Aygun Umran, Yagin Fatma Hilal, Yagin Burak, Yasar Seyma, Colak Cemil, Ozkan Ahmet Selim, Ardigò Luca Paolo
Department of Anesthesiology and Reanimation, Malatya Yesilyurt Hasan Calık State Hospital, Malatya 44929, Turkey.
Department of Biostatistics and Medical Informatics, Faculty of Medicine, Inonu University, Malatya 44280, Turkey.
Diagnostics (Basel). 2024 Feb 20;14(5):457. doi: 10.3390/diagnostics14050457.
This study aims to develop an interpretable prediction model based on explainable artificial intelligence to predict bacterial sepsis and discover important biomarkers. A total of 1572 adult patients, 560 of whom were sepsis positive and 1012 of whom were negative, who were admitted to the emergency department with suspicion of sepsis, were examined. We investigated the performance characteristics of sepsis biomarkers alone and in combination for confirmed sepsis diagnosis using Sepsis-3 criteria. Three different tree-based algorithms-Extreme Gradient Boosting (XGBoost), Light Gradient Boosting Machine (LightGBM), Adaptive Boosting (AdaBoost)-were used for sepsis prediction, and after examining comprehensive performance metrics, descriptions of the optimal model were obtained with the SHAP method. The XGBoost model achieved accuracy of 0.898 (0.868-0.929) and area under the ROC curve (AUC) of 0.940 (0.898-0.980) with a 95% confidence interval. The five biomarkers for predicting sepsis were age, respiratory rate, oxygen saturation, procalcitonin, and positive blood culture. SHAP results revealed that older age, higher respiratory rate, procalcitonin, neutrophil-lymphocyte count ratio, C-reactive protein, plaque, leukocyte particle concentration, as well as lower oxygen saturation, systolic blood pressure, and hemoglobin levels increased the risk of sepsis. As a result, the Explainable Artificial Intelligence (XAI)-based prediction model can guide clinicians in the early diagnosis and treatment of sepsis, providing more effective sepsis management and potentially reducing mortality rates and medical costs.
本研究旨在基于可解释人工智能开发一种可解释的预测模型,以预测细菌性脓毒症并发现重要的生物标志物。共检查了1572例成年患者,其中560例脓毒症呈阳性,1012例呈阴性,这些患者因疑似脓毒症而被收入急诊科。我们使用Sepsis-3标准研究了单独及联合使用脓毒症生物标志物进行确诊脓毒症诊断的性能特征。使用三种不同的基于树的算法——极端梯度提升(XGBoost)、轻量级梯度提升机(LightGBM)、自适应提升(AdaBoost)——进行脓毒症预测,并在检查综合性能指标后,用SHAP方法获得了最优模型的描述。XGBoost模型的准确率为0.898(0.868 - 0.929),ROC曲线下面积(AUC)为0.940(0.898 - 0.980),95%置信区间。预测脓毒症的五个生物标志物为年龄、呼吸频率、血氧饱和度、降钙素原和血培养阳性。SHAP结果显示,年龄较大、呼吸频率较高、降钙素原、中性粒细胞与淋巴细胞计数比值、C反应蛋白、斑块、白细胞颗粒浓度,以及较低的血氧饱和度、收缩压和血红蛋白水平会增加脓毒症风险。因此,基于可解释人工智能(XAI)的预测模型可以指导临床医生对脓毒症进行早期诊断和治疗,提供更有效的脓毒症管理,并有可能降低死亡率和医疗成本。