# Association of the blood urea nitrogen to serum albumin ratio and 28-day all-cause mortality in patients with cardiac arrest: a retrospective cohort study using the MIMIC-IV database

**Authors:** Gaosheng Zhou, Yayuan Tan, Xueli Li, Yixun Wang, Dingdeng Wang, Min Liu

PMC · DOI: 10.3389/fcvm.2025.1609059 · 2025-06-06

## TL;DR

This study found that a higher blood urea nitrogen to serum albumin ratio is linked to increased 28-day mortality in cardiac arrest patients.

## Contribution

The study identifies a novel non-linear association between BAR and mortality in cardiac arrest patients.

## Key findings

- Higher BAR at admission was significantly associated with increased 28-day mortality risk.
- A nonlinear relationship was found between BAR and mortality (P = 0.003).
- Each 1-unit increase in BAR (≤17.981) raised death risk by 5.7%.

## Abstract

The blood urea nitrogen to serum albumin ratio (BAR) has been identified as a novel indicator of both inflammatory and nutritional status, exhibiting a correlation with adverse cardiovascular outcomes.

To explore the association between the BAR and 28-day all-cause mortality in cardiac arrest patients who achieved return of spontaneous circulation (ROSC) and were admitted to the intensive care unit (ICU).

Data for patients with cardiac arrest were obtained from the Medical Information Mart for Intensive Care IV database. The outcome was 28-day all-cause mortality. Multivariable-adjusted Cox regression analysis, curve fitting, and threshold effects analysis were used to assess the relationship between the BAR and 28-day all-cause mortality in patients with cardiac arrest in the intensive care unit.

A total of 793 patients were included and divided into tertiles based on the BAR (Q1, Q2, Q3); 8-day all-cause mortality rates were 37.5%, 53.4%, and 63.8%, respectively (P < 0.001). A higher BAR at initial admission was significantly associated with an increased 28-day all-cause mortality risk. Results from the adjusted Models 2, 3, 4, and 5 were consistent with those of Model 1. Subgroup analysis revealed no interactions in age, sex, renal disease, liver disease, vasoactive drug use, ventilation, race, aids, malignant cancer, diabetes, peptic ulcer disease, rheumatic disease, chronic pulmonary disease, cerebrovascular disease, peripheral vascular disease, congestive heart failure and myocardial infarct between the BAR and 28-day all-cause mortality. Restricted cubic spline analysis revealed a nonlinear association between the BAR and 28-day all-cause mortality (P = 0.003). With BAR ≤ 17.981, each 1-unit increase in the BAR was associated with a 5.7% higher risk of death [95% CI (1.012–1.105), P < 0.05].

This study identified a non-linear relationship between the BAR and 28-day all-cause mortality in patients with cardiac arrest.

## Linked entities

- **Diseases:** cardiac arrest (MONDO:0000745), renal disease (MONDO:0005240), liver disease (MONDO:0005154), AIDS (MONDO:0012268), diabetes (MONDO:0005015), peptic ulcer disease (MONDO:0004247), rheumatic disease (MONDO:0005554), cerebrovascular disease (MONDO:0011057), peripheral vascular disease (MONDO:0005294), congestive heart failure (MONDO:0005009), myocardial infarct (MONDO:0005068)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** malignant cancer (MESH:D009369), cardiac arrest (MESH:D006323), congestive heart failure (MESH:D006333), renal disease (MESH:D007674), liver disease (MESH:D008107), inflammatory (MESH:D007249), cerebrovascular disease (MESH:D002561), peptic ulcer disease (MESH:D010437), chronic pulmonary disease (MESH:D002908), diabetes (MESH:D003920), peripheral vascular disease (MESH:D016491), myocardial infarct (MESH:D009203), rheumatic disease (MESH:D012216)
- **Chemicals:** vasoactive drug (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12179132/full.md

---
Source: https://tomesphere.com/paper/PMC12179132