AI Article Synopsis

  • Delayed graft function (DGF) is a frequent issue after kidney transplants, often requiring surveillance biopsies to assess the condition of the graft.
  • This study analyzed 356 biopsies from 335 deceased donor transplant recipients during the DGF period to identify histological findings and risk factors affecting graft outcomes.
  • Key findings revealed that acute tubular necrosis, acute rejection, and borderline changes were common in biopsies, with recipient age and DGF duration linked to rejection risk, while anti-thymocyte globulin therapy was protective.

Article Abstract

Delayed graft function (DGF) is a common complication of kidney transplantation and frequently leads to the necessity of surveillance biopsies. The purpose of this study is to describe the histological findings in surveillance biopsies of deceased donor kidney transplant recipients and evaluate the risk factors for graft outcomes. This is a monocentric, retrospective study including kidney transplant recipients that underwent a graft biopsy during the DGF period between January 2006 and July 2019. 356 biopsies were performed in 335 deceased donor transplant recipients. Biopsies were analyzed according to the Banff classification. The main histological findings were: acute tubular necrosis in 150 biopsies (42.1%), acute rejection in 96 biopsies (26.9%), and borderline findings in 91 biopsies (25.5%). In the multivariate analysis, recipient age ( = 0.028) and DGF duration ( = 0.005) were associated with rejection, antibody-induction with anti-thymocyte globulin (ATG) was protective ( = 0.001). The occurrence of rejection was associated with lower death-censored graft survival (log-rank; = 0.009). Surveillance biopsies of kidney grafts experiencing DGF remain an essential tool for the care of kidney transplant recipients. The recipient's age and duration of DGF are independent risk factors for acute rejection, while antibody-induction therapy with ATG is associated with protection from its occurrence.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988887PMC
http://dx.doi.org/10.3389/ti.2022.10344DOI Listing

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