ArticleFrontiers in cardiovascular medicine2026
Construction and subgroup validation of a predictive model for IVIG-resistance in kawasaki disease.
Article in Frontiers in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: Kawasaki disease is an acute immune vasculitis, and intravenous immunoglobulin (IVIG) therapy was an important treatment method, although a small proportion of children exhibited IVIG resistance. Our study aimed to construct a risk model for Kawasaki disease with IVIG resistance and to validate it across different clinical characteristic subgroups, with the goal of optimizing personalized and precise management to improve patient outcomes. Methods: We first compared various factors between the groups with and without IVIG resistance. Then, we used LASSO analysis to screen for factors that significantly predicted outcomes. The selected factors were used to develop the risk model. We evaluated the model using ROC curves, calibration curves, and decision curve analysis, and conducted internal validation through 5-fold cross-validation. Finally, we performed subgroup analyses based on age, sex, and other factors. Results: Through univariate analysis, LASSO analysis, and correlation analysis, we identified WBC, PLT, CRP, fever days, PLR, and ALT as key factors in constructing the risk model. The model achieved an area under the curve of 0.816 (95% CI: 0.775-0.857). Additionally, calibration curves, DCA, and 5-fold cross-validation demonstrated that the model had good predictive performance. The model's effectiveness was also satisfactory across various subgroups. Conclusions: Our study successfully constructed a risk model for Kawasaki disease with IVIG resistance in the Chinese population. The model demonstrated strong predictive ability and was validated across multiple subgroups, showing potential clinical application value.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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 OpenQuestion graph.