Cold ischemia is a major determinant of acute rejection and renal graft survival in the modern era of immunosuppressionCold ischemia is a major determinant of acute rejection and renal graft survival in the modern era of immunosuppression
Faculty of Medicine and Health Sciences
Publication type
Baltimore, Md,
Human medicine
Source (journal)
Transplantation. - Baltimore, Md, 1963, currens
85(2008):7s:[S], p. S3-S9
Target language
English (eng)
Full text (Publishers DOI)
Background. The aim of our study was to examine, in a recent cohort of kidney transplant recipients who have received modern inummosuppressive therapy, the respective role of cold ischernia time (CIT) and delayed graft function (DGF) on acute rejection (AR) rates and long-term graft survival. Methods. We retrospectively reviewed the charts of 611 renal transplantations between 1996 and 2005. Most patients received a calcineurin inhibitor as maintenance therapy, either cyclosporine (43%) or tacrolimus (52%) and 76% of the patients received an antilymphocyte induction therapy. Study endpoints were DGF, first-year AR, and long-term graft survival. Uni- and multivariate analyses were performed to determine factors that may have influenced the study outcomes. Results. DGF was observed in 16.2% of patients. Both older donor age and longer CIT were significant risk factors for DGF. DGF rates were similar whether patients received a calcineurin inhibitor before transplantation or not. AR occurred in 16.5% of grafts during the first year. Independent predictors of AR by multivariate analysis were duration of dialysis, CIT, current panel-reactive lymphocytotoxic antibody more than 5%, and the number of human leukocyte antigen-A, B, and DR mismatches. Each hour of cold ischernia increases the risk of rejection by 4%. With respect to death-censored graft survival, three pretransplant parameters emerged as independent predictors of graft loss: younger recipient age, peak panel-reactive lymphocytotoxic antibody more than 5% and longer CIT. The detrimental effect of CIT on graft survival was entirely because of its propensity to trigger AR. When AR was added to the multivariate Cox model, CIT was no longer significant whereas first-year AR became the most important predictor of graft loss (Hazards ratio, 4.6). Conclusion. Shortening CIT will help to decrease not only DGF rates but also AR incidence and hence graft loss. Patients with prolonged CIT should receive adequate immunosuppression, possibly with antilymphocyte preparations, to prevent AR occurrence.