Groetzner Jan, Kaczmarek Ingo, Landwehr Peter, Mueller Markus, Daebritz Sabine, Lamm Peter, Meiser Bruno, Reichart Bruno
Department of Cardiac Surgery, Ludwig Maximilians University Hospital Grosshadern, Marchioninistrasse 15, D-81377 Munich, Germany.
Eur J Cardiothorac Surg. 2004 Mar;25(3):333-41. doi: 10.1016/j.ejcts.2003.11.030.
Calcineurin inhibitor (CNI)-related renal failure is a common problem after cardiac transplantation (HTx). The aim of this prospective study was to evaluate the safety and efficacy of a completely CNI-free immunosuppressive regimen [mycophenolate mofetil (MMF) and sirolimus (Sir)] in HTx-recipients with late post-transplant renal impairment.
Since 2001, 30 HTx-patients (25 men, 6 women; 0.2-14.2 years after transplantation) with CNI-based immunosuppression and a serum creatinine >1.9 mg/dl were included in the study. Creatinine and cystatin levels were monitored to detect renal function. Conversion was started with 6 mg Sir or 500 mg MMF according to the pre-existing regimen and was continued with the dose adjusted to achieve target trough levels between 8 and 14 ng/ml (Sir) or 1.5 and 4 microg/ml (mycophenolate). Subsequently, the CNIs were tapered down and stopped. Clinical follow-up included endomyocardial biopsies, echocardiography and laboratory studies. Additionally, every HTx-patient treated at our centre between 1996 and 2001 due to chronic renal failure without immunosuppressive conversion and fulfilling the inclusion criteria were retrospectively analysed and acted as control group.
Patient demographics and 1-year survival [93 (conversion) vs 90% (control)] were compared. No acute rejection episode was detected in either group. Renal function improved significantly in the conversion group (creatinine: 3.18+/-0.71 vs 2.22+/-0.79 mg/dl, P=0.001; cystatin pre- vs post-conversion: 2.95+/-1.06 vs 2.02+/-1.1 mg/l, P=0.01). In three patients haemodialysis therapy was stopped completely after conversion. In the control group renal impairment was deteriorating, creatinine increased from 2.44+/-0.8 to 3.28+/-1 mg/dl (P=0.01). In 10 out of 33 patients chronic haemodialysis had to be initiated within 1 year. Although side effects of CNI-free immunosuppression were common (76%), no patient had to be excluded due to adverse effects.
Conversion from CNI-based immunosuppression to MMF and Sir in HTx-patients with chronic renal failure was safe, preserved graft function and improved renal function.
钙调神经磷酸酶抑制剂(CNI)相关的肾衰竭是心脏移植(HTx)后常见的问题。这项前瞻性研究的目的是评估在移植后期出现肾功能损害的HTx受者中,完全无CNI免疫抑制方案[霉酚酸酯(MMF)和西罗莫司(Sir)]的安全性和有效性。
自2001年起,30例接受基于CNI免疫抑制治疗且血清肌酐>1.9 mg/dl的HTx患者(25例男性,6例女性;移植后0.2 - 14.2年)被纳入研究。监测肌酐和胱抑素水平以检测肾功能。根据原有的治疗方案,开始使用6 mg西罗莫司或500 mg霉酚酸酯进行转换治疗,并持续调整剂量以达到目标谷浓度,西罗莫司为8至14 ng/ml,霉酚酸为1.5至4 μg/ml。随后,逐渐减少并停用CNI。临床随访包括心内膜心肌活检、超声心动图和实验室检查。此外,对1996年至2001年期间在本中心因慢性肾衰竭接受治疗且未进行免疫抑制转换并符合纳入标准的每例HTx患者进行回顾性分析,并作为对照组。
比较了患者的人口统计学特征和1年生存率[转换组为93%,对照组为90%]。两组均未检测到急性排斥反应。转换组的肾功能显著改善(肌酐:3.18±0.71 vs 2.22±0.79 mg/dl,P = 0.001;转换前与转换后的胱抑素:2.95±1.06 vs 2.02±1.1 mg/l,P = 0.01)。3例患者在转换治疗后完全停止了血液透析治疗。对照组的肾功能损害在恶化,肌酐从2.44±0.8升高至3.28±1 mg/dl(P = 0.01)。33例患者中有10例在1年内不得不开始进行慢性血液透析。尽管无CNI免疫抑制的副作用很常见(76%),但没有患者因不良反应而被排除。
在慢性肾衰竭的HTx患者中,从基于CNI的免疫抑制转换为MMF和西罗莫司是安全的,可保留移植肾功能并改善肾功能。