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Adjustment of the GRACE Score and SHAP Analysis in STEMI Patients
Jin Cao1, Jingyi Liu2, Xiaoqiang Wang3
1College of Mathematics, Taiyuan University of Technology, Taiyuan, Shanxi 030024, PR China.
Insights
This study refines the GRACE risk score for ST-segment elevation myocardial infarction (STEMI) patients. The new GRACE-STEMI score improves mortality prediction and identifies novel risk groups for personalized care.
Area of Science:
- Cardiology
- Medical Informatics
- Biostatistics
Background:
- The Global Registry of Acute Coronary Events (GRACE) risk score is established for acute coronary syndrome but needs refinement for ST-segment elevation myocardial infarction (STEMI).
- Accurate risk stratification is crucial for managing STEMI patients and predicting major cardiovascular events.
Purpose of the Study:
- To develop and validate an adjusted GRACE risk score specifically for STEMI patients to enhance mortality prediction.
- To identify key predictors of out-of-hospital all-cause death (ACD) in STEMI patients.
Main Methods:
- Retrospective analysis of ACD incidence and correlation with GRACE score indicators.
- Adjustment of GRACE scores by reducing contributions from insignificant indicators.
- Development of the GRACE-STEMI score using a Stacking ensemble method with multiple regression models.
- Validation using SHAP (Shapley Additive exPlanations) analysis for interpretability.
Main Results:
- Identified nine key variables influencing the adjusted GRACE score: LA, LVEF, neutrophil percentage, lymphocytes, urea, systolic pressure, admission heart rate, age, and Killip classification.
- The GRACE-STEMI adjusted model achieved an adjusted R2 of 0.7886 and a C-index of 0.8521.
- The model demonstrated strong performance on the test set with MSE of 250.8 and RMSE of 15.84.
- SHAP analysis confirmed model interpretability and identified novel risk factors.
Conclusions:
- The GRACE-STEMI score adjusted model provides a more precise tool for risk stratification and mortality prediction in STEMI patients.
- Integration of SHAP analysis enhances interpretability and aids in identifying new risk groups for personalized clinical decision-making.
- This refined score represents a clinically relevant advancement for STEMI patient management.
Background:
The GRACE (Global Registry of Acute Coronary Events) risk score is a well-established tool for predicting major cardiovascular events in patients with acute coronary syndrome. However, its application in acute ST-segment elevation myocardial infarction (STEMI) requires refinement to enhance its predictive accuracy in clinical settings.
Methods:
In this study, we conducted a retrospective analysis of the incidence of out-of-hospital all-cause death (ACD), calculated the correlation and significance of the GRACE score indicators with ACD, and reduced the scores corresponding to insignificant and low-correlation indicators to adjust the scores for survive patients. Using the adjusted GRACE score as the target variable, we trained and optimized and integrated the multiple regression models using the Stacking method(named GRACE-STEMI score adjusted model). Additionally, we performed supplementary SHAP (SHapley Additive exPlanations) analysis.
Results:
The study ultimately identified nine key variables affecting the adjusted GRACE score: LA, LVEF, neutrophil percentage, lymphocytes, urea, systolic pressure, admission heart rate, age, and Killip classification. Furthermore, by employing the Stacking method to integrate the three best-performing regression models on the training set, the GRACE-STEMI score adjusted model achieved an adjusted R2 score of 0.7886, a C-index of 0.8521, an MSE (Mean Squared Error) of 250.8, and an RMSE (Root Mean Squared Error) of 15.84 on the test set. The model's interpretability was also successfully validated through SHAP analysis.
Conclusions:
The GRACE-STEMI score adjusted model offers a clinically relevant advancement, providing a more precise tool for risk stratification and mortality prediction in STEMI patients. The integration of SHAP analysis not only enhances the model's interpretability but also facilitates the identification of novel risk groups, contributing to personalized clinical decision-making.
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