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接受环孢素微乳剂治疗的心脏和肝脏移植患者的C2监测史。

History of C2 monitoring in heart and liver transplant patients treated with cyclosporine microemulsion.

作者信息

Cantarovich M, Barkun J, Giannetti N, Cecere R, Besner J-G, Tchervenkov J

机构信息

Department of Medicine, Royal Victoria Hospital, McGill Univesity Health Center, Montréal, Québec, Canada.

出版信息

Transplant Proc. 2004 Mar;36(2 Suppl):442S-447S. doi: 10.1016/j.transproceed.2004.01.004.

Abstract

Therapeutic drug monitoring of CsA has evolved since the introduction of CsA microemulsion. The purpose of the present review is to summarize the history of CsA concentration 2 hours postdose (C2) monitoring in heart and liver transplantation. C2 has been shown to be the best single time point that correlates with the area-under-the-curve, with a correlation coefficient (r2) ranging between .83 and.93. C2 monitoring (300 to 600 ng/mL) has resulted in a significant clinical benefit in long-term heart and liver transplant patients compared to trough level (C0) monitoring. Moreover, a C2 range of 300 to 600 ng/mL resulted in a similar calcineurin inhibition compared to a C2 range of 700 to 1000 ng/mL or a C0 range of 100 to 200 ng/mL while being less injurious to renal function. In de novo liver transplant patients not receiving induction therapy, the achievement of a target C2 of 850 to 1400 ng/mL by postoperative day 3 has resulted in a low acute rejection rate. Furthermore, C2 monitoring has been associated with a lower rejection rate in hepatitis C virus (HCV)-negative patients and with an overall lesser severity of acute rejection compared to C0 monitoring. In de novo heart transplant patients who receive antithymocyte globulin induction, a lower C2 range may be sufficient to prevent rejection and renal dysfunction. Future studies should help to fine-tune the optimal C2 range in heart or liver transplant patients receiving induction therapy and different maintenance immunosuppressive combinations.

摘要

自环孢素微乳剂引入以来,环孢素(CsA)的治疗药物监测不断发展。本综述的目的是总结心脏和肝移植中环孢素给药后2小时浓度(C2)监测的历史。C2已被证明是与曲线下面积相关性最好的单一时间点,相关系数(r2)在0.83至0.93之间。与谷浓度(C0)监测相比,C2监测(300至600 ng/mL)已在长期心脏和肝移植患者中产生了显著的临床益处。此外,与700至1000 ng/mL的C2范围或100至200 ng/mL的C0范围相比,300至600 ng/mL的C2范围在抑制钙调神经磷酸酶方面效果相似,同时对肾功能的损害较小。在未接受诱导治疗的初治肝移植患者中,术后第3天达到850至1400 ng/mL的目标C2可导致较低的急性排斥反应发生率。此外,与C0监测相比,C2监测与丙型肝炎病毒(HCV)阴性患者较低的排斥反应发生率以及急性排斥反应的总体严重程度较低相关。在接受抗胸腺细胞球蛋白诱导的初治心脏移植患者中,较低的C2范围可能足以预防排斥反应和肾功能障碍。未来的研究应有助于微调接受诱导治疗和不同维持免疫抑制组合的心脏或肝移植患者的最佳C2范围。

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