Todd Rachel, van Leeuwen Leonie, Rosowicz Andrew, Irizar Aritz, Arvelakis Antonios, DiNorcia Joseph, Facciuto Marcelo, Moon Jang, Rocha Chiara, Tabrizian Parissa, Kim-Schluger Leona, Florman Sander S, Akhtar M Zeeshan
Recanati/Miller Transplantation Institute, The Mount Sinai Hospital, New York, New York, USA.
Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Clin Transplant. 2025 Aug;39(8):e70282. doi: 10.1111/ctr.70282.
Normothermic machine perfusion (NMP) is increasing the safe utilization of donation after circulatory death livers. Historically, tissue plasminogen activator (tPA) has been administered intraoperatively to DCD graft recipients to reduce non-anastomotic biliary complications (NAS). Treating the liver during NMP offers a potentially safer administration, preventing systemic treatment of the recipient. In this retrospective study, we explore our center's experience of giving tPA with FFP during NMP and its effects on clinical chemistries during perfusion, intraoperative transfusions, and post-operative outcomes and clinical chemistries.
One hundred and twenty-seven livers were perfused using the OrganOx metra, including 56 DCD livers (tPA + NMP-DCD) that received a bolus of 10 mg tPA followed by a 90-min infusion of 40 mg. Sixty-five livers from donation after brain death donors underwent NMP without tPA (NMP-DBD). A historical, propensity-matched cohort of 78 livers from non-NMP DCD donor livers (n = 51) were an additional comparator group (tPA-DCD).
Intraoperative transfusions, 30-day and 3-month patient survival, and 30-day and 3-month graft survival were not statistically different between the tPA-NMP-DCD and NMP-DBD groups, except for cell saver volumes (p = 0.0034). Less platelets and cryoprecipitate transfusions were observed in the tPA-NMP-DCD livers compared to historical tPA-DCD livers (p = 0.0021 and 0.0046, respectively). One incidence of primary non-function occurred in the tPA-DCD group, and the tPA-NMP-DCD arm had one case of ischemic cholangiopathy required re-transplant. There was a higher reoperation rate for hematoma evacuation in the NMP-DBD cohort. Minimum follow-up time was 5 months.
Our results continue to lend support to NMP providing a platform for administering tPA to donor livers, curtailing a potential risk to the recipient.
Administration of tissue plasminogen activator (tPA) can be safely administered during normothermic machine perfusion. For centers who traditionally deploy tPA in recipients for DCD donor livers, delivering during NMP is an alternative safer option sparing the reciepient from exposure.
常温机器灌注(NMP)正在提高心脏死亡后供肝的安全利用率。从历史上看,组织纤溶酶原激活剂(tPA)已在术中用于心脏死亡后供肝移植受者,以减少非吻合口胆管并发症(NAS)。在NMP期间对肝脏进行处理提供了一种潜在更安全的给药方式,避免了对受者进行全身治疗。在这项回顾性研究中,我们探讨了本中心在NMP期间给予tPA联合新鲜冰冻血浆(FFP)的经验及其对灌注期间临床化学指标、术中输血、术后结局和临床化学指标的影响。
使用OrganOx metra对127例肝脏进行灌注,其中包括56例心脏死亡后供肝(tPA + NMP - DCD),给予10 mg tPA推注,随后90分钟输注40 mg。65例脑死亡后供体的肝脏在未使用tPA的情况下进行NMP(NMP - DBD)。另外一个对照队列是78例非NMP心脏死亡后供肝(n = 51),采用倾向性匹配法进行匹配(tPA - DCD)。
tPA - NMP - DCD组和NMP - DBD组在术中输血、30天和3个月患者生存率以及30天和3个月移植物生存率方面无统计学差异,但细胞回收血量除外(p = 0.0034)。与历史tPA - DCD肝脏相比,tPA - NMP - DCD肝脏的血小板和冷沉淀输注量更少(分别为p = 0.0021和0.004)。tPA - DCD组发生1例原发性无功能,tPA - NMP - DCD组有1例缺血性胆管病需要再次移植。NMP - DBD队列中血肿清除的再次手术率更高。最短随访时间为5个月。
我们的结果继续支持NMP为向供肝给药tPA提供一个平台,减少对受者的潜在风险。
组织纤溶酶原激活剂(tPA)可在常温机器灌注期间安全给药。对于传统上在心脏死亡后供肝移植受者中使用tPA的中心,在NMP期间给药是一种更安全的选择,可避免受者接触。