A time-incorporated SOFA score-based machine learning model for predicting mortality in critically ill patients: A multicenter, real-world study

接收机工作特性 医学 逻辑回归 沙发评分 重症监护 病危 支持向量机 重症监护室 急诊医学 梯度升压 机器学习 重症监护医学 人工智能 随机森林 计算机科学 内科学
作者
Yang Liu,Kun Gao,Hongbin Deng,Tong Ling,Jiajia Lin,Xianqiang Yu,Xiangwei Bo,Jing Zhou,Lin Gao,Peng Wang,Jiajun Hu,Jian Zhang,Zhihui Tong,Yuxiu Liu,Yinghuan Shi,Lu Ke,Yang Gao,Weiqin Li
出处
期刊:International Journal of Medical Informatics [Elsevier BV]
卷期号:163: 104776-104776 被引量:19
标识
DOI:10.1016/j.ijmedinf.2022.104776
摘要

Organ dysfunction (OD) assessment is essential in intensive care units (ICUs). However, current OD assessment scores merely describe the number and the severity of each OD, without evaluating the duration of organ injury. The objective of this study is to develop and validate a machine learning model based on the Sequential Organ Failure Assessment (SOFA) score for the prediction of mortality in critically ill patients. Data from the eICU Collaborative Research Database and Medical Information Mart for Intensive Care (MIMIC) -III were mixed for model development. The MIMIC-IV and Nanjing Jinling Hospital Surgical ICU database were used as external test set A and set B, respectively. The outcome of interest was in-ICU mortality. A modified SOFA model incorporating time-dimension (T-SOFA) was stepwise developed to predict ICU mortality using extreme gradient boosting (XGBoost), support vector machine, random forest and logistic regression algorithms. Time-dimensional features were calculated based on six consecutive SOFA scores collected every 12 h within the first three days of admission. The predictive performance was assessed with the area under the receiver operating characteristic curves (AUROC) and calibration plot. A total of 82,132 patients from the real-world datasets were included in this study, and 7,494 patients (9.12%) died during their ICU stay. The T-SOFA M3 that incorporated the time-dimension features and age, using the XGBoost algorithm, significantly outperformed the original SOFA score in the validation set (AUROC 0.800 95% CI [0.787–0.813] vs. 0.693 95% CI [0.678–0.709], p < 0.01). Good discrimination and calibration were maintained in the test set A and B, with AUROC of 0.803, 95% CI [0.791–0.815] and 0.830, 95% CI [0.789–0.870], respectively. The time-incorporated T-SOFA model could significantly improve the prediction performance of the original SOFA score and is of potential for identifying high-risk patients in future clinical application.
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