2018
DOI: 10.1016/j.nefroe.2017.12.003
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Validation of KDRI/KDPI for the selection of expanded criteria kidney donors

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Cited by 8 publications
(7 citation statements)
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“…Third, the (L)KDPI in the investigated cohort correlated well with chronic lesions such as arteriosclerosis, glomerulosclerosis and IF/TA giving reason to expected lower graft quality of marginal donor kidneys, which was shown previously (34). This correlation was also observed in a study on pre-implantation biopsies (35). Kidney grafts can also be evaluated by pretransplant donor biopsies, but due to a high heterogeneity in biopsy-technique, histological evaluation, and study design no valuable recommendation can be derived to include pretransplant donor biopsies into daily routine (36).…”
Section: Discussionsupporting
confidence: 80%
“…Third, the (L)KDPI in the investigated cohort correlated well with chronic lesions such as arteriosclerosis, glomerulosclerosis and IF/TA giving reason to expected lower graft quality of marginal donor kidneys, which was shown previously (34). This correlation was also observed in a study on pre-implantation biopsies (35). Kidney grafts can also be evaluated by pretransplant donor biopsies, but due to a high heterogeneity in biopsy-technique, histological evaluation, and study design no valuable recommendation can be derived to include pretransplant donor biopsies into daily routine (36).…”
Section: Discussionsupporting
confidence: 80%
“…A critic of this KDPI based rule is that a high KDPI in pediatric donors is because of low weight, height, and age but kidneys are histologic pristine, and as shown in this study hyperfiltration injury is of limited impact. This is in stark comparison to high KDPI adult kidneys, which often present some chronic kidney injury [23,24]. Considering the high thrombosis rate, one issue is the transplantation of SPD into pediatric recipients, where vascular anastomosis involving small-donor arteries may increase the risk of thrombosis [25].…”
Section: Discussionmentioning
confidence: 99%
“…The second goal of KDRI introduction was to limit the percentage of discarded kidneys [ 13 ]. Nevertheless, in the USA and in some European countries the in-depth quality assessment of marginal kidneys is based mainly on the pre-implantation biopsy [ 7 , 14 , 15 ], the utility of which for predicting transplant outcomes is limited [ 16 , 17 ]. On the other hand, it has been suggested that chronic histological changes identified in early post-reperfusion biopsies better correlate with graft outcomes [ 18 , 19 ].…”
Section: Introductionmentioning
confidence: 99%