Department of Gastroenterology and Hepatology, University Medical Center of Utrecht, P.O. Box 85500, 3508 GA Utrecht, The Netherlands.
Department of Gastroenterology and Hepatology, University Medical Center of Utrecht, P.O. Box 85500, 3508 GA Utrecht, The Netherlands; Department of Internal Medicine and Infectious Diseases, University Medical Center of Utrecht, Utrecht, The Netherlands.
Clin Res Hepatol Gastroenterol. 2016 Nov;40(5):622-630. doi: 10.1016/j.clinre.2015.12.014. Epub 2016 Feb 8.
Adherence is essential in antiviral therapy for chronic hepatitis C. We investigated the effect of real-time medication monitoring on adherence to ribavirin.
In this randomized controlled trial, patients in the intervention group received a medication dispenser that monitored ribavirin intake real-time during 24 weeks PEG-interferon/ribavirin±boceprevir or telaprevir. Patients in the control group received standard-of-care. Adherence was also measured by pill count.
Seventy-two patients were assigned to either intervention (n=35) or control groups (n=37). Median adherence by pill count was 96% (range: 43%-100%) with 30 (94%) of patients exhibiting≥80% adherence. Perfect adherence (i.e. 100%) was similar in intervention and control groups: 22 (85%) vs. 15 (75%) (P=0.47). Adherences by real-time medication monitoring and by pill count did not correlate (R=0.19, P=0.36). No predictors of poor adherence could be identified. Ribavirin trough levels after 8 weeks (median: 2.4 vs. 2.7mg/L, P=0.30) and 24 weeks (median: 3.0 vs. 3.0mg/L, P=0.69), and virological responses did not differ between intervention and control groups.
Adherence to ribavirin during PEG-interferon containing therapy in chronic hepatitis C is high. Real-time medication monitoring did not influence adherence to ribavirin, plasma ribavirin levels or virological responses.
在慢性丙型肝炎的抗病毒治疗中,依从性至关重要。我们研究了实时药物监测对利巴韦林依从性的影响。
在这项随机对照试验中,干预组的患者在 24 周的聚乙二醇干扰素/利巴韦林±博赛泼维或特拉泼维治疗期间使用药物分配器实时监测利巴韦林的摄入。对照组的患者接受标准护理。通过药片计数来衡量依从性。
72 名患者被分配到干预组(n=35)或对照组(n=37)。通过药片计数得出的中位依从率为 96%(范围:43%-100%),其中 30 名(94%)患者的依从率≥80%。干预组和对照组的完美依从率(即 100%)相似:22 名(85%)与 15 名(75%)(P=0.47)。实时药物监测和药片计数的依从性没有相关性(R=0.19,P=0.36)。无法确定不良依从的预测因素。第 8 周(中位数:2.4 与 2.7mg/L,P=0.30)和第 24 周(中位数:3.0 与 3.0mg/L,P=0.69)的利巴韦林谷浓度以及病毒学应答在干预组和对照组之间没有差异。
在慢性丙型肝炎的含聚乙二醇干扰素治疗中,利巴韦林的依从性很高。实时药物监测并没有影响利巴韦林的依从性、血浆利巴韦林水平或病毒学应答。