McDiarmid S V, Farmer D A, Goldstein L I, Martin P, Vargas J, Tipton J R, Simmons F, Busuttil R W
Department of Surgery, University of California, Los Angeles, USA.
Transplantation. 1995 Dec 27;60(12):1443-50. doi: 10.1097/00007890-199560120-00013.
The safety of steroid withdrawal in orthotopic liver transplant (OLT) recipients has been studied in a prospective trial with a comparison control group. Sixty-four recipients of ABO-compatible grafts (42 adults, 22 children) were randomized into a steroid withdrawal (SW) group and a control group. Inclusion criteria included survival > one year post-OLT and no rejection > six months after OLT. Exclusion criteria included previous graft loss secondary to rejection, > two episodes of documented rejection, patients transplanted for autoimmune hepatitis, and patients unable to receive azathioprine. Target HPLC cyclosporine levels in both groups were 100-200 ng/ml. Thirty-three patients entered the SW group and 31 the control group at a mean of 3.5 years after OLT; follow-ups were 592 and 527 days, respectively. Two patients in each group developed biopsy-proven rejection. In the SW group one patient rejected at three months, the other at nine months. Both rejection episodes resolved with only reinstitution of oral prednisone. Of the two patients who rejected in the control group (one at 7 months, one at 11 months) one required conversion to tacrolimus and the other intravenous steroids. There were no significant differences between the two groups for prednisone, azathioprine, cyclosporine doses, cyclosporine levels, liver function tests, and white blood cell counts at base line compared with 12 months. Fasting serum cholesterol in the SW group decreased from 194 +/- 44 mg/dl at baseline to 175 +/- 37 mg/dl at one year, whereas in the control group cholesterol rose from 180 +/- 48 mg/dl to 193 +/- 44 mg/dl. In pediatric patients no significant difference in age-adjusted height velocities over one year was seen between the two groups. We concluded that dual therapy with cyclosporine and azathioprine in stable long-term liver allograft recipients is not associated with an increase in rejection incidence. Prednisone withdrawal may be associated with an improvement in lipid profiles.
一项前瞻性试验通过设立对照比较组,对原位肝移植(OLT)受者停用类固醇的安全性进行了研究。64例接受ABO血型相容移植物的受者(42例成人,22例儿童)被随机分为类固醇撤药(SW)组和对照组。纳入标准包括OLT术后存活超过1年且OLT术后6个月内无排斥反应。排除标准包括既往因排斥反应导致移植物丢失、有记录的排斥反应发作超过2次、因自身免疫性肝炎接受移植的患者以及无法接受硫唑嘌呤的患者。两组的目标高效液相色谱法环孢素水平均为100 - 200 ng/ml。33例患者在OLT术后平均3.5年进入SW组,31例进入对照组;随访时间分别为592天和527天。两组各有2例患者经活检证实发生排斥反应。在SW组,1例患者在3个月时发生排斥反应,另1例在9个月时发生。两次排斥反应均仅通过重新给予口服泼尼松得以缓解。在对照组发生排斥反应的2例患者中(1例在7个月时,1例在11个月时),1例需要换用他克莫司,另1例需要静脉使用类固醇。与12个月时相比,两组在基线时的泼尼松、硫唑嘌呤、环孢素剂量、环孢素水平、肝功能检查和白细胞计数方面均无显著差异。SW组的空腹血清胆固醇从基线时的194±44 mg/dl降至1年时的175±37 mg/dl,而对照组的胆固醇从180±48 mg/dl升至193±44 mg/dl。在儿科患者中,两组在1年的年龄校正身高增长速度方面未见显著差异。我们得出结论,对于稳定的长期肝移植受者,环孢素和硫唑嘌呤联合治疗与排斥反应发生率增加无关。停用泼尼松可能与脂质谱改善有关。