Uriarte-Pinto Moisés, Navarro-Aznarez Herminia, De La Llama-Celis Natalia, Arazo-Garcés Piedad, Martínez-Sapiña Ana María, Abad-Sazatornil María Reyes
Pharmacy Department, Miguel Servet University Hospital, Paseo Isabel la Católica, 1-3, 50009, Saragossa, Spain.
Unit of Infectious Diseases, Miguel Servet University Hospital, Paseo Isabel la Católica, 1-3, 50009, Saragossa, Spain.
Int J Clin Pharm. 2018 Jun;40(3):608-616. doi: 10.1007/s11096-018-0621-0. Epub 2018 Mar 20.
Background HIV-HCV coinfection produces high morbi-mortality. Direct-acting antivirals (DAAs) have shown high efficacy, although special attention should be paid to the risk of drug interactions. However, due to the lack of representativeness of coinfected patients in clinical trials, it is important to know real-world results. Objective To evaluate DAA treatment effectiveness in coinfected patients. We also analyse safety profile of DAA treatment and drug interactions between HCV and HIV therapy. Setting Descriptive study carried in a tertiary hospital of Spain Method HIV-HCV coinfected patients treated with DAAs between November 2014 and June 2016 were included. Main outcome measure Efficacy was measured in terms of sustained virologic response at week 12 after the end of therapy. Adverse events that led to treatment discontinuation were registered to evaluate the safety profile, and also drug interactions between DAAs and antiretroviral treatment were evaluated. Results Main HCV genotypes were 1a (34.9%) and 4 (24.5%). 51.9% were HCV previously treated, 54.7% had grade 4 liver fibrosis. SVR12 was reported in 90.6%. HCV treatment was well tolerated and there were no discontinuations because of adverse events. 30.2% of HIV treatments had to be modified before DAA treatment was started due to interactions, HIV suppression was not compromised. Conclusion DAA treatment in coinfected patients seems to be highly effective and secure. Evaluation of drug interactions must be a priority in order to maximize effectiveness and avoid toxicity.
HIV-HCV合并感染导致高病残率和死亡率。直接作用抗病毒药物(DAA)已显示出高效性,尽管应特别关注药物相互作用的风险。然而,由于临床试验中合并感染患者缺乏代表性,了解真实世界的结果很重要。目的:评估DAA治疗合并感染患者的有效性。我们还分析了DAA治疗的安全性概况以及HCV与HIV治疗之间的药物相互作用。地点:在西班牙一家三级医院进行的描述性研究方法:纳入2014年11月至2016年6月期间接受DAA治疗的HIV-HCV合并感染患者。主要结局指标:在治疗结束后第12周根据持续病毒学应答来衡量疗效。记录导致治疗中断的不良事件以评估安全性概况,同时评估DAA与抗逆转录病毒治疗之间的药物相互作用。结果:主要HCV基因型为1a(34.9%)和4型(24.5%)。51.9%的患者既往接受过HCV治疗,54.7%有4级肝纤维化。12周持续病毒学应答率为90.6%。HCV治疗耐受性良好,无因不良事件导致的治疗中断。30.2%的HIV治疗在开始DAA治疗前因相互作用而必须调整,HIV抑制未受影响。结论:DAA治疗合并感染患者似乎高效且安全。为了最大化有效性并避免毒性,药物相互作用的评估必须是优先事项。