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首页> 外文期刊>BMC Infectious Diseases >Adherence to response-guided pegylated interferon and ribavirin for people who inject drugs with hepatitis C virus genotype 2/3 infection: the ACTIVATE study
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Adherence to response-guided pegylated interferon and ribavirin for people who inject drugs with hepatitis C virus genotype 2/3 infection: the ACTIVATE study

机译:遵守响应引导的聚乙二醇干扰素和利巴韦林,用于用丙型肝炎病毒基因型注射药物2/3感染的人:激活研究

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Background The aims of this analysis were to investigate treatment completion and adherence among people with ongoing injecting drug use or receiving opioid substitution therapy (OST) in a study of response-guided therapy for chronic HCV genotypes 2/3 infection. Methods ACTIVATE was a multicenter clinical trial recruited between 2012 and 2014. Participants with genotypes 2/3 were treated with directly observed peg-interferon alfa-2b (PEG-IFN) and self-administered ribavirin for 12 (undetectable HCV RNA at week 4) or 24?weeks (detectable HCV RNA at week 4). Outcomes included treatment completion, PEG-IFN adherence, ribavirin adherence, and sustained virological response (SVR, undetectable HCV RNA >12?weeks post-treatment). Results Among 93 people treated, 59% had recently injected drugs (past month), 77% were receiving OST and 56% injected drugs during therapy. Overall, 76% completed treatment. Mean on-treatment adherence to PEG-IFN and ribavirin were 98.2% and 94.6%. Overall, 6% of participants missed >1 dose of PEG-IFN and 31% took Conclusions This study demonstrated a high adherence to directly observed PEG-IFN and self-administered ribavirin among people with ongoing injecting drug use or receiving OST. These data also suggest that shortening therapy from 24 to 12?weeks can lead to improved treatment completion. Treatment completion was associated with improved response to therapy. ACTIVATE trial registration number: NCT01364090 - May 31, 2011
机译:背景技术该分析的目的是调查持续注射药物使用或接受阿片类药物替代治疗(OST)的人们对慢性HCV基因型2/3感染的响应引导治疗的治疗完成和粘附。方法激活是2012年和2014年间招聘的多中心临床试验。基因型2/3的参与者用直接观察到的PEG-干扰素ALFA-2b(PEG-IFN)和自我施用的利巴韦林进行12个(第4周不可检测的HCV RNA)或24周(第4周的可检测的HCV RNA)。结果包括治疗完成,PEG-IFN粘附,利巴韦仑粘附和持续的病毒学反应(SVR,未检测到的HCV RNA>后处理后12?周数)。结果93人在治疗93人中,59%最近注射了药物(过去一个月),77%是在治疗期间接受OST和56%的注射药物。总体而言,76%完成治疗。对PEG-IFN和利巴韦林的平均治疗粘附为98.2%和94.6%。总体而言,6%的参与者遗漏> 1剂量的PEG-IFN和31%的结论本研究表明,直接观察到持续注射药物使用或接受OST的人们中直接观察到的PEG-IFN和自我施用的利巴韦林的高粘附性。这些数据还表明,从24到12岁以下的缩短治疗时间可能导致治疗完成改善。治疗完成与改善对治疗的反应有关。激活试用注册号:NCT01364090 - 2011年5月31日

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