SGPGIMS, Lucknow, India.
Int Urol Nephrol. 2010 Jun;42(2):279-84. doi: 10.1007/s11255-009-9601-6. Epub 2009 Jun 26.
To compare the incidence of immediate surgical complications after renal transplantation between mycophenolate mofetil (MMF group)-based and mTOR inhibitors (mTOR group)-based immunosuppressive regimens.
The preoperative parameters in the recipients, rejection rates and surgical complications within 12 months in the recipients were analyzed in 80 patients who had live related renal transplantation. The immunosuppressive regimen was based on MMF (MMF, prednisolone, cyclosporine) in 40 patients and mTOR inhibitors (sirolimus/everolimus, prednisolone, cyclosporine) in 40 patients.
The baseline characteristics were comparable between the two groups. Infective complications (urinary tract infections, pulmonary infections and superficial wound infection) occurred in 27.5% (11/40) and 12.5% (5/40) of patients from MMF and mTORI groups, respectively (P = 0.096). Patients in mTORI group had significantly more wound dehiscence (8/40 i.e., 20%) than in MMF group (1/40 i.e., 2.5%) (P = 0.014). There was no significant difference in the occurrence of clinically significant or symptomatic lymphoceles that needed intervention (3 vs. 2). The hospital stay was significantly prolonged in mTORI group mainly because of wound-related problems (35 vs. 24 days).
In the post-renal transplant setting, use of mTORI results in significantly higher wound complications compared to that of MMF leading to prolonged hospital stay. There is no significant difference in infective complications or lymphocele incidence between these two immunosuppressive regimens.
比较吗替麦考酚酯(MMF 组)和 mTOR 抑制剂(mTOR 组)为基础的免疫抑制方案在肾移植后即刻手术并发症的发生率。
对 80 例活体亲属肾移植患者的受者术前参数、12 个月内排斥率和手术并发症进行分析。40 例患者采用 MMF(MMF、泼尼松、环孢素),40 例患者采用 mTOR 抑制剂(西罗莫司/依维莫司、泼尼松、环孢素)作为免疫抑制方案。
两组基线特征无差异。MMF 组和 mTORI 组的感染性并发症(尿路感染、肺部感染和浅表伤口感染)发生率分别为 27.5%(11/40)和 12.5%(5/40)(P=0.096)。mTORI 组的伤口裂开发生率(8/40,即 20%)明显高于 MMF 组(1/40,即 2.5%)(P=0.014)。需要干预的临床显著或有症状的淋巴囊肿发生率无显著差异(3 例比 2 例)。mTORI 组的住院时间明显延长,主要是由于伤口相关问题(35 天比 24 天)。
在肾移植后,与 MMF 相比,mTORI 导致的伤口并发症发生率显著增加,导致住院时间延长。这两种免疫抑制方案在感染性并发症或淋巴囊肿发生率方面无显著差异。