Abstract:Summary
Prolonged cold ischemia time (CIT) is associated with delayed graft function and worse kidney transplant (KT) outcome, but the effect of CIT on long‐term allograft survival in KT from younger donors has not been well established. We investigated the predictive value of CIT exposure on long‐term death‐censored graft loss in 829 KT recipients from younger donors (<50 years) that were performed in our center between 1991 and 2005. Overall death‐censored graft failure rate was significantly higher in CIT≥1… Show more
“…Similar to our findings, among post‐transplant factors, the adverse impact of DGF and acute rejection on long‐term outcomes has also been described by numerous authors (15, 20, 25, 26). However, these factors are not available for decision making during a kidney offer.…”
“…Similar to our findings, among post‐transplant factors, the adverse impact of DGF and acute rejection on long‐term outcomes has also been described by numerous authors (15, 20, 25, 26). However, these factors are not available for decision making during a kidney offer.…”
“…However, shipped allografts with no HLA mismatches had similar graft survival compare to locally‐transplanted allografts with no HLA mismatches. This finding is consistent with a single‐centre study demonstrating that extended cold ischaemic time was independently associated with increased graft loss in renal transplantation (cold ischaemic time ≥19 h compared to <19 h; relative risk 1.5, 95% CI 1.1–2.1, P = 0.023) 5 . In addition, longer duration of allograft ischaemia has been associated with increased risk of DGF and rejection but this association is inconsistent 6,7 .…”
“…These results have been confirmed by additional studies [16,17]. In addition, inflammation, oxidative stress and the apoptotic machinery activated by reperfusion may exacerbate the renal hypoxic insult [18].…”
Our data reveal, for the first time, that sulodexide, alone or combined to low doses of everolimus, may hinder EMT in renal cells following hypoxia or minimize fibrotic complications due to high dosage of mammalian target of rapamycin inhibitors.
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