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Published on: June 21, 2024
Routine Doppler Ultrasonography Does Not Differentiate Acute Tubular Necrosis and Rejection in Early Pediatric Kidney
Ihtisham Ahmad1, Priyank Yadav2, Dheidan Alshammari3
1Temerty Faculty of Medicine, University of Toronto, Toronto, Canada.
Resistive index (RI) measurements do not reliably distinguish acute tubular necrosis (ATN) from rejection in pediatric kidney transplants (KT). Temporal RI trends reflect hemodynamic adaptation, not graft pathology, limiting its use as a standalone diagnostic tool.
Area of Science:
- Nephrology
- Pediatric Transplantation
- Diagnostic Imaging
Background:
- Distinguishing acute tubular necrosis (ATN) from rejection in pediatric kidney transplant (KT) recipients is challenging, often requiring invasive biopsies.
- Doppler ultrasound-derived resistive index (RI) is a noninvasive tool for assessing graft status, but its diagnostic value in children is not well-established.
Purpose of the Study:
- To evaluate the utility of RI in differentiating ATN from rejection in pediatric KT recipients.
- To assess the diagnostic accuracy of established RI thresholds in this population.
Main Methods:
- Retrospective cohort study of 296 pediatric KT recipients from 2000-2021.
- Patients were categorized into uncomplicated, ATN, or rejection groups based on biopsy results.
- RI was measured at multiple time points post-transplant (24h, 3, 6, 12 months); linear mixed-effects models analyzed temporal trends.
Main Results:
- No significant difference in median RI was observed between ATN and rejection groups for either surveillance or clinically indicated biopsies.
- Established RI thresholds (0.7, 0.8) lacked specificity for differentiating complications.
- RI showed a temporal increase post-transplant and inverse correlation with recipient age but no association with ATN or rejection.
Conclusions:
- RI thresholds and temporal trends are insufficient to differentiate ATN from rejection in pediatric KT.
- The observed temporal RI increase likely represents systemic hemodynamic adaptation, not graft-specific pathology.
- Multimodal approaches integrating RI with clinical and biochemical markers are needed for improved noninvasive graft monitoring.
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