Matas Arthur J, Kandaswamy Raja, Humar Abhinav, Payne William D, Dunn David L, Najarian John S, Gruessner Rainer W G, Gillingham Kristen J, McHugh Lois E, Sutherland David E R
Department of Surgery, University of Minnesota, Minneapolis, USA.
Ann Surg. 2004 Sep;240(3):510-6; discussion 516-7. doi: 10.1097/01.sla.0000137140.79206.d0.
Concern exists that prednisone-free maintenance immunosuppression in kidney transplant recipients will increase acute and/or chronic rejection.
From October 1, 1999, through February 29, 2004, at our center, 477 kidney transplant recipients (341 living donor, 136 cadaver) discontinued prednisone on postoperative day 6, per our protocol. Immunosuppression consisted of polyclonal antibody (Thymoglobulin) for 5 days, prednisone intraoperatively and for 5 days, a calcineurin inhibitor, and either sirolimus or mycophenolate mofetil. We compared outcome with that of historical controls who did not discontinue prednisone.
The recipients on prednisone-free maintenance immunosuppression had excellent 4-year actuarial patient survival (92%), graft survival (90%), acute rejection-free graft survival (86%), and chronic rejection-free graft survival (95%). The mean serum creatinine level (+/- SD) at 1 year was 1.6 +/- 0.6; at 4 years, 1.6 +/- 0.6. We noted that 8% of recipients had cytomegalovirus (CMV) disease; 4.5%, fractures; 2.8%, cataracts; 1%, posttransplant diabetes; 0.2%, avascular necrosis; 0.2%, posttransplant lymphoproliferative disease; and 0%, polyomavirus. In all, 85% of kidney recipients with functioning grafts remain prednisone-free as of April 1, 2004. As compared with historical controls, the recipients on prednisone-free maintenance immunosuppression had better patient (P = 0.02) and graft survival (P < 0.0001) and lower rates of acute (P = 0.0004) and chronic (P = 0.02) rejection. In addition, they had a significantly lower rate of CMV disease (P < 0.0001), cataracts (P < 0.0001), posttransplant diabetes (P < 0.0001), and avascular necrosis (P = 0.0003).
Prednisone-related side effects can be minimized without maintenance immunosuppression; our prednisone-free recipients do not have increased acute or chronic rejection.
人们担心肾移植受者停用泼尼松进行维持性免疫抑制会增加急性和/或慢性排斥反应。
1999年10月1日至2004年2月29日,在我们中心,477例肾移植受者(341例活体供肾,136例尸体供肾)按照我们的方案在术后第6天停用泼尼松。免疫抑制方案包括使用多克隆抗体(即复宁)5天、术中及术后使用泼尼松5天、一种钙调神经磷酸酶抑制剂以及西罗莫司或霉酚酸酯。我们将这些患者的结局与未停用泼尼松的历史对照者进行了比较。
接受无泼尼松维持性免疫抑制的受者4年实际患者生存率(92%)、移植物生存率(90%)、无急性排斥反应的移植物生存率(86%)和无慢性排斥反应的移植物生存率(95%)均良好。1年时血清肌酐水平的均值(±标准差)为1.6±0.6;4年时为1.6±0.6。我们注意到8%的受者发生了巨细胞病毒(CMV)疾病;4.5%发生骨折;2.8%发生白内障;1%发生移植后糖尿病;0.2%发生缺血性坏死;0.2%发生移植后淋巴细胞增殖性疾病;0%发生多瘤病毒感染。截至2004年4月1日,所有移植肾功能良好的肾移植受者中,85%仍未使用泼尼松。与历史对照者相比,接受无泼尼松维持性免疫抑制的受者患者生存率(P = 0.02)和移植物生存率(P < 0.0001)更高,急性(P = 0.0004)和慢性(P = 0.02)排斥反应发生率更低。此外,他们的CMV疾病(P < 0.0001)、白内障(P < 0.0001)、移植后糖尿病(P < 0.0001)和缺血性坏死(P = 0.0003)发生率显著更低。
在不进行维持性免疫抑制的情况下,泼尼松相关的副作用可降至最低;我们的无泼尼松受者并未出现急性或慢性排斥反应增加的情况。