Key result
Early albumin linked to ~32% lower 28-day mortality in patients with sepsis and heart failure.
Why the study?
The association between albumin administration during the first 24 h after ICU admission and all-cause mortality in patients with sepsis and concurrent HF required investigation.
Does early albumin administration within the first 24 hours of ICU admission reduce 28-day all-cause mortality in critically ill adults with sepsis and concurrent heart failure?
Cohort (n=4,063)
No
Does early albumin administration within the first 24 hours of ICU admission reduce 28-day all-cause mortality in critically ill adults with sepsis and concurrent heart failure?
In critically ill patients with sepsis and concurrent heart failure, early albumin infusion within 24 hours of ICU admission was observationally associated with an approximately 30% relative hazard reduction in 28-, 90-, and 365-day all-cause mortality without reducing crystalloid fluid volume.
Answers are grounded in this paper and cite their sources.
Should not yet change practice in sepsis with heart failure; leaves open confirmation in randomized trials.
We retrospectively examined the association between albumin administration during the first 24 h after intensive care unit (ICU) admission and all-cause mortality in patients with sepsis and concurrent heart failure (HF) using MIMIC-IV version 3.1. The cohort included 4063 adults, of whom 432 were in the early-albumin group and 3631 were in the control group. The primary endpoint was 28-day all-cause mortality after ICU admission; secondary mortality endpoints were 90- and 365-day all-cause mortality. The primary analysis used multivariable Cox proportional-hazards models in the full cohort, with analyses in the fixed propensity-score-matched cohort providing supportive evidence. In the full cohort, early albumin administration was associated with lower all-cause mortality at 28 days (adjusted hazard ratio [HR], 0.68; 95% confidence interval [CI], 0.55–0.85; P < 0.001), 90 days (adjusted HR, 0.71; 95% CI, 0.59–0.86; P < 0.001), and 365 days (adjusted HR, 0.70; 95% CI, 0.59–0.82; P < 0.001). Directionally consistent associations were observed in the matched Cox models. Early albumin administration was not associated with lower documented volumes of major isotonic crystalloids (0.9% saline plus lactated Ringer’s) during the first 48 h after ICU admission. In this retrospective cohort, early albumin administration during the first 24 h after ICU admission was associated with lower 28-, 90-, and 365-day all-cause mortality, but not with lower documented major isotonic crystalloid administration. These findings are observational and do not establish causality.
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Liu et al. (2026) conducted a cohort in Sepsis and concurrent heart failure (n=4,063). Early albumin administration (within 24 hours of ICU admission) vs. No albumin administration during the first 24 hours after ICU admission was evaluated on 28-day all-cause mortality after ICU admission (HR 0.68, 95% CI 0.55–0.85, p=<0.001). Early albumin administration within 24 hours of ICU admission was associated with lower 28-day all-cause mortality (adjusted HR 0.68, 95% CI 0.55–0.85; P < 0.001) in patients with sepsis and heart failure.
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