Nacif Lucas Souto, David André Ibrahim, Pinheiro Rafael Soares, Diniz Marcio Augusto, Andraus Wellington, Cruz Ruy Jorge, D'Albuquerque Luiz A Carneiro
Faculdade de Medicina da Universidade de São Paulo, Department of Gastroenterology, Liver and Gastrointestinal Transplant Division, São Paulo, SP, Brazil.
Clinics (Sao Paulo). 2014 Nov;69(11):745-9. doi: 10.6061/clinics/2014(11)07.
Orthotopic liver transplantation has improved survival in patients with end-stage liver disease; however, therapeutic strategies that achieve ideal immunosuppression and avoid early complications are lacking. To correlate the dose and level of Tacrolimus with early complications, e.g., rejection, infection and renal impairment, after liver transplantation. From November 2011 to May 2013, 44 adult liver transplant recipients were studied in this retrospective comparative study.
The most frequent indication for liver transplantation was hepatitis C cirrhosis (47.7%), with a higher prevalence observed in male patients (68.18%). The ages of the subjects ranged from 19-71 and the median age was 55.5 years. The mean length of the hospital stay was 16.1±9.32 days and the mean Model for End-stage Liver Disease score was 26.18±4.28. There were five cases of acute cellular rejection (11.37%) and 16 cases of infection (36.37%). The blood samples that were collected and analyzed over time showed a significant correlation between the Tacrolimus blood level and the deterioration of glomerular filtration rate and serum creatinine (p<0.05). Patients with infections had a higher serum level of Tacrolimus (p = 0.012). The dose and presence of rejection were significantly different (p = 0.048) and the mean glomerular filtration rate was impaired in patients who underwent rejection compared with patients who did not undergo rejection (p = 0.0084).
Blood Tacrolimus levels greater than 10 ng/ml were correlated with impaired renal function. Doses greater than 0.15 mg/kg/day were associated with the prevention of acute cellular rejection but predisposed patients to infectious disease.
原位肝移植提高了终末期肝病患者的生存率;然而,目前缺乏能实现理想免疫抑制并避免早期并发症的治疗策略。本研究旨在探讨肝移植后他克莫司的剂量和血药浓度水平与早期并发症(如排斥反应、感染和肾功能损害)之间的相关性。在这项回顾性比较研究中,选取了2011年11月至2013年5月间44例成年肝移植受者进行研究。
肝移植最常见的指征是丙型肝炎肝硬化(47.7%),男性患者更为多见(68.18%)。研究对象年龄在19至71岁之间,中位年龄为55.5岁。平均住院时间为16.1±9.32天,终末期肝病模型平均评分为26.18±4.28。发生急性细胞排斥反应5例(11.37%),感染16例(36.37%)。随着时间推移采集并分析的血样显示,他克莫司血药浓度水平与肾小球滤过率及血清肌酐的恶化之间存在显著相关性(p<0.05)。感染患者的他克莫司血清水平较高(p = 0.012)。排斥反应的剂量及发生率存在显著差异(p = 0.048),与未发生排斥反应的患者相比,发生排斥反应的患者平均肾小球滤过率受损(p = 0.0084)。
他克莫司血药浓度大于10 ng/ml与肾功能损害相关。剂量大于0.15 mg/kg/天可预防急性细胞排斥反应,但会使患者易患感染性疾病。