Institute of Medicine, School of Medicine, Chung-Shan Medical University, 110, Sec.1, Jian-Guo N. Road, Taichung 402, Taiwan.
World J Surg. 2012 Jan;36(1):222-8. doi: 10.1007/s00268-011-1312-3.
The purpose of the present study was to evaluate graft and patient survival and long-term outcomes of primary endoluminal stenting (PES) as an initial treatment for transplant renal artery stenosis (TRAS).
From December 1999 to March 2010, 744 consecutive patients undergoing renal transplantation were enrolled. Patients were divided into one of two groups: the study group, comprised of 18 patients who underwent PES for TRAS > 60%, and a control group, including the remaining 726 recipients who did not develop TRAS post-transplantation. Primary outcome measures were death-censored graft failure and all-cause mortality. The immediate and long-term effects of PES were evaluated by assessing blood pressure (BP) control and biochemical graft function.
The technical success rate for PES was 100%, and minor complication occurred in only one case (5.6% of the study group). With a mean follow-up of 7.1 ± 3.7 and 6.9 ± 2.4 years in the study and control groups, respectively, 4 patients in the study group and 113 patients in the control group reached the primary outcome (log rank P = 0.418). The reduction in stenosis resulted in immediate improvement in BP control and graft function, which persisted throughout the 6 year follow-up period. Restenosis occurred in only one patient (5.6%), but restenosis was not the cause of graft failure.
This study indicated that both the long-term graft and patient survival were as good in TRAS patients treated with PES as in patients without TRAS. The data also supported the use of PES as an initial treatment for TRAS.
本研究旨在评估原发性腔内支架置入术(PES)作为移植肾动脉狭窄(TRAS)初始治疗的移植物和患者存活率及长期结局。
1999 年 12 月至 2010 年 3 月,共纳入 744 例连续接受肾移植的患者。患者分为两组:研究组 18 例,TRAS>60%行 PES;对照组 726 例,移植后未发生 TRAS。主要终点为死亡相关移植物失功和全因死亡率。通过评估血压(BP)控制和生化移植物功能,评估 PES 的即刻和长期效果。
PES 的技术成功率为 100%,仅 1 例(研究组的 5.6%)发生轻微并发症。研究组和对照组的平均随访时间分别为 7.1±3.7 年和 6.9±2.4 年,研究组有 4 例和对照组有 113 例达到主要终点(对数秩 P=0.418)。狭窄的减轻导致即刻改善血压控制和移植物功能,这种改善在 6 年的随访期间持续存在。仅 1 例(5.6%)发生再狭窄,但再狭窄不是移植物失功的原因。
该研究表明,TRAS 患者行 PES 治疗的长期移植物和患者存活率与无 TRAS 患者相当。该数据也支持 PES 作为 TRAS 的初始治疗。