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A Retrospective Cohort Study on 28-Day Mortality in Immunosuppressed Sepsis: An Interpretability-Based Predictive Model Using MIMIC-IV V2.2

医学 回顾性队列研究 心理干预 败血症 急诊医学 队列 队列研究 儿科 梅德林 重症监护医学 生存分析 内科学 比例危险模型 预测模型 死亡率 试验预测值
作者
Zhiru Zhong,Huiwei He,Zhiying Lin
出处
期刊:Shock [Lippincott Williams & Wilkins]
卷期号:65 (3): 348-359
标识
DOI:10.1097/shk.0000000000002721
摘要

BACKGROUND: Sepsis in immunosuppressed patients is associated with significantly higher mortality rates, yet predictive models tailored to this high-risk population remain limited. This study aims to develop an interpretable machine learning model to predict 28-day mortality in immunosuppressed sepsis patients, with a focus on model transparency and clinical applicability. METHODS: A retrospective cohort study was conducted using clinical, laboratory, and demographic data from immunosuppressed sepsis patients. Feature selection was performed using LASSO regression, followed by the development of predictive models, including XGBoost. The model's performance was evaluated using the area under the receiver operating characteristic curve (AUROC). To enhance clinical interpretability, Shapley additive explanations (SHAP) were employed to provide insights into the contribution of individual features to mortality predictions. RESULTS: The final model identified key predictors of 28-day mortality, including lactate levels, red cell distribution width, platelet count, and Sequential Organ Failure Assessment score. XGBoost demonstrated superior predictive accuracy with an AUROC of 0.93 (95% confidence interval: 0.90-0.96), outperforming other models. SHAP analysis revealed that elevated lactate levels and reduced platelet counts were strong risk factors for mortality, while lower lactate and higher platelet counts were protective. The model's interpretability provided clear insights into the role of each predictor, facilitating individualized risk stratification. CONCLUSION: The XGBoost model, combined with SHAP analysis, offers an accurate and interpretable tool for predicting 28-day mortality in immunosuppressed sepsis patients. This approach enhances clinical decision-making by providing transparent insights into the factors driving mortality risk, thus supporting personalized and timely interventions aimed at improving patient outcomes.
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