Impact of Extraction Time During Donation After Circulatory Death Organ Procurement on Kidney Function After Transplantation in The Netherlands.


Journal

Transplantation direct
ISSN: 2373-8731
Titre abrégé: Transplant Direct
Pays: United States
ID NLM: 101651609

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 20 01 2023
revised: 03 08 2023
accepted: 05 08 2023
medline: 13 10 2023
pubmed: 13 10 2023
entrez: 13 10 2023
Statut: epublish

Résumé

In The Netherlands, 60% of deceased-donor kidney offers are after donation after circulatory death. Cold and warm ischemia times are known risk factors for delayed graft function (DGF) and inferior allograft survival. Extraction time is a relatively new ischemia time. During procurement, cooling of the kidneys is suboptimal with ongoing ischemia. However, evidence is lacking on whether extraction time has an impact on DGF if all ischemic periods are included. Between 2012 and 2018, 1524 donation after circulatory death kidneys were procured and transplanted in The Netherlands. Donation and transplantation-related data were obtained from the database of the Dutch Transplant Foundation. The primary outcome parameter was the incidence of DGF. In our cohort, extraction time ranged from 14 to 237 min, with a mean of 62 min (SD 32). In multivariate logistic regression analysis, extraction time was an independent risk factor for incidence of DGF (odds ratio per minute increase 1.008; 95% confidence interval, 1.003-1.013; Considering all known ischemic periods during the donation after the circulatory death process, prolonged kidney extraction time increased the risk of DGF after kidney transplantation.

Sections du résumé

Background UNASSIGNED
In The Netherlands, 60% of deceased-donor kidney offers are after donation after circulatory death. Cold and warm ischemia times are known risk factors for delayed graft function (DGF) and inferior allograft survival. Extraction time is a relatively new ischemia time. During procurement, cooling of the kidneys is suboptimal with ongoing ischemia. However, evidence is lacking on whether extraction time has an impact on DGF if all ischemic periods are included.
Methods UNASSIGNED
Between 2012 and 2018, 1524 donation after circulatory death kidneys were procured and transplanted in The Netherlands. Donation and transplantation-related data were obtained from the database of the Dutch Transplant Foundation. The primary outcome parameter was the incidence of DGF.
Results UNASSIGNED
In our cohort, extraction time ranged from 14 to 237 min, with a mean of 62 min (SD 32). In multivariate logistic regression analysis, extraction time was an independent risk factor for incidence of DGF (odds ratio per minute increase 1.008; 95% confidence interval, 1.003-1.013;
Conclusions UNASSIGNED
Considering all known ischemic periods during the donation after the circulatory death process, prolonged kidney extraction time increased the risk of DGF after kidney transplantation.

Identifiants

pubmed: 37829246
doi: 10.1097/TXD.0000000000001538
pmc: PMC10566979
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e1538

Informations de copyright

Copyright © 2023 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc.

Déclaration de conflit d'intérêts

The authors declare no funding or conflicts of interest.

Références

Am J Transplant. 2011 Oct;11(10):2093-109
pubmed: 21883901
BJS Open. 2021 Jan 8;5(1):
pubmed: 33609374
Lancet. 2004 Nov 13-19;364(9447):1814-27
pubmed: 15541456
Am J Transplant. 2017 Mar;17(3):724-732
pubmed: 27593738
Transpl Int. 2022 Feb 09;35:10186
pubmed: 35221788
Transplantation. 2019 Apr;103(4):e79-e88
pubmed: 30418426
Transplantation. 2005 May 15;79(9):1195-9
pubmed: 15880069
Ann Surg. 2019 Apr;269(4):712-717
pubmed: 29166361
Br J Surg. 2020 Jun;107(7):e235
pubmed: 32383499
J Nephrol Ther. 2012;2012(Suppl 4):
pubmed: 32913667
Transplant Proc. 2010 Dec;42(10):3963-5
pubmed: 21168600
Ann Transl Med. 2016 Oct;4(20):397
pubmed: 27867949
Am J Transplant. 2011 Nov;11(11):2279-96
pubmed: 21929642
Transplantation. 2018 Nov;102(11):e466-e471
pubmed: 30048397
Br J Surg. 2020 Jan;107(1):87-95
pubmed: 31573084
Transplantation. 2007 Feb 15;83(3):247-53
pubmed: 17297393
Am J Transplant. 2016 Jan;16(1):181-93
pubmed: 26361242
Am J Transplant. 2016 Feb;16(2):700-3
pubmed: 26414911

Auteurs

Erika van Straalen (E)

Division of Hepatopancreatobiliary and Transplant Surgery, Department of Surgery, Erasmus Medical Center Transplant Institute, Rotterdam, The Netherlands.

Elsaline Rijkse (E)

Division of Hepatopancreatobiliary and Transplant Surgery, Department of Surgery, Erasmus Medical Center Transplant Institute, Rotterdam, The Netherlands.

AnneLoes van Staa (A)

Research Center Innovations in Care, Rotterdam University of Applied Sciences, The Netherlands.

Paul M Rebers (PM)

Division of Hepatopancreatobiliary and Transplant Surgery, Department of Surgery, Erasmus Medical Center Transplant Institute, Rotterdam, The Netherlands.

Hanneke J A M Hagenaars (HJAM)

Division of Hepatopancreatobiliary and Transplant Surgery, Department of Surgery, Erasmus Medical Center Transplant Institute, Rotterdam, The Netherlands.

Jacqueline van de Wetering (J)

Department of Nephrology, Erasmus Medical Center Transplant Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Jan N M Ijzermans (JNM)

Division of Hepatopancreatobiliary and Transplant Surgery, Department of Surgery, Erasmus Medical Center Transplant Institute, Rotterdam, The Netherlands.

Robert C Minnee (RC)

Division of Hepatopancreatobiliary and Transplant Surgery, Department of Surgery, Erasmus Medical Center Transplant Institute, Rotterdam, The Netherlands.

Classifications MeSH