A multicenter machine learning model for predicting ICU mortality in mechanically ventilated patients: development and external validation.

IF 5.5 3区 医学 Q2 MEDICAL INFORMATICS
Yi Zhang, Xu Chen, Xinghan Tian, Hui Zhao
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引用次数: 0

Abstract

Background: Accurate early prediction of mortality in mechanically ventilated intensive care unit (ICU) patients remains challenging due to disease heterogeneity and dynamic clinical trajectories. Traditional severity scoring systems have limited flexibility and generalizability. This study aimed to develop and externally validate a machine learning-based model using routinely available clinical variables to predict ICU mortality in mechanically ventilated patients.

Methods: A retrospective multicenter cohort study was conducted using the MIMIC database as the development cohort, with external validation performed in the eICU Collaborative Research Database and an independent institutional cohort. Adult ICU patients receiving invasive mechanical ventilation were included. A two-step feature selection strategy combining least absolute shrinkage and selection operator (LASSO) regression and recursive feature elimination was applied to identify robust predictors. Six machine learning algorithms were compared, and a random forest model was selected. Model performance was evaluated using discrimination, calibration, decision curve analysis, time-dependent area under the curve (AUC), and concordance index (C-index). Model interpretability was assessed using SHAP analysis.

Results: A total of 21 predictors were selected for model development. The random forest model demonstrated superior overall performance compared with alternative algorithms. In external validation, the model showed favorable early discrimination, with near-perfect AUC values during the first 48 hours in the local cohort and consistently acceptable performance in the eICU cohort. Predictive performance attenuated over time, particularly in the local cohort, whereas temporal stability was observed in the multicenter dataset. Calibration and decision curve analyses supported the reliability and clinical utility of the model. Key predictors included age, markers of respiratory dysfunction, metabolic stress, organ failure, and treatment intensity.

Conclusions: The proposed random forest model provides accurate and interpretable admission-time risk stratification for ICU mortality in mechanically ventilated patients. We recommend its use as an admission triage and screening tool for identifying high-risk patients within the first 48 hours of ICU admission. While predictive performance declined over time, the model demonstrated robust early risk stratification and generalizability across independent cohorts, highlighting its potential value for early clinical decision support in critical care settings.

Clinical trial number: Not applicable. This study was an observational retrospective cohort study and was not registered as a clinical trial.

预测ICU机械通气患者死亡率的多中心机器学习模型:开发和外部验证。
背景:由于疾病异质性和动态临床轨迹,对机械通气重症监护病房(ICU)患者死亡率的准确早期预测仍然具有挑战性。传统的严重性评分系统具有有限的灵活性和通用性。本研究旨在开发并外部验证基于机器学习的模型,该模型使用常规可用的临床变量来预测机械通气患者的ICU死亡率。方法:采用MIMIC数据库作为发展队列进行回顾性多中心队列研究,并在eICU合作研究数据库和独立机构队列中进行外部验证。纳入接受有创机械通气的ICU成人患者。采用最小绝对收缩和选择算子(LASSO)回归和递归特征消除相结合的两步特征选择策略来识别稳健的预测因子。比较了6种机器学习算法,选择了随机森林模型。通过判别、校准、决策曲线分析、随时间变化的曲线下面积(AUC)和一致性指数(C-index)来评估模型的性能。采用SHAP分析评估模型可解释性。结果:共选择21个预测因子进行模型开发。与其他算法相比,随机森林模型表现出更好的整体性能。在外部验证中,该模型显示出良好的早期识别能力,在本地队列中,前48小时的AUC值接近完美,在eICU队列中,该模型的表现始终可以接受。预测性能随着时间的推移而减弱,特别是在本地队列中,而在多中心数据集中观察到时间稳定性。校正和决策曲线分析支持了模型的可靠性和临床实用性。关键预测因素包括年龄、呼吸功能障碍标志物、代谢应激、器官衰竭和治疗强度。结论:所提出的随机森林模型为ICU机械通气患者的死亡率提供了准确且可解释的入院时间风险分层。我们建议将其作为入院分诊和筛查工具,用于在ICU入院前48小时内识别高危患者。虽然预测性能随着时间的推移而下降,但该模型在独立队列中显示出强大的早期风险分层和通用性,突出了其在重症监护环境中早期临床决策支持的潜在价值。临床试验号:不适用。本研究是一项观察性回顾性队列研究,未注册为临床试验。
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来源期刊
CiteScore
7.20
自引率
5.70%
发文量
297
审稿时长
1 months
期刊介绍: BMC Medical Informatics and Decision Making is an open access journal publishing original peer-reviewed research articles in relation to the design, development, implementation, use, and evaluation of health information technologies and decision-making for human health.
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