Long-term outcome of adding mycophenolate mofetil to tacrolimus for nephrotoxicity following liver transplantation

被引:27
作者
Jain, A
Vekatramanan, R
Eghtesad, B
Gadomski, M
Mohanka, R
Marcos, A
Fung, J
机构
[1] Univ Rochester, Strong Mem Hosp, Dept Surg, Rochester, NY 14642 USA
[2] Univ Pittsburgh, Thomas E Starzl Transplantat Inst, Dept Surg, Pittsburgh, PA USA
[3] Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
关键词
liver transplantation; nephrotoxicity; tacrolimus; mycophenolate mofetil;
D O I
10.1097/01.TP.0000173994.63299.63
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Mycophenolate mofetil (MMF) has no known nephrotoxicity. This report examines the outcome in patients who received MMF for renal impairment on tacrolimus-based immunosuppression. From 1995 to 1996, twelve liver transplantation (LTx) patients (mean age 54.6 years) with serum creatinine > 1.8 mg/dl were included in the study. MMF was introduced and tacrolimus dose was reduced by 30-50%. Each patient was followed for 6 years. Renal function showed improvement in seven patients, deterioration in four, and no change in one patient. Overall mean serum creatinine decreased from 2.5 to 1.9 mg/dl at 6 months but increased to 2.2 mg/dl at 18 to 24 months. After that, renal function remained stable for 72 months. lothalamate clearance showed 18.5% improvement at I year. Three patients developed renal failure. Six patients died in the follow-up period. Addition of MMF with reduced tacrolimus dose resulted in sustained improvement in renal function in 58% of patients.
引用
收藏
页码:859 / 864
页数:6
相关论文
共 19 条
[1]
Evaluation of renal function in transplant patients on tacrolimus therapy [J].
Agarwala, S ;
Culligan, E ;
Jain, A ;
McCauley, J ;
Shapiro, R ;
Chakrabarti, P ;
Burckart, G ;
Venkataramanan, R .
JOURNAL OF CLINICAL PHARMACOLOGY, 2002, 42 (07) :798-805
[2]
[Anonymous], 1994, Lancet, V344, P423
[3]
Improvement of acute and chronic renal dysfunction in liver transplant patients after substitution of calcineurin inhibitors by mycophenolate mofetil [J].
Barkmann, A ;
Nashan, B ;
Schmidt, HHJ ;
Böker, KHW ;
Emmanouilidis, N ;
Rosenau, J ;
Bahr, MJ ;
Hoffmann, MW ;
Manns, MP ;
Klempnauer, J ;
Schlitt, HJ .
TRANSPLANTATION, 2000, 69 (09) :1886-1890
[4]
BUSUTTIL RW, 1994, NEW ENGL J MED, V331, P1110
[5]
End-stage renal disease (ESRD) after orthotopic liver transplantation (OLTX) using calcineurin-based immunotherapy - Risk of development and treatment [J].
Gonwa, TA ;
Mai, ML ;
Melton, LB ;
Hays, SR ;
Goldstein, RM ;
Levy, MF ;
Klintmalm, GB .
TRANSPLANTATION, 2001, 72 (12) :1934-1939
[6]
GRINYO J, 1995, LANCET, V345, P1321
[7]
Conversion of liver transplant recipients on cyclosporine with renal impairment to mycophenolate mofetil [J].
Herrero, JI ;
Quiroga, J ;
Sangro, B ;
Girala, M ;
Gomez-Manero, N ;
Pardo, F ;
Alvarez-Cienfuegos, J ;
Prieto, J .
LIVER TRANSPLANTATION AND SURGERY, 1999, 5 (05) :414-420
[8]
Use of mycophenolate mofetil in liver transplant recipients experiencing renal dysfunction on cyclosporine or tacrolimus-randomized, prospective, multicenter study results [J].
Hodge, EE ;
Reich, DJ ;
Clavien, PA ;
Kim-Schluger, L .
TRANSPLANTATION PROCEEDINGS, 2002, 34 (05) :1546-1547
[9]
IWATSUKI S, 1988, TRANSPLANT P, V20, P498
[10]
What have we learned about primary liver transplantation under tacrolimus immunosuppression? Long-term follow-up of the first 1000 patients [J].
Jain, A ;
Reyes, J ;
Kashyap, R ;
Rohal, S ;
Abu-Elmagd, K ;
Starzl, T ;
Fung, J .
ANNALS OF SURGERY, 1999, 230 (03) :441-448