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A new prediction diagnosis model of incomplete Kawasaki disease based on data mining with big data
Zhen Yang1,2,3, Bo Pan1,2,3, Jia Liu1
1Department of Cardiology Children's Hospital of Chongqing Medical University Chongqing China.
Insights
Early prediction of incomplete Kawasaki disease (IKD) in children is crucial. This study identified key risk factors like UA (uric acid) to improve early IKD diagnosis and treatment in pediatric patients.
Area of Science:
- Pediatrics
- Rheumatology
- Clinical Diagnostics
Background:
- Incomplete Kawasaki disease (IKD) presents diagnostic challenges due to atypical symptoms.
- Distinguishing IKD from other febrile illnesses is critical for timely and appropriate treatment.
- Early identification of IKD can prevent severe complications.
Purpose of the Study:
- To investigate independent risk factors for the early prediction of IKD in children.
- To develop age-specific predictive models for IKD.
- To identify novel biomarkers for IKD diagnosis.
Main Methods:
- Retrospective analysis of 809 children with IKD and 2427 children with other febrile diseases.
- Development of age-specific predictive models using univariate analysis.
- Validation of predictive models using ROC curve analysis and new datasets.
Main Results:
- Identified distinct sets of independent risk factors for IKD across different age groups (0-24 months, 24-60 months, and >60 months).
- Key predictors include CRP, LDH, UA, TP, ALB, RDA, PLT, HGB, and MCHC, varying by age group.
- Uric acid (UA) emerged as a novel independent risk factor for IKD.
- Predictive models demonstrated good performance with AUC values ranging from 0.7 to 0.88 across age groups and datasets.
Conclusions:
- Age-specific risk factor models can significantly aid in the early prediction of IKD.
- UA is a newly identified, valuable biomarker for IKD diagnosis.
- These findings support personalized diagnostic strategies for IKD in pediatric care.
Abstract:
Kawasaki disease (KD) is an acute, self-limited febrile illness occurring in children. In actual clinical situations, unlike complete Kawasaki disease (CKD), incomplete Kawasaki disease (IKD) lacks typical symptoms and is difficult to distinguish from many febrile illnesses, which poses a challenge to accurate diagnosis and misleading the treatment. Therefore, we investigated the independent risk factors for early prediction of IKD in children. In this research, 809 children suffering from IKD were recruited from the Children's Hospital of Chongqing Medical University from 2007 to 2017, as well as 2427 children were related to febrile diseases, divided into the IKD group and the other related febrile disease group. According to the results of univariate analysis, the study population was divided into three age groups to develop group-specific models that demonstrated more effective performance. Finally, the 0-24 months old group obtained eight independent risk factors: CRP, LDH, UA, TP, ALB, RDA, PLT, and HGB, with the ROC curve showing an AUC of 0.862 in the predictive model and 0.88 in the new dataset. Meanwhile, LDH, UA, ALB, PLT, and MCHC were in the 24-60 months old group, among which AUC was 0.83 in the predictive model and 0.82 in the new dataset; the older group obtained LDH, UA, MCHC, and PLT, with an AUC of 0.7 in the predictive model and 0.8 in the new dataset. Particularly, UA is a new independent risk factor of IKD. These findings offer valuable insights into guiding the personalized diagnosis of IKD in pediatric patients.
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