Grebely Jason, Dore Gregory J, Zeuzem Stefan, Aspinall Richard J, Fox Raymond, Han Lingling, McNally John, Osinusi Anu, Brainard Diana M, Subramanian G Mani, Natha Macky, Foster Graham R, Mangia Alessandra, Sulkowski Mark, Feld Jordan J
The Kirby Institute, University of New South Wales Australia, Sydney.
Johann Wolfgang Goethe University Medical Center, Frankfurt am Main, Germany.
Clin Infect Dis. 2016 Dec 1;63(11):1479-1481. doi: 10.1093/cid/ciw579. Epub 2016 Aug 23.
In this analysis of the ASTRAL trials (non-opioid substitution therapy [OST], n = 984; OST, n = 51) evaluating the once-daily, pan-genotypic regimen of sofosbuvir/velpatasvir for hepatitis C virus infection, OST did not impact completion, adherence, sustained virologic response (SVR12), or safety. SVR12 was 96% (95% confidence interval, 87%, >99%) in those receiving OST.
在这项对ASTRAL试验(非阿片类替代疗法[OST],n = 984;阿片类替代疗法,n = 51)的分析中,评估了索磷布韦/维帕他韦每日一次的泛基因型方案用于丙型肝炎病毒感染的情况,阿片类替代疗法对完成率、依从性、持续病毒学应答(SVR12)或安全性没有影响。接受阿片类替代疗法的患者中,SVR12为96%(95%置信区间,87%,>99%)。