巴西肝移植中心早期同种异体移植功能障碍的术中危险因素:一项回顾性研究。

IF 0.8
Geisiane Custódio, Andrew Maykon Massutti, Sofia Stein Corrêa da Cunha, Cristiane Bauermann Leitão, Tatiana Helena Rech
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引用次数: 0

摘要

背景:早期同种异体移植物功能障碍(EAD)是肝移植的严重并发症。多种供体、受体和术中危险因素导致其发展。本研究旨在评估术中EAD危险因素对肝移植受者临床预后的影响。方法:本回顾性研究纳入脑死亡供体和成人肝移植受者。通过交叉列表促进了供体与受体的匹配,并记录了供体、受体和手术过程的综合临床和实验室数据。主要评价指标为EAD。次要结局是解剖变异与出血量和输血需求、ICU和住院时间、再移植以及12个月后患者和移植物存活之间的关系。结果:2019年1月至2021年12月期间,共有228名患者接受了脑死亡供体的肝脏移植。EAD的发生率为25%。在单变量分析中,肝移植脂肪变性、既往腹部手术、Roux-in-Y胆道重建、总移植时间、出血量和所有类型血液制品的需求与EAD相关。然而,在调整终末期肝病模型(MELD)评分后,只有Roux-in-Y胆道重建(OR 4.58, 95% CI 1.63-12.83, P = 0.004)和总移植时间(OR 1.01, 95% CI 1.003-1.014, P = 0.002)与EAD持续相关。解剖变异与EAD、出血增加、输血需求或其他临床结果无关。结论:Roux-in-Y胆道重建和总移植时间与EAD的发生有关,而解剖动脉变异与EAD的发生无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intraoperative Risk Factors of Early Allograft Dysfunction at a Liver Transplantation Center in Brazil: A Retrospective Study.

Background: Early allograft dysfunction (EAD) is a serious complication of liver transplantation. Multiple donor, recipient, and intraoperative risk factors contribute to its development. This study aims to assess the impact of intraoperative risk factors for EAD on clinical outcomes of liver transplant recipients.

Methods: This retrospective study enrolled brain-dead donors and adult liver graft recipients. Recipient-donor matching was facilitated via a crossover list, and comprehensive clinical and laboratory data were recorded for donors, recipients, and surgical procedures. The primary outcome assessed was EAD. Secondary outcomes were the association between anatomical variants with bleeding volume and need for blood transfusions, length of ICU and hospital stay, retransplantation, and patient and graft survival after 12 months.

Results: A total of 228 patients underwent liver transplants from brain-dead donors between January 2019 and December 2021. The incidence of EAD was 25%. In the univariate analysis, liver graft steatosis, previous abdominal surgery, biliary reconstruction in Roux-in-Y, total transplantation time, bleeding volume, and the need for all types of blood products were associated with EAD. However, after adjustment for the Model for End Stage Liver Disease (MELD) score, only biliary reconstruction in Roux-in-Y (OR 4.58, 95% CI 1.63-12.83, P = .004) and total transplantation time (OR 1.01, 95% CI 1.003-1.014, P = .0002) persisted in association with EAD. Anatomical variants were not associated with EAD, increased bleeding and the need for blood transfusions or other clinical outcomes.

Conclusions: Biliary reconstruction in Roux-in-Y and total transplantation time were associated with EAD development while anatomical artery variants were not.

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