同种异体移植失败的风险评分:它们在循环性死亡后的捐赠肝受体中仍然有用吗?

Mohamed H Mohamed Chairi, Mónica Mogollón González, Jennifer Triguero Cabrera, Inmaculada Segura Jiménez, Maria T Villegas Herrera, Jesús M Villar Del Moral
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引用次数: 0

摘要

背景:由热缺血和冷缺血时间决定的循环死亡后捐献肝移植与早期移植物功能障碍的高风险相关。必须有精确的标准来识别这种并发症,以便指导治疗策略。目的:验证肝移植(LT) DCD移植患者不同的移植物和受体生存评分。方法:2013年11月至2022年11月,对65例对照DCD供体移植的LT患者进行回顾性观察性单中心研究。采用英国(UK)风险评分、早期同种异体移植功能障碍(EAD) Olthoff评分和早期同种异体移植功能模型(MEAF)评分来评估移植后移植物和受体生存的风险。为了进行生存分析,我们使用Kaplan-Meier方法,并使用log-rank (Mantel-Cox)检验比较亚组之间的差异。结果:65例患者纳入研究。英国风险评分并不能预测受体或移植物的存活。而在70岁以上的供者中(18.4%),它能显著预测移植物存活(P < 0.05)。Kaplan-Meier生存曲线显示,与其他组相比,无效组6个月、2年和5年移植物存活率显著下降至50% (log-rank为8.806,P < 0.05)。EAD Olthoff和MEAF评分不能预测受体或移植物的存活。根据Kaplan-Meier生存曲线,MEAF评分≥7的患者在6个月、2年和5年的移植存活率均低于MEAF评分较低的患者(log-rank为4.667,P < 0.05)。结论:在我们的研究中,UK DCD风险评分和MEAF评分都具有预测移植物存活的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk scores for allograft failure: Are they still useful in liver recipients from donation after circulatory death?

Background: Liver grafts from donation after circulatory death (DCD) are associated with a higher risk of early graft dysfunction, determined by the warm ischemia and cold ischemia times. It is essential to have precise criteria to identify this complication in order to guide therapeutic strategies.

Aim: To validate different graft and recipient survival scores in patients undergoing liver transplantation (LT) with DCD grafts.

Methods: A retrospective and observational unicentric study was conducted on 65 LT patients with grafts obtained from controlled DCD donors from November 2013 to November 2022. The United Kingdom (UK) risk score, early allograft dysfunction (EAD) Olthoff score, and model for early allograft function (MEAF) score were used to evaluate the risk of graft and recipient survival post-transplant. For survival analysis purposes, we used the Kaplan-Meier method, and the differences between subgroups were compared using the log-rank (Mantel-Cox) test.

Results: Sixty-five patients were included in the study. The UK risk score did not demonstrate predictive capacity for recipient or graft survival. However, in donors aged over 70 years old (18.4%), it significantly predicted graft survival (P < 0.05). According to Kaplan-Meier survival curves, graft survival rates at 6 months, 2 years, and 5 years in the futility group dramatically decreased to 50% compared to the other groups (log-rank 8.806, P < 0.05). The EAD Olthoff and MEAF scores did not demonstrate predictive capacity for recipient or graft survival. Based on Kaplan-Meier survival curves, patients with a MEAF score ≥ 7 had a lower graft survival rate at 6 months, 2 years, and 5 years compared to patients with a lower MEAF score (log-rank 4.667, P < 0.05).

Conclusion: In our series, both UK DCD risk score and MEAF score showed predictive capability for graft survival.

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