ArticleTranslational pediatrics2026
A nomogram model for early recognition of acute necrotizing encephalopathy: a retrospective study.
Article in Translational pediatrics, 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
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Acute necrotizing encephalopathy (ANE) is an infection-associated encephalopathy characterized by acute onset and poor prognosis. Currently, there is a lack of effective prediction models for its early identification. To address this gap, we developed and validated a nomogram model for the early identification of ANE in pediatric patients. Methods: This retrospective study analyzed children presenting with seizures or consciousness disorders following coronavirus disease 2019 (COVID-19) or influenza infection at Children's Hospital of Soochow University between November 2021 and February 2024. The single-center patient data were stratified into ANE/non-ANE groups, and then randomly divided into training and validation cohorts at a 7:3 ratio for internal validation. Logistic and least absolute shrinkage and selection operator (LASSO) regression were used to identify risk factors for ANE, and a nomogram was subsequently developed. The model's performance was validated using the area under the curve (AUC) and the area under the precision-recall curve (AUPRC), and further validated through calibration curve and decision curve analysis (DCA). Results: Altered consciousness, aspartate aminotransferase (AST), lactate dehydrogenase (LDH), and blood urea nitrogen (BUN) were independently associated with ANE development. A nomogram model incorporating these four factors demonstrated high predictive performance, with AUC values of 0.961 and 0.978, and AUPRC values of 0.792 and 0.809 in the training and validation cohorts, respectively. Calibration curves, DCA, and clinical impact curves further indicated the model's accuracy in predicting ANE onset. Conclusions: Our nomogram model provides a novel tool for the early identification of children at high risk of ANE, assisting clinicians in formulating timely interventions to improve patient prognosis.
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.