Dixon Celeste G, Trujillo Rivera Eduardo A, Patel Anita K, Pollack Murray M
Department of Pediatrics, Division of Critical Care Medicine, Children's National Hospital, George Washington University School of Medicine and Health Sciences, Washington, DC, United States.
Front Pediatr. 2025 Apr 4;13:1549836. doi: 10.3389/fped.2025.1549836. eCollection 2025.
Renal dysfunction is common in critically ill children and increases morbidity and mortality risk. Diagnosis and management of renal dysfunction relies on creatinine, a delayed marker of renal injury. We aimed to develop and validate a machine learning model using routinely collected clinical data to predict 24-hour creatinine change in critically ill children before change is observed clinically.
Retrospective cohort study of 39,932 pediatric intensive care unit encounters in a national multicenter database from 2007 to 2022. A neural network was trained to predict <50% or ≥50% creatinine change in the next 24 h. Admission demographics, routinely measured vital signs, laboratory tests, and medication use variables were used as predictors for the model. Data set was randomly split at the encounter level into model development (80%) and test (20%) sets. Performance and clinical relevance was assessed in the test set by accuracy of prediction classification and confusion matrix metrics.
The cohort had a male predominance (53.8%), median age of 8.0 years (IQR 1.9-14.6), 21.0% incidence of acute kidney injury, and 2.3% mortality. The overall accuracy of the model for predicting change of <50% or ≥50% was 68.1% (95% CI 67.6%-68.7%). The accuracy of classification improved substantially with higher creatinine values from 29.9% (CI 28.9%-31.0%) in pairs with an admission creatinine <0.3 mg/dl to 90.0-96.3% in pairs with an admission creatinine of ≥0.6 mg/dl. The model had a negative predictive value of 97.2% and a positive predictive value of 7.1%. The number needed to evaluate to detect one true change ≥50% was 14.
24-hour creatinine change consistent with acute kidney injury can be predicted using routine clinical data in a machine learning model, indicating risk of significant renal dysfunction before it is measured clinically. Positive predictive performance is limited by clinical reliance on creatinine.
肾功能障碍在危重症儿童中很常见,会增加发病和死亡风险。肾功能障碍的诊断和管理依赖于肌酐,这是一种肾损伤的延迟标志物。我们旨在开发并验证一种机器学习模型,该模型使用常规收集的临床数据来预测危重症儿童在临床上观察到肌酐变化之前24小时内的肌酐变化情况。
对2007年至2022年国家多中心数据库中39,932例儿科重症监护病房病例进行回顾性队列研究。训练一个神经网络来预测未来24小时内肌酐变化<50%或≥50%的情况。入院时的人口统计学数据、常规测量的生命体征、实验室检查和用药变量被用作该模型的预测指标。数据集在病例层面随机分为模型开发集(80%)和测试集(20%)。通过预测分类的准确性和混淆矩阵指标在测试集中评估模型的性能和临床相关性。
该队列中男性占主导(53.8%),中位年龄为8.0岁(四分位间距1.9 - 14.6),急性肾损伤发生率为21.0%,死亡率为2.3%。预测<50%或≥50%变化的模型总体准确率为68.1%(95%置信区间67.6% - 68.7%)。随着肌酐值升高,分类准确率显著提高,入院肌酐<0.3mg/dl的配对中为29.9%(置信区间28.9% - 31.0%),入院肌酐≥0.6mg/dl的配对中为90.0% - 96.3%。该模型的阴性预测值为97.2%,阳性预测值为7.1%。检测到一次≥50%的真实变化所需评估的病例数为14例。
使用机器学习模型中的常规临床数据可以预测与急性肾损伤一致的24小时肌酐变化情况,这表明在临床测量之前就存在显著肾功能障碍的风险。阳性预测性能受到临床对肌酐依赖的限制。