# C-reactive Protein to Albumin Ratio and Fluid Overload as Predictors of Mortality in Comparison to Pediatric Risk of Mortality (PRISM) III Score in Critically Ill Children in a Tertiary Care Hospital: A Prospective Cohort Study

**Authors:** Ankita Mandal, Keerti Swarnkar, Shikha Malik

PMC · DOI: 10.7759/cureus.102158 · 2026-01-23

## TL;DR

This study shows that the CRP to albumin ratio is a useful and low-cost predictor of mortality and complications in critically ill children, similar to the PRISM III score.

## Contribution

The study introduces the CRP-to-albumin ratio as a novel, cost-effective predictor of mortality and MODS in critically ill children.

## Key findings

- Non-survivors had a significantly higher CRP-to-albumin ratio than survivors.
- A CRP-to-albumin ratio of 10.73 showed high sensitivity and specificity for mortality.
- The ratio was strongly correlated with the PRISM III score and predicted MODS risk.

## Abstract

Objectives: To study the predictive value of the C-reactive protein (CRP) to albumin ratio and fluid overload for the development of Multiple Organ Dysfunction Syndrome (MODS) and mortality in critically ill children, and compare it with the Pediatric Risk of Mortality (PRISM) III score.

Methods: This prospective cohort study was conducted in the pediatric intensive care unit (PICU) of a tertiary care hospital in central India. PRISM-III scoring, CRP, and albumin level were done within 24 hours of admission. Early and cumulative fluid overload were calculated. Sensitivity and specificity were calculated for the CRP-to-albumin ratio and fluid overload for MODS and mortality, and compared with the PRISM III score.

Results: We enrolled 102 critically ill children. The median CRP-to-albumin ratio was significantly higher in non-survivors than survivors (25.30 vs. 3.37, respectively) (p-value <0.001). At a cut-off value of 10.73, it has 72.6% sensitivity and 79.3% specificity. Patients with a ratio of 9.25 or higher were at a significant risk of developing MODS (p <0.0001). CRP-to-albumin ratio is also associated with increased risk for mechanical ventilation and inotrope use. Furthermore, we established a strong positive correlation (coefficient: 0.44; p<0.0001) between the CRP-to-albumin ratio and PRISM III score. Though fluid balance was statistically insignificant for the development of MODS and mortality, it varied significantly between the length of PICU stay (p = 0.007).

Conclusions: CRP to albumin ratio is an inexpensive but statistically significant biomarker having comparable discriminatory power to that of PRISM III score for assessing critically ill children, and fluid imbalance is a significant indicator of duration of PICU stay.

## Linked entities

- **Proteins:** LOC100189571 (uncharacterized LOC100189571)
- **Diseases:** Multiple Organ Dysfunction Syndrome (MONDO:0043726)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, C1QA (complement C1q A chain) [NCBI Gene 712] {aka C1QD1}, PRDM6 (PR/SET domain 6) [NCBI Gene 93166] {aka KMT8C, PDA3, PRISM}
- **Diseases:** protein-losing enteropathy (MESH:D011504), congenital heart disease (MESH:D006330), rheumatology (MESH:D012216), malabsorption syndrome (MESH:D008286), III (MESH:C537189), PRISM III (MESH:D003643), oncology (MESH:D000072716), sepsis (MESH:D018805), infectious disease (MESH:D003141), necrotizing enterocolitis (MESH:D020345), acute lung injury (MESH:D055371), Fluid Overload (MESH:D019190), Critically Ill (MESH:D016638), trauma (MESH:D014947), chronic liver disease (MESH:D008107), inflammation (MESH:D007249), nephrotic syndrome (MESH:D009404), respiratory illnesses (MESH:D012140), neurology (MESH:D009461), metabolic disorders (MESH:D008659), MODS (MESH:D009102), severe acute malnutrition (MESH:D000067011), acute kidney injury (MESH:D058186), hypoalbuminemia (MESH:D034141)
- **Chemicals:** lysophosphatidylcholine (MESH:D008244), bromocresol green (MESH:D001961), bromocresol purple (MESH:D001962)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12925612/full.md

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Source: https://tomesphere.com/paper/PMC12925612