ArticleTranslational pediatrics2026
Development and internal validation of a prognostic nomogram for poor outcomes in neonatal bacterial meningitis.
Article in Translational pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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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.
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Who cites it
2 citing papers in PubMed.
- Response to letter regarding "Development and internal validation of a prognostic nomogram for poor outcomes in neonatal bacterial meningitis".Translational pediatrics · 2026Article
- Risk stratification regarding an unfavourable course of bacterial meningitis in newborns requires consideration of all influencing factors.Translational pediatrics · 2026Article
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3 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Background: Neonatal bacterial meningitis (NBM) remains a life-threatening condition with considerable mortality and long-term neurodevelopmental impairment. Early prognostic assessment is challenging, and prediction models tailored to neonates are limited. This study aimed to develop and internally validate a prognostic nomogram for predicting poor outcomes in neonates with bacterial meningitis. Methods: A retrospective cohort study was conducted including 214 neonates diagnosed with bacterial meningitis between 2011 and 2024. Independent predictors of poor outcome were identified using Firth penalized logistic regression to reduce small-sample bias. A prognostic nomogram was developed and internally validated using bootstrap resampling to assess model performance. Results: Among the 214 neonates, 83 (38.8%) experienced poor outcomes. Lower gestational age, seizures, elevated cerebrospinal fluid (CSF) protein, and reduced CSF glucose were independently associated with poor prognosis. The model demonstrated good discrimination, with an area under the curve (AUC) of 0.79 [95% confidence interval (CI): 0.72-0.85] and an optimism-corrected C-index of 0.77 after bootstrap validation. Calibration analysis showed good agreement between predicted and observed probabilities. Decision curve analysis suggested net clinical benefit across threshold probabilities ranging from 0.05 to 0.65. Conclusions: This model integrates inflammatory biomarkers reflecting central nervous system injury with clinical parameters, providing a potential bridge between pathophysiological mechanisms and bedside risk stratification. External validation in independent cohorts is warranted prior to routine clinical application.
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