Evidence map›Paper›PMID 40722434›Full record

ArticleBioengineering (Basel, Switzerland)2025

A Multi-Stage Framework for Kawasaki Disease Prediction Using Clustering-Based Undersampling and Synthetic Data Augmentation: Cross-Institutional Validation with Dual-Center Clinical Data in Taiwan.

Heng-Chih Huang, Chuan-Sheng Hung, Chun-Hung Richard Lin, Yi-Zhen Shie, Cheng-Han Yu, Ting-Hsin Huang

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Heng-Chih HuangDepartment of Computer Science and Engineering, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.ORCID 0009-0005-8233-7081
Chuan-Sheng HungDepartment of Computer Science and Engineering, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.ORCID 0009-0008-6290-0967
Chun-Hung Richard LinDepartment of Computer Science and Engineering, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.ORCID 0000-0003-0840-394X
Yi-Zhen ShieDepartment of Computer Science and Engineering, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.
Cheng-Han YuDepartment of Computer Science and Engineering, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.
Ting-Hsin HuangDepartment of Computer Science and Engineering, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.ORCID 0000-0002-6338-4908

Funding

National Science and Technology Council of TAIWAN NSTC 113-2622-E-110-017
6 · The paper itself

Abstract

Kawasaki disease (KD) is a rare yet potentially life-threatening pediatric vasculitis that, if left undiagnosed or untreated, can result in serious cardiovascular complications. Its heterogeneous clinical presentation poses diagnostic challenges, often failing to meet classical criteria and increasing the risk of oversight. Leveraging routine laboratory tests with AI offers a promising strategy for enhancing early detection. However, due to the extremely low prevalence of KD, conventional models often struggle with severe class imbalance, limiting their ability to achieve both high sensitivity and specificity in practice. To address this issue, we propose a multi-stage AI-based predictive framework that incorporates clustering-based undersampling, data augmentation, and stacking ensemble learning. The model was trained and internally tested on clinical blood and urine test data from Chang Gung Memorial Hospital (CGMH, n = 74,641; 2010-2019), and externally validated using an independent dataset from Kaohsiung Medical University Hospital (KMUH, n = 1582; 2012-2020), thereby supporting cross-institutional generalizability. At a fixed recall rate of 95%, the model achieved a specificity of 97.5% and an F1-score of 53.6% on the CGMH test set, and a specificity of 74.7% with an F1-score of 23.4% on the KMUH validation set. These results underscore the model's ability to maintain high specificity even under sensitivity-focused constraints, while still delivering clinically meaningful predictive performance. This balance of sensitivity and specificity highlights the framework's practical utility for real-world KD screening.

Indexed as

class imbalanceclusteringdata augmentationensemble learningKawasaki disease

Identifiers

PMID40722434
PMCPMC12292631

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.