...
首页> 外文期刊>Transplantation Proceedings >Sirolimus-based immunosuppressive therapy in liver transplant recipient with tacrolimus-related chronic renal insufficiency.
【24h】

Sirolimus-based immunosuppressive therapy in liver transplant recipient with tacrolimus-related chronic renal insufficiency.

机译:基于西罗莫司的免疫抑制疗法在他克莫司相关的慢性肾功能不全的肝移植受者中。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

BACKGROUND: While providing potent immunosuppression for liver transplant recipients, calcineurin inhibitors (CNI) exhibit nephrotoxicity as a major side effect. The purpose of this study was to evaluate the safety and efficacy of conversion from CNI to sirolimus (SRL) among liver transplant recipients with CNI-induced chronic nephrotoxicity. METHODS: Between January 2004 and June 2005, we performed conversion in 16 recipients after a median period of 8.5 months after liver transplantation. The indication for conversion was CNI-related nephrotoxicity with a serum creatinine (sCr) value 132.6 umol/L. Renal function was measured before and after conversion to SRL. Clinical and laboratory data related to the clinical course of the patients were recorded to investigate the safety and efficacy of conversion. RESULTS: Sixteen patients were converted to SRL after developing nephrotoxicity. Their renal function improved gradually after conversion. The levels of sCr decreased significantly within the first 30 days (164.1 +/- 12.48 micromol/L to 130.1 +/- 5.573 micromol/L), and over the next 60 days after conversion (97.86 +/- 11.69 micromol/L to 90.7 +/- 8.95 micromol/L) (P .01). Similarly, the mean glomerular filtration rate (GFR) increased significantly during the same period. Four recipients experienced hypercholesterolemia, 1 with ankle edema, and 1 with acute rejection. The median follow-up was 2.4 years. No patient discontinued SRL due to side effects. No patient needed dialysis or kidney transplantation during the study period. CONCLUSIONS: SRL is a safe, effective replacement agent as primary immunosuppressive therapy following withdrawal of CNIs in liver transplant recipients with CNI-induced chronic nephrotoxicity.
机译:背景:钙调神经磷酸酶抑制剂(CNI)在为肝移植受者提供有效的免疫抑制作用时,显示出肾毒性是主要的副作用。这项研究的目的是评估由CNI引起的慢性肾毒性的肝移植受者从CNI转换为西罗莫司(SRL)的安全性和有效性。方法:从2004年1月至2005年6月,我们在中位肝移植8.5个月后对16位接受者进行了转化。转化的指征是CNI相关的肾毒性,血清肌酐(sCr)值> 132.6 umol / L。在转换为SRL之前和之后测量肾功能。记录与患者临床病程相关的临床和实验室数据,以研究转换的安全性和有效性。结果:16名患者发生肾毒性后转为SRL。转换后其肾功能逐渐改善。在转化后的30天内,sCr含量显着降低(从164.1 +/- 12.48 micromol / L降至130.1 +/- 5.573 micromol / L),并在转化后的60天内(97.86 +/- 11.69 micromol / L降至90.7 +/- 8.95 micromol / L)(P <.01)。同样,平均肾小球滤过率(GFR)在同一时期显着增加。四位接受者经历了高胆固醇血症,其中一位患有踝部水肿,另一位经历了急性排斥反应。中位随访时间为2。4年。没有患者因副作用而停药。在研究期间,没有患者需要透析或肾脏移植。结论:SRL是一种安全,有效的替代药物,可作为具有CNI诱导的慢性肾毒性的肝移植受者撤回CNI后作为主要的免疫抑制疗法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号