Predicting Major Adverse Cardiovascular Events After Cardiac Surgery Using Combined Clinical, Laboratory, and
Mladjan Golubovic1,2, Velimir Peric1,2, Marija Stosic1,2
1Clinic of Cardiovascular Surgery, University Clinical Center Nis, 18000 Nis, Serbia.
Insights
This study developed a machine learning model to predict major adverse cardiovascular events (MACE) after heart surgery, integrating novel echocardiographic and biochemical markers for improved risk stratification.
Area of Science:
- Cardiology
- Medical Informatics
- Biomedical Engineering
Background:
- Major adverse cardiovascular events (MACE) are a leading cause of mortality post-cardiac surgery.
- Current risk models often lack comprehensive assessment of atrial mechanics and biomarkers.
- Improved preoperative risk stratification is crucial for patient outcomes.
Purpose of the Study:
- To develop an interpretable machine learning model for predicting perioperative MACE.
- To integrate clinical, biochemical, and novel echocardiographic features into the predictive model.
- To identify key physiological markers influencing cardiovascular risk.
Main Methods:
- Retrospective analysis of 131 patients undergoing major cardiac surgery.
- Development of an Extreme Gradient Boosting (XGBoost) classifier.
- Utilized SHapley Additive exPlanations (SHAPs) for model interpretability.
Main Results:
- The machine learning model demonstrated robust performance with an average AUC of 0.846 ± 0.092 and F1-score of 0.807 ± 0.096.
- Key predictors included total atrial conduction time, mitral/tricuspid annular orifice areas, and HDL cholesterol.
- The model provided clinically intuitive insights into individual risk profiles.
Conclusions:
- Combining echocardiography, biochemistry, and machine learning offers potential for individualized cardiovascular risk prediction.
- Novel parameters significantly enhance predictive performance, even in patients with preserved left ventricular function.
- Prospective validation in larger cohorts is needed for clinical integration.
Abstract:
Background and Objectives: Despite significant advances in surgical techniques and perioperative care, major adverse cardiovascular events (MACE) remain a leading cause of postoperative morbidity and mortality in patients undergoing coronary artery bypass grafting and/or aortic valve replacement. Accurate preoperative risk stratification is essential yet often limited by models that overlook atrial mechanics and underutilized biomarkers. Materials and Methods: This study aimed to develop an interpretable machine learning model for predicting perioperative MACE by integrating clinical, biochemical, and echocardiographic features, with a particular focus on novel physiological markers. A retrospective cohort of 131 patients was analyzed. An Extreme Gradient Boosting (XGBoost) classifier was trained on a comprehensive feature set, and SHapley Additive exPlanations (SHAPs) were used to quantify each variable's contribution to model predictions. Results: In a stratified 80:20 train-test split, the model initially achieved an AUC of 1.00. Acknowledging the potential for overfitting in small datasets, additional validation was performed using 10 independent random splits and 5-fold cross-validation. These analyses yielded an average AUC of 0.846 ± 0.092 and an F1-score of 0.807 ± 0.096, supporting the model's stability and generalizability. The most influential predictors included total atrial conduction time, mitral and tricuspid annular orifice areas, and high-density lipoprotein (HDL) cholesterol. These variables, spanning electrophysiological, structural, and metabolic domains, significantly enhanced discriminative performance, even in patients with preserved left ventricular function. The model's transparency provides clinically intuitive insights into individual risk profiles, emphasizing the significance of non-traditional parameters in perioperative assessments. Conclusions: This study demonstrates the feasibility and potential clinical value of combining advanced echocardiographic, biochemical, and machine learning tools for individualized cardiovascular risk prediction. While promising, these findings require prospective validation in larger, multicenter cohorts before being integrated into routine clinical decision-making.
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