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Updated: Jul 2, 2026

Using a Chemical Biopsy for Graft Quality Assessment
Published on: June 17, 2020
Delayed graft function and long-term outcomes after deceased donor kidney transplantation: insights from mate-kidney
Oscar A Garcia Valencia1, Ahmed Zeen Alabedeen Alrifai1, Mohammed Y Mahgoub1
1Department of Medicine, Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, United States.
Abstract:
Delayed graft function (DGF) is a frequent complication after deceased donor kidney transplantation, yet its long-term impact remains understudied. Heterogeneous populations, short follow-up, and inadequate control of donor-related factors have limited prior studies. Using the Scientific Registry of Transplant Recipients (2005-2024), we evaluated the association between DGF and long-term graft outcomes, including a mate-kidney (same donor, discordant DGF status) analysis to isolate its independent effect. We identified 103,678 dialysis-dependent deceased donor kidney recipients maintained on tacrolimus and mycophenolate. Mixed-effects Cox models, adjusted for donor, recipient, immunologic, and procurement factors. DGF occurred in 30.1% of recipients and was associated with increased death-censored graft failure (HR 1.40; 95% CI 1.33-1.47) and overall graft failure (HR 1.27; 95% CI 1.23-1.31). DGF recipients had higher rejection rates at 6 (6.0% vs. 4.7%) and 12 months (8.9% vs. 7.3%), longer hospital stay, and higher 1-year rehospitalization. In the mate-kidney analysis (6,818 donors), DGF remained strongly associated with death-censored graft failure (HR 1.58; 95% CI 1.39-1.80) and overall graft failure (HR 1.35; 95% CI 1.25-1.46), confirming the independent effect of DGF. DGF is a strong predictor of adverse long-term outcomes irrespective of rejection and warrants targeted prevention strategies and intensified follow-up.
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