Fang Chuxuan, Dong Chunqiang, Huang Kaiyong, Wen Ningyu, Chen Yiyu, Tang Shuangyi
Department of Pharmacy, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Department of Organ Transplantation, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Front Pharmacol. 2024 Nov 21;15:1473891. doi: 10.3389/fphar.2024.1473891. eCollection 2024.
This study aims to explore the factors influencing tacrolimus intrapatient variability (TAC-IPV) and its association with 1-year post-transplant outcomes in pediatric liver transplant recipients.
Clinical and biological data of pediatric patients after liver transplantation were collected. The patients were divided into high- and low-IPV groups according to the median TAC-IPV for statistical comparisons. Factors with < 0.05 in univariate analysis were introduced into binomial logistic regression analysis. Correlation analysis was used to test the connections between the Tac-IPV and outcomes within 1 year after liver transplantation (LT), and Kaplan-Meier was used to draw the survival curves.
A total of 116 children underwent 746 measurements of TAC trough concentrations. The median TAC-IPV was 32.31% (20.81%, 46.77%). Hematocrit ( = 0.017) and concomitant medications ( = 0.001) were identified as independent influencing factors for TAC-IPV. The incidence of transplant rejection ( = 0.008), CMV infection ( < 0.001), and hospital admission due to infection ( = 0.003) were significantly higher in the high-IPV group than in the low-IPV group. Kaplan-Meier survival analysis suggests that after considering the time factor, high IPV (IPV > 32.31%) was still significantly associated with transplant rejection (HR = 3.17 and = 0.005) and CMV infection (HR = 2.3 and < 0.001) within 1 year after LT.
The study highlights the significant variation in TAC-IPV among children post-liver transplantation, emphasizing the impact of hematocrit levels and concomitant medications on TAC-IPV. Elevated TAC-IPV is associated with increased risks of transplant rejection, CMV infection, and readmission due to infection in the first year after liver transplantation. Close monitoring of patients with high TAC-IPV is recommended to promptly detect adverse reactions and provide timely intervention and treatment.
本研究旨在探讨影响小儿肝移植受者他克莫司个体内变异(TAC-IPV)的因素及其与移植后1年结局的关联。
收集小儿肝移植术后患者的临床和生物学数据。根据TAC-IPV中位数将患者分为高IPV组和低IPV组进行统计学比较。单因素分析中P<0.05的因素纳入二项逻辑回归分析。采用相关性分析检验肝移植(LT)后1年内Tac-IPV与结局之间的联系,并采用Kaplan-Meier法绘制生存曲线。
共116例儿童接受了746次TAC谷浓度测量。TAC-IPV中位数为32.31%(20.81%,46.77%)。血细胞比容(P=0.017)和合并用药(P=0.001)被确定为TAC-IPV的独立影响因素。高IPV组移植排斥反应发生率(P=0.008)、巨细胞病毒(CMV)感染率(P<0.001)和因感染住院率(P=0.003)均显著高于低IPV组。Kaplan-Meier生存分析表明,考虑时间因素后,高IPV(IPV>32.31%)在LT后1年内仍与移植排斥反应(HR=3.17,P=0.005)和CMV感染(HR=2.3,P<0.001)显著相关。
该研究突出了小儿肝移植后TAC-IPV的显著差异,强调了血细胞比容水平和合并用药对TAC-IPV的影响。TAC-IPV升高与肝移植后第一年移植排斥反应、CMV感染和因感染再入院风险增加相关。建议密切监测高TAC-IPV患者,以便及时发现不良反应并提供及时干预和治疗。