Central and Northern Adelaide Renal and Transplantation Services, Adelaide, SA, Australia.
Australia and New Zealand Dialysis and Transplant (ANZDATA) Registry, Adelaide, SA, Australia.
Transpl Int. 2019 Nov;32(11):1151-1160. doi: 10.1111/tri.13472. Epub 2019 Jul 9.
Delayed graft function (DGF) in deceased donor kidney transplantation is associated with worse outcomes. DGF has been less well studied in live donor transplantation. We aimed to examine the risk factors for DGF, and associations between DGF and short- and long-term outcomes in live donor kidney transplant recipients. Using data from the Australia and New Zealand Dialysis and Transplant (ANZDATA) Registry, we included live donor kidney transplants performed in Australia and New Zealand over 2004-2015 and excluded pediatric recipients (n = 440), pathological donors (n = 97), grafts that failed in the first week (as a proxy for primary non function; n = 38), and grafts with missing DGF data (n = 46). We used multivariable logistic regression to identify the risk factors for DGF and the association between DGF and rejection at 6 months; Cox proportional hazards models to examine the relationship between DGF and patient and graft survival; and linear regression to examine the association between DGF and eGFR at 1 year. DGF occurred in 77 (2.3%) of 3358 transplants. Risk factors for DGF included right-sided kidney [odds ratio (OR) 2.00 (95% CI 1.18, 3.40)], donor BMI [OR 1.06 per kg/m (95% CI 1.01, 1.12)]; increasing time on dialysis and total ischemic time [OR 1.09 per hour (1.00, 1.17)]. DGF was associated with increased risk of rejection at 6 months [OR 2.37 (95% CI 1.41, 3.97)], worse patient survival [HR 2.14 (95% CI 1.21, 3.80)] and graft survival [HR 1.98 (95% CI 1.27, 3.10)], and worse renal function at 1 year [Coefficient -9.57 (95% CI -13.5, -5.64)]. DGF is uncommon after live donor kidney transplantation, but associated with significantly worse outcomes. The only modifiable risk factors identified were kidney side and total ischemic time.
在尸体供肾移植中,移植物延迟功能(DGF)与较差的结局相关。在活体供肾移植中,DGF 的研究较少。我们旨在研究 DGF 的危险因素,以及 DGF 与活体供肾移植受者短期和长期结局之间的关系。我们使用澳大利亚和新西兰透析和移植(ANZDATA)登记处的数据,纳入了 2004 年至 2015 年在澳大利亚和新西兰进行的活体供肾移植,排除了儿科受者(n=440)、病理性供者(n=97)、移植在第一周失败的(作为原发性无功能的替代指标;n=38)以及缺少 DGF 数据的移植(n=46)。我们使用多变量逻辑回归来确定 DGF 的危险因素,以及 DGF 与 6 个月时排斥反应之间的关系;Cox 比例风险模型来检查 DGF 与患者和移植物存活率之间的关系;线性回归来检查 DGF 与 1 年时 eGFR 的关系。在 3358 例移植中,77 例(2.3%)发生 DGF。DGF 的危险因素包括右侧肾脏[比值比(OR)2.00(95%CI 1.18,3.40)]、供者 BMI[OR 每公斤体重增加 1.06(95%CI 1.01,1.12)];透析时间和总缺血时间延长[OR 每小时增加 1.09(95%CI 1.00,1.17)]。DGF 与 6 个月时排斥反应的风险增加相关[OR 2.37(95%CI 1.41,3.97)],患者存活率[HR 2.14(95%CI 1.21,3.80)]和移植物存活率[HR 1.98(95%CI 1.27,3.10)]较差,以及 1 年时肾功能较差[系数-9.57(95%CI-13.5,-5.64)]。在活体供肾移植后,DGF 并不常见,但与结局明显较差相关。唯一确定的可改变的危险因素是肾脏侧和总缺血时间。