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重症肺炎并发呼吸衰竭预测模型的构建

Construction of a prediction model for severe pneumonia complicate with respiratory failure

  • 摘要:
    目的  探讨重症社区获得性肺炎(community-acquired pneumonia,CAP)并发呼吸衰竭(respiratory failure,RF)的预测因素,构建临床预测模型并进行内部验证。
    方法  回顾性选择2022年9月至2024年12月武汉科技大学附属天佑医院重症CAP患者350例,按照7∶3随机分为训练集(n=245)和验证集(n=105),并根据是否并发RF分为RF组和非RF组。采用LASSO回归分析优化变量选择,多因素logistic回归分析构建预测模型并进行内部验证。
    结果 单因素回归分析显示男性、高血压、糖尿病、冠心病、年龄、CURB-65评分、白细胞计数、中性粒细胞计数、C反应蛋白(C-reactive protein,CRP)、淀粉样蛋白A、降钙素原和住院天数是重症肺炎并发RF的危险因素;白蛋白水平是重症肺炎并发RF的保护因素。经LASSO回归分析,最终将CURB-65评分、白蛋白水平和CRP纳入预测模型,受试者工作特征曲线在训练集和验证集中的曲线下面积分别为0.903和0.919。校准曲线分析中训练集和验证集均显示出非常好的拟合度,Hosmer-Lemeshow拟合优度检验显示训练集和验证集中的预测值与真实值间均无显著性差异,阈值概率均为0.01~0.99。
    结论  CURB-65评分、白蛋白水平及CRP是重症肺炎并发RF的独立预测因素,基于上述预测因素建立的重症肺炎并发RF的临床预测模型具有良好的区分度、校准度、拟合度及临床实用性。

     

    Abstract:
    Objective  To explore predictive factors of severe community-acquired pneumonia (CAP) complicated with respiratory failure (RF) and to develop and internally validate a clinical prediction model.
    Methods A retrospective study was conducted on 350 patients with severe CAP admitted to Tianyou Hospital Affiliated to Wuhan University of Science and Technology from September 2022 to December 2024. Patients were randomly divided into a training set (n=245) and a validation set (n=105) in a 7∶3 ratio, and further categorized into RF and non-RF groups. LASSO regression was applied to optimize variable selection. Multivariate logistic analysis was used to construct the prediction model, followed by internal validation.
    Results Univariate regression analysis identified male, hypertension, diabetes, coronary heart disease, age, CURB-65 score, white blood cell count, neutrophil count, C-reactive protein (CRP), serum amyloid A, procalcitonin, and hospital stay as risk factors for RF in severe CAP, while albumin level was a protective factor. LASSO regression selected CURB-65 score, albumin level, and CRP for inclusion in the final model. The area under the receiver operating characteristic curve was 0.903 in the training set and 0.919 in the validation set. Calibration curve analysis demonstrated excellent agreement between predicted and observed probabilities in both sets, and Hosmer-Lemeshow goodness-of-fit tests indicated no significant deviations. Threshold probabilities ranged from 0.01 to 0.99 in both training and validation sets.
    Conclusions CURB-65 score, albumin level, and CRP are independent predictors of RF in severe CAP. The clinical prediction model based on these factors exhibits strong discrimination, calibration, goodness-of-fit, and clinical utility.

     

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