上呼吸道感染继发肺部感染的列线图模型构建与验证

Construction of nomogram model for secondary pulmonary infection following upper respiratory tract infection and its validation

  • 摘要:
    目的 探讨基于血常规参数、肌酸激酶同工酶(CK-MB)、神经元特异性烯醇化酶(NSE)构建的危险因素模型对上呼吸道感染继发肺部感染的预测价值,以实现早期风险识别,为临床预防和干预提供依据。
    方法 回顾性分析2024年1-12月于中国人民解放军海军第九〇五医院就诊的141例上呼吸道感染患者为研究对象,以病原学结果为金标准,根据患者肺部感染情况分为肺炎组(n=52)和非肺炎组(n=89)。以多因素logistic回归分析筛选危险因素,建立危险因素模型分析预测价值并构建列线图模型验证。
    结果 白细胞计数(WBC)、CK-MB、NSE水平均偏高,血小板计数(PLT)水平偏低均为上呼吸道感染继发肺部感染的危险因素(P<0.05);WBC、CK-MB、PLT、NSE联合预测上呼吸道感染继发肺部感染的曲线下面积(AUC)高于WBC、CK-MB、PLT、NSE单独预测(P<0.05);基于上呼吸道感染继发肺部感染的危险因素构建列线图模型,141例患者按7∶3的比例分为训练集和验证集,训练集99例,验证集42例,列线图模型训练集和验证集受试者工作特征曲线的AUC分别为0.882(0.813~0.950)和0.814(0.662~0.951);以bootstrap法抽样1 000次,绘制校准曲线以评价模型一致性,结果显示,列线图模型预测价值与实际相近;绘制临床决策曲线进一步评估模型临床实用价值,横坐标表示阈概率,纵坐标表示净收益,可见列线图在40%~100%具有更高正收益。
    结论 基于血常规参数、CK-MB、NSE构建上呼吸道感染继发肺部感染的危险因素模型预测价值较高。

     

    Abstract:
    OBJECTIVE  To explore the predictive value of a risk factor model based on blood routine parameters, creatine kinase isoenzyme (CK-MB) and neuron-specific enolase (NSE) for secondary pulmonary infection following upper respiratory tract infection, thereby achieving early risk identification and providing evidences for clinical prevention and intervention.
    METHODS  A retrospective analysis was conducted on 141 patients with upper respiratory tract infection treated at the 905 Hospital of the People's Liberation Army Navy from Jan. 2024 to Dec. 2024, where etiological findings were considered as the gold standard. Patients were divided into a pneumonia group (n=52) and a non-pneumonia group (n=89) based on pulmonary infection status. Multivariate logistic regression analysis was employed to screen for risk factors, establish a risk factor model, evaluate its predictive value, and construct a nomogram model for validation.
    RESULTS  Elevated white blood cell count (WBC), CK-MB and NSE levels, as well as decreased platelet (PLT) levels, were identified as risk factors for secondary pulmonary infection following upper respiratory tract infection (P<0.05). The area under the curve (AUC) for the combined prediction of this infection by WBC, CK-MB, PLT and NSE was higher than that of individual predictions (P<0.05). A nomogram model was constructed based on the risk factors for this infection. The 141 patients were divided into a training set (n=99) and a validation set (n=42) at a ratio of 7∶3. The AUCs of the receiver operating characteristic curves for the nomogram model in the training and validation sets were 0.882 (0.813–0.950) and 0.814 (0.662–0.951), respectively. Bootstrap sampling with 1,000 resamples was performed, and a calibration curve was plotted to evaluate the consistency of the model. The results showed that the predicted values of the nomogram were close to the actual observations. A clinical decision curve was further plotted to assess the clinical utility of the model, with threshold probability on the x-axis and net benefit on the y-axis. The nomogram was found to provide higher net benefit in the threshold probability range of 40%-100%.
    CONCLUSION  The risk factor model for secondary pulmonary infection following upper respiratory tract infection, constructed based on routine blood parameters, CK-MB and NSE, demonstrates high predictive value.

     

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