Bedside clinical prediction tool for mortality in critically ill children

Kanokkarn Sunkonkit1,2,3, Chatree Chai-Adisaksopha2,3,4, Rungrote Natesirinilkul5

  • 1Department of Pediatrics, Division of Pulmonary and Sleep Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

Plos One
|April 24, 2025
PubMed

Insights

A new score using clinical data and hemogram predicts mortality in critically ill children. This tool helps identify high-risk pediatric intensive care unit (PICU) patients for better resource allocation.

Area of Science:

  • Pediatric Critical Care Medicine
  • Clinical Prediction Modeling
  • Hemostasis and Thrombosis

Background:

  • Pediatric intensive care unit (PICU) mortality remains a significant challenge.
  • Identifying high-risk pediatric patients is crucial for resource allocation.
  • Predictive tools are needed to improve outcomes for critically ill children.

Purpose of the Study:

  • To develop a prediction score for 28-day PICU mortality.
  • To utilize clinical parameters and hemogram data for risk stratification.
  • To identify key predictors of mortality in critically ill children.

Main Methods:

  • Retrospective study of children (1 month to 18 years) admitted to the PICU.
  • Data collected between January 2018 and December 2022.
  • Multivariable logistic regression used to develop the prediction score, assessing calibration and discrimination.

Main Results:

  • The prediction score incorporates male gender, vasoactive drug use, and red blood cell distribution width (RDW) and platelet distribution width (PDW) levels.
  • Scores range from 0 to 8, with a cutoff of 5 identifying high-risk patients.
  • The model showed excellent discrimination (AuROC 0.86) with 82.8% sensitivity and 73.1% specificity.

Conclusions:

  • A novel score combining clinical and hemogram data can predict 28-day mortality in critically ill children.
  • The developed score shows potential for clinical application in risk stratification.
  • External validation is recommended before widespread clinical implementation.
Abstract