Why the study?
Coexisting HFrEF and COPD complicates management and worsens prognosis, prompting this analysis of the association between COPD and HF treatment optimization, long-term clinical outcomes, mortality, and HF readmissions.
Does concomitant COPD worsen long-term mortality, HF readmissions, and HF treatment optimization in patients with HFrEF?
Cohort (n=375)
Does concomitant COPD worsen long-term mortality, HF readmissions, and HF treatment optimization in patients with HFrEF?
Concomitant COPD in patients with HFrEF is associated with significantly higher 5-year all-cause mortality, HF-related mortality, and HF readmissions despite similar beta-blocker and ivabradine dose optimization.
Answers are grounded in this paper and cite their sources.
Comorbid COPD flags HFrEF patients for intensified monitoring; extends prognostic data but leaves open whether COPD therapies improve survival.
Background: The coexistence of heart failure with reduced ejection fraction (HFrEF) and chronic obstructive pulmonary disease (COPD) is a common health problem that complicates therapeutic management and worsens prognosis. Our aim was to analyse the association between COPD and HF treatment optimization, long-term clinical outcomes, mortality, and HF readmissions. Methods: A retrospective, observational study comparing two cohorts: HFrEF with COPD versus HFrEF without COPD. Beta-blocker (BB) and ivabradine dose optimization were assessed in both groups, and inhaled treatment was assessed in patients with COPD. Clinical outcomes during follow-up were analyzed using Kaplan–Meier methods and Cox proportional hazards regression. Results: 375 patients were included, of whom 71 had COPD (18.9%). No significant differences were observed between groups in BB or ivabradine dose optimization. After 60 months of follow-up, patients with COPD had higher rates of all-cause mortality (40.8% vs. 25.6%; p = 0.014), HF-related mortality (33.8% vs. 18.4%; p = 0.006), and HF readmission (50.7% vs. 35.2%; p = 0.014). COPD remained significantly associated with adverse clinical outcomes in multivariable Cox regression analysis. Among patients with COPD, dual inhaled therapy was the most common regimen (54.9%), followed by triple inhaled therapy (32.4%). Conclusions: In our cohort of patients with HFrEF, concomitant COPD was associated with higher mortality and HF readmission rates despite similar BB and ivabradine dose optimization between groups. These findings highlight the importance of COPD in the clinical management of patients with HFrEF, although the observational design of the study precludes causal conclusions. Further studies are warranted to clarify the relationship between COPD, HF outcomes, and treatment patterns.
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Caño et al. (2026) conducted a cohort in Heart failure with reduced ejection fraction (HFrEF) (n=375). Concomitant chronic obstructive pulmonary disease (COPD) vs. HFrEF without COPD was evaluated on All-cause mortality at 60 months (p=0.014).
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