Key result
High red cell distribution width-to-albumin ratio linked to ~5.8-fold higher in-hospital mortality in ADHF-HFrEF.
Why the study?
Early risk stratification is challenging in ICD recipients hospitalized with ADHF-HFrEF, and the prognostic significance of the red cell distribution width-to-albumin ratio (RAR) in this population was unknown.
Does admission red cell distribution width-to-albumin ratio (RAR) predict all-cause in-hospital mortality in implantable cardioverter-defibrillator recipients hospitalized with acute decompensated heart failure with reduced ejection fraction?
Cohort (n=514)
Blinded outcome assessment
No
Does admission red cell distribution width-to-albumin ratio (RAR) predict all-cause in-hospital mortality in implantable cardioverter-defibrillator recipients hospitalized with acute decompensated heart failure with reduced ejection fraction?
Admission red cell distribution width-to-albumin ratio (RAR > 4.05) is a strong, independent, and readily available predictor of in-hospital mortality in ICD recipients hospitalized with acute decompensated HFrEF.
Background Early risk stratification remains a major challenge in implantable cardioverter-defibrillator (ICD) recipients hospitalized with acute decompensated heart failure with reduced ejection fraction (ADHF-HFrEF). The red cell distribution width-to-albumin ratio (RAR), a composite biomarker integrating inflammatory and nutritional status, has emerged as a promising prognostic marker in cardiovascular disease. However, its prognostic significance in ICD recipients hospitalized with ADHF-HFrEF remains unknown. This study aimed to evaluate the association between admission RAR and in-hospital mortality in this high-risk population. Methods This retrospective observational cohort study included 514 consecutive ICD recipients hospitalized with ADHF-HFrEF between January 2022 and March 2025. Admission RAR was calculated by dividing red cell distribution width (%) by serum albumin (g/dL). The primary outcome was all-cause in-hospital mortality. Independent predictors of mortality were identified using multivariable logistic regression analysis, and the discriminative performance of RAR was assessed using receiver operating characteristic (ROC) curve analysis. Results Among the 514 patients, 78 (15.2%) died during hospitalization. Admission RAR was significantly higher in non-survivors than in survivors (4.58 ± 1.56 vs. 3.42 ± 0.80, p < 0.001). After multivariable adjustment, age (OR 1.060, 95% CI 1.029–1.091; p < 0.001), serum creatinine (OR 1.570, 95% CI 1.205–2.045; p = 0.001), serum sodium (OR 0.773, 95% CI 0.718–0.832; p < 0.001), C-reactive protein (OR 1.013, 95% CI 1.004–1.021; p = 0.003), and RAR > 4.05 (OR 5.812, 95% CI 2.980–11.335; p < 0.001) were independently associated with in-hospital mortality. RAR demonstrated good discriminatory performance for predicting in-hospital mortality (AUC 0.813, 95% CI 0.773–0.848; p < 0.001). Conclusion Admission RAR was independently associated with in-hospital mortality in ICD recipients hospitalized with ADHF-HFrEF. As a simple, inexpensive, and routinely available biomarker, RAR may complement early admission risk stratification in this particularly vulnerable patient population. Prospective multicenter studies are warranted to externally validate these findings.
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Tunca et al. (2026) conducted a cohort in Acute decompensated heart failure with reduced ejection fraction (ADHF-HFrEF) in implantable cardioverter-defibrillator (ICD) recipients (n=514). Admission red cell distribution width-to-albumin ratio (RAR) > 4.05 vs. Admission RAR <= 4.05 was evaluated on All-cause in-hospital mortality (OR 5.812, 95% CI 2.980-11.335, p=<0.001). Admission red cell distribution width-to-albumin ratio >4.05 independently predicted in-hospital mortality (OR 5.812, p<0.001) in ICD recipients hospitalized with ADHF-HFrEF.
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