Machine Learning for Mortality Prediction in Pediatric Myocarditis

被引:10
作者
Chou, Fu-Sheng [1 ]
Ghimire, Laxmi, V [2 ]
机构
[1] Loma Linda Univ, Sch Med, Dept Pediat, Loma Linda, CA 92350 USA
[2] Lakes Reg Gen Hosp, Laconia, NH USA
关键词
pediatric myocarditis; mortality; machine learning; predictive modeling; random forest; extracorporeal membrane oxygenation; OUTCOMES;
D O I
10.3389/fped.2021.644922
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Pediatric myocarditis is a rare disease. The etiologies are multiple. Mortality associated with the disease is 5-8%. Prognostic factors were identified with the use of national hospitalization databases. Applying these identified risk factors for mortality prediction has not been reported. Methods: We used the Kids' Inpatient Database for this project. We manually curated fourteen variables as predictors of mortality based on the current knowledge of the disease, and compared performance of mortality prediction between linear regression models and a machine learning (ML) model. For ML, the random forest algorithm was chosen because of the categorical nature of the variables. Based on variable importance scores, a reduced model was also developed for comparison. Results: We identified 4,144 patients from the database for randomization into the primary (for model development) and testing (for external validation) datasets. We found that the conventional logistic regression model had low sensitivity (similar to 50%) despite high specificity (>95%) or overall accuracy. On the other hand, the ML model struck a good balance between sensitivity (89.9%) and specificity (85.8%). The reduced ML model with top five variables (mechanical ventilation, cardiac arrest, ECMO, acute kidney injury, ventricular fibrillation) were sufficient to approximate the prediction performance of the full model. Conclusions: The ML algorithm performs superiorly when compared to the linear regression model for mortality prediction in pediatric myocarditis in this retrospective dataset. Prospective studies are warranted to further validate the applicability of our model in clinical settings.
引用
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页数:8
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