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心脏死亡器官捐献肾因冷缺血时间导致延迟移植肾功能的结果。

Outcomes of DCD kidneys with CIT-induced delayed graft function.

作者信息

Zaphiros Nikolas H, Nie Jing, Alchaer Michael W, Kayler Liise K

机构信息

Department of Surgery, University at Buffalo, Buffalo, New York, USA.

Transplant and Kidney Care Regional Center of Excellence, Erie County Medical Center, Buffalo, New York, USA.

出版信息

Clin Transplant. 2023 Apr;37(4):e14918. doi: 10.1111/ctr.14918. Epub 2023 Feb 10.

Abstract

Donation after circulatory death (DCD) kidneys are exposed to warm ischemia, which, coupled with cold ischemia time (CIT) exacerbates delayed graft function (DGF) and is possibly associated with worse graft survival. To analyze the risk of CIT-induced DGF on DCD kidney outcomes, we evaluated national data between 2008 and 2018 of adult kidney-only recipients of paired DCD kidneys where one kidney recipient experienced DGF and the other did not. Of 5602 paired DCD kidney recipients, multivariate analysis between recipients with higher CIT relative to lower CIT showed that increasing CIT differences had a significant dose-dependent effect on overall graft survival. The graft survival risk was minimal with CIT differences of ≥1-h (adjusted hazard ratio [aHR] 1.07, 95% CI .95- 1.20, n = 5602) and ≥5-h (aHR 1.09, 95% CI .93-1.29, n = 2710) and became significant at CIT differences of ≥10-h (aHR 1.37, 95% CI 1.05-1.78, n = 1086) and ≥15-h (aHR 1.78, 95% CI 1.15-2.77, n = 1086). Between each of the four delta-CIT levels of shorter and longer CIT, there were no statistically significant differences in the proportion of acute rejection. These results suggest that in the setting of DCD kidney transplantation (KTX), DGF, specifically mediated by prolonged CIT, impacts long-term graft outcomes.

摘要

心脏死亡后器官捐献(DCD)的肾脏会经历热缺血,再加上冷缺血时间(CIT),会加剧移植肾功能延迟(DGF),并可能与更差的移植肾存活相关。为了分析CIT诱导的DGF对DCD肾结局的风险,我们评估了2008年至2018年全国范围内仅接受成对DCD肾的成年肾移植受者的数据,其中一名肾移植受者发生了DGF,另一名没有。在5602对DCD肾移植受者中,对CIT较高与较低的受者进行多变量分析显示,CIT差异增加对总体移植肾存活有显著的剂量依赖性影响。CIT差异≥1小时(调整后风险比[aHR]1.07,95%置信区间0.95 - 1.20,n = 5602)和≥5小时(aHR 1.09,95%置信区间0.93 - 1.29,n = 2710)时,移植肾存活风险最小,而在CIT差异≥10小时(aHR 1.37,95%置信区间1.05 - 1.78,n = 1086)和≥15小时(aHR 1.78,95%置信区间1.15 - 2.77,n = 1086)时变得显著。在较短和较长CIT的四个CIT差值水平之间,急性排斥反应的比例没有统计学上的显著差异。这些结果表明,在DCD肾移植(KTX)中,特别是由延长的CIT介导的DGF会影响长期移植肾结局。

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