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首页> 外文期刊>Clinical and experimental nephrology >Randomized comparative trial of mizoribine versus mycophenolate mofetil in combination with tacrolimus for living donor renal transplantation
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Randomized comparative trial of mizoribine versus mycophenolate mofetil in combination with tacrolimus for living donor renal transplantation

机译:咪唑立滨与吗替麦考酚酯联合他克莫司治疗活体肾移植的随机比较试验

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摘要

Background: Mizoribine (MZR) was approved in 1984 in Japan for the suppression of rejection in renal transplantation with an approved administration dosage of 1-3 mg/kg/day. The action of MZR resembles that of mycophenolate mofetil (MMF), but MZR dosing is markedly lower than that of MMF. To examine whether higher dosing of MZR could obtain efficacy similar to MMF in renal transplantation, we conducted a comparative study of MZR and MMF using a high daily dose of MZR. Methods: A prospective, randomized comparative study of MZR versus MMF using tacrolimus (FK) and steroids as the base was conducted in 35 patients who had undergone living-donor renal transplantation (ABO-incompatible patients were not included) at 8 institutions in Japan between July 2005 and June 2007. Starting doses were 12 mg/kg/day for MZR and 2 g/day for MMF. Dosages of FK and steroids were set according to the protocol of each institution. Results: Patient and graft survival rate at 1 year after transplantation was 100 in each group, with no significant difference in rejection rate apparent between groups. Adverse events found in both groups were characteristic, frequently involving infection and digestive organ disorder in the MMF group and elevated uric acid levels in the MZR group. Conclusions: Based on these results, MZR and MMF are considered almost equivalent in terms of efficacy and safety.
机译:背景:咪唑立滨 (MZR) 于 1984 年在日本被批准用于抑制肾移植中的排斥反应,批准给药剂量为 1-3 mg/kg/天。MZR的作用类似于吗替麦考酚酯(MMF),但MZR的剂量明显低于MMF。为了检查较高剂量的 MZR 是否可以在肾移植中获得与 MMF 相似的疗效,我们使用高日剂量的 MZR 对 MZR 和 MMF 进行了比较研究。方法:2005 年 7 月至 2007 年 6 月期间,在日本 8 家机构对 35 例接受活体肾移植的患者(不包括 ABO 不相容的患者)进行了 MZR 与 MMF 的前瞻性随机比较研究。MZR 的起始剂量为 12 mg/kg/天,MMF 的起始剂量为 2 g/天。FK和类固醇的剂量根据每个机构的方案设定。结果:各组移植后1年患者和移植物存活率为100%,两组间排斥反应率无显著差异。两组均有特征性不良事件,MMF组常有感染和消化器官紊乱,MZR组尿酸水平升高。结论:基于这些结果,MZR和MMF在疗效和安全性方面几乎相当。

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