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To evaluate virological response to telaprevir or boceprevir in combination with pegylated interferon and ribavirin and resistance mutations to NS3/4A inhibitors in hepatitis C virus-human immunodeficiency virus (HCV-HIV) coinfected patients in a real life setting.Patients with HCV genotype 1-HIV coinfection followed in Nice University Hospital internal medicine and infectious diseases departments who initiated treatment including pegylated interferon and ribavirin (PegIFN/RBV) + telaprevir or boceprevir, according to standard treatment protocols, between August 2011 and October 2013 entered this observational study. Patient data were extracted from an electronic database (Nadis(®)). Liver fibrosis was measured by elastometry (Fibroscan(®)) with the following cut-off values: F0-F1: < 7.1 kPa, F2: 7.1-9.5 kPa, F3: 9.5-14.5 kPa, F4: ≥ 14.5 kPa. The proportion of patients with sustained virological response (SVR) twelve weeks after completing treatment, frequency and type of adverse events, and NS3/4A protease inhibitor mutations were described.Forty-one patients were included: 13 (31.7

作者:Alissa, Naqvi;Valérie, Giordanengo;Brigitte, Dunais;Francine, de Salvador-Guillouet;Isabelle, Perbost;Jacques, Durant;Pascal, Pugliese;Aline, Joulié;Pierre Marie, Roger;Eric, Rosenthal

来源:World journal of hepatology 2015 年 7卷 18期

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作者:
Alissa, Naqvi;Valérie, Giordanengo;Brigitte, Dunais;Francine, de Salvador-Guillouet;Isabelle, Perbost;Jacques, Durant;Pascal, Pugliese;Aline, Joulié;Pierre Marie, Roger;Eric, Rosenthal
来源:
World journal of hepatology 2015 年 7卷 18期
标签:
Boceprevir Hepatitis C virus-human immunodeficiency virus coinfection Resistance mutations Telaprevir
To evaluate virological response to telaprevir or boceprevir in combination with pegylated interferon and ribavirin and resistance mutations to NS3/4A inhibitors in hepatitis C virus-human immunodeficiency virus (HCV-HIV) coinfected patients in a real life setting.Patients with HCV genotype 1-HIV coinfection followed in Nice University Hospital internal medicine and infectious diseases departments who initiated treatment including pegylated interferon and ribavirin (PegIFN/RBV) + telaprevir or boceprevir, according to standard treatment protocols, between August 2011 and October 2013 entered this observational study. Patient data were extracted from an electronic database (Nadis(®)). Liver fibrosis was measured by elastometry (Fibroscan(®)) with the following cut-off values: F0-F1: < 7.1 kPa, F2: 7.1-9.5 kPa, F3: 9.5-14.5 kPa, F4: ≥ 14.5 kPa. The proportion of patients with sustained virological response (SVR) twelve weeks after completing treatment, frequency and type of adverse events, and NS3/4A protease inhibitor mutations were described.Forty-one patients were included: 13 (31.7