重症肺炎短期死亡风险预测模型的构建与验证

Development and validation of a short-term mortality risk prediction model for severe pneumonia

  • 摘要:
    背景 重症肺炎患者病情危重,病死率高,对该群体进行早期干预能显著改善其预后。
    目的 探索重症监护室中肺炎患者的死亡预测因素,构建短期死亡(7 d死亡)风险预测模型并进行临床应用。
    方法 基于美国MIMIC-Ⅳ数据库,收集2008 — 2022年4 247例重症肺炎患者相关临床信息,按3∶1的比例随机划分为训练集(n=3 185)和验证集(n=1 062)。在训练集中基于LASSO回归筛选特征构建5种机器学习模型并验证,包括logistic回归、弹性网络、随机森林、极限梯度提升和轻量梯度提升,并在验证集中进行评估。结合受试者工作特征(receiver operating characteristic,ROC)曲线、校准曲线、临床决策曲线分析(decision curve analysis,DCA)、敏感度、特异度及阴性预测值(negative predictive value,NPV)等指标综合评估并筛选最佳模型,并与序贯器官衰竭评分(sequential organ failure assessment,SOFA)进行比较。基于最终模型制作列线图以增强模型解释性,并构建在线网页计算器以增加临床实用性。
    结果 LASSO回归最终纳入9个关键特征:pH、年龄、血尿素氮、血氧饱和度、乳酸、活化部分凝血活酶时间(activated partial thromboplastin time,APTT)、抗凝治疗、感染类型和抗病原体治疗。5种机器学习模型中,logistic回归模型在验证集中综合性能表现最佳(AUC=0.82,95% CI:0.77 ~ 0.88;NPV=0.99,95% CI:0.97 ~ 0.99),校准曲线和DCA曲线提示该模型有良好的稳定性和临床适用性。Logistic回归模型的Brier评分为0.042,校准斜率为0.944,截距为0.027,Hosmer-Lemeshow拟合优度检验提示拟合良好(P=0.768),且预测性能显著优于SOFA评分(DeLong检验,P<0.05)。
    结论 本研究构建并验证了一个基于机器学习的重症肺炎短期死亡风险临床预测模型。该模型具有较高的预测效能与临床实用性,可以辅助临床早期决策和风险评估。

     

    Abstract:
    Background Patients with severe pneumonia are in critical condition and have a high mortality rate; early intervention in this population can significantly improve prognosis.
    Objective To identify risk factors for mortality in patients with pneumonia in intensive care units, develop a predictive model for short-term mortality (death within 7 days), and apply this model in clinical practice.
    Methods Clinical data on 4 247 critically ill pneumonia patients were collected from the MIMIC-Ⅳ database (2008 — 2022). Data were randomly divided into a training set (n=3 185) and a validation set (n=1 062) in a 3:1 ratio. Five machine learning models were constructed using features selected via LASSO regression: logistic regression, elastic net (Enet), random forest (RF), extreme gradient boosting (XGBoost), and light gradient boosting machine (LightGBM). The optimal model was comprehensively evaluated using receiver operating characteristic (ROC) curves, calibration curves, decision curve analysis (DCA), sensitivity, specificity, and negative predictive value (NPV), with comparative analysis against the SOFA score. Model interpretability was enhanced through a nomogram for individualized risk visualization, and an online web calculator was developed to improve clinical utility.
    Results The final model incorporated nine key features: pH, age, blood urea nitrogen, oxygen saturation, lactate, activated partial thromboplastin time (APTT), anticoagulant therapy, type of infection, and anti-pathogen treatment. Among the five models, the logistic regression model demonstrated the best overall performance in the validation set (AUC=0.82, 95% CI: 0.77 - 0.88; NPV=0.99, 95% CI: 0.97 - 0.99), with the calibration curve and DCA confirming good stability and clinical applicability. Logistic regression model had a Brier score of 0.042, a calibration slope of 0.944, and an intercept of 0.027; the Hosmer-Lemeshow goodness-of-fit test indicated good fit (P=0.768), and its predictive performance was significantly superior to that of the SOFA score (DeLong test, P < 0.05). The study further deployed the final model as an online web-based calculator for rapid assessment of short-term mortality risk in patients with severe pneumonia.
    Conclusion This study constructed and validated a machine learning-based clinical predictive model for short-term mortality risk in severe pneumonia. The model demonstrates high predictive efficacy and clinical utility, supporting early clinical decision-making and risk assessment.

     

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