Multicenter validation of the liver graft assessment following transplantation (L-GrAFT) score for assessment of early allograft dysfunction

Multicenter validation of the liver graft assessment following transplantation (L-GrAFT) score for assessment of early allograft dysfunction
复制标题

DOI:
10.1016/j.jhep.2020.09.015
复制
发表时间:
2021-03-15
影响因子:
25.7
通讯作者:
Busuttil, Ronald W.
Busuttil, Ronald W.
中科院分区:
医学1区
文献类型:
--
作者:
Agopian, Vatche G.;Markovic, Daniela;Busuttil, Ronald W.

文献摘要

被引文献

相似文献

背景与目的:肝移植(LT)后早期同种异体移植物功能障碍(EAD)对移植物和患者结局产生负面影响。之前我们报道了在单中心衍生队列中,移植后肝移植评估(L-GrAFT 7)风险评分上级二元EAD或早期同种异体移植功能模型(MEAF)评分,用于估计3个月无移植失败生存率。在此,我们试图从外部验证L-GrAFT 7,并将其预后性能与EAD和MEAF进行比较。方法:在美国3中心验证队列中比较L-GrAFT 7,EAD和MEAF的准确性(n = 3,201)和欧洲器官保存联盟(科普)常温机器灌注(NMP)试验队列(n = 222);结果:与衍生队列相比,验证和NMP试验队列中的患者具有较低的受体中位MELD评分,不太可能需要移植前住院、肾脏替代治疗或机械通气;总体而言,1年的疗效优于上级(90%和95% vs. 84%)和无移植失败(88%和93% vs. 81%)存活率,3个月移植物失败的发生率较低(7.4%和4.0% vs. 11.1%; p = IVa(HR 4.99,p = 0.011))并发症; LT后住院时间结论:我们已经验证了L-GrAFT 7风险评分作为3个月肝移植失败的可推广的、高度准确的、个体化的风险评估上级现有评分。L-GrAFT 7可以标准化早期肝移植功能的分级,并作为转化研究中的临床终点(www.lgraft.com)。在总计3,423例接受肝移植的独立多中心美国和欧洲队列中,移植后肝移植评估(L-GrAFT)风险评分被验证为早期同种异体移植物功能的上级指标,可准确区分3个月移植物无衰竭生存期和肝移植后并发症。(C)2020年欧洲肝脏研究协会。Elsevier B. V.出版,保留所有权利。
Background & Aims: Early allograft dysfunction (EAD) following liver transplantation (LT) negatively impacts graft and patient outcomes. Previously we reported that the liver graft assessment following transplantation (L-GrAFT7) risk score was superior to binary EAD or the model for early allograft function (MEAF) score for estimating 3-month graft failure-free survival in a single center derivation cohort. Herein, we sought to externally validate L-GrAFT7, and compare its prognostic performance to EAD and MEAF.Methods: Accuracies of L-GrAFT7, EAD, and MEAF were compared in a 3-center US validation cohort (n = 3,201), and a Consortium for Organ Preservation in Europe (COPE) normothermic machine perfusion (NMP) trial cohort (n = 222); characteristics were compared to assess generalizability.Results: Compared to the derivation cohort, patients in the validation and NMP trial cohort had lower recipient median MELD scores; were less likely to require pretransplant hospitalization, renal replacement therapy or mechanical ventilation; and had superior 1-year overall (90% and 95% vs. 84%) and graft failure-free (88% and 93% vs. 81%) survival, with a lower incidence of 3-month graft failure (7.4% and 4.0% vs. 11.1%; p = IVa (HR 4.99, p = 0.011) complications; post-LT length of hospitalization (p = 0.002); and renal replacement therapy (odds ratio 3.62, p = 0.016).Conclusions: We have validated the L-GrAFT7 risk score as a generalizable, highly accurate, individualized risk assessment of 3-month liver allograft failure that is superior to existing scores. L-GrAFT7 may standardize grading of early hepatic allograft function and serve as a clinical endpoint in translational studies (www.lgraft.com).Lay summary: Early allograft dysfunction negatively affects outcomes following liver transplantation. In independent multicenter US and European cohorts totaling 3,423 patients undergoing liver transplantation, the liver graft assessment following transplantation (L-GrAFT) risk score is validated as a superior measure of early allograft function that accurately discriminates 3-month graft failure-free survival and post-liver transplantation complications. (C) 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.