Postcontrast Acute Kidney Injury in Pediatric Patients: A Cohort Study

Jennifer S McDonald1, Robert J McDonald1, Cheryl L Tran2

  • 1Department of Radiology, Mayo Clinic, Rochester, MN.

Insights

This study found very low rates of acute kidney injury (AKI), dialysis, and death in pediatric patients receiving iodinated contrast material for CT scans. The risks were not detectably different from those not receiving contrast, though an effect cannot be ruled out.

Area of Science:

  • Pediatric Nephrology
  • Radiology
  • Clinical Outcomes Research

Background:

  • The safety of iodinated contrast material in pediatric patients undergoing computed tomography (CT) scans is not well-established.
  • Assessing risks such as acute kidney injury (AKI), dialysis, and mortality is crucial for informed clinical decision-making.

Purpose of the Study:

  • To investigate the incidence of postcontrast AKI, dialysis therapy, and death in pediatric patients receiving intravenous iodinated contrast material.
  • To compare these outcomes between contrast-enhanced and unenhanced CT scans in a pediatric cohort.

Main Methods:

  • A retrospective cohort study was conducted on pediatric patients (<18 years) undergoing contrast-enhanced or unenhanced CT scans.
  • Propensity score analysis was used to compare risks of AKI, dialysis, and death between the two groups, adjusting for relevant covariates.
  • AKI was defined using KDIGO criteria based on serum creatinine.

Main Results:

  • The study identified 2,201 pediatric patients (1,773 contrast, 428 noncontrast).
  • Rates of AKI and dialysis in the contrast group were 3.3% and 0.1%, respectively.
  • After propensity score adjustment, no significant differences in the risk of AKI, dialysis, or death were observed between contrast and noncontrast groups. All severe AKI cases had alternative causes.

Conclusions:

  • Postcontrast AKI, dialysis therapy, and death occurred at very low rates in this pediatric cohort undergoing contrast-enhanced CT.
  • While not detectably different from the noncontrast group, the study's limitations (small sample size, low event rates) preclude ruling out a potential effect of contrast material.
  • Further research with larger cohorts may be needed to definitively assess contrast-related risks in pediatric patients.
Abstract

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