Abstract:Objective: To analyze the clinical value of laboratory test indicators in the early diagnosis of neonatal sepsis (NS).Methods: Ninety-one patients with NS and 79 healthy infants treated in our hospital from September 2020 to October 2023 were enrolled in this research. The infants were divided into the control group (n=79) and sepsis group (n=91). The detection results of blood indexes were compared between the two groups. Multivariate logistic regression was used to identify the independent risk factors of NS. The receiver operating characteristic (ROC) curve was plotted to analyze the diagnostic value of laboratory indexes on NS.Results: The total number of white blood cells (WBC), neutrophilicgranulocyte (Neu), neutrophil-lymphocyte ratio (NLR), monocyte-lymphocyte ratio (MLR), procalcitonin (PCT), and C-reactive protein (CRP) in sepsis group were higher than those in control group (P<0.05), while the total number of lymphocyte (Lym) and lymphocyte-leukocyte ratio (LLR) were lower than those in control group (P<0.05), but there was no statistical difference in the total number of monocyte (Mono) between the two groups (P>0.05). Multivariate logistic regression analysis showed that WBC, Neu, Lym, PCT, and CRP were independent risk factors for neonatal NS (P<0.05). ROC curve analysis found that the area under the curve (AUC) of the combination of WBC, Neu, Lym, PCT, and CRP in predicting the occurrence of NS was the highest at 0.960, higher than that detected by the above indicators alone.Conclusion: WBC, Neu, Lym, PCT, and CRP are independent risk factors for neonatal NS, and combined detection has the highest efficiency in the early diagnosis of NS.
杨清玉, 杨续, 李维春. 实验室检测指标对新生儿败血症早期诊断的评估价值[J]. 河北医学, 2024, 30(9): 1530-1533.
YANG Qingyu, YANG Xu, LI Weichun. Assessment of the Value of Laboratory Test Indicators for the Early Diagnosis of Neonatal Sepsis. HeBei Med, 2024, 30(9): 1530-1533.
[1] Yilmaz Oztorun Z.Evaluation of haematological parameters and uric acid in the diagnosis of late onset neonatal sepsis[J].Cureus,2023,15(5):39691. [2] Milton R,Gillespie D,Dyer C,et al.Neonatal sepsis and mortality in low-income and middle-income countries from a facility-based birth cohort:an international multisite prospective observational study[J].Lancet Glob Health,2022,10(5):661-672. [3] Odabasi IO,Bulbul A.Neonatal sepsis[J].Sisli Etfal Hastan Tip Bul,2020,54(2):142-158. [4] Celik IH,Hanna M,Canpolat FE,et al.Diagnosis of neonatal sepsis:the past,present and future[J].Pediatr Res,2022,91(2):337-350. [5] Dierikx T,Budding A,Bos M,et al.Potential of molecular culture in early onset neonatal sepsis diagnosis:a proof of principle study[J].Microorganisms,2023,11(4):960. [6] 中华医学会儿科学分会新生儿学组,余加林,吴仕孝.新生儿败血症诊疗方案[J].中华儿科杂志,2003,41(12):897-899. [7] Huang C,Chen J,Zhan X,et al.Clinical value of laboratory biomarkers for the diagnosis and early identification of culture-positive sepsis in neonates[J].Inflamm Res,2023(16):5111-5124. [8] 王丽娟,朱兵兵,徐浩.降钙素原、C-反应蛋白及白细胞参数联合测定对新生儿败血症的早期诊断[J].基因组学与应用生物学,2020,39 (8):3803-3809. [9] Newman TB,Puopolo KM,Wi S,et al.Interpreting complete blood counts soon after birth in newborns at risk for sepsis[J].Pediatrics,2010,126(5):903-909. [10] 陈章宇,朱惠芳,罗开源.脐血CRP、PCT、IL-6对新生儿早发型败血症的诊断价值分析[J].中国现代医学杂志,2022,32 (8):6-10. [11] Jimoh AK,Bolaji OB,Adelekan A,et al.Clinical utility of procalcitonin and C-reactive protein in the management of neonatal sepsis in a resource-limited nigerian hospital[J].Niger Clin Pract,2023,26(12):1895-1901. [12] Anugu NR,Khan S.Comparing the diagnostic accuracy of procalcitonin and C-reactive protein in neonatal sepsis:a systematic review[J].Cureus,2021,13(11):19485.