Donor specific antibody surveillance among pediatric kidney transplant programs: A report from the improving renal outcome collaborative

Author:

Steinbach Emily J.1ORCID,Barletta Gina M.2ORCID,Patel Hiren P.3ORCID,Hooper David K.45ORCID,Garro Rouba6ORCID,Harshman Lyndsay A.1ORCID

Affiliation:

1. Division of Nephrology, Dialysis, and Transplantation University of Iowa Stead Family Children's Hospital Iowa City Iowa USA

2. Department of Pediatric Nephrology Phoenix Children's Hospital Phoenix Arizona USA

3. Division of Nephrology and Hypertension Nationwide Children's Hospital Columbus Ohio USA

4. Division of Nephrology and Hypertension Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

5. University of Cincinnati College of Medicine Cincinnati Ohio USA

6. Emory School of Medicine Children's Healthcare of Atlanta Atlanta Georgia USA

Abstract

AbstractBackgroundKidney 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.MethodsPediatric 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.Results29/30 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.ConclusionsThis 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.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Wiley

Subject

Transplantation,Pediatrics, Perinatology and Child Health

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