Abstract

Kawasaki disease (KD) is a form of systemic vasculitis that occurs in children under the age of 5 years old. Due to prolonged fever and elevated inflammatory markers that are found in both KD and sepsis, the treatment approach differs for each. We enrolled a total of 420 children (227 KD and 193 sepsis) in this study. Logistic regression and a nomogram model were used to analyze the laboratory markers. We randomly selected 247 children as the training modeling group and 173 as the validation group. After completing a logistic regression analysis, white blood cell (WBC), anemia, procalcitonin (PCT), C-reactive protein (CRP), albumin, and alanine transaminase (ALT) demonstrated a significant difference in differentiating KD from sepsis. The patients were scored according to the nomogram, and patients with scores greater than 175 were placed in the high-risk KD group. The area under the curve of the receiver operating characteristic curve (ROC curve) of the modeling group was 0.873, sensitivity was 0.893, and specificity was 0.746, and the ROC curve in the validation group was 0.831, sensitivity was 0.709, and specificity was 0.795. A novel nomogram prediction model may help clinicians differentiate KD from sepsis with high accuracy.

Highlights

  • Kawasaki disease (KD) is a form of systemic vasculitis that occurs in children under the age of 5 years old

  • Kawasaki disease (KD), known as cutaneous mucosal lymph node syndrome, is an acute, self-limiting vasculitis that is common in children under the age of 5 years old, with coronary aneurysms occurring in about 25% of untreated cases

  • We enrolled a total of 420 children in this study, including 254 males (60.5%), 166 females (39.5%), 227 KD patients (54.0%), and 193 sepsis patients (46.0%)

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Summary

Introduction

Kawasaki disease (KD) is a form of systemic vasculitis that occurs in children under the age of 5 years old. As well as effective treatment, can help reduce coronary artery lesions (CAL) and improve intravenous immunoglobulin (IVIG) treatment r­ esponse[3,4]. Both the etiology and pathogenesis of KD remain unclear. Antibiotics are unnecessary and ineffective for KD patients, while IVIG infusion with follow-up cardiac ultrasonography are the main treatment methods for ­KD2. Both KD and sepsis are characterized by fever and elevated inflammatory markers in the acute stage, but the treatments are very different.

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