Evidence map›Paper›PMID 41476738›Full record

ArticlePediatric discovery2025

A new prediction diagnosis model of incomplete Kawasaki disease based on data mining with big data.

Zhen Yang, Bo Pan, Jia Liu, Haolin Wang, Jie Tian

Abstract read
In one paragraph

Article in Pediatric discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

5 authors.

Zhen YangDepartment of Cardiology Children's Hospital of Chongqing Medical University Chongqing China.ORCID https://orcid.org/0009-0000-4726-081X
Bo PanDepartment of Cardiology Children's Hospital of Chongqing Medical University Chongqing China.ORCID https://orcid.org/0009-0001-2139-1632
Jia LiuDepartment of Cardiology Children's Hospital of Chongqing Medical University Chongqing China.
Haolin WangCollege of Medical Informatics Chongqing Medical University Chongqing China.
Jie TianDepartment of Cardiology Children's Hospital of Chongqing Medical University Chongqing China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

age groupingdata miningincomplete Kawasaki diseaseindependent risk factorsprediction model

Identifiers

PMID41476738
PMCPMC12753023

What Socratic holds

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LicenceCC BY
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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.