Monday, March 30, 2026

GBM model predicts postoperative delirium in elderly CHD patients with 0.856 AUC

Key Takeaway
Consider higher CFS grade, lower MMSE score, and higher AIS score as significant predictors when assessing POD risk in elderly CHD patients undergoing non-cardiac surgery.

This retrospective cohort study aimed to develop a machine learning-based predictive model for postoperative delirium (POD) in elderly patients with coronary heart disease (CHD) undergoing non-cardiac surgery, as this population is at significantly increased risk and no specific prediction method exists. Data from elderly CHD patients were collected and split into training and validation sets in a 7:3 ratio. Feature selection was performed using the Boruta algorithm, LASSO regression, and multiple logistic regression. Ten machine learning models were constructed and compared. A total of 861 patients were included, with a POD incidence of 16.6% (143/861). Seven key predictive features were identified. Among the ten models, the gradient boosting model (GBM) demonstrated superior performance. The area under the receiver operating characteristic curve (AUC) for the GBM was 0.856 (95% confidence interval: 0.796-0.916). The model also showed relatively good performance on decision curve analysis, calibration curve, specificity, sensitivity, accuracy, F1 score, and Brier score. Shapley additive interpretation (SHAP) plots indicated that higher Clinical Frailty Scale (CFS) grade, lower Mini-mental State Examination (MMSE) score, and higher Athens Insomnia Scale (AIS) score were significant predictors that enhanced the model's ability. Based on the GBM model, the researchers developed an easy-to-use calculator for predicting POD risk. The study concludes by stating the developed GBM model is reliable for predicting POD in this population but requires external validation before clinical application. The trial was registered in the Chinese Clinical Trial Registry (ChiCTR2500097325) on 17/02/2025.

View Original Abstract ↓
BackgroundPatients with advanced age and coronary heart disease (CHD) are at significantly increased risk for postoperative delirium (POD). However, there is no method to predict POD in elderly patients with CHD.MethodsDate from elderly patients with CHD who underwent non-cardiac surgery was collected. The dataset is subdivided into training and validation sets at a ratio of 7:3. Boruta algorithm, least absolute shrinkage and selection operator (LASSO) regression and multiple logistic regression analysis were used to select features. Machine learning method was used to construct a model for predicting the occurrence of POD. Receiver operating characteristic (ROC) curve, decision curve, calibration curve, specificity, sensitivity, accuracy, F1 score and Brier score were used to compare the predictive performance of these machine learning models, and the interpretability of the models was evaluated by Shapley additive interpretation (SHAP).ResultsA total of 861 patients were included in the study. The incidence of POD was 16.6% (143/861). Seven key features were identified. Ten machine learning models were constructed. Among the models, gradient boosting model (GBM) performed better. The area under the ROC curve (AUC) is 0.856 (95% confidence interval [CI]: 0.796-0.916). The decision curve, calibration curve, specificity, sensitivity, accuracy, F1 score and Brier score were also relatively good. SHAP plots of GBM showed that Clinical Frailty Scale (CFS) grade, Mini-mental State Examination (MMSE) score, and Athens Insomnia Scale (AIS) score were significant predictors of POD in elderly CHD patients, and an easy-to-use calculator for predicting the risk of POD was developed based on the GBM model.ConclusionThis study developed a reliable GBM model for predicting the occurrence of POD in elderly patients with CHD. Higher CFS grade, lower MMSE score and higher AIS score significantly enhanced the predictive ability of the model. External validation of our model is needed before it can be applied in a clinical setting.Trial registrationRegistration number of the Chinese Clinical Trial Registry: ChiCTR2500097325, Registration Date: 17/02/2025.