# Evaluation of the Course of Acute-Phase Reactants in the Postoperative Period of Newborns and Their Diagnostic Utility in Identifying Postoperative Sepsis

**Authors:** Erkan Deniz, Leyla Sero, Duygu Tuncel, Nilufer Okur

PMC · DOI: 10.3390/diagnostics16040545 · Diagnostics · 2026-02-12

## TL;DR

This study evaluates how CRP and PCT levels change after surgery in newborns and their usefulness in detecting postoperative sepsis.

## Contribution

The study provides time-dependent diagnostic thresholds for CRP and PCT in postoperative neonatal sepsis detection.

## Key findings

- PCT showed the highest diagnostic accuracy at 72 hours post-surgery with an AUC of 0.911.
- CRP also demonstrated good diagnostic performance with AUC values between 0.802 and 0.838.
- A multiparametric, time-dependent approach is more reliable than single-parameter interpretation for diagnosing neonatal sepsis.

## Abstract

Background/Objectives: Neonatal sepsis remains a major diagnostic challenge, particularly in postoperative infants where systemic inflammatory responses may mimic infection; therefore, reliable biomarkers are urgently needed to distinguish sepsis from normal post-surgical changes. Methods: This prospective cohort study included 135 neonates who underwent surgery without preoperative signs of infection. Serum levels of C-reactive protein (CRP) and procalcitonin (PCT) were measured preoperatively and at 24, 72 and 120 h postoperatively. Patients were classified as having proven sepsis based on positive blood cultures or clinical sepsis using European Medicines Agency (EMA) neonatal sepsis scoring. Biomarker levels were compared between septic and non-septic infants, and diagnostic performance was evaluated using receiver operating characteristic analysis. Results: Sixteen infants had proven sepsis and twenty-five had clinical sepsis. Both CRP and PCT levels showed a significant rise in septic infants at 72 h postoperatively (p < 0.01) and remained elevated at 120 h. PCT demonstrated the highest diagnostic accuracy at 72 h (AUC 0.911; threshold 1.2 µg/L; sensitivity 83%; specificity 84%), while CRP also showed good performance (AUC 0.802–0.838). Conclusions: CRP, PCT and albumin are valuable postoperative sepsis markers; however, single-parameter interpretation is insufficient, and a multiparametric, time-dependent approach provides superior diagnostic reliability in neonatal sepsis.

## Full-text entities

- **Genes:** CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, MUC1 (mucin 1, cell surface associated) [NCBI Gene 4582] {aka ADMCKD, ADMCKD1, ADTKD2, CA 15-3, CD227, Ca15-3}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** respiratory distress (MESH:D012128), Neonatal sepsis (MESH:D000071074), congenital diaphragmatic hernia (MESH:D065630), diabetes (MESH:D003920), preeclampsia (MESH:D011225), myelomeningocele (MESH:D008591), injury to (MESH:D014947), Postoperative systemic inflammation (MESH:D007249), oligohydramnios (MESH:D016104), GP infections (MESH:D016908), esophageal atresia (MESH:D004933), septic shock (MESH:D012772), hydrocephalus (MESH:D006849), chorioamnionitis (MESH:D002821), tissue injury (MESH:D017695), Postoperative Sepsis (MESH:D018805), proinflammatory cytokines (MESH:D000080424), bacterial infection (MESH:D001424), depression (MESH:D003866), necrotizing enterocolitis (MESH:D020345), GN infections (MESH:D016905), infected (MESH:D007239), HELLP syndrome (MESH:D017359), bacteremia (MESH:D016470), premature rupture of membranes (MESH:D005322), polyhydramnios (MESH:D006831), viral infections (MESH:D014777)
- **Chemicals:** lactate (MESH:D019344), cefazolin (MESH:D002437), Cezol (-)
- **Species:** Klebsiella pneumoniae (species) [taxon 573], Enterobacter cloacae (species) [taxon 550], Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12939169/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939169/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939169/full.md

---
Source: https://tomesphere.com/paper/PMC12939169