Artificial intelligence differentiates abdominal Henoch‐Schönlein purpura from acute appendicitis in children

Author:

Nie Dan1,Zhan Yishan2,Xu Kun2,Zou Haibo1,Li Kehao1,Chen Leifeng3,Chen Qiang2,Zheng Weiming4,Peng Xiaojie4,Yu Mengjie5ORCID,Zhang Shouhua1

Affiliation:

1. Department of General Surgery Jiangxi Provincial Children's Hospital Nanchang Jiangxi China

2. Department of Rheumatology and Immunology Jiangxi Provincial Children's Hospital Nanchang Jiangxi China

3. Department of General Surgery Second Affiliated Hospital of Nanchang University Nanchang Jiangxi China

4. Department of Nephrology Jiangxi Provincial Children's Hospital Nanchang Jiangxi China

5. Key Laboratory of Drug Metabolism and Pharmacokinetics China Pharmaceutical University Nanjing Jiangsu China

Abstract

AbstractObjectiveThis study aims to construct an artificial intelligence (AI) model capable of effectively discriminating between abdominal Henoch‐Schönlein purpura (AHSP) and acute appendicitis (AA) in pediatric patients.MethodsA total of 6965 participants, comprising 2201 individuals with AHSP and 4764 patients with AA, were enrolled in the study. Additionally, 53 laboratory indicators were taken into consideration. Five distinct artificial intelligence (AI) models were developed employing machine learning algorithms, namely XGBoost, AdaBoost, Gaussian Naïve Bayes (GNB), MLPClassifier (MLP), and support vector machine (SVM). The performance of these prediction models was assessed through receiver operating characteristic (ROC) curve analysis, calibration curve assessment, and decision curve analysis (DCA).ResultsWe identified 32 discriminative indicators (p < .05) between AHSP and AA. Five indicators, namely the lymphocyte ratio (LYMPH ratio), eosinophil ratio (EO ratio), eosinophil count (EO count), neutrophil ratio (NEUT ratio), and C‐reactive protein (CRP), exhibited strong performance in distinguishing AHSP from AA (AUC ≥ 0.80). Among the various prediction models, the XGBoost model displayed superior performance evidenced by the highest AUC (XGBoost = 0.895, other models < 0.89), accuracy (XGBoost = 0.824, other models < 0.81), and Kappa value (XGBoost = 0.621, other models < 0.60) in the validation set. After optimization, the XGBoost model demonstrated remarkable diagnostic performance for AHSP and AA (AUC > 0.95). Both the calibration curve and decision curve analysis suggested the promising clinical utility and net benefits of the XGBoost model.ConclusionThe AI‐based machine learning model exhibits high prediction accuracy and can differentiate AHSP and AA from a data‐driven perspective.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

Rheumatology

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