The impact of cyclosporine dose and level on acute rejection and patient and graft survival in liver transplant recipients

被引:19
作者
Wiesner, RH
Goldstein, RM
Donovan, JP
Miller, CM
Lake, JR
Lucey, MR
机构
[1] Mayo Clin & Mayo Fdn, Rochester, MN 55905 USA
[2] Mayo Med Sch, Rochester, MN USA
[3] Baylor Univ, Med Ctr, Dallas, TX USA
[4] Univ Nebraska, Med Ctr, Dept Internal Med, Omaha, NE USA
[5] Mt Sinai Med Ctr, New York, NY 10029 USA
[6] Univ Calif San Francisco, Liver Transplantat Program, San Francisco, CA 94143 USA
[7] Univ Penn, Med Ctr, Liver Transplant Program, Philadelphia, PA 19104 USA
来源
LIVER TRANSPLANTATION AND SURGERY | 1998年 / 4卷 / 01期
关键词
D O I
10.1002/lt.500040105
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
A multicenter, retrospective analysis of 623 liver transplant recipients was performed to define safe and effective cyclosporine doses and blood levels at various times after transplantation. Patient and graft survival were assessed as efficacy parameters, and serum creatinine and cholesterol levels as safety parameters, The mean daily cyclosporine dose was 12.1 mg/kg/d at 1 month posttransplantation and 5.5 mg/kg/d after 1 year, After 4 years, the mean cyclosporine dose was maintained at 4.0 mg/kg/d, Mean cyclosporine blood levels showed a similar trend, Patient and graft survival after 4 years of cyclosporine maintenance therapy were 72% and 67%, respectively, Both serum creatinine and cholesterol levels were stable over the study period, and neither correlated with cyclosporine dose, The cumulative incidence of biopsy-proven acute cellular rejection was 59% for early (<6 months) episodes and 21% for late (greater than or equal to 6 months) episodes, Patient and graft survival did not differ significantly between patients experiencing early or late acute rejection episodes and those who did using univariate analysis, The high patient and graft survival, low rejection rates, and lack of significant renal dysfunction or hypercholesterolemia suggest that the cyclosporine doses and blood levels described are safe and therapeutically effective. Copyright (C) 1998 by the American Association for the Study of Liver Diseases.
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收藏
页码:34 / 41
页数:8
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