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肾移植术后1年选择性停用环孢素。

Elective cyclosporine withdrawal 1 year after renal transplantation.

作者信息

Heim-Duthoy K L, Chitwood K K, Tortorice K L, Massy Z A, Kasiske B L

机构信息

Drug Evaluation Unit, Hennepin County Medical Center, Minneapolis, MN.

出版信息

Am J Kidney Dis. 1994 Nov;24(5):846-53. doi: 10.1016/s0272-6386(12)80680-9.

Abstract

Whether the risks of acute rejection after elective cyclosporine (CsA) withdrawal in renal transplantation outweigh the potential benefits is unclear. We examined results for 236 patients who underwent transplantation between January 1986 and June 1991. Patients were treated with prophylactic CsA, prednisone, and azathioprine, and had grafts that functioned at least 1 year. We elected to withdraw CsA after 1 year in 192 patients who were rejection free for 12 months. Thirty-four patients elected to continue CsA. In 1988 a protocol that tapered CsA over 6 weeks was abandoned when eight (29.6%) of the first 27 patients developed acute rejection within 6 months. We then adopted a 12-week CsA taper preceded by 1 month of increased azathioprine (2.5 mg/d as tolerated) and followed by increased prednisone (30 mg/d for 1 week, 20 mg/d for 1 week, 15 mg/day for 6 months, then 15 mg/d on alternate days). With this protocol the incidence of postwithdrawal acute rejection within 6 months was reduced to 9.1% among 165 patients (P < 0.01 v 6-week taper). Actuarial 5-year graft survival (patients living with a functioning graft) was 81.7% for patients left on CsA, 88.9% for patients tapered over 6 weeks, and 81.5% for patients tapered over 12 weeks (P > 0.05). We also examined risk factors for acute rejection after CsA withdrawal using a Cox proportional hazards model and found that the relative risk of acute rejection within 6 months of taper was approximately two times greater for each DR mismatch (P < 0.001). We conclude that CsA withdrawal has not affected renal allograft survival at our center.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在肾移植中,择期停用环孢素(CsA)后急性排斥反应的风险是否超过潜在益处尚不清楚。我们研究了1986年1月至1991年6月期间接受移植的236例患者的结果。患者接受了预防性CsA、泼尼松和硫唑嘌呤治疗,且移植肾至少有1年的功能。我们选择在192例无排斥反应达12个月的患者中于1年后停用CsA。34例患者选择继续使用CsA。1988年,当最初27例患者中有8例(29.6%)在6个月内发生急性排斥反应时,一个在6周内逐渐减少CsA用量的方案被放弃。然后我们采用了一个12周逐渐减少CsA用量的方案,在此之前1个月增加硫唑嘌呤用量(根据耐受情况增至2.5mg/d),之后增加泼尼松用量(30mg/d持续1周,20mg/d持续1周,15mg/d持续6个月,然后隔日15mg/d)。采用该方案后,165例患者在停药后6个月内急性排斥反应的发生率降至9.1%(与6周逐渐减量方案相比,P<0.01)。存活且移植肾功能良好的患者5年移植肾存活率,继续使用CsA的患者为81.7%,6周逐渐减量的患者为88.9%,12周逐渐减量的患者为81.5%(P>0.05)。我们还使用Cox比例风险模型研究了停用CsA后急性排斥反应的危险因素,发现每一个DR错配在逐渐减量后6个月内急性排斥反应的相对风险大约增加两倍(P<0.001)。我们得出结论,在我们中心,停用CsA并未影响肾移植的存活。(摘要截短于250词)

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