Association of Albumin–Bilirubin (ALBI) Grade With 28-Day All-Cause Mortality in Patients With Acute Respiratory Distress Syndrome: A Retrospective Analysis of the MIMIC-IV Database

The albumin–bilirubin (ALBI) grade, a validated prognostic tool in cancers such as hepatocellular carcinoma, has not been evaluated in acute respiratory distress syndrome (ARDS). This retrospective cohort study, utilizing data from the MIMIC-IV (v3.0) database, aimed to assess ALBI’s predictive valu...

Full description

Saved in:
Bibliographic Details
Main Authors: Weixiao Chen, Qingzhou Chen, Zhiwei Tang, Zhibo Li, Weiyan Chen, Xuming Xiong, Deliang Wen, Zhenhui Zhang
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/mi/9930648
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The albumin–bilirubin (ALBI) grade, a validated prognostic tool in cancers such as hepatocellular carcinoma, has not been evaluated in acute respiratory distress syndrome (ARDS). This retrospective cohort study, utilizing data from the MIMIC-IV (v3.0) database, aimed to assess ALBI’s predictive value for 28-day all-cause mortality in 338 adult ARDS patients admitted to the ICU. Patients were stratified into survivors (209 cases) and nonsurvivors (129 cases), with a 28-day mortality rate of 38.2%. Multivariable Cox regression identified ALBI as an independent predictor of 28-day mortality (HR = 1.46, 95% CI: 1.09–1.95, p=0.011). Receiver operating characteristic (ROC) analysis yielded an area under the curve (AUC) of 61.1% (95% CI: 54.7%–67.4%) with an optimal ALBI cutoff of −1.681; Kaplan–Meier (KM) survival curves confirmed significantly higher mortality in patients with ALBI ≥−1.681 versus ALBI <−1.681 (p=0.0098). Subgroup analyses revealed no significant interactions between ALBI and clinical variables (interaction p: 0.672–0.85). These findings demonstrate ALBI’s utility as a novel, independent prognostic marker for short-term mortality risk in ARDS patients.
ISSN:1466-1861