Admission Circulating Cell-Free DNA Levels as a Prognostic Factor in Pediatric Burns

D Halpern1, A Cohen2, N Sharon2

  • 1Joyce & Irving Goldman Medical School, Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheba, Israel.

Insights

Admission levels of cell-free DNA (cfDNA) show promise in assessing pediatric burn severity. Higher cfDNA levels correlate with more severe burns and longer hospital stays, offering a potential new objective measure for burn care.

Area of Science:

  • Biochemistry
  • Pediatric Medicine
  • Trauma Care

Background:

  • Pediatric burn injuries represent a significant source of trauma with lasting effects.
  • Current methods for evaluating burn extent upon admission lack precision.
  • Circulating cell-free DNA (cfDNA) is emerging as a potential biomarker for tissue damage in burn management.

Purpose of the Study:

  • To investigate the utility of cfDNA levels at admission as a prognostic indicator for pediatric burn severity and patient outcomes.
  • To establish cfDNA as an objective tool for assessing burn injury severity.

Main Methods:

  • Quantified cfDNA levels in 38 pediatric burn patients and 12 matched controls using a direct fluorometric assay.
  • Compared cfDNA levels between burn patients and controls, and between partial-thickness and full-thickness burns.
  • Analyzed correlations between cfDNA levels and hospitalization duration, surgical procedures, and PICU admission.

Main Results:

  • Pediatric burn patients exhibited significantly higher admission cfDNA levels than controls (p=0.03).
  • Full-thickness burns showed significantly higher cfDNA levels compared to partial-thickness burns (p=0.01).
  • cfDNA levels significantly correlated with hospitalization duration (R=0.42, p<0.01) and need for surgery (R=0.40, p<0.01).

Conclusions:

  • Admission cfDNA levels may serve as a valuable objective tool for assessing pediatric burn severity.
  • The findings suggest cfDNA is a promising novel method for pediatric burn assessment.
  • Further research with larger cohorts and age-standardized healthy children is needed to validate cfDNA as a prognostic factor.
Abstract

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