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首页> 外文期刊>Transplantation Proceedings >Improvement of renal graft function after conversion from a calcineurin inhibitor including immunosuppression to a mycophenolate sodium including regimen: A 4-year follow-up
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Improvement of renal graft function after conversion from a calcineurin inhibitor including immunosuppression to a mycophenolate sodium including regimen: A 4-year follow-up

机译:从钙调神经磷酸酶抑制剂(包括免疫抑制)转变为麦考酚酸钠(包括治疗方案)后改善肾移植功能:4年随访

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摘要

Background: The most common immunosuppressive regimens after renal transplantation include calcineurin inhibitors (CNI). However, due to renal toxicity long-term graft survival does not seem to be positively affected by CNIs. Methods: In the present study, we investigated 17 patients, in which the CNI immunosuppression was converted to a CNI-free, mycophenolate sodium (MPS) regimen. Conversion was performed due to progressive impairment of the graft function from suspected CNI toxicity. We retrospectively analyzed graft function as well as toxicity and surrogate markers for 4 years before and 4 years after conversion using a repeated-measures mixed model data analysis and/or a paired sample t-test. Results: The mean time point of therapy conversion was 11.2 ?? 4.6 years after transplantation. Within 1 month of CNI discontinuation, allograft function improved significantly, remaining at a significant level for 2 years. The estimated glomerular filtration rate increased from 43.4 ?? 14.8 to a maximum of 55.7 ?? 21.7 mL/min at 1 year after conversion (P =.0027). After 4 years, the end of the observation period, renal function was similar to the baseline. There were no significant side effects. Conclusion: These data suggested that, when chronic CNI-toxicity is suspected, renal allograft recipients may benefit from CNI withdrawal in favor of a MPS-including immunosuppressive regimen. ? 2013 Elsevier Inc.
机译:背景:肾移植后最常见的免疫抑制方案包括钙调神经磷酸酶抑制剂(CNI)。但是,由于肾毒性,CNIs似乎并未对移植物的长期存活产生积极影响。方法:在本研究中,我们调查了17名患者,其中CNI免疫抑制被转换为无CNI的麦考酚酸钠(MPS)方案。由于怀疑的CNI毒性导致移植物功能逐渐受损,因此进行了转化。我们使用重复测量混合模型数据分析和/或配对样本t检验对转换前4年和转换后4年的移植物功能以及毒性和替代标志物进行了回顾性分析。结果:治疗转换的平均时间点为11.2 ??。移植后4。6年。在CNI停用后1个月内,同种异体移植功能显着改善,并维持2年的显着水平。估计的肾小球滤过率从43.4? 14.8至最大55.7 ??转化后1年的流速为21.7 mL / min(P = .0027)。观察期结束4年后,肾功能与基线相似。没有明显的副作用。结论:这些数据表明,当怀疑存在慢性CNI毒性时,肾同种异体移植受者可能会受益于CNI停药而转而接受包括MPS在内的免疫抑制方案。 ? 2013爱思唯尔公司

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