儿童腺病毒肺炎重症的危险因素及其预测模型构建

Risk factors for severe adenovirus pneumonia in children and construction of its predictive model

  • 摘要:
    目的 分析儿童腺病毒肺炎(AP)重症的危险因素,并构建列线图。
    方法 选择2023年11月-2024年4月南京医科大学附属儿童医院感染科收治的108例AP患儿,根据其病情程度分为重症组(n=38)与非重症组(n=70),采用logistic回归分析归纳儿童AP重症的危险因素;用R软件绘制列线图,采用受试者工作特征(ROC)曲线、校准曲线、Hosmer-Lemeshow拟合优度检验评估列线图。
    结果 贫血(OR=4.370,95%CI:1.370~13.941,P=0.013)、先天性心脏病(OR=4.036,95%CI:1.277~12.754,P=0.017)、多重感染(OR=4.984,95%CI:1.546~16.069,P=0.007)、肺实变(OR=17.492,95%CI:5.288~57.864,P<0.001)是儿童AP重症的危险因素。预测儿童AP重症的列线图ROC曲线下面积为0.896(95%CI:0.838~0.954)。校准曲线斜率接近1,且Hosmer-Lemeshow拟合优度检验χ2=7.754,P=0.355。
    结论 贫血、先天性心脏病、多重感染、肺实变是儿童AP重症的危险因素,依此构建的列线图可个体化预测儿童AP重症的风险,以指导采取个体化干预措施。

     

    Abstract:
    OBJECTIVE To analyze the risk factors for severe adenovirus pneumonia (AP) in children and construct a nomogram.
    METHODS A total of 108 children with AP admitted to the Department of Infectious Diseases at Children′s Hospital of Nanjing Medical University from Nov. 2023 to Apr. 2024 were selected and divided into a severe group (n=38) and a non-severe group (n=70) based on disease severity. Logistic regression analysis was used to identify the risk factors for severe AP in children. A nomogram was developed by R software, and its performance was evaluated by the receiver operating characteristic (ROC) curve, calibration curve and Hosmer-Lemeshow goodness-of-fit test.
    RESULTS Anemia (OR=4.370, 95% CI: 1.370-13.941, P=0.013), congenital heart disease (OR=4.036, 95% CI: 1.277-12.754, P=0.017), multiple infection (OR=4.984, 95% CI: 1.546-16.069, P=0.007) and pulmonary consolidation (OR=17.492, 95% CI: 5.288-57.864, P < 0.001) were identified as risk factors for severe AP in children. The area under the ROC curve of the nomogram for predicting severe AP in children was 0.896 (95% CI: 0.838-0.954). The slope of calibration curve was close to 1, and the Hosmer-Lemeshow goodness-of-fit test yielded χ2=7.754, P=0.355.
    CONCLUSIONS Anemia, congenital heart disease, multiple infection and pulmonary consolidation are risk factors for severe AP in children. The constructed nomogram enables individualized prediction of severe AP risk in children, thereby guiding personalized interventions.

     

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