# Platelet-to-C-reactive protein ratio stratifies surgical risk and mortality in necrotizing enterocolitis neonates with portal venous gas

**Authors:** Xinyin Zhang, Huan Wei, Qi Tan, Zhengli Wang, Zhenhua Guo, Wei Liu, Jian Cao

PMC · DOI: 10.3389/fped.2025.1686076 · Frontiers in Pediatrics · 2026-01-02

## TL;DR

A blood test measuring platelet-to-C-reactive protein ratio helps predict the need for surgery and risk of death in newborns with a severe intestinal condition.

## Contribution

The study introduces the platelet-to-C-reactive protein ratio as a novel biomarker for predicting surgical need and mortality in NEC patients with portal venous gas.

## Key findings

- The PCR was an independent predictor of surgical intervention with an AUC of 0.84 and a cutoff of ≤4.84 × 10⁹/mg.
- PCR also predicted 30-day mortality with an AUC of 0.80 and a cutoff of ≤2.57 × 10⁹/mg.
- The PCR outperformed individual parameters in predicting outcomes for NEC-PVG patients.

## Abstract

Portal venous gas (PVG) represents a severe complication of necrotizing enterocolitis (NEC), typically signaling disease progression and a poor prognosis. While PVG has traditionally been regarded as an indication for surgical intervention in NEC, accumulating clinical evidence indicates that not all cases require operative management. Currently, surgical decision-making for NEC neonates with PVG primarily relies on subjective clinical assessments by physicians, resulting in substantial management uncertainty. The platelet-to-C-reactive protein ratio (PCR), an objective and convenient biomarker integrating information on disseminated intravascular coagulation and systemic inflammation, has demonstrated predictive value in neonatal sepsis and other conditions. However, the utility of the PCR has not yet been explored in NEC-PVG patients. This study retrospectively evaluates the predictive value of the PCR for surgical intervention and prognosis in this high-risk population, aiming to facilitate early identification and improve clinical outcomes.

This retrospective single-center cohort study analyzed 186 neonates diagnosed with NEC (Bell stage ≥ IIa) and ultrasonographically confirmed PVG (2021–2024). We evaluated the PCR, calculated at the time of PVG diagnosis, for predicting surgical intervention and 30-day mortality by employing multivariate logistic regression (which included collinearity assessment and bootstrap validation) to identify independent factors and receiver operating characteristic (ROC) analysis to assess predictive performance and determine optimal cutoff values, supplemented by sensitivity analyses.

The cohort demonstrated a surgical intervention rate of 37.10% (69/186) and a 30-day mortality of 13.98% (26/186). Multivariate analysis identified the PCR as an independent predictor for both surgical intervention (adjusted odds ratio (aOR) = 0.77, 95% CI: 0.69–0.86) and mortality (aOR = 0.80, 95% CI: 0.69–0.92). ROC curve analysis established PCR thresholds of ≤4.84 × 109/mg for surgical intervention (AUC 0.84; sensitivity 80%, specificity 85%) and ≤2.57 × 109/mg for mortality prediction (AUC 0.80; sensitivity 69%, specificity 91%).

This study suggests that the PCR is a promising predictor of surgical intervention and mortality risk in NEC-PVG patients, demonstrating superior predictive performance compared to individual parameters. Based on these findings, we propose the incorporation of PCR testing into standard clinical monitoring protocols, using 4.84 × 109/mg as a potential cutoff value to inform therapeutic decision-making. This approach may improve the clinical management and outcomes in this high-risk population.

## Linked entities

- **Diseases:** necrotizing enterocolitis (MONDO:0004639)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** PVG (MESH:D011007), systemic inflammation (MESH:D007249), disseminated intravascular coagulation (MESH:D004211), sepsis (MESH:D018805), NEC (MESH:D020345)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12808459/full.md

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Source: https://tomesphere.com/paper/PMC12808459