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首页> 外文期刊>Frontiers in Pediatrics >Comparison of Machine Learning Models for Prediction of Initial Intravenous Immunoglobulin Resistance in Children With Kawasaki Disease
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Comparison of Machine Learning Models for Prediction of Initial Intravenous Immunoglobulin Resistance in Children With Kawasaki Disease

机译:川崎病儿童初始静脉内免疫球蛋白抗性预测机器学习模型的比较

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Background: We aimed to construct an optimal machine learning (ML) method for predicting intravenous immunoglobulin (IVIG) resistance in children with Kawasaki disease (KD) using commonly available clinical and laboratory variables. Methods: We retrospectively collected 98 clinical records of hospitalized children with KD (2–109 months of age). We found that 20 (20%) children were resistant to initial IVIG therapy. We trained three ML techniques, including logistic regression, linear support vector machine, and eXtreme gradient boosting with 10 variables against IVIG resistance. Moreover, we estimated the predictive performance based on nested 5-fold cross-validation (CV). We also selected variables using the recursive feature elimination method and performed the nested 5-fold CV with selected variables in a similar manner. We compared ML models with the existing system regardless of their predictive performance. Results: The results of the area under the receiver operator characteristic curve were in the range of 0.58–0.60 in the all-variable model and 0.60–0.75 in the select-model. The specificities were more than 0.90 and higher than those in existing scoring systems, but the sensitivities were lower. Conclusions: Three ML models based on demographics and routine laboratory variables did not provide reliable performances. Additional biomarkers are likely to be needed to generate an effective prediction model.
机译:背景:使用常用的临床和实验室变量,构建用于预测川崎病(KD)儿童静脉内免疫球蛋白(IVIG)抗性的最佳机器学习(ML)方法。方法:我们回顾性地收集了98名住院儿童的临床记录,患有KD(2-109个月)。我们发现20名(20%)儿童抵抗初始IVIG治疗。我们培训了三毫升技术,包括Logistic回归,线性支持向量机,以及极端梯度升高,10个变量抵抗IVIG电阻。此外,我们估计了基于嵌套5倍交叉验证(CV)的预测性能。我们还使用递归特征消除方法选择变量,并以类似的方式执行具有所选变量的嵌套5倍CV。我们将ML模型与现有系统进行比较,无论其预测性能如何。结果:接收器操作员特征曲线下区域的结果在“全变模型”中的0.58-0.60的范围为0.58-0.60。选择模型中的0.60-0.75。特异性大于0.90,高于现有评分系统的特异性,但敏感性较低。结论:基于人口统计和常规实验室变量的三毫升模型没有提供可靠的表现。可能需要额外的生物标志物来产生有效的预测模型。

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