ArticleFrontiers in cellular and infection microbiology2025
A machine learning model for robust prediction of sepsis-induced coagulopathy in critically ill patients with sepsis.
Article in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.
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Who cites it
5 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Biomarkers and clinical factors associated with sepsis-induced coagulopathy: A systematic review and meta-analysis.Science progress · 2026Pooled it
- Development and Validation of an Interpretable Machine Learning Model to Predict Mortality in Patients With Sepsis-Induced Coagulopathy: Multicenter Cohort Study.JMIR medical informatics · 2026Article
- The vasoactive-age adjusted sepsis-induced coagulopathy score predicts 28-day new-onset multiple organ dysfunction syndrome in patients with sepsis: a single-centre retrospective cohort study.Frontiers in medicine · 2026Article
- Explainable machine learning for predicting venous thromboembolism in septic shock patients.Frontiers in immunology · 2026Article
- Association of the atherogenic index of plasma with in-hospital mortality in patients with sepsis-induced coagulopathy.Lipids in health and disease · 2025Article
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7 authors.
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Abstract
Introduction: Sepsis-induced coagulopathy (SIC) is a common disease in patients with sepsis. It denotes higher mortality rates and a poorer prognosis in these patients. This study aimed to develop a practical machine learning (ML) model for the prediction of the risk of SIC in critically ill patients with sepsis. Methods: In this retrospective cohort study, patients were extracted from the Medical Information Mart for Intensive Care IV (MIMIC-IV) database and the Inner Mongolia Autonomous Region People's Hospital database. Sepsis and SIC were defined based on the Sepsis-3 criteria and the criteria developed based on the International Society of Thrombosis and Haemostasis (ISTH), respectively. We compared nine ML models using the Sequential Organ Failure Assessment (SOFA) score in terms of SIC prediction ability. Optimal model selection was based on the superior performance metrics exhibited by the model on the training dataset, the internal validation dataset, and the external validation dataset. Results: Of the 15,479 patients in MIMIC-IV included in the final cohort, a total of 6,036 (38.9%) patients developed SIC during sepsis. We selected 17 features to construct ML prediction models. The gradient boosting machine (GBM) model was deemed optimal as it achieved high predictive accuracy and reliability across the training, internal, and external validation datasets. The areas under the curve of the GBM model were 0.773 (95%CI = 0.765-0.782) in the training dataset, 0.730 (95%CI = 0.715-0.745) in the internal validation dataset, and 0.966 (95%CI = 0.938-0.994) in the external validation dataset. The Shapley Additive Explanations (SHAP) values illustrated the prediction results, indicating that total bilirubin, red cell distribution width (RDW), systolic blood pressure (SBP), heparin, and blood urea nitrogen (BUN) were risk factors for progression to SIC in patients with sepsis. Conclusions: We developed an optimal and operable ML model that was able to predict the risk of SIC in septic patients better than the SOFA scoring models.
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