开发和验证基于机器学习的模型,用于预测 COVID-19 住院患者中的医护相关细菌/真菌感染:一项回顾性队列研究

Min Wang, Wenjuan Li, Hui Wang, Peixin Song
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引用次数: 0

摘要

COVID-19 和细菌/真菌并发感染给人类健康带来了重大挑战。然而,目前还缺乏良好的工具来预测合并感染风险,以帮助临床工作。我们旨在研究 COVID-19 患者中细菌/真菌合并感染的风险因素,并开发机器学习模型来估计合并感染的风险。在这项回顾性队列研究中,我们招募了2023年1月1日至7月31日期间在中国一家三甲医院确诊为COVID-19的成年住院患者,并收集了入院时的基线信息。所有数据按 7:3 的比例随机分为训练集和测试集。我们在训练集中建立了合并感染的广义线性模型和随机森林模型,并在测试集中评估了模型的性能。我们还进行了决策曲线分析,以评估临床适用性。共有 1244 名患者被纳入训练队列,其中包括 62 例医护相关细菌/真菌感染;534 名患者被纳入测试队列,其中包括 22 例感染。我们发现,与无合并症的患者相比,有合并症(糖尿病、神经系统疾病)的患者发生合并感染的风险更高(OR = 2.78,95%CI = 1.61-4.86;OR = 1.93,95%CI = 1.11-3.35)。留置中心静脉导管或导尿管也与合并感染的风险增加有关(OR = 2.53,95%CI = 1.39-4.64;OR = 2.28,95%CI = 1.24-4.27)。PCT>0.5纳克/毫升的患者受感染的几率是普通人的2.03倍(95%CI = 1.41-3.82)。有趣的是,IL-6 浓度小于 10 pg/ml 的患者合并感染的风险也更高(OR = 1.69,95%CI = 0.97-2.94)。基线肌酐水平较低的患者发生细菌/真菌合并感染的风险较低(OR = 0.40,95%CI = 0.22-0.71)。广义线性模型和随机森林模型显示出良好的接收者操作特征曲线(ROC = 0.87,95%CI = 0.80-0.94;ROC = 0.88,95%CI = 0.82-0.93),准确性、灵敏度和特异性分别为 0.86vs0.75、0.82vs0.86、0.87vs0.74。相应的校准评估 P 统计量分别为 0.883 和 0.769。我们的机器学习模型具有很强的预测能力,可作为有效的临床决策支持工具,用于识别有细菌/真菌合并感染风险的COVID-19患者,并指导抗生素用药。IL-6 等细胞因子的水平可能会影响细菌/真菌合并感染的状况。
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Development and validation of machine learning-based models for predicting healthcare-associated bacterial/fungal infections among COVID-19 inpatients: a retrospective cohort study
COVID-19 and bacterial/fungal coinfections have posed significant challenges to human health. However, there is a lack of good tools for predicting coinfection risk to aid clinical work. We aimed to investigate the risk factors for bacterial/fungal coinfection among COVID-19 patients and to develop machine learning models to estimate the risk of coinfection. In this retrospective cohort study, we enrolled adult inpatients confirmed with COVID-19 in a tertiary hospital between January 1 and July 31, 2023, in China and collected baseline information at admission. All the data were randomly divided into a training set and a testing set at a ratio of 7:3. We developed the generalized linear and random forest models for coinfections in the training set and assessed the performance of the models in the testing set. Decision curve analysis was performed to evaluate the clinical applicability. A total of 1244 patients were included in the training cohort with 62 healthcare-associated bacterial/fungal infections, while 534 were included in the testing cohort with 22 infections. We found that patients with comorbidities (diabetes, neurological disease) were at greater risk for coinfections than were those without comorbidities (OR = 2.78, 95%CI = 1.61–4.86; OR = 1.93, 95%CI = 1.11–3.35). An indwelling central venous catheter or urinary catheter was also associated with an increased risk (OR = 2.53, 95%CI = 1.39–4.64; OR = 2.28, 95%CI = 1.24–4.27) of coinfections. Patients with PCT > 0.5 ng/ml were 2.03 times (95%CI = 1.41–3.82) more likely to be infected. Interestingly, the risk of coinfection was also greater in patients with an IL-6 concentration < 10 pg/ml (OR = 1.69, 95%CI = 0.97–2.94). Patients with low baseline creatinine levels had a decreased risk of bacterial/fungal coinfections(OR = 0.40, 95%CI = 0.22–0.71). The generalized linear and random forest models demonstrated favorable receiver operating characteristic curves (ROC = 0.87, 95%CI = 0.80–0.94; ROC = 0.88, 95%CI = 0.82–0.93) with high accuracy, sensitivity and specificity of 0.86vs0.75, 0.82vs0.86, 0.87vs0.74, respectively. The corresponding calibration evaluation P statistics were 0.883 and 0.769. Our machine learning models achieved strong predictive ability and may be effective clinical decision-support tools for identifying COVID-19 patients at risk for bacterial/fungal coinfection and guiding antibiotic administration. The levels of cytokines, such as IL-6, may affect the status of bacterial/fungal coinfection.
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