Key result
Higher hemoglobin-to-albumin ratio predicts ~7% greater 28-day mortality in critically ill patients with AF.
Why the study?
Existing risk scores offer limited prognostic value for mortality in critically ill patients with AF, and the prognostic utility of hemoglobin-to-albumin ratio in this population is unknown.
Does a higher hemoglobin-to-albumin ratio predict increased mortality in critically ill patients with atrial fibrillation?
Cohort (n=7,801)
No
Does a higher hemoglobin-to-albumin ratio predict increased mortality in critically ill patients with atrial fibrillation?
Effect estimate: HR 1.07 (95% CI 1.03-1.11)
p-value: p=<0.001
The hemoglobin-to-albumin ratio is an independent predictor of short- and long-term mortality in critically ill patients with atrial fibrillation, offering a simple, routinely available prognostic biomarker.
May aid risk stratification in ICU AF; leaves open incremental value beyond existing scores pending validation.
Atrial fibrillation (AF) is common in critically ill patients and contributes to poor outcomes. Existing risk scores provide limited prognostic value for overall mortality. The hemoglobin-to-albumin ratio (HAR), reflecting hematologic and nutritional-inflammatory status, may serve as a novel prognostic biomarker in this setting. We performed a retrospective cohort study using the Medical Information Mart for Intensive Care IV database (version 3.1). Adult intensive care unit patients with AF were included, excluding those with multiple admissions, hospital stay <24 hours, or missing laboratory data. The primary outcome was 28-day all-cause mortality, and the secondary outcome was 360-day mortality. Patients were stratified by HAR quartiles. Kaplan–Meier analysis, Cox proportional hazards models, and restricted cubic splines were applied. Subgroup analyses assessed consistency across clinical strata. A total of 7801 patients were included (median age 75 years; 40.9% male). The 28- and 360-day mortality rates were 20.1% and 25.9%, respectively. Higher HAR was associated with increased mortality (log-rank P < .001). In fully adjusted Cox models, HAR independently predicted 28-day mortality (hazard ratio: 1.07, 95% confidence interval: 1.03–1.11) and 360-day mortality (hazard ratio: 1.07, 95% confidence interval: 1.04–1.11). Restricted cubic splines showed an approximately linear relationship. Subgroup analyses indicated stronger associations in older patients, those not receiving beta-blockers, and in amiodarone users at 360 days. HAR is an independent predictor of short- and long-term mortality in critically ill AF patients. As a simple and routinely available biomarker, HAR may enhance risk stratification beyond conventional clinical tools. Further prospective and multicenter studies are warranted to validate these findings.
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Sun et al. (2026) conducted a cohort in Atrial fibrillation in critically ill patients (n=7,801). Hemoglobin-to-albumin ratio (HAR) vs. Lower HAR was evaluated on 28-day all-cause mortality (HR 1.07, 95% CI 1.03-1.11, p=<0.001). Higher hemoglobin-to-albumin ratio independently predicted 28-day all-cause mortality in critically ill patients with atrial fibrillation (HR 1.07; 95% CI 1.03–1.11).
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