Impact of donor transaminases on liver transplant utilisation and unnecessary organ discard: national registry cohort study.

Frontiers in transplantation Pub Date : 2024-09-04 eCollection Date: 2024-01-01 DOI:10.3389/frtra.2024.1458996
Joseph J Dobbins, Samuel J Tingle, Jennifer Mehew, Emily R Thompson, Georgios Kourounis, Stuart McPherson, Steve A White, Colin H Wilson
{"title":"Impact of donor transaminases on liver transplant utilisation and unnecessary organ discard: national registry cohort study.","authors":"Joseph J Dobbins, Samuel J Tingle, Jennifer Mehew, Emily R Thompson, Georgios Kourounis, Stuart McPherson, Steve A White, Colin H Wilson","doi":"10.3389/frtra.2024.1458996","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Donor liver transaminases (ALT and AST) have been used to decline livers for transplant, despite evidence that they do not influence transplant outcomes. This study assesses the effect that raised donor transaminases have on the unnecessary decline of livers.</p><p><strong>Methods: </strong>This retrospective cohort study used the National Health Service registry on adult liver transplantation (2016-2019). Logistic regression models were built to assess the impact of donor transaminases on the utilisation of organs donated following brain stem death (DBD) and circulatory death (DCD). A further model was used to simulate the impact on liver decline if raised donor ALT was not used to make utilisation decisions.</p><p><strong>Results: </strong>5,424 adult livers were offered for transplant, of which 3,605 were utilised (2,841 DBD, 764 DCD). In multivariable analysis, adjusted for key factors, increasing peak donor ALT independently increased the odds of liver decline (DBD aOR = 1.396, 1.305-1.494, <i>p</i> < 0.001, DCD aOR = 1.162, 1.084-1.246, <i>p</i> < 0.001). AST was also a significant predictor of liver decline. 18.5% of livers from DBD donors with ALT > 40 U/L (<i>n</i> = 1,683) were declined for transplantation. In this group, our model predicted a 48% (38%-58%) decrease in decline if raised donor ALT was excluded from these decisions. This represents an additional 37 (30-45) liver transplants every year in the UK.</p><p><strong>Conclusions: </strong>Raised donor ALT increased the likelihood of liver decline. As it does not influence transplant outcome, avoiding donor ALT-based organ decline is an immediate and effective way to expand the donor pool.</p>","PeriodicalId":519976,"journal":{"name":"Frontiers in transplantation","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11421386/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in transplantation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/frtra.2024.1458996","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Donor liver transaminases (ALT and AST) have been used to decline livers for transplant, despite evidence that they do not influence transplant outcomes. This study assesses the effect that raised donor transaminases have on the unnecessary decline of livers.

Methods: This retrospective cohort study used the National Health Service registry on adult liver transplantation (2016-2019). Logistic regression models were built to assess the impact of donor transaminases on the utilisation of organs donated following brain stem death (DBD) and circulatory death (DCD). A further model was used to simulate the impact on liver decline if raised donor ALT was not used to make utilisation decisions.

Results: 5,424 adult livers were offered for transplant, of which 3,605 were utilised (2,841 DBD, 764 DCD). In multivariable analysis, adjusted for key factors, increasing peak donor ALT independently increased the odds of liver decline (DBD aOR = 1.396, 1.305-1.494, p < 0.001, DCD aOR = 1.162, 1.084-1.246, p < 0.001). AST was also a significant predictor of liver decline. 18.5% of livers from DBD donors with ALT > 40 U/L (n = 1,683) were declined for transplantation. In this group, our model predicted a 48% (38%-58%) decrease in decline if raised donor ALT was excluded from these decisions. This represents an additional 37 (30-45) liver transplants every year in the UK.

Conclusions: Raised donor ALT increased the likelihood of liver decline. As it does not influence transplant outcome, avoiding donor ALT-based organ decline is an immediate and effective way to expand the donor pool.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
供体转氨酶对肝移植利用率和不必要的器官丢弃的影响:全国登记队列研究。
背景:供体肝脏转氨酶(谷丙转氨酶和谷草转氨酶)一直被用于拒绝移植肝脏,尽管有证据表明它们不会影响移植结果。本研究评估了捐献者转氨酶升高对不必要的肝脏衰竭的影响:这项回顾性队列研究使用了国家卫生服务局的成人肝移植登记表(2016-2019 年)。建立了逻辑回归模型,以评估供体转氨酶对脑干死亡(DBD)和循环死亡(DCD)后捐献器官利用率的影响。另一个模型用于模拟如果不使用捐赠者升高的谷丙转氨酶来做出利用决定,对肝脏衰退的影响:共提供了 5424 个成人肝脏用于移植,其中 3605 个得到利用(2841 个 DBD,764 个 DCD)。在对主要因素进行调整后的多变量分析中,供体ALT峰值的增加会独立增加肝脏衰竭的几率(DBD aOR = 1.396, 1.305-1.494, p p 40 U/L(n = 1,683))。在这组患者中,如果将供体 ALT 升高排除在这些决定之外,我们的模型预测肝功能下降率将下降 48% (38%-58%)。这意味着英国每年将增加37例(30-45例)肝移植:供体ALT升高会增加肝功能衰退的可能性。由于ALT不会影响移植结果,因此避免供体ALT升高导致器官衰竭是扩大供体库的一个直接有效的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Antibiotic subclasses differentially perturb the gut microbiota in kidney transplant recipients. Walter Brendel and the dawn of transplantation research in Germany. Propionic acid supplementation promotes the expansion of regulatory T cells in patients with end-stage renal disease but not in renal transplant patients. Impact of donor transaminases on liver transplant utilisation and unnecessary organ discard: national registry cohort study. The role of C4d and donor specific antibodies in face and hand transplantation-a systematic review.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1