Bessa Adrieli B, Felipe Claudia R, Hannun Pedro, Sayuri Priscila, Felix Maria Julia, Ruppel Priscila, Ferreira Alexandra N, Cristelli Marina P, Viana Laila, Mansur Juliana B, Basso Geovana, Aguiar Wilson Ferreira, Tedesco-Silva Hélio, Medina-Pestana José
Divisions of *Nephrology and †Urology, Hospital do Rim, Universidade Federal de São Paulo, Brazil.
Ther Drug Monit. 2016 Aug;38(4):447-55. doi: 10.1097/FTD.0000000000000299.
This study evaluated the influence of pharmaceutical care (PhC) in the intra-individual variability of dose-corrected whole blood tacrolimus (TAC) trough concentrations, adherence to immunosuppressive therapy and clinical outcomes.
We randomized 128 kidney transplant recipients to receive PhC consisted of predefined instructions provided by a pharmacist (PhC group, n = 64) or standard nurse staff instructions (control group, n = 64) from day 3 to day 90 after kidney transplantation. The study was powered to detect at least 50% reduction in the coefficient of variation (%CV), calculated from 6 dose-corrected whole blood TAC trough concentrations, in the PhC group. Patient adherence was evaluated using Basel Assessment of Adherence to Immunosuppressive Medication Scale (BAASIS) questionnaire.
There was no difference in the %CV comparing PhC and control group (31.4% ± 12.3% versus 32.5% ± 16.1%, P = 0.673). There were no differences in the proportion of patients showing TAC concentrations within predefined target concentrations in each study visit. There was no difference in the proportion of nonadherent patients at day 28 (17% versus 26%, P = 0.135) and day 90 (27% versus 25%, P = 0.457) based on BAASIS questionnaire answers, respectively. There were no differences in clinical outcomes.
Universal PhC in addition to standard nurse staff instruction was not associated with reduced intra-individual variability of dose-corrected whole blood TAC trough concentrations or improved adherence.
本研究评估了药学服务(PhC)对剂量校正的全血他克莫司(TAC)谷浓度个体内变异性、免疫抑制治疗依从性及临床结局的影响。
我们将128例肾移植受者随机分为两组,从肾移植术后第3天至第90天,一组接受由药剂师提供的预定义指导的药学服务(PhC组,n = 64),另一组接受标准护士指导(对照组,n = 64)。该研究旨在检测PhC组中由6次剂量校正的全血TAC谷浓度计算得出的变异系数(%CV)至少降低50%。使用巴塞尔免疫抑制药物依从性评估量表(BAASIS)问卷评估患者依从性。
PhC组和对照组的%CV无差异(31.4% ± 12.3%对32.5% ± 16.1%,P = 0.673)。在每次研究访视中,TAC浓度处于预定义目标浓度范围内的患者比例无差异。根据BAASIS问卷答案,在第28天(17%对26%,P = 0.135)和第90天(27%对25%,P = 0.457),非依从患者的比例无差异。临床结局也无差异。
除标准护士指导外的通用药学服务与剂量校正的全血TAC谷浓度个体内变异性降低或依从性改善无关。