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Outcomes with transplanting kidneys offered through expedited allocation.

Authors :
Jadlowiec CC
Ohara SY
Punukollu R
Wagler J
Ruch B
Kumm K
Budhiraja P
Me HM
Mathur AK
Reddy KS
Khamash H
Heilman R
Source :
Clinical transplantation [Clin Transplant] 2023 Nov; Vol. 37 (11), pp. e15094. Date of Electronic Publication: 2023 Aug 10.
Publication Year :
2023

Abstract

Introduction: Expedited out-of-sequence deceased donor kidney allocation is a strategy to avoid discards after early placement attempts have been unsuccessful. Our study aimed to assess outcomes and characteristics of these transplanted kidneys.<br />Methods: KDPI matching was performed between expedited allocation (EA) and standard allocation (SA) deceased donor kidney transplants performed at our center.<br />Results: Between 2018 and 2021, there were 225 EA offers, and 189 (84%) were transplanted. EA recipients were older (p = .007) and had shorter dialysis vintage (p < .0001). EA kidneys were likely to be nationally allocated (p < .001), have AKI (p < .0001) and longer CIT (p < .0001). There were no differences in EA and SA time-zero kidney biopsies (ci, p = .07; ct, p = .89; cv, p = .95; ah, p = .79). EA kidneys had more DGF (p = .0006), but there were no differences in DGF duration (p = .83), hospital length of stay (p = .43), 1- and 2-year eGFR (p = .16, p = .99), patient (p = .34), or death-censored graft (p = .66) survival.<br />Conclusion: During this study period, our center transplanted 189 kidneys through EA following local-regional declines. These kidneys often came from AKI donors and had more DGF but had similar outcomes to KDPI-matched SA kidneys. Although it has been suggested that EA has the potential to worsen transplant disparities, transplant center level decisions on organ acceptance contribute to these variations.<br /> (© 2023 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1399-0012
Volume :
37
Issue :
11
Database :
MEDLINE
Journal :
Clinical transplantation
Publication Type :
Academic Journal
Accession number :
37563488
Full Text :
https://doi.org/10.1111/ctr.15094