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Published on: September 22, 2023
A nomogram for predicting coronary artery lesions in patients with Kawasaki disease
Wenjie Xuan1, Yinping Yao, Yayun Wang
1Department of Pediatrics, Shaoxing People's Hospital (Shaoxing Hospital, Zhejiang University School of Medicine), Shaoxing, China.
Insights
Kawasaki disease (KD) patients with prolonged fever, elevated C-reactive protein, and lower hemoglobin/albumin are at higher risk for coronary artery lesions (CAL). A predictive model aids in rapid CAL risk assessment.
Area of Science:
- Pediatrics
- Cardiology
- Rheumatology
Background:
- Kawasaki disease (KD) is an acute systemic vasculitis with potential coronary artery lesions (CAL).
- The etiology of KD remains unidentified, necessitating predictive tools for CAL risk.
Purpose of the Study:
- To construct and validate a predictive model for coronary artery lesions (CAL) in Kawasaki disease (KD) patients.
- To identify independent risk factors for CAL development in KD.
Main Methods:
- Retrospective collection of clinical and laboratory data from KD patients (January 2016 - June 2023).
- Development of a predictive nomogram using logistic regression on a training set.
- Validation of the nomogram's performance using calibration and ROC curves in a verification set.
Main Results:
- Younger age, fever duration ≥10 days, elevated C-reactive protein, and lower hemoglobin/albumin were independent risk factors for CAL.
- The predictive nomogram demonstrated good discriminatory power (AUC 0.764 in training set, 0.798 in verification set).
Conclusions:
- A predictive nomogram incorporating five key risk factors can facilitate individualized CAL risk assessment in KD patients.
- This tool aids clinicians in early identification and management of KD patients at risk for CAL.
Abstract:
As an acute systemic vasculitis, Kawasaki disease (KD) could develop coronary artery lesions (CAL) sometimes. However, its etiology was still unidentified. This study was to construct a predictive model based on clinical features and laboratory parameters, and then perform a rapid risk assessment of CAL. We collected clinical and laboratory data retrospectively for all patients with KD who were hospitalized at our hospital from January 2016 to June 2023. All the patients were divided into CAL and non-CAL groups and then randomly assigned to a training set and a verification set. The independent risk variables of CAL were identified by univariate analysis and multivariate logistic regression analysis of the training set. These components were then utilized to build a predictive nomogram. Calibration curve and receiver operating characteristic curve were used to evaluate the performance of the model. The predictive nomogram was further validated in the verification set. In the training set, 49 KD patients (19.9%) showed CAL. Compared with the non-CAL group, the proportion of fever days ≥ 10, C-reactive protein and total bilirubin were significantly higher in the CAL group, whereas age was younger, hemoglobin and albumin were lower. Younger age, fever days ≥ 10, higher C-reactive protein, lower hemoglobin and albumin were identified as independent risk factors for CAL in KD patients. The nomogram constructed using these factors showed satisfactory calibration degree and discriminatory power (the area under the curve, 0.764). In the verification set, the area under the curve was 0.798. Younger age, fever days ≥ 10, lower hemoglobin and albumin levels, higher C-reactive protein levels were independent risk factors for CAL in KD patients. The predictive nomogram constructed utilizing 5 relevant risk factors could be conveniently used to facilitate the individualized prediction of CAL in KD patients.
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