Donor Diabetes and Prolonged Cold Ischemia Time Synergistically Increase the Risk of Graft Failure After Liver Transplantation
Authors
Bruggenwirth, Isabel M. A.Dolgin, Natasha H.
Porte, Robert J.
Bozorgzadeh, Adel
Martins, Paulo N.A.
UMass Chan Affiliations
Department of Quantitative Health SciencesDepartment of Surgery, Division of Organ Transplantation
Document Type
Journal ArticlePublication Date
2017-06-12Keywords
Endocrine System DiseasesEndocrinology, Diabetes, and Metabolism
Nutritional and Metabolic Diseases
Surgery
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Show full item recordAbstract
BACKGROUND: Both prolonged cold ischemia time (CIT) and donor history of diabetes mellitus (DM) are associated with reduced graft survival after liver transplantation. However, it is unknown whether the adverse effect of prolonged CIT on posttransplant graft survival is more pronounced after transplant with DM versus non-DM donor grafts. METHODS: The study sample included 58 226 liver transplant recipients (2002-2015) from the Scientific Registry of Transplant Recipients. Multivariable Cox survival regression with interaction analysis was used to quantify the extent to which history of donor DM (n = 6478) potentiates the adverse effect of prolonged ( > /=8 hours) CIT (n = 18 287) on graft survival. RESULTS: Donor DM and CIT 8 hours or longer were each associated with increased risk of graft failure (GF) (adjusted hazard ratio [aHR], 1.19; 95% confidence interval [CI], 1.06-1.35 and aHR, 1.42; 95% CI, 1.32-1.53, respectively) compared with transplanted grafts without either risk factor. However, the combination of DM and CIT 8 hours or longer was associated with a higher risk of GF than either factor alone (aHR, 1.79; 95% CI, 1.55-2.06) and had a synergy index of 1.30. The interaction was significant on a multiplicative scale in the later postoperative period, days 31 to 365 (P = 0.047). CONCLUSIONS: These results suggest that liver grafts from DM donors are more susceptible to the adverse effects of prolonged CIT than livers from non-DM donors. We need to be cognizant that they are more susceptible to ischemic injury, and this may be considered during the allocation process.Source
Transplant Direct. 2017 Jun 12;3(7):e173. doi: 10.1097/TXD.0000000000000692. eCollection 2017 Jul. Link to article on publisher's siteDOI
10.1097/TXD.0000000000000692Permanent Link to this Item
http://hdl.handle.net/20.500.14038/40379PubMed ID
28706976Related Resources
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Copyright © 2017 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc.Distribution License
http://creativecommons.org/licenses/by-nc-nd/4.0/ae974a485f413a2113503eed53cd6c53
10.1097/TXD.0000000000000692
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Except where otherwise noted, this item's license is described as Copyright © 2017 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc.

