The association between MMF and risk of progressive renal dysfunction and death in adult liver transplant recipients with HCV

被引:7
|
作者
Lake, John [1 ,2 ]
Patel, Dharmesh [3 ]
David, Kristin [4 ]
Richwine, Jason [4 ]
Morris, Jonathan [4 ]
机构
[1] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Med Ctr, Liver Transplantat Program, Minneapolis, MN 55455 USA
[3] Roche Labs, Nutley, NJ USA
[4] ProSanos Corp, Harrisburg, PA USA
关键词
chronic kidney disease; hepatitis C; immunosuppression; liver transplantation; mycophenolate mofetil; CHRONIC KIDNEY-DISEASE; MYCOPHENOLATE-MOFETIL; THERAPY; CYCLOSPORINE; IMPROVEMENT; TACROLIMUS; SURVIVAL; EFFICACY; FAILURE; IMPACT;
D O I
10.1111/j.1399-0012.2008.00916.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
The impact of a three-drug regimen including mycophenolate mofetil (MMF) vs. a two-drug (no MMF) regimen on progressive renal dysfunction (PRD) in liver transplant recipients with hepatitis C virus (HCV) infection has not been well described. Adults with HCV who received a primary liver transplant between January 1, 2000 and December. 31, 2005 and were discharged from the hospital on a three-drug regimen [CNI+MMF+steroids (S)] (n = 4 946) were compared with those discharged on two-drug regimen (CNI+S) (n = 3 884). Time to PRD (defined by a post-transplant 25% decline in estimated GFR, based on the four-variable MDRD equation) and recipient death were evaluated using Kaplan-Meier analysis. Cox proportional hazards regression was used to estimate the risk for post-transplant PRD and death after controlling for baseline characteristics and extended steroid use. The two groups were similar in baseline characteristics. The percentage of recipients on three- vs. two-drug regimen without PRD was higher, 36.8% vs. 31.9%, (p < 0.001), at three yrs post-transplant; three-drug therapy was associated with a 6% lower adjusted risk of PRD. The death rate and adjusted risk for death was lower for recipients on a three- vs. two-drug regimen. Liver transplant recipients with HCV on a MMF-containing regimen are at a lower risk for PRD and death compared with recipients on a regimen not including MMF.
引用
收藏
页码:108 / 115
页数:8
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