Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania, School of Medicine, Philadelphia, PA 19104-6021, USA.
Transplantation. 2011 Jun 15;91(11):1211-7. doi: 10.1097/TP.0b013e318218d59a.
Transmission of human immunodeficiency virus and hepatitis C to transplant recipients has drawn attention of the use of allografts from seronegative donors at increased risk for blood-borne viral infection (DIRVI).
We performed a cohort study of 7803 kidney transplant recipients whose kidneys were recovered through one of two organ procurement organizations from 1996 to 2007. Detailed organ procurement organization data on donor risk factors were linked to recipient data from the Organ Procurement and Transplantation Network.
Median recipient follow-up was 3.9 years. Three hundred sixty-eight (5%) patients received DIRVI kidneys, a third of which were procured from donors with a history of injection drug use or commercial sex work. Compared with standard criteria kidney recipients, DIRVI kidney recipients were more likely to be human immunodeficiency virus positive or black. In multivariable Cox regression, using DIRVI recipients as the reference, recipients of standard criteria donor kidneys had lower mortality (hazard ratio [HR] 0.71, P<0.01) and no difference in death-censored allograft failure (HR 1.09, P=0.62), whereas recipients of expanded criteria donor kidneys had no significant difference in mortality (HR 0.98, P=0.83) but a higher allograft failure rate (HR 1.93, P<0.01). High-quality data on posttransplant recipient viral testing were not available.
DIRVI kidney recipients experienced higher mortality than standard criteria kidney recipients. This finding could be explained if sicker patients received DIRVI kidneys (i.e., residual confounding) or the less likely possibility of undetected transmission of viral infections. Given the limitations of registry data used in this analysis, prospective studies are needed to further elucidate these findings.
人类免疫缺陷病毒和丙型肝炎向移植受者的传播引起了人们对使用来自血液传播病毒感染风险增加的血清阴性供体的同种异体移植物的关注(DIRVI)。
我们对 1996 年至 2007 年间通过两个器官采购组织之一获得肾脏的 7803 名肾移植受者进行了队列研究。详细的器官采购组织数据中有关供体危险因素的信息与从器官采购和移植网络获得的受者数据相关联。
中位受者随访时间为 3.9 年。368 例(5%)患者接受了 DIRVI 肾脏,其中三分之一来自有注射吸毒或商业性工作史的供者。与标准标准肾脏受者相比,DIRVI 肾脏受者更可能是 HIV 阳性或黑人。在多变量 Cox 回归中,以 DIRVI 受者为参照,标准标准供体肾脏受者的死亡率较低(风险比[HR]0.71,P<0.01),且无死亡受者的移植物失败率差异(HR 1.09,P=0.62),而扩展标准供体肾脏受者的死亡率无显著差异(HR 0.98,P=0.83),但移植物失败率较高(HR 1.93,P<0.01)。接受移植后受者病毒检测的高质量数据不可用。
与标准标准肾脏受者相比,DIRVI 肾脏受者的死亡率更高。如果接受 DIRVI 肾脏的患者病情更严重(即残余混杂),或者更有可能检测不到病毒感染的传播,则可以解释这一发现。鉴于本分析中使用的登记数据的局限性,需要进行前瞻性研究以进一步阐明这些发现。