基于LASSO回归对早产儿晚发型败血症风险预测模型的建立与评价

Establishment and evaluation of a risk prediction model for premature late-onset sepsis in preterm infants based on LASSO regression

  • 摘要:
    背景  晚发型败血症是造成早产儿不良事件和死亡的主要原因之一,对其进行早期评估和预测至关重要。
    目的  探索早产儿晚发型败血症发生的危险因素并构建预测早产儿晚发型败血症发生风险的列线图模型。
    方法  回顾性分析2019年1月—2023年6月于解放军总医院第七医学中心出生并于出生后立即转入新生儿重症病房住院治疗的早产儿,根据诊断分为晚发型败血症组和非败血症组,并收集患儿母亲孕期资料、患儿基本资料、临床资料等,以2022年12月为时间截点划分为建模组和验证组,对建模组使用LASSO回归模型进行变量筛选,将具有统计学意义的因素构建列线图预测模型。使用受试者操作特征(ROC)曲线、曲线下面积(AUC)、C统计量及校准曲线对预测模型的区分度、准确度进行临床效能评估。对验证组采用受试者操作特征曲线(ROC)的曲线下面积(AUC)评估区分度并计算模型的敏感度和特异度。并应用300次bootstrap重抽样对模型进行内部验证。
    结果  建模组共纳入734例早产儿(105例早产儿晚发型败血症),验证组133例(13例早产儿晚发型败血症),其中建模组通过LASSO回归分析发现患儿出生体重、胎龄、Apgar评分(10 min)、支气管肺发育不良史、坏死性小肠结肠炎、呼吸窘迫综合征、气管插管为早产儿晚发型败血症发生的危险因素。构建列线图模型,通过绘制ROC曲线,发现该预测模型的AUC为0.748(95% CI:0.694 ~ 0.802),C-index值为0.761,提示该模型具有良好的区分度和精准度。重抽样内部验证所得到的C-index的值为0.744,提示该模型具有良好的稳定性,在验证人群,对列线图预测模型进行外部验证,其ROC曲线 AUC为0.843(95% CI:0.742 ~ 0.944),提示模型的预测性能良好。
    结论  出生体重、胎龄、Apgar评分(10 min)、支气管肺发育不良史、坏死性小肠结肠炎、呼吸窘迫综合征、气管插管构建的预测模型具有良好的预测效能。

     

    Abstract:
    Background Late-onset sepsis is one of the main causes of adverse events and mortality in premature infants, and its early evaluation and prediction are essential.
    Objective To explore the risk factors for late-onset sepsis in premature infants and construct a nomogram model to predict the risk of late-onset sepsis in premature infants.
    Methods Retrospective analysis was perfomed in preterm infants who were born at the Seventh Medical Center of Chinese PLA General Hospital from January 2019 to June 2023 and transferred to the neonatal intensive care unit for hospitalization immediately after birth, and they were divided into late-stage sepsis group and non-sepsis group according to the diagnosis. The pregnancy data of mothers, basic data of the infants, and their clinical data were collected. Taking December 2022 as the cut-off point, they were divided into modeling group and validation group, and the modeling group was screened for variables using the LASSO regression model, and the statistically significant factors were constructed into a column-line graph prediction model. Clinical efficacy of the predictive model was assessed for differentiation and accuracy using subject operating characteristic (ROC) curves, area under the curve (AUC), C-statistic, and calibration curves. For the validation group, the area under the curve (AUC) of the subject's work characteristic curve (ROC) was used to assess the discrimination and calculate the sensitivity and specificity of the model. And 300 times bootstrap resampling was applied for internal validation of the model.
    Results A total of 734 preterm infants (105 cases of late-onset sepsis in preterm infants) were included in the modeling group and 133 cases (13 cases of late-onset sepsis in preterm infants) were included in the validation group. LASSO regression analysis found that the child's birth weight, gestational age, Apgar score (10 min), history of bronchopulmonary dysplasia, necrotizing small intestinal colitis, respiratory distress syndrome, and endotracheal intubation were the risk factors for the development of late-onset sepsis in preterm infants in the modeling group. A column-line graphical model was constructed, and by plotting the ROC curve, the AUC of the predictive model was 0.748 (95% CI: 0.694-0.802) and the C-index value was 0.761, suggesting that the model had a good degree of differentiation and precision. The C-index value obtained from the resampling internal validation was 0.744, suggesting that the model had good stability, and in the validation population, the external validation of the column-line graph prediction model had a ROC curve AUC of 0.843 (95% CI: 0.742-0.944), suggesting that the model had good predictive performance.
    Conclusion The prediction model constructed based on birth weight, gestational age, Apgar score (10 min), bronchopulmonary dysplasia history, necrotizing enterocolitis, respiratory distress syndrome and endotracheal intubation has good predictive performance, but further external validation is needed.

     

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