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A donor risk index for graft loss in pediatric living donor kidney transplantation.

Heather L WasikCozumel S PruetteRebecca L RuebnerMara Ann McAdams-DeMarcoSheng ZhouAlicia M NeuDorry L SegevAllan B Massie
Published in: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons (2019)
Pediatric kidney transplant candidates often have multiple potential living donors (LDs); no evidence-based tool exists to compare potential LDs, or to decide between marginal LDs and deceased donor (DD) kidney transplantation (KT). We developed a pediatric living kidney donor profile index (P-LKDPI) on the same scale as the DD KDPI by using Cox regression to model the risk of all-cause graft loss as a function of living donor characteristics and DD KDPI. HLA-B mismatch (adjusted hazard ratio [aHR] per mismatch = 1.04 1.271.55 ), HLA-DR mismatch (aHR per mismatch = 1.02 1.231.49 ), ABO incompatibility (aHR = 1.20 3.268.81 ), donor systolic blood pressure (aHR per 10 mm Hg = 1.01 1.071.18 ), and donor estimated GFR (eGFR; aHR per 10 mL/min/1.73 m2 = 0.88 0.940.99 ) were associated with graft loss after LDKT. Median (interquartile range [IQR]) P-LKDPI was -25 (-56 to 12). 68% of donors had P-LKDPI <0 (less risk than any DD kidney) and 25% of donors had P-LKDPI >14 (more risk than median DD kidney among pediatric KT recipients during the study period). Strata of LDKT recipients of kidneys with higher P-LKDPI had a higher cumulative incidence of graft loss (39% at 10 years for P-LDKPI ≥20, 28% for 20> P-LKDPI ≥-20, 23% for -20 > P-LKDPI ≥-60, 19% for P-LKDPI <-60 [log rank P < .001]). The P-LKDPI can aid in organ selection for pediatric KT recipients by allowing comparison of potential LD and DD kidneys.
Keyphrases
  • kidney transplantation
  • blood pressure
  • small cell lung cancer
  • heart failure
  • risk factors
  • type diabetes
  • metabolic syndrome
  • young adults
  • epidermal growth factor receptor
  • heart rate
  • glycemic control