Lehner Lukas J, Reinke Petra, Hörstrup Jan H, Rath Thomas, Suwelack Barbara, Krämer Bernhard K, Budde Klemens, Banas Bernhard
Department of Nephrology and Medical Intensive Care, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Department of Nephrology and Intensive Care Medicine, Humboldt-University, Berlin, Germany.
Clin Transplant. 2018 Jan;32(1). doi: 10.1111/ctr.13142. Epub 2018 Jan 5.
This study assessed adherence to prolonged-release tacrolimus (PR-T)-based immunosuppression during routine maintenance of renal transplant recipients in Germany. Patients had received PR-T for ≥1 month at inclusion. Data were collected during four visits (V): baseline (V1), 6 (V2), 12 (V3), and 18 (V4) months. Composite primary endpoint: nonadherence at V4, defined as self-reported nonadherence on the Basel Assessment of Adherence with Immunosuppressive Medication Scale (BAASIS ), investigator-rated nonadherence, and/or V4 tacrolimus trough level outside a predefined range. Secondary endpoints: individual BAASIS items, incidence of rejection, kidney function, and safety. Overall, 153 adult kidney recipients (mean [standard deviation] time post-transplant 5.8 [4.6] years) were included. Nonadherence was high at V4 (67.7% [95% confidence interval 58.9%, 75.6%]). Medication-taking adherence was 86.9% and 91.3% at V1 and V4, respectively; adherence to timing of medication intake was 58.2% and 58.3%, with little evidence of missed doses/drug holidays. Investigators rated adherence "good" in 85.6% of patients (V4). Two (1.3%) patients had acute rejection episodes. Kidney function remained stable (mean creatinine clearance, V1: 62.1 mL/min; V4: 65.3 mL/min). Investigators rated effectiveness of PR-T as "very good"/"good" in 91.5% of patients. Most patients (94.7%) found PR-T dosing more convenient than immediate-release tacrolimus. PR-T was well tolerated with high medication persistence.
本研究评估了德国肾移植受者在常规维持治疗期间对基于缓释他克莫司(PR-T)的免疫抑制治疗的依从性。纳入的患者接受PR-T治疗≥1个月。在四次访视(V)期间收集数据:基线(V1)、6个月(V2)、12个月(V3)和18个月(V4)。复合主要终点:V4时的不依从,定义为在巴塞尔免疫抑制药物依从性评估量表(BAASIS)上自我报告的不依从、研究者评定的不依从和/或V4时他克莫司谷浓度超出预定义范围。次要终点:BAASIS各单项、排斥反应发生率、肾功能和安全性。总共纳入了153例成年肾移植受者(移植后平均[标准差]时间为5.8[4.6]年)。V4时的不依从率很高(67.7%[95%置信区间58.9%,75.6%])。V1和V4时的服药依从性分别为86.9%和91.3%;服药时间的依从性分别为58.2%和58.3%,几乎没有漏服剂量/药物假期的证据。研究者在85.6%的患者(V4)中评定依从性为“良好”。两名(1.3%)患者发生急性排斥反应。肾功能保持稳定(平均肌酐清除率,V1:62.1 mL/分钟;V4:65.3 mL/分钟)。研究者在91.5%的患者中评定PR-T的有效性为“非常好”/“良好”。大多数患者(94.7%)发现PR-T给药比速释他克莫司更方便。PR-T耐受性良好,药物持续性高。