Long-term outcome of a prospective randomized trial of conversion from cyclosporine to azathioprine treatment one year after renal transplantation

被引:52
作者
MacPhee, IAM [1 ]
Bradley, JA [1 ]
Briggs, JD [1 ]
Junor, BJR [1 ]
MacPherson, SG [1 ]
McMillan, MA [1 ]
Rodger, RSC [1 ]
Watson, MA [1 ]
机构
[1] Univ Glasgow, Western Infirm, Renal Transplant Unit, Glasgow G11 6NT, Lanark, Scotland
关键词
D O I
10.1097/00007890-199811150-00013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Since the introduction of cyclosporine (CsA), 1-year renal allograft survival has improved, but concern persists about the long-term adverse effects of CsA, especially with respect to renal function and blood pressure, This randomized controlled trial was set up to establish whether withdrawal of CsA would alter long-term outcome. Methods. Adult patients who, at 1 year after renal transplantation, had a stable serum creatinine of less than 300 mu mol/L and who had not had acute rejection within the last; 6 months were eligible for entry. Patients were randomized either to continue on CsA (n=114) or to stop CsA and start azathioprine (Aza, n=102), All patients remained on prednisolone, Median follow-up was 93 months after transplantation (range: 52-133 months), Results. Theres was no significant difference in actuarial 10-year patient or graft survival (Kaplan-Meier), despite an increased incidence of acute rejection within the first few months after conversion, Median serum creatinine was lower in the Aza group (Aza: 119 mu mol/L; CsA: 153 mu mol/L at 5 years after randomization, P=0.0002). The requirement for antihypertensive treatment was also reduced after conversion to Ate; 75% of patients required antihypertensive treatment at the start of the study, decreasing to 55% from 1 year after randomization in the Aza group and increasing to >80% in the CsA group (55% (Aza) and 84% (CsA) at 6 years after randomization, P<0.005). Conclusions. Conversion from CsA to Aza at 1 year after renal transplantation results in improvement in both blood pressure control and renal allograft function, and is not associated with significant adverse effects on long-term patient or graft survival.
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页码:1186 / 1192
页数:7
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