Langness Jacob A, Nguyen Matthew, Wieland Amanda, Everson Gregory T, Kiser Jennifer J
Jacob A Langness, Matthew Nguyen, Amanda Wieland, Gregory T Everson, Jennifer J Kiser, Hepatology and Transplant Clinic, University of Colorado Hospital, Aurora, CO 80045, United States.
World J Gastroenterol. 2017 Mar 7;23(9):1618-1626. doi: 10.3748/wjg.v23.i9.1618.
To quantify drug-drug-interactions (DDIs) encountered in patients prescribed hepatitis C virus (HCV) treatment, the interventions made, and the time spent in this process.
As standard of care, a clinical pharmacist screened for DDIs in patients prescribed direct acting antiviral (DAA) HCV treatment between November 2013 and July 2015 at the University of Colorado Hepatology Clinic. HCV regimens prescribed included ledipasvir/sofosbuvir (LDV/SOF), paritaprevir/ritonavir/ombitasvir/dasabuvir (OBV/PTV/r + DSV), simeprevir/sofosbuvir (SIM/SOF), and sofosbuvir/ribavirin (SOF/RBV). This retrospective analysis reviewed the work completed by the clinical pharmacist in order to measure the aims identified for the study. The number and type of DDIs identified were summarized with descriptive statistics.
Six hundred and sixty four patients (83.4% Caucasian, 57% male, average 56.7 years old) were identified; 369 for LDV/SOF, 48 for OBV/PTV/r + DSV, 114 for SIM/SOF, and 133 for SOF/RBV. Fifty-one point five per cent of patients were cirrhotic. Overall, 5217 medications were reviewed (7.86 medications per patient) and 781 interactions identified (1.18 interactions per patient). The number of interactions were fewest for SOF/RBV (0.17 interactions per patient) and highest for OBV/PTV/r + DSV (2.48 interactions per patient). LDV/SOF and SIM/SOF had similar number of interactions (1.28 and 1.48 interactions per patient, respectively). Gastric acid modifiers and vitamin/herbal supplements commonly caused interactions with LDV/SOF. Hypertensive agents, analgesics, and psychiatric medications frequently caused interactions with OBV/PTV/r + DSV and SIM/SOF. To manage these interactions, the pharmacists most often recommended discontinuing the medication (28.9%), increasing monitoring for toxicities (24.1%), or separating administration times (18.2%). The pharmacist chart review for each patient usually took approximately 30 min, with additional time for more complex patients.
DDIs are common with HCV medications and management can require medication adjustments and increased monitoring. An interdisciplinary team including a clinical pharmacist can optimize patient care.
量化接受丙型肝炎病毒(HCV)治疗的患者中出现的药物相互作用(DDI)、所采取的干预措施以及该过程所花费的时间。
作为标准治疗,一名临床药剂师于2013年11月至2015年7月在科罗拉多大学肝病诊所对接受直接抗病毒药物(DAA)HCV治疗的患者进行了DDI筛查。所开具的HCV治疗方案包括来迪派韦/索磷布韦(LDV/SOF)、帕利哌韦/利托那韦/奥比他韦/达沙布韦(OBV/PTV/r + DSV)、西米普明/索磷布韦(SIM/SOF)以及索磷布韦/利巴韦林(SOF/RBV)。这项回顾性分析审查了临床药剂师完成的工作,以衡量本研究确定的目标。通过描述性统计总结了所识别出的DDI的数量和类型。
共识别出664例患者(83.4%为白种人,57%为男性,平均年龄56.7岁);其中369例接受LDV/SOF治疗,48例接受OBV/PTV/r + DSV治疗,114例接受SIM/SOF治疗,133例接受SOF/RBV治疗。51.5%的患者患有肝硬化。总体而言,共审查了5217种药物(每位患者7.86种药物),识别出781种相互作用(每位患者1.18种相互作用)。SOF/RBV的相互作用数量最少(每位患者0.17种相互作用),而OBV/PTV/r + DSV的相互作用数量最多(每位患者2.48种相互作用)。LDV/SOF和SIM/SOF的相互作用数量相似(分别为每位患者1.28种和1.48种相互作用)。胃酸调节剂以及维生素/草药补充剂常与LDV/SOF发生相互作用。降压药、镇痛药和精神科药物常与OBV/PTV/r + DSV以及SIM/SOF发生相互作用。为处理这些相互作用,药剂师最常建议停用药物(28.9%)、增加毒性监测(24.1%)或分开给药时间(18.2%)。药剂师对每位患者的病历审查通常需要约30分钟,病情较复杂的患者则需要更多时间。
HCV药物治疗中DDI很常见,管理可能需要调整用药并加强监测。包括临床药剂师在内的跨学科团队可以优化患者护理。