将稳定的肾移植受者转换为通用的他克莫司是可行和安全的,但必须进行监测。

IF 0.9 Q3 SURGERY
Journal of Transplantation Pub Date : 2017-01-01 Epub Date: 2017-01-26 DOI:10.1155/2017/5646858
Fernando González, René López, Elizabeth Arriagada, René Carrasco, Natalia Gallardo, Eduardo Lorca
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引用次数: 5

摘要

背景。他克莫司是用于肾移植患者的主要免疫抑制药物。在智利卫生部授权实施这一转变后,我们研究了用仿制药替代品牌产品是一个有争议的问题。方法。41例稳定的接受肾移植的Prograf (Astellas)患者以1:1的剂量比例切换到通用的他克莫司(Sandoz),随访长达8个月。所有其他药物维持正常操作。结果。切换后,他克莫司剂量及其谷血水平均未发生显著变化,但血清肌酐变化明显:1.62±0.90 mg/dL vs 1.75±0.92 mg/dL (p < 0.001)。同时,进行了5例移植活检,其中2例出现细胞急性排斥反应。通过适当的治疗,有9例感染发作得到满意的治疗。随访期间无患者或移植物丢失。结论。从品牌他克莫司切换到非专利他克莫司(山德士)是可行的,似乎是安全的,但必须由治疗医生仔细监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Switching Stable Kidney Transplant Recipients to a Generic Tacrolimus Is Feasible and Safe, but It Must Be Monitored.

Background. Tacrolimus is the primary immunosuppressive drug used in kidney transplant patients. Replacing brand name products with generics is a controversial issue that we studied after a Chilean Ministry of Health mandate to implement such a switch. Methods. Forty-one stable Prograf (Astellas) receiving kidney transplant patients were switched to a generic tacrolimus (Sandoz) in a 1 : 1 dose ratio and were followed up for up to 8 months. All other drugs were maintained as per normal practice. Results. Neither tacrolimus doses nor their trough blood levels changed significantly after the switch, but serum creatinine did: 1.62 ± 0.90 versus 1.75 ± 0.92 mg/dL (p < 0.001). At the same time, five graft biopsies were performed, and two of them showed cellular acute rejection. There were nine infectious episodes treated satisfactorily with proper therapies. No patient or graft was lost during the follow-up time period. Conclusion. Switching from brand name tacrolimus to a generic tacrolimus (Sandoz) is feasible and appears to be safe, but it must be monitored carefully by treating physicians.

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5
审稿时长
16 weeks
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