Parker Brian M, Cywinski Jacek B, Alster Joan M, Irefin Samuel A, Popovich Marc, Beven Michael, Fung John J
Department of General Anesthesiology, Cleveland Clinic, Cleveland, OH 44195, USA.
Liver Transpl. 2008 Jan;14(1):46-52. doi: 10.1002/lt.21308.
Twenty adult patients undergoing orthotopic liver transplantation (OLT) were enrolled in this study, with the noninvasive indocyanine green plasma disappearance rate (ICG-PDR) measured both during and after OLT to assess the relationship between ICG-PDR and the ability of patients to achieve therapeutic postoperative tacrolimus immunosuppressant blood levels. Liver function was determined at both 2 and 18 hours post reperfusion with the ICG-PDR k value (1/min). Postoperative standard serum measures of liver function as well as liver biopsies were also collected and analyzed. The median ICG-PDR k value for the study group at 2 hours post reperfusion was 0.20 (0.16, 0.27), whereas at 18 hours post reperfusion, it was 0.22 (0.18, 0.35). The median change in the k value between the two ICG-PDR measurements was 0.05 (-0.02, 0.07) with P = 0.02. There was an interaction between the postoperative day 1 (18 hours post reperfusion) ICG-PDR k value and the linear increase in the tacrolimus blood level, such that the greater the k value was, the more gradual the observed rise was in tacrolimus over time [that is, the longer it took to achieve a therapeutic blood level (>12 ng/mL), P = 0.003]. Of the 16 patients that received tacrolimus, comparable dosing on a per kilogram body weight basis was observed. Also, no significant association between ICG-PDR k values and postoperative liver biopsy results was seen. This study demonstrates that the ICG-PDR measurement is a modality with the potential to assist in achieving adequate blood levels of tacrolimus following OLT.
本研究纳入了20例接受原位肝移植(OLT)的成年患者,在OLT期间及术后均测量无创性吲哚菁绿血浆消失率(ICG-PDR),以评估ICG-PDR与患者术后达到他克莫司免疫抑制药物治疗血药浓度能力之间的关系。在再灌注后2小时和18小时测定肝功能及ICG-PDR的k值(1/分钟)。还收集并分析了术后肝功能的标准血清指标以及肝活检结果。研究组在再灌注后2小时的ICG-PDR k值中位数为0.20(0.16,0.27),而在再灌注后18小时为0.22(0.18,0.35)。两次ICG-PDR测量之间k值的中位数变化为0.05(-0.02,0.07),P = 0.02。术后第1天(再灌注后18小时)的ICG-PDR k值与他克莫司血药浓度的线性增加之间存在交互作用,即k值越大,他克莫司随时间的升高越缓慢[也就是说,达到治疗血药浓度(>12 ng/mL)所需的时间越长,P = 0.003]。在接受他克莫司治疗的16例患者中,观察到基于每千克体重的给药剂量相当。此外,未发现ICG-PDR k值与术后肝活检结果之间存在显著关联。本研究表明,ICG-PDR测量是一种有可能有助于在OLT后达到足够他克莫司血药浓度的方法。