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Performance of PRISM III and PELOD-2 scores in a pediatric intensive care unit

Jean-Pierre Gonçalves1,2, Milton Severo3,4, Carla Rocha5

  • 1Pediatric Intensive Care Unit, Pediatric Integrated Hospital, São João Hospital, Alameda Professor Hernâni Monteiro, 4200-319, Porto, Portugal. pierre_3.14r@hotmail.com.

Insights

The Pediatric Risk of Mortality III (PRISM III) and Pediatric Logistic Organ Dysfunction 2 (PELOD-2) scores showed good mortality prediction in a Portuguese pediatric intensive care unit. However, PELOD-2 requires recalibration for improved reliability.

Area of Science:

  • Pediatric intensive care
  • Clinical epidemiology
  • Health services research

Background:

  • Pediatric Risk of Mortality III (PRISM III) and Pediatric Logistic Organ Dysfunction (PELOD) scores are established tools for assessing pediatric intensive care unit (PICU) performance and predicting mortality.
  • The newer Pediatric Logistic Organ Dysfunction 2 (PELOD-2) score has demonstrated good discrimination and calibration in previous validations.
  • This study evaluates and recalibrates these scores within a specific Portuguese pediatric population.

Purpose of the Study:

  • To compare the predictive performance of the PRISM III and PELOD-2 scores for mortality in a Portuguese PICU.
  • To recalibrate the PELOD-2 score for the Portuguese population to enhance its predictive accuracy.
  • To assess the discrimination and calibration of both scoring systems.

Main Methods:

  • A prospective cohort study was conducted, including 556 consecutive patients admitted to a PICU between January 2011 and December 2012.
  • The performance of PRISM III and PELOD-2 was evaluated using standardized mortality ratio, discrimination (Area Under the Receiver Operating Characteristic curve), and calibration (Hosmer and Lemeshow goodness-of-fit test).
  • Statistical analysis was performed to compare the observed mortality with the predicted mortality from both scores.

Main Results:

  • Both PRISM III and PELOD-2 demonstrated good discrimination, with Area Under the ROC Curve values of 0.92 and 0.94, respectively.
  • The observed mortality was 29 patients, while PRISM III predicted 30.8 deaths and PELOD-2 predicted 22.1 deaths.
  • The Hosmer and Lemeshow test indicated good calibration for PRISM III (p=0.282) but poor calibration for PELOD-2 (p=0.022).

Conclusions:

  • Both PRISM III and PELOD-2 exhibit strong discriminatory power for mortality prediction in the studied pediatric intensive care unit population.
  • The PELOD-2 score requires recalibration to improve its reliability and accuracy in this specific Portuguese cohort.
  • PRISM III demonstrated adequate calibration, suggesting its suitability for use in this population without immediate recalibration.
Abstract