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Real-world efficacy and safety of ritonavir-boosted paritaprevir, ombitasvir, dasabuvir ± ribavirin for hepatitis C genotype 1 - final results of the REV1TAL study.
Antiviral Therapy ( IF 1.2 ) Pub Date : 2017-4-20 , DOI: 10.3851/imp3168
John Lubel 1, 2 , Simone Strasser 3 , Katherine A Stuart 4 , Gregory Dore 5 , Alexander Thompson 6, 7 , Stephen Pianko 8 , Steven Bollipo 9 , Joanne L Mitchell 10 , Vincenzo Fragomeli 11 , Tracey Jones 9 , Sarah Chivers 2 , Paul Gow 12 , David Iser 6 , Miriam Levy 13 , Edmund Tse 14 , Alessia Gazzola 10 , Wendy Cheng 15 , Saroj Nazareth 15 , Sam Galhenage 16 , Amanda Wade 17 , Martin Weltman 11 , Alan Wigg 18 , Gerry MacQuillan 19, 20 , Joe Sasadeusz 21 , Jacob George 22, 23 , Amany Zekry 24 , Stuart K Roberts 10 ,
Affiliation  

Limited data exist on the outcomes of ritonavir-boosted paritaprevir with ombitasvir and dasabuvir (PrOD) ± ribavirin in a real-world setting. The aim of this study was to compare the efficacy and safety of PrOD-based therapy in hepatitis C genotype 1 patients with and without cirrhosis, and to explore pre-treatment factors predictive of sustained viral response (SVR) and serious adverse events (SAEs) on treatment.

中文翻译:

利托那韦增强的paritaprevir,ombitasvir,dasabuvir±利巴韦林对丙型肝炎基因型1的真实疗效和安全性-REV1TAL研究的最终结果。

在真实环境中,使用利托那韦增强的帕利他普韦与ombitasvir和dasabuvir(PrOD)±利巴韦林的疗效相关的数据有限。这项研究的目的是比较基于PrOD的疗法在有和没有肝硬化的C型基因型1型肝炎患者中的疗效和安全性,并探讨预测持续病毒应答(SVR)和严重不良事件(SAE)的治疗前因素。在治疗上。
更新日期:2020-08-21
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