Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
National Engineering Research Center for Big Data Technology and System, Services Computing Technology and System Lab, Cluster and Grid Computing Lab, School of Computer Science and Technology, Huazhong University of Science and Technology, Wuhan, China.
Front Cell Infect Microbiol. 2021 Mar 2;10:586054. doi: 10.3389/fcimb.2020.586054. eCollection 2020.
The outbreak of coronavirus disease 2019 (COVID-19) has become a global public health concern. Many inpatients with COVID-19 have shown clinical symptoms related to sepsis, which will aggravate the deterioration of patients' condition. We aim to diagnose Viral Sepsis Caused by SARS-CoV-2 by analyzing laboratory test data of patients with COVID-19 and establish an early predictive model for sepsis risk among patients with COVID-19.
This study retrospectively investigated laboratory test data of 2,453 patients with COVID-19 from electronic health records. Extreme gradient boosting (XGBoost) was employed to build four models with different feature subsets of a total of 69 collected indicators. Meanwhile, the explainable Shapley Additive ePlanation (SHAP) method was adopted to interpret predictive results and to analyze the feature importance of risk factors.
The model for classifying COVID-19 viral sepsis with seven coagulation function indicators achieved the area under the receiver operating characteristic curve (AUC) 0.9213 (95% CI, 89.94-94.31%), sensitivity 97.17% (95% CI, 94.97-98.46%), and specificity 82.05% (95% CI, 77.24-86.06%). The model for identifying COVID-19 coagulation disorders with eight features provided an average of 3.68 (±) 4.60 days in advance for early warning prediction with 0.9298 AUC (95% CI, 86.91-99.04%), 82.22% sensitivity (95% CI, 67.41-91.49%), and 84.00% specificity (95% CI, 63.08-94.75%).
We found that an abnormality of the coagulation function was related to the occurrence of sepsis and the other routine laboratory test represented by inflammatory factors had a moderate predictive value on coagulopathy, which indicated that early warning of sepsis in COVID-19 patients could be achieved by our established model to improve the patient's prognosis and to reduce mortality.
2019 年冠状病毒病(COVID-19)的爆发已成为全球公共卫生关注的焦点。许多 COVID-19 住院患者表现出与脓毒症相关的临床症状,这将使患者病情恶化。我们旨在通过分析 COVID-19 患者的实验室检测数据来诊断由 SARS-CoV-2 引起的病毒性败血症,并为 COVID-19 患者的脓毒症风险建立早期预测模型。
本研究回顾性调查了 2453 例 COVID-19 患者的电子病历实验室检测数据。采用极端梯度提升(XGBoost)构建了四个模型,每个模型均使用 69 个采集指标的不同特征子集。同时,采用可解释性 Shapley Additive ePlanation(SHAP)方法解释预测结果,并分析危险因素的特征重要性。
使用 7 项凝血功能指标对 COVID-19 病毒败血症进行分类的模型,其受试者工作特征曲线下面积(AUC)为 0.9213(95%CI,89.94-94.31%),灵敏度为 97.17%(95%CI,94.97-98.46%),特异性为 82.05%(95%CI,77.24-86.06%)。使用 8 个特征识别 COVID-19 凝血障碍的模型,可提前平均 3.68(±)4.60 天进行预警预测,AUC 为 0.9298(95%CI,86.91-99.04%),灵敏度为 82.22%(95%CI,67.41-91.49%),特异性为 84.00%(95%CI,63.08-94.75%)。
我们发现凝血功能异常与脓毒症的发生有关,以炎症因子为代表的其他常规实验室检测对凝血障碍具有中等预测价值,这表明我们建立的模型可以实现对 COVID-19 患者脓毒症的早期预警,改善患者预后,降低死亡率。