Andres Axel, Livingstone Scott, Kin Tatsuya, Campbell Patricia M, Senior Peter A, Kneteman Norman M, Bigam David, Shapiro A M James
a Department of Surgery ; University of Alberta ; Edmonton , Alberta , Canada.
b Department of Medicine ; University of Alberta ; Edmonton , Alberta , Canada.
Islets. 2015;7(6):e1126036. doi: 10.1080/19382014.2015.1126036.
For selected patients with type 1 diabetes, β-cell replacement is the treatment of choice, either by islet transplantation (ITX) or whole pancreas transplantation (PTX). When either modality fails, current practice is to consider retransplantation, or return to exogenous insulin. We investigate outcomes with PTX after failed ITX (PAI), and ITX after failed PTX (IAP). All patients receiving PAI or IAP at a single institution were identified. Donor and recipient variables were documented, including transplant outcomes analyzed for insulin requirement and metabolic control. Five subjects were listed for PAI, and 2 received transplants. Of the 4 listed for IAP, 3 have received transplants. The mean waitlist time was 4.5 ± 4.1 y for PAI and 0.35 ±0 .4 y for IAP (p = 0.08). Metabolic control was excellent after PAI, with 2/2 insulin-independent. After IAP, 1/2 achieved insulin independence and good metabolic control after 2 islet infusions. The third could not receive 2(nd) infusion and presented c-peptide levels < 0.1 nmol/L. Both strategies are feasible. The outcomes after PAI in our center must be offset by much longer waitlist time due to the sensitization status of these patients. Data from multicentre experience will allow more robust comparative outcomes to be made, the current observations being restricted to a limited patient set.
对于部分1型糖尿病患者,β细胞替代是首选治疗方法,可通过胰岛移植(ITX)或全胰腺移植(PTX)进行。当这两种方式均失败时,目前的做法是考虑再次移植,或恢复使用外源性胰岛素。我们研究了胰岛移植失败后进行全胰腺移植(PAI)以及全胰腺移植失败后进行胰岛移植(IAP)的结果。确定了在单一机构接受PAI或IAP的所有患者。记录了供体和受体的变量,包括针对胰岛素需求和代谢控制分析的移植结果。有5名受试者被列入PAI名单,2人接受了移植。在列入IAP名单的4人中,有3人接受了移植。PAI的平均等待名单时间为4.5±4.1年,IAP为0.35±0.4年(p=0.08)。PAI后代谢控制良好,2/2实现了胰岛素非依赖。IAP后,2例中有1例在2次胰岛输注后实现了胰岛素非依赖且代谢控制良好。第3例无法接受第2次输注,且C肽水平<0.1nmol/L。两种策略都是可行的。由于这些患者的致敏状态,我们中心PAI后的结果必须被更长的等待名单时间所抵消。多中心经验的数据将使我们能够得出更有力的比较结果,目前的观察仅限于有限的患者群体。