Normothermic regional perfusion in controlled DCD liver procurement: Outcomes of the Swedish national implementation protocol.

IF 4.7 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Liver Transplantation Pub Date : 2024-11-01 Epub Date: 2024-07-23 DOI:10.1097/LVT.0000000000000434
Emil Bluhme, Markus Gäbel, Lilia Martinez de la Maza, Vera Nilsén, Karin Hildebrand, Jenni Jarsäter, Cecilia Bååth, Matilda Proos, Antonio Romano, Christina Villard, Gabriel C Oniscu, Niklas Gustafsson, Monica Thompson, Christoffer Hansson, Margareta Löfstedt, Jonas Andersson Lindholm, Lars Falk, William Bennet, Carl Jorns
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Abstract

Liver transplantation (LTX) using donors after controlled circulatory death (cDCD) is associated with poorer graft survival and increased incidence of nonanastomotic biliary strictures (NASs) compared to livers procured from brain-dead donors (DBD). The use of normothermic regional perfusion (NRP) during cDCD procurement may improve posttransplant outcomes and reduce the incidence of NAS. In Sweden, cDCD LTX was introduced through a national pilot protocol with mandatory NRP. This study aims to evaluate the outcome of cDCD LTX during the pilot period. Donor and recipient data were collected on all cDCD liver transplants during the pilot period between January 2020 to December 2022. Outcome on NAS, patient and graft survival, early allograft dysfunction, acute kidney injury, and comprehensive complication index was compared to a matched cohort of 28 patients transplanted with a DBD liver between 2018 and 2022. Eighteen patients were transplanted with a liver from a cDCD donor after using NRP. The mean functional warm ischemia time was 29 ± 6 minutes. The mean lactate reduction during NRP was 8.7 ± 2.4 mmol/L, and the end NRP perfusate alanine aminotransferase was 1.4 ± 1 µkat/L. When comparing recipients of cDCD liver transplant to DBD, no significant differences were observed in the incidence of NAS, patient and graft survival, comprehensive complication index, early allograft dysfunction, or acute kidney injury. Study protocol magnetic resonance cholangiopancreatography in cDCD patients showed no signs of subclinical biliary strictures. Evaluation of the Swedish national pilot of cDCD LTX with mandatory NRP shows comparable outcomes to a matched DBD cohort with 94.4% 1-year patient and graft survival and no incidence of NAS within the first year.

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在受控 DCD 肝脏采集中进行常温区域灌注:瑞典国家实施协议的成果。
与脑死亡捐献者(DBD)的肝脏相比,使用受控循环死亡(cDCD)后的捐献者进行肝脏移植的移植物存活率较低,非吻合口胆道狭窄(NAS)的发生率也较高。在cDCD肝移植过程中使用常温区域灌注(NRP)可改善移植后的预后并降低NAS的发生率。瑞典通过国家试点方案引入了 cDCD 肝移植,并强制实施 NRP。本研究旨在评估试点期间 cDCD 肝移植的效果。在 2020 年至 2022 年 12 月的试点期间,收集了所有 cDCD 肝移植的捐献者和受者数据。将NAS、患者和移植物存活率、早期同种异体功能障碍、急性肾损伤和综合并发症指数等方面的结果与2018-2022年间接受DBD肝移植的28名匹配队列患者进行了比较。18名患者在使用NRP后移植了来自cDCD供体的肝脏。平均功能性温缺血时间为29±6分钟。NRP期间平均乳酸减少量为(8.7±2.4)mmol/L,NRP末灌注液ALT为(1.4±1)μkat/L。将cDCD肝移植受者与DBD进行比较,在NAS发生率、患者和移植物存活率、综合并发症指数、早期同种异体功能障碍和急性肾损伤方面均未观察到显著差异。研究方案对 cDCD 患者进行的 MRCP 检查未发现亚临床胆道狭窄的迹象。对瑞典全国 cDCD 肝移植试点项目进行的评估显示,强制性 NRP 的结果与匹配的 DBD 队列相当,患者和移植物一年存活率为 94.4%,第一年内无 NAS 发生。
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来源期刊
Liver Transplantation
Liver Transplantation 医学-外科
CiteScore
7.40
自引率
6.50%
发文量
254
审稿时长
3-8 weeks
期刊介绍: Since the first application of liver transplantation in a clinical situation was reported more than twenty years ago, there has been a great deal of growth in this field and more is anticipated. As an official publication of the AASLD, Liver Transplantation delivers current, peer-reviewed articles on liver transplantation, liver surgery, and chronic liver disease — the information necessary to keep abreast of this evolving specialty.
期刊最新文献
Management of the liver transplant candidate with high cardiac risk: Multidisciplinary best practices and recommendations. An international, multicenter, survey-based analysis of practice and management of acute liver failure. Utility of scores to predict alcohol use after liver transplant: Take them with a grain of salt. Intensive locoregional therapy before liver transplantation for colorectal cancer liver metastasis: A novel pretransplant protocol. Association of psychosocial risk factors and liver transplant evaluation outcomes in metabolic dysfunction-associated steatotic liver disease.
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