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肝移植术后慢性肾功能不全患者由钙调磷酸酶抑制剂转换为依维莫司后肾功能的改善。

Improvement of renal function after the switch from a calcineurin inhibitor to everolimus in liver transplant recipients with chronic renal dysfunction.

机构信息

Liver Transplantation Unit, Hospital Clinico Universitario de Santiago, Santiago de Compostela, Spain.

出版信息

Liver Transpl. 2009 Dec;15(12):1792-7. doi: 10.1002/lt.21920.

Abstract

Chronic renal dysfunction is a frequent and severe complication in solid-organ transplant recipients. Calcineurin inhibitors (CNIs) are the main pathogenic factors of renal dysfunction. Switching from CNIs to nonnephrotoxic drugs, such as mammalian target of rapamycin inhibitors (everolimus and sirolimus), can improve renal function in these patients, but available data about the efficacy and safety of everolimus in liver transplant recipients are scarce. Twenty-one liver transplant recipients (19 males, mean age = 60.6 +/- 7.8 years) with chronic renal dysfunction (creatinine >or= 1.5 mg/dL) were prospectively included. The basal creatinine values were 1.79 +/- 0.39 mg/dL (range = 1.50-2.90 mg/dL). The basal creatinine clearance, evaluated with the Cockroft-Gault formula, was 54.64 +/- 12.47 mL/minute. Everolimus was initiated at a dosage of 0.75 mg twice daily, with target levels of 3 to 8 ng/mL. The withdrawal of CNIs was initiated after the target levels of everolimus were reached. Periodic controls of the weight, arterial pressure, liver function tests, serum creatinine, everolimus levels, proteinuria, creatinine clearance, and glomerular filtration rate at days 30, 90, 180, and 360 were made. After a median follow-up of 19.8 months, the respective creatinine values at 30, 90, 180, and 360 days were 1.68 +/- 0.40 (P = 0.012 with respect to basal values), 1.67 +/- 0.34 (P = 0.107), 1.70 +/- 0.41 (P = 0.521), and 1.57 +/- 0.30 mg/dL (P = 0.047). The respective creatinine clearance values at 30, 90, 180, and 360 days were 58.64 +/- 16.50 (P = 0.013 with respect to basal values), 59.49 +/- 13.27 (P = 0.028), 59.82 +/- 16.83 (P = 0.124), and 64.46 +/- 16.79 mL/minute (P = 0.025). CNIs were withdrawn in 20 recipients (95.2%). Rejection was not detected in any case. In conclusion, the application in liver transplant recipients with chronic renal dysfunction of an immunosuppressive protocol with everolimus and the withdrawal of CNIs was associated with an initial improvement of renal function tests without an increase in the risk of rejection.

摘要

慢性肾功能障碍是实体器官移植受者中常见且严重的并发症。钙调神经磷酸酶抑制剂(CNIs)是肾功能障碍的主要致病因素。将 CNIs 转换为非肾毒性药物,如雷帕霉素靶蛋白抑制剂(依维莫司和西罗莫司),可改善这些患者的肾功能,但关于依维莫司在肝移植受者中的疗效和安全性的数据很少。21 例(男性 19 例,平均年龄 60.6 +/- 7.8 岁)慢性肾功能障碍(肌酐 >or= 1.5 mg/dL)的肝移植受者前瞻性纳入研究。基础肌酐值为 1.79 +/- 0.39 mg/dL(范围 = 1.50-2.90 mg/dL)。用 Cockroft-Gault 公式评估的基础肌酐清除率为 54.64 +/- 12.47 mL/minute。依维莫司起始剂量为每日 2 次,每次 0.75 毫克,目标浓度为 3 至 8 ng/mL。在达到依维莫司的目标浓度后,开始停用 CNIs。在第 30、90、180 和 360 天进行体重、动脉压、肝功能试验、血清肌酐、依维莫司水平、蛋白尿、肌酐清除率和肾小球滤过率的定期监测。中位随访 19.8 个月后,第 30、90、180 和 360 天的肌酐值分别为 1.68 +/- 0.40(与基础值相比,P = 0.012)、1.67 +/- 0.34(P = 0.107)、1.70 +/- 0.41(P = 0.521)和 1.57 +/- 0.30 mg/dL(P = 0.047)。第 30、90、180 和 360 天的肌酐清除率值分别为 58.64 +/- 16.50(与基础值相比,P = 0.013)、59.49 +/- 13.27(P = 0.028)、59.82 +/- 16.83(P = 0.124)和 64.46 +/- 16.79 mL/minute(P = 0.025)。20 例(95.2%)受者停用了 CNIs。在任何情况下都未检测到排斥反应。总之,在慢性肾功能障碍的肝移植受者中应用依维莫司和停用 CNIs 的免疫抑制方案与肾功能试验的初始改善相关,而排斥反应的风险没有增加。

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