Machine Learning Models Using Hospital Admission Characteristics Do Not Optimally Predict Nosocomial Infection Development in a Global Cirrhosis Cohort.

Scott Silvey,Ashok K Choudhury,Patrick S Kamath,Qing Xie,Florence Wong,Peter C Hayes,Wai-Kay Seto,Umang Arora,Garima Singhal,Dinesh Jothimani,Sumeet Asrani,Adrian Gadano,Dinc Dincer,Alberto Queiroz Farias,Daneille Adebayo,José Antonio Velarde-Ruiz Velasco,Adam Doyle,Anand V Kulkarni,Nabil Debzi,Jawaid Shaw,Sezgin Barutcu,Hailemicheal Desalgn,Dominik Bettinger,Ponan Claude Regis Lah,Andres Duarte-Rojo,Dilara Turan,Lei Wang,Rene Male Velazquez,Xin Zheng,Sevda Aghayaeva,Zeki Karasu,Coskun Demirtas,Chenghai Liu,Jacqueline Cordova-Gallardo,Bin Xu,Aabha Nagral,Haibing Gao,Harendran Elangovan,James Fung,Neil Rajorya,Xinrui Wang,Helena Katchmann,Dibyalochan Praharaj,Sanjiv Mahadeva,Yongfang Jiang,Katina Zheng,Kessarin Thanapirom,C E Eapen,Radha K Dhiman,Mingqin Lu,Marco Arrese,Minghua Su,Sarai Gonzalez Hueso,Chuanwu Zhu,Hanna Aberra,Henok Fisseha,Hiang Keat Tan,Caiyan Zhao,Ningping Zhang,Sunil Taneja,Aloysious D Aravinthan,Amey Sonavane,Anoop Saraya,Cameron Gofton,Gerry MacQuillan,Gustavo Pereira,K Rajender Reddy,Shiv K Sarin,Zhujun Cao,Mark Topazian,Ramazan Idilman,Aldo Torre,Jacob George,Mario Alvares da Silva,Brian J Bush,Jasmohan S Bajaj,
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Abstract

BACKGROUND Nosocomial infections (NI) in cirrhosis are associated with high mortality but could be preventable. Logistic regression (LR) models have failed to identify high-risk patients. We aimed to develop machine learning (ML) models to predict NI. METHODS The CLEARED consortium consists of prospectively enrolled cirrhosis inpatients from >120 centers. Using day-of-admission clinical data, three ML approaches[Random Forest (RF), Extreme Gradient Boosting (XGBoost), and Neural Networks (NN)] were used to predict NI. Data were split 80:20 for training and testing stratified by the outcome. Models were compared using Area-under-Receiver-operating-characteristic curve (AUC). RESULTS 8,263 patients (55.90±13.34 years; 64.1% men) from 127 centers in 37 countries were included. NI developed in 869 (10.5%) a median of 6 (4-11) days post-admission. Major NIs were respiratory (29.6%) and urinary tract infection (15.7%), and spontaneous bacterial peritonitis (13.5%). NIs occurred more frequently in patients from low/low-middle income countries and those with severe liver disease, alcohol etiology, and admission infections. NIs were associated with inpatient mortality (31.9% vs. 8.1%, p<0.001) and liver transplantation (4.8% vs. 1.9%, p<0.001). While the RF model (AUC 0.69) showed good calibration (Brier score 0.09), outperforming XGBoost, NN, and LR models (AUC 0.66 for all; LR comparison p = 0.043), no model achieved AUC ≥0.80 for clinical utility. At 10% predicted probability threshold, RF model demonstrated only 75.4% sensitivity, 52.9% specificity, and 15.9% PPV. CONCLUSIONS NIs cannot be accurately predicted from day-of-admission data using ML models, even in a large, prospective, global cirrhosis cohort. Every hospitalized patient with cirrhosis should receive protocolized infection-control measures.
使用住院特征的机器学习模型不能最优地预测全球肝硬化队列中医院感染的发展。
背景:肝硬化患者的医院感染(NI)与高死亡率相关,但可以预防。Logistic回归(LR)模型未能识别出高危患者。我们的目标是开发机器学习(ML)模型来预测NI。方法:clear研究由来自bbb120中心的肝硬化住院患者组成。根据入院当天的临床数据,使用三种ML方法[随机森林(RF),极端梯度增强(XGBoost)和神经网络(NN)]来预测NI。训练和测试按结果分层,数据按80:20分割。采用面积-接收器下-工作特性曲线(AUC)对模型进行比较。结果纳入37个国家127个中心的8263例患者(55.90±13.34岁,男性64.1%)。869例(10.5%)患者在入院后6(4-11)天中位数出现NI。主要的NIs为呼吸道感染(29.6%)、尿路感染(15.7%)和自发性细菌性腹膜炎(13.5%)。NIs更常见于低收入/中低收入国家的患者以及患有严重肝病、酒精病因和入院感染的患者。NIs与住院死亡率(31.9% vs. 8.1%, p<0.001)和肝移植(4.8% vs. 1.9%, p<0.001)相关。虽然RF模型(AUC 0.69)显示出良好的校准(Brier评分0.09),优于XGBoost、NN和LR模型(AUC均为0.66;LR比较p = 0.043),但没有模型达到AUC≥0.80的临床应用。在10%的预测概率阈值下,RF模型的灵敏度仅为75.4%,特异性为52.9%,PPV为15.9%。结论:即使在一个大型的、前瞻性的、全球肝硬化队列中,使用ML模型也不能从入院当日的数据中准确预测snis。每位住院的肝硬化患者都应接受相应的感染控制措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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