摘要
目的探讨应用以环孢素(cyclosporine,CsA)为基础免疫抑制剂的慢性移植肾肾病(chronic allograft nephropathy,CAN)患者转换为他克莫司(tacrolimus,FK506)联合麦考酚吗乙酯(mycophenolate mofetil,MMF)治疗的疗效及安全性。方法使用CsA为基础免疫抑制方案的CAN患者76例,转换为FK506+MMF,随访6个月,根据移植肾穿刺病理结果将患者分为伴有慢性排斥反应组(CR组,41例)和不伴有慢性排斥反应组(non-CR组,35例)。观察两组的疗效及不良反应。结果 CR组好转27例(66%),稳定9例(22%),无效5例(12%);non-CR组好转11例(31%),稳定15例(43%),无效9例(26%),CR组疗效优于non-CR组(P<0.05)。CR组和non-CR组转换后,24h尿蛋白定量均有所降低,高血压和高脂血症的病例数有所减少,而且未出现继发性高血糖、严重感染等不良反应。结论 CAN患者使用FK506+MMF替代CsA为基础的免疫抑制剂方案是安全有效的。
Objective To investigate the efficacy and safety of converting cyclosporine(CsA)-based immunosuppressant regimen to tacrolimus(FK506)plus mycophenolate mofetil(MMF)in renal transplantation patients with chronic allograft nephropathy(CAN).Methods Seventy-six cases of CAN were followed up for 6 month,who converted to FK506+MMF from CsA.All cases were divided into chronic rejection(CR)group(n =41)and non-CR group(n =35)according to the pathological results of transplanted kidney.The efficacy and adverse reaction were observed between the two groups.Results In CR group,the renal function were improved in 27 cases(66 %),stable in 9 cases(22 %)and even worse in 5 cases(12 %).In non-CR group,the renal function were improved in 11 cases(31 %),stable in 15 cases(43 %)and even worse in another 9 cases(26 %).The efficacy of immunosuppressant conversion in CR group was more obvious than that in non-CR group(P 0.05).The amount of 24-hour urine protein excretion was reduced compared with the pre-conversion in both CR group and non-CR group.Compared with pre-conversion,the incidence of hypertension and hyperlipidemia were also reduced.There was no case with new onset post transplantation hyperglycaemia as well as with serve infection.Conclusion It suggests that converting to FK506+MMF from CsA-based regimen is safe and effective in treating renal transplantation patients with CAN.
出处
《器官移植》
CAS
2010年第6期342-344,380,共4页
Organ Transplantation
基金
广东省自然科学基金(06024438)
关键词
肾移植
慢性移植肾肾病
慢性排斥反应
他克莫司
麦考酚吗乙酯
环孢素
Renal transplantation
Chronic allograft nephropathy
Chronic rejection
Tacrolimus
Mycophenolate mofetil
Cyclosporine