Development and validation of a deep interpretable network for continuous acute kidney injury prediction in critically ill patients

被引:3
作者
Yang, Meicheng [1 ]
Liu, Songqiao [2 ,3 ]
Hao, Tong [2 ]
Ma, Caiyun [1 ]
Chen, Hui [2 ]
Li, Yuwen [1 ]
Wu, Changde [2 ]
Xie, Jianfeng [2 ]
Qiu, Haibo [2 ]
Li, Jianqing [1 ,4 ,5 ]
Yang, Yi [2 ,6 ]
Liu, Chengyu [1 ,5 ]
机构
[1] Southeast Univ, Sch Instrument Sci & Engn, State Key Lab Digital Med Engn, Nanjing, Peoples R China
[2] Southeast Univ, Zhongda Hosp, Sch Med, Dept Crit Care Med,Jiangsu Prov Key Lab Crit Care, Nanjing, Peoples R China
[3] Nanjing Lishui Peoples Hosp, Zhongda Hosp, Dept Crit Care Med, Lishui Branch, Nanjing, Peoples R China
[4] Nanjing Med Univ, Sch Biomed Engn & Informat, Nanjing, Peoples R China
[5] 2 Sipailou Rd, Nanjing 210096, Jiangsu Provinc, Peoples R China
[6] 87 Dingjiaqiao, Nanjing 210009, Jiangsu Provinc, Peoples R China
关键词
Acute kidney injury; Critical care; Predictive model; External validation; Model interpretation; ARTIFICIAL-INTELLIGENCE; NEURAL-NETWORKS; MANAGEMENT; SCORE;
D O I
10.1016/j.artmed.2024.102785
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Early detection of acute kidney injury (AKI) may provide a crucial window of opportunity to prevent further injury, which helps improve clinical outcomes. This study aimed to develop a deep interpretable network for continuously predicting the 24 -hour AKI risk in real-time and evaluate its performance internally and externally in critically ill patients. A total of 21,163 patients' electronic health records sourced from Beth Israel Deaconess Medical Center (BIDMC) were first included in building the model. Two external validation populations included 3025 patients from the Philips eICU Research Institute and 2625 patients from Zhongda Hospital Southeast University. A total of 152 intelligently engineered predictors were extracted on an hourly basis. The prediction model referred to as DeepAKI was designed with the basic framework of squeeze -and -excitation networks with dilated causal convolution embedded. The integrated gradients method was utilized to explain the prediction model. When performed on the internal validation set (3175 [15 %] patients from BIDMC) and the two external validation sets, DeepAKI obtained the area under the curve of 0.799 (95 % CI 0.791-0.806), 0.763 (95 % CI 0.755-0.771) and 0.676 (95 % CI 0.668-0.684) for continuousAKI prediction, respectively. For model interpretability, clinically relevant important variables contributing to the model prediction were informed, and individual explanations along the timeline were explored to show how AKI risk arose. The potential threats to generalisability in deep learning -based models when deployed across health systems in real -world settings were analyzed.
引用
收藏
页数:10
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