Breslin Nadine T, Salerno David M, Topkara Veli K, Latif Farhana, Restaino Susan, Takeda Koji, Takayama Hiroo, Farr Maryjane, Colombo Paolo C, Jennings Douglas L
1 Department of Pharmacy, NewYork-Presbyterian Hospital, New York, NY, USA.
2 Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Prog Transplant. 2019 Jun;29(2):129-134. doi: 10.1177/1526924819835840. Epub 2019 Mar 7.
Amiodarone use prior to heart transplant is independently associated with a higher rate of severe primary graft dysfunction and in-hospital mortality. Amiodarone may also alter the pharmacokinetics of medications metabolized via cytochrome P450. No data exist regarding the interaction between pretransplant amiodarone and tacrolimus concentrations.
Single-center retrospective study of transplant patients between January 1, 2014, and June 30, 2016. A therapeutic tacrolimus concentration was defined as a trough level between 8 and 15 ng/mL for 2 consecutive days. The primary outcome was the tacrolimus therapeutic weight-based dosing requirements (mg/kg/day) for patients receiving amiodarone prior to transplant when compared to those without prior receipt of amiodarone. Secondary outcomes include the incidence of cellular rejection and mortality within 6 months posttransplant.
Multi-organ transplant recipients (n = 3), retransplants (n = 9), those who died prior to a therapeutic level (n = 1), and those receiving amiodarone posttransplant (n = 7) were excluded from the analysis. Of the 80 patients included, 34 (42%) received amiodarone prior to transplant. Patient characteristics were similar, with the exception of primary graft dysfunction incidence (38% in amiodarone vs 8.5% in control, P = .001). The median therapeutic dose was 0.1 (interquartile range [IQR]: 0.07-0.12) versus 0.13 (IQR: 0.09-0.17) in the amiodarone and control groups, respectively, ( P < .01). No significant difference in mortality or rejection was noted.
Patients receiving amiodarone prior to transplant require a lower weight-based dose of tacrolimus.
心脏移植前使用胺碘酮与严重原发性移植物功能障碍发生率较高及住院死亡率独立相关。胺碘酮还可能改变经细胞色素P450代谢的药物的药代动力学。目前尚无关于移植前胺碘酮与他克莫司浓度之间相互作用的数据。
对2014年1月1日至2016年6月30日期间的移植患者进行单中心回顾性研究。将治疗性他克莫司浓度定义为连续2天谷浓度在8至15 ng/mL之间。主要结局是与未预先接受胺碘酮的患者相比,移植前接受胺碘酮的患者基于体重的他克莫司治疗剂量需求(mg/kg/天)。次要结局包括移植后6个月内细胞排斥反应发生率和死亡率。
多器官移植受者(n = 3)、再次移植者(n = 9)、在达到治疗水平前死亡者(n = 1)以及移植后接受胺碘酮者(n = 7)被排除在分析之外。在纳入的80例患者中,34例(42%)移植前接受了胺碘酮。患者特征相似,但原发性移植物功能障碍发生率除外(胺碘酮组为38%,对照组为8.5%,P = 0.001)。胺碘酮组和对照组的中位治疗剂量分别为0.1(四分位间距[IQR]:0.07 - 0.12)和0.13(IQR:0.09 - 0.17),(P < 0.01)。在死亡率或排斥反应方面未观察到显著差异。
移植前接受胺碘酮的患者基于体重的他克莫司剂量需求较低。