Key result
SGLT2i, RAASi, finerenone, and GLP-1RA benefit HF and CKD patients, with kidney declines rarely requiring discontinuation.
Why the study?
Heart failure and chronic kidney disease frequently coexist, elevating clinical risks, but many challenges remain in diagnosing and managing them in combination.
This KDIGO conference report emphasizes the need for integrated management of coexisting HF and CKD, highlighting that initial hemodynamic declines in kidney function with HF therapies should not prompt discontinuation.
HF therapies should not be stopped for small kidney declines in CKD; reinforces integrated cardiorenal care and need for trials in advanced stages.
Heart failure (HF) and chronic kidney disease (CKD) frequently coexist, which elevates the risks of hospitalization, disease progression, and death. Despite advances in treating each condition independently, many challenges remain in diagnosing and managing them in combination. In March 2024, Kidney Disease: Improving Global Outcomes (KDIGO) held the Controversies Conference on Kidney Disease and Heart Failure: Recent Advances and Current Challenges. Discussions highlighted the complex, bidirectional relationship between HF and CKD, including shared risk factors and overlapping pathophysiology as well as nuances in interpreting biomarkers such as natriuretic peptides and serum creatinine. Sodium-glucose cotransporter-2 inhibitors, renin-angiotensin-aldosterone system inhibitors, and emerging agents such as finerenone and glucagon-like peptide-1 receptor agonists can have benefits in both populations of patients with HF and CKD, though evidence in advanced CKD remains limited. Importantly, small declines in kidney function after initiating guideline-directed HF therapies generally do not require discontinuation, as these declines are often hemodynamic in nature and not associated with poor outcomes. The group highlighted the need for CKD-specific HF diagnostic thresholds and refined acute kidney injury definitions in HF. It is important for future cardiovascular and kidney trials to include relevant end points, such as kidney function trajectories, symptom burden, and quality of life. To improve care for individuals with HF and CKD, a more integrated approach to management, rooted in individualization, clinical context, and shared therapeutic goals, is needed.
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Lam et al. (2026) studied this question. SGLT2 inhibitors, RAAS inhibitors, finerenone, and GLP-1 receptor agonists benefit patients with heart failure and CKD, with small kidney declines after HF therapy rarely requiring discontinuation.
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