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Received:December 26, 2025 Published Online:May 01, 2026
Received:December 26, 2025 Published Online:May 01, 2026
中文摘要: 目的 探讨床旁颅脑超声联合血清胶质纤维酸性蛋白(GFAP)对窒息早产儿脑损伤诊断及神经发育结局的预后评估价值,为早期识别高危患儿,优化临床管理提供依据。方法 采用前瞻性观察性研究方法,连续纳入江阴市人民医院2023年2月至2024年12月收治的窒息早产儿100例设为研究组;另选取同期收治的、胎龄相匹配的无窒息史早产儿100例设为对照组。研究组根据床旁颅脑超声及临床神经症状综合判定为脑损伤(n=80)与非脑损伤(n=20)。所有患儿均于生后3 d内完成床旁颅脑超声检查及血清GFAP检测;脑损伤组进一步根据纠正胎龄6个月的Gesell发育诊断量表中发育商(DQ)结果进一步分为预后良好(DQ≥76,n=46)与预后不良(DQ≤75,n=34)两个亚组;比较各组超声异常率及 GFAP 水平;绘制受试者工作特征(ROC)曲线分析各指标诊断及预测效能,计算曲线下面积(AUC)及其95%置信区间;采用多因素logistic回归分析预后不良的独立预测因素。结果 研究组中脑损伤患儿的超声异常率及GFAP水平均分别高于非脑损伤患儿及对照组(P<0.017)。预后不良亚组的超声异常率及GFAP水平亦高于预后良好亚组(P<0.05)。ROC曲线分析显示,超声联合GFAP诊断脑损伤的 AUC 为 0.949(95%CI :0.886~0.983),灵敏度 94.00%,特异度 91.00%;预测预后不良的 AUC 为0.974(95%CI :0.900~0.998),灵敏度94.59%,特异度95.24%。多因素logistic回归分析显示,校正胎龄、窒息程度后,床旁颅脑超声异常(OR =4.213,95%CI :1.828~9.710)与血清 GFAP 水平≥3.09 ng/mL(OR =4.859,95%CI :1.453~16.252)是窒息早产儿发生神经发育不良(预后不良)的独立危险因素。结论 床旁颅脑超声联合血清GFAP检测可提高对窒息早产儿脑损伤的早期识别能力,并对神经发育结局具有较好的预测价值。超声异常与高GFAP水平是预后不良的独立预测因素。
Abstract:Objective To explore the value of bedside cranial ultrasound(BCUS)combined with serum glial fibrillary acidic protein(GFAP)in the diagnosis of brain injury and prognostic assessment of neurodevelopmental outcomes in asphyxiated premature infants,to provide a basis for early identification of high-risk infants and optimization of clinical management. Methods Using a prospective observational study method,100 asphyxiated premature infants admitted to Jiangyin People??s Hospital from February 2023 to December 2024 were successively enrolled as the study group,and100 gestational age-matched premature infants without asphyxia admitted in the same period were served as the control group. Based on BCUS findings and clinical neurological symptoms,the study group was further divided into brain injury subgroup(n=80)and non - brain injury subgroup(n=20). All infants underwent BCUS examination and serum GFAP detection within 3 days after birth. The brain injury subgroup was further classified into good prognosis[developmental quotient(DQ)≥76,n=46]and poor prognosis(DQ≤75,n=34)subgroups according to the DQ Results of Gesell Developmental Schedules at the corrected gestational age of 6 months. The rates of BCUS abnormalities and serum GFAP levels were compared among all groups. Receiver operating characteristic(ROC)curves were plotted to analyze the diagnostic and predictive efficacy of each index,and the area under the curve(AUC)and its 95%CI were calculated. Multivariable logistic regression analysis was used to identify the independent predictors of poor prognosis.Results The rates of BCUS abnormalities and serum GFAP levels in the brain injury subgroup were significantly higher than those in the non-brain injury subgroup and the control group(P<0.017),respectively. The above two indicators in the poor prognosis subgroup were also higher than those in the good prognosis subgroup(P<0.05). ROC curve analysis showed that BCUS combined with GFAP had an AUC of 0.949(95%CI :0.886-0.983)for diagnosing brain injury,with a sensitivity of 94.00% and a specificity of 91.00%;for predicting poor prognosis,the AUC was 0.974(95%CI :0.900-0.998),with a sensitivity of 94.59% and a specificity of 95.24%. Multivariate logistic regression analysis showed that after adjusting for corrected gestational age and asphyxia degree,abnormal BCUS findings(OR =4.213,95%CI :1.828-9.710)and serum GFAP level ≥3.09 ng/mL(OR =4.859,95%CI :1.453-16.252)were independent predictors of poor neurodevelopmental outcome in asphyxiated premature infants. Conclusion Bedside cranial ultrasound combined with serum GFAP can improve the ability of early identification of brain injury in asphyxiated premature infants and has a good predictive value for neurodevelopmental outcomes. Abnormal BCUS findings and elevated serum GFAP level are independent predictors of poor prognosis.
keywords: Premature infant,Asphyxiated Brain injury Bedside cranial ultrasound Serum glial fibrillary acidic protein Developmental quotient Neurodereropmental disorder
文章编号: 中图分类号:R722 文献标志码:A
基金项目:江苏省卫生健康委科研项目(ZQ2024009)
| Author Name | Affiliation |
| LI Ting,WU Yuyun | Department of Ultrasound,Jinagyin Hospital Affiliated to Nanjong University Jiangyin People??s Hospital,Wuxi,Jiangsu 214400,China |
| Author Name | Affiliation |
| LI Ting,WU Yuyun | Department of Ultrasound,Jinagyin Hospital Affiliated to Nanjong University Jiangyin People??s Hospital,Wuxi,Jiangsu 214400,China |
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