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肾移植受者无类固醇免疫抑制及普乐可复单药治疗:一项前瞻性多中心试验的中期分析

Steroid-free immunosuppression in kidney transplant recipients and prograf monotherapy: an interim analysis of a prospective multicenter trial.

作者信息

Bäckman L, Aselius H, Lindberger K, Svensson L, Strömbom U, Olausson E, Hadimeri H, Deurell S-I, Norrby J, Gäbel M, Ebermark A, Olausson M

机构信息

Department of Transplantation and Liver Surgery, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

Transplant Proc. 2006 Oct;38(8):2654-6. doi: 10.1016/j.transproceed.2006.07.026.

Abstract

This report described an interim analysis of a investigator-driven multicenter trial in renal transplant recipients: the Prospective Quality of life Renal Transplantation Switch Study; Tacrolimus-based immunosuppression ("PQRST study"). Patients included in the trial initially treated with cyclosporine-based immunosuppression after renal transplantation who experienced side effects, such as hypertension, hyperlipidemia, hypertrichosis, or other adverse reactions, were converted to a tacrolimus-based immunosuppressive regimen (n = 31). Steroids were subsequently discontinued between 3 and 6 months after the conversion. As of today 19/31 (50%) patients have been successfully weaned off steroids with the remaining patients in this process. In this interim analysis, with a follow-up ranging from 1 to 18 months both patient and graft survivals were 100%. No patient experienced an acute rejection episode; none of the grafts were lost. Blood pressure decreased in 22/31 (71%) of the patients. No patient developed de novo diabetes or other serious side effect related to the conversion. Three patients were withdrawn from the trial because of side effects: bleeding, depression, and proteinuria. However, none of these adverse events were felt to be directly related to the change of the immunosuppressive regimen to tacrolimus monotherapy. In conclusion, conversion from cyclosporine to tacrolimus-based therapy was safe and well tolerated; it may improve the cardiovascular risk profile after kidney transplantation.

摘要

本报告描述了一项由研究者发起的针对肾移植受者的多中心试验的中期分析

前瞻性肾移植生活质量转换研究;基于他克莫司的免疫抑制治疗(“PQRST研究”)。该试验纳入的患者最初在肾移植后接受基于环孢素的免疫抑制治疗,出现了如高血压、高脂血症、多毛症或其他不良反应等副作用,随后转换为基于他克莫司的免疫抑制方案(n = 31)。在转换后3至6个月期间停用类固醇。截至目前,19/31(50%)的患者已成功停用类固醇,其余患者仍在该过程中。在本次中期分析中,随访时间为1至18个月,患者和移植物存活率均为100%。没有患者发生急性排斥反应;没有移植物丢失。22/31(71%)的患者血压下降。没有患者出现新发糖尿病或与转换相关的其他严重副作用。三名患者因副作用退出试验:出血、抑郁和蛋白尿。然而,这些不良事件均被认为与免疫抑制方案转换为他克莫司单药治疗无直接关系。总之,从环孢素转换为基于他克莫司的治疗是安全且耐受性良好的;它可能改善肾移植后的心血管风险状况。

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