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Nephrology Dialysis Transplantation, Vol 13, Issue 3 704-710, Copyright © 1998 by Oxford University Press


ORIGINAL ARTICLES

Race and delayed kidney allograft function

H Feldman, J Burns, D Roth, J Berlin, L Szczech, R Gayner, S Kushner, K Brayman and R Grossman
Center for Clinical Epidemiology and Biostatistics and the Department of Biostatistics and Epidemiology, Renal Electrolyte and Hypertension Division, Department of Medicine, University of Pennsylvania, Philadelphia, PA, USA; Division of Nephrology, St Lukes Hospital, Bethlehem, PA, USA; Health Management Services, SmithKline Beecham, Philadelphia, PA, USA; Department of Surgery, University of Pennsylvania, Philadelphia, PA, USA; Corresponding author at: University of Pennsylvania Medical Center, Center for Clinical Epidemiology and Biostatistics, 720 Blockley Hall, 423 Guardian Drive, Philadelphia, PA 19104-6201, USA

Background: Allograft survival among black recipients is poorer than among whites. Delayed allograft function is associated with a significant reduction in renal allograft survival. The relationship between delayed allograft function and black race is incompletely specified and was the focus of this investigation. Methods: A non-concurrent study of 325 recipients of cadaveric allografts followed for the occurrence of delayed allograft function defined as dialysis during the first week following transplantation for the principal analysis. A secondary definition of delayed allograft function was formulated based on the serum creatinine 2 weeks after transplantation. Unadjusted and adjusted logistic regression analysis were used to examine the unconfounded relationship between race and delayed allograft function. Results: Fifty-seven of 91 (62.6%) black recipients experienced delayed allograft function compared to 113 of 234 (48.3%) whites. The odds ratio for black race as a predictor of delayed allograft function was 1.80, P=0.02, (95% CI, 1.09, 2.85). This finding was stable despite adjustment for other predictors of delayed allograft function in a multivariate model, but the precision of this estimate was less (P=0.10) because of missing data. Additionally, adjusted models with imputed values for missing covariates, models using a secondary definition of delayed allograft function, and models excluding patients whose cyclosporin therapy was delayed, all consistently demonstrated a similar association between black race and delayed allograft function. Conclusions: This study demonstrated an increased risk of delayed allograft function among black recipients. This relationship may play a role in the poorer allograft outcomes experienced by black recipients. Given the negative effect of delayed allograft function on allograft survival, efforts to identify its modifiable risk factors should be a high priority. Key words: cadaveric allograft; delayed allograft function; kidney transplantation; logistic regression analysis
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