AI Article Synopsis

  • Kidney transplantation is the preferred treatment for children with end-stage kidney disease, with advancements in immunosuppression and donor-specific antibody (DSA) testing improving graft survival, though monitoring practices vary among centers.
  • A survey conducted among pediatric transplant nephrologists revealed that most centers monitor DSA every three months in the first year post-transplant, using antibody levels and creatinine increase as key indicators for patient management.
  • The findings highlight variability in practices, with many centers planning increased monitoring and immunosuppression after dnDSA detection, suggesting a need for standardized guidelines in pediatric kidney transplant care.

Article Abstract

Background: Kidney transplantation (KT) is the preferred treatment for children with end-stage kidney disease. Recent advances in immunosuppression and advances in donor specific antibody (DSA) testing have resulted in prolonged allograft survival; however, standardized approaches for surveillance DSA monitoring and management of de novo (dn) DSA are widely variable among pediatric KT programs.

Methods: Pediatric transplant nephrologists in the multi-center Improving Renal Outcomes Collaborative (IROC) participated in a voluntary, web-based survey between 2019 and 2020. Centers provided information pertaining to frequency and timing of routine DSA surveillance and theoretical management of dnDSA development in the setting of stable graft function.

Results: 29/30 IROC centers responded to the survey. Among the participating centers, screening for DSA occurs, on average, every 3 months for the first 12 months post-transplant. Antibody mean fluorescent intensity and trend most frequently directed changes in patient management. Increased creatinine above baseline was reported by all centers as an indication for DSA assessment outside of routine surveillance testing. 24/29 centers would continue to monitor DSA and/or intensify immunosuppression after detection of antibodies in the setting of stable graft function. In addition to enhanced monitoring, 10/29 centers reported performing an allograft biopsy upon detection of dnDSA, even in the setting of stable graft function.

Conclusions: This descriptive report is the largest reported survey of pediatric transplant nephrologist practice patterns on this topic and provides a reference for monitoring dnDSA in the pediatric kidney transplant population.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305844PMC
http://dx.doi.org/10.1111/petr.14498DOI Listing

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