文章摘要
儿童肺炎支原体肺炎合并气道黏液栓临床预测模型的构建及验证
Construction and Validation of a Clinical Prediction Model for Airway Mucus Plug in Children with Mycoplasma Pneumoniae Pneumonia
投稿时间:2026-01-17  
DOI:10.3969/j.issn.1000-0399.2026.08.011
中文关键词: 儿童  肺炎支原体肺炎  黏液栓  预测模型  列线图
英文关键词: Children  Mycoplasma pneumoniae pneumonia  Mucus plug  prediction model  Nomogram
基金项目:
作者单位E-mail
王颖 安徽合肥 安徽省儿童医院呼吸科  
黄璇 安徽合肥 安徽省儿童医院呼吸科  
曹芳 安徽合肥 安徽省儿童医院呼吸科  
罗明鑫 安徽合肥 安徽省儿童医院呼吸科  
魏文 安徽合肥 安徽省儿童医院呼吸科 ahsetyyww@126.com 
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中文摘要:
      目的 通过收集肺炎支原体肺炎(MPP)患儿临床特征、实验室检查及胸部CT结果,建立儿童MPP并发气道黏液栓的预测模型并进行验证。方法 回顾性分析2023年1月至2024年12月在安徽省儿童医院呼吸科接受电子纤维支气管镜检查的241例MPP患儿资料,按是否合并气道黏液栓分为黏液栓组(n=88)与无黏液栓组(n=153)。收集两组MPP患儿血常规计算全身炎症指数(SII)、中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR),并统计C反应蛋白(CRP)、乳酸脱氢酶(LDH)、D-二聚体、肝功能,胸部CT及临床资料、支气管镜检查报告,通过单因素分析筛选出有统计学差异的指标,并采用多因素logistic回归构建列线图模型,以受试者工作特征(ROC)曲线评估预测效能。结果 单因素分析结果显示,两组MPP患儿的住院天数、抗生素使用天数、发热天数,中性粒细胞数及比率、淋巴细胞数,CRP、LDH、D-二聚体、谷丙转氨酶(ALT)、谷草转氨酶(AST)、SII、PLR、NLR,胸腔积液数、支气管堵塞,差异有统计学意义(P<0.05)。多因素logistic回归分析结果指出,发热天数、D-二聚体、SII、NLR、胸腔积液是MPP患儿合并气道黏液栓的独立危险因素(P<0.05)。利用发热天数、D-二聚体、SII、NLR、胸腔积液建立MPP患儿并发气道内黏液栓的列线图预测模型,AUC=0.865(95%CI:0.817~0.912),约登指数为0.563,灵敏度为73.9%,特异度为82.4%。结论 将发热天数、D-二聚体、SII、NLR、胸腔积液建立列线图预测模型,可用于预测MPP患儿合并气道黏液栓。
英文摘要:
      Objective To build and verify a prediction model which can predict airway mucus plugs in children with mycoplasma pneumoniae pneumonia via collecting clinical features, laboratory test results and chest CT findings of these children. Methods A retrospective analysis was performed on the clinical data of 241 children admitted to the Respiratory Department of Anhui Children's Hospital from January 2023 to December 2024. All children had mycoplasma pneumoniae pneumonia and received flexible bronchoscopy, then they were divided into two groups. The first group had 88 children with airway mucus plugs. The second group had 153 children without airway mucus plugs. The clinical data and blood test results were collected. Systemic immune-inflammation index, neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio were detected. C-reactive protein, lactate dehydrogenase, D-dimer, liver function indicators, chest CT results and bronchoscopy reports were also recorded. Univariate analysis was used to screen different indicators. Multivariate logistic regression was used to make a nomogram model. The receiver operating characteristic curve was employed to check the prediction effect. Results Two groups showed clear differences in length of hospital stay, antibiotic treatment time, fever duration, blood cell indicators, C-reactive protein, lactate dehydrogenase, D-dimer, liver function indicators, inflammation indexes, pleural effusion and bronchial obstruction. All differences had statistical significance. Further regression analysis confirmed five independent risk factors, namely, fever duration, D-dimer, systemic immune-inflammation index, neutrophil-to-lymphocyte ratio and pleural effusion. The new nomogram model showed good performance. Its area under curve was 0.865. The 95% confidence interval ranged from 0.817 to 0.912. Its Youden index was 0.563. Its sensitivity reached 73.9%. Its specificity reached 82.4%.Conclusion The nomogram model uses fever duration, D-dimer, systemic immune-inflammation index, neutrophil-to-lymphocyte ratio and pleural effusion. It can effectively predict the risk of airway mucus plugs in children with mycoplasma pneumoniae pneumonia.
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