Abstract:Objective To investigate the predictive value of the EOS Risk Calculator (SRC) combined with serum C-reactive protein (CRP) and procalcitonin (PCT) levels in early-onset sepsis (EOS) in neonates.Methods This study included 286 neonates with a gestational age of ≥ 34 weeks, born at Rui'an People's Hospital between January 2021 and December 2021. The neonates were divided into two groups: Group A and Group B, with a 1:1 ratio. Group A received SRC-assisted antibiotic management, while Group B received antibiotics based on standard neonatal sepsis treatment protocols. The SRC scores at admission, length of hospital stay, antibiotic usage rate, and incidence of complications were compared between the two groups. Among the 286 neonates, 95 were diagnosed with EOS and classified as the EOS group, while the remaining 191 uninfected neonates served as the control group. Risk scores and serum levels of CRP and PCT were assessed in both groups. The predictive efficacy of the EOS Risk Calculator combined with serum CRP and PCT for EOS was evaluated using a Receiver Operating Characteristic (ROC) curve analysis.Results Group A had significantly higher SRC scores at admission, shorter hospital stays, and lower antibiotic usage and complication rates compared to Group B (P < 0.05). The EOS group had higher risk scores and serum levels of CRP and PCT than the control group (P < 0.05). The ROC curve analysis demonstrated that the combination of SRC scores with serum CRP and PCT levels provided the highest predictive value for EOS, with a sensitivity of 97.0% (95% CI: 0.871, 0.981) and specificity of 90.8% (95% CI: 0.891, 0.965). The area under the ROC curve was 0.973 (95% CI: 0.949, 0.997), surpassing the predictive value of individual markers.Conclusion The EOS Risk Calculator combined with serum CRP and PCT levels exhibits high sensitivity and specificity in predicting EOS in neonates. This approach can improve diagnostic accuracy for EOS, reduce unnecessary antibiotic use, and lower the incidence of complications, offering significant clinical value for the early identification and treatment of EOS in neonates.