Key result
Advanced CKD-associated excess mortality in HF declined over time, driven by reductions in HFpEF.
Why the study?
Patients with advanced CKD and HF are systematically underrepresented in clinical trials. Whether contemporary care has improved outcomes in this high-risk group, particularly among HFpEF patients, remains incompletely defined.
Does the excess all-cause mortality risk associated with advanced CKD (eGFR 15–45 mL/min/1.73m²) attenuate over time (2016–2025 vs 2009–2016) in patients with heart failure, particularly those with HFpEF?
Cohort (n=15,381)
No
Does the excess all-cause mortality risk associated with advanced CKD (eGFR 15–45 mL/min/1.73m²) attenuate over time (2016–2025 vs 2009–2016) in patients with heart failure, particularly those with HFpEF?
In a large real-world heart failure cohort, the excess mortality risk associated with advanced CKD narrowed significantly between 2009–2016 and 2016–2025 specifically among patients with HFpEF, coinciding with increased uptake of contemporary guideline-directed therapies.
Attenuated excess mortality with advanced CKD in HFpEF may inform updated risk models; extends observational data but leaves causal mechanisms and practice change open.
Background Patients with advanced chronic kidney disease (CKD) and heart failure (HF) are systematically underrepresented in clinical trials despite comprising a substantial proportion of real-world HF populations [1]. Whether contemporary care has translated into improved outcomes in this high-risk group particularly among heart failure with preserved ejection fraction (HFpEF) patients, in whom cardiorenal pathophysiology is central remains incompletely defined [2–5]. Purpose To evaluate temporal changes in the mortality risk associated with advanced CKD in a real-world HF population, and to determine whether these trends differ according to HF phenotype, with particular focus on HFpEF. Methods We performed a retrospective cohort study of 15,381 HF patients in the SHEBAHEART registry (January 2009–October 2025) at a tertiary care center. Patients were stratified by kidney function: advanced CKD (eGFR 15–45 mL/min/1.73m²) versus non-advanced CKD (eGFR ≥45 mL/min/1.73m²). Temporal trends were evaluated by comparing an early (2009–2016) and late (2016–2025) period. The primary outcome was all-cause mortality, assessed using Kaplan–Meier methods and Cox proportional hazards models with period-by-CKD interaction terms; analyses were further stratified by HF phenotype (HFpEF vs HFrEF). Results Among 15,381 patients (age 72±14 years, 60% male), 3,595 (23%) had advanced CKD. Over a median 3.6-year follow-up, 5,018 (33%) patients died. Advanced CKD was consistently associated with higher mortality. Overall, the excess mortality risk associated with advanced CKD attenuated over time (HR 1.80 [95% CI 1.69–1.91] in 2009–2016 vs 1.66 [1.53–1.81] in 2016–2025; p for interaction=0.06). This temporal improvement was driven by HFpEF, where the advanced CKD-associated excess risk declined substantially (HR 1.73 to 1.48; p for interaction=0.003). In contrast, HFrEF patients demonstrated only minimal change over time (HR 1.84 to 1.81). Uptake of contemporary HF therapies increased in the later era, including broader use of guideline-directed agents among patients with advanced CKD [2–4]. Conclusions In this large single-center real-world HF cohort, advanced CKD remained associated with markedly higher mortality; however, the relative excess risk narrowed over the past decade, with the clearest improvement observed in HFpEF. These findings are consistent with increasing implementation of contemporary HF strategies in routine practice and support proactive use of evidence-based therapies in HFpEF patients with advanced CKD [2–4].Spline HFrEF vs HFpEF
No takes yet. Share an insight, caveat, or question.
Hochstein et al. (2026) conducted a cohort in Heart failure and chronic kidney disease (n=15,381). Advanced CKD (eGFR 15-45 mL/min/1.73m²) across temporal eras (2016-2025 vs 2009-2016) vs. Non-advanced CKD (eGFR ≥45 mL/min/1.73m²) was evaluated on All-cause mortality (HR 1.66 (2016-2025) vs HR 1.80 (2009-2016), 95% CI 1.53-1.81, p=0.06 for interaction). Advanced CKD-associated excess mortality risk in HF declined over time (HR 1.80 to 1.66; p=0.06), driven by a substantial reduction in HFpEF patients (HR 1.73 to 1.48; p for interaction=0.003).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: