symptoms and prevented hospital admissions. Evidence suggests that combined cardiology-nephrology clinics may help improve management of patients with HFrEF and CKD. A multidisciplinary approach may be necessary for implementation of evidence-based therapy.
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