Immunosuppression based on mycophenolate mofetil in stable liver transplanted patients

被引:21
作者
Bilbao, Itxarone [1 ]
Castells, Luis
Rojas, Luis
Cancino, Jorge
Dopazo, Cristina
Castro, Ernest
Pou, Leonor
Andino, Ricardo
Margarit, Carlos
机构
[1] Univ Autonoma Barcelona, Liver Transplant Unit, Dept Gen Surg, Hosp Valle Hebron, Barcelona, Spain
[2] Univ Autonoma Barcelona, Hosp Vall Hebron, Hepatol Unit, Dept Internal Med, E-08193 Barcelona, Spain
[3] Univ Autonoma Barcelona, Hosp Vall Hebron, Dept Biochem, E-08193 Barcelona, Spain
关键词
mycophenolate mofetil; liver transplantation; stable patients; conversion; nephrotoxicity;
D O I
10.1016/j.intimp.2006.09.022
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aim: To analyze our results With mycophenolate mofetil (MMF) in stable liver transplantation (LT) patients presenting with adverse events (AE) related to prolonged use of calcineurin inhibitors (CNI). Methods: Conversion to MMF was performed in 56 out of 323 LT patients from 91-02: 24 (43%) were converted to MMF in monotherapy and 32 (57%) to MMF+low doses of CNI. The indication for conversion was chronic renal insufficiency (CRI) in all patients. The mean time between AE and conversion was 38.7 +/- 30 months (r: 2-101 m). Post-conversion follow-up was 39 20 months (r: 3-72 m). Results: The calculated creatinine clearance (Crauckoft), improved significantly in all patients. In those converted to MMF, improvement was seen during the first IS months for Urea and during the first 6 months for creatinine. In patients converted to MMF+CNI, improvement was maintained throughout the conversion period for both Urea and creatinine. Eleven (19.6%) patients underwent acute rejection (2 severe episodes in the MMF group and 1 death). Hypertension was present in 31 patients but only improved in 4 (7%). Dyslipemia was found in 12 and improved in 4 (7%). DM was present in 14 and improved in 1 (2%). Conclusions: Conversion to MMF in monotherapy is useful in stable LT patients with CRI due to CNI, although this result is offset by more severe rejections. Therefore, for AE secondary to CNI, we propose all early conversion to MMF+low doses of CNI as a first step. If liver function remains stable and AEs persist or progress, conversion to MMF in monotherapy is recommended, as a second step, with close monitoring of the patient. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1977 / 1983
页数:7
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