| Autor: |
Mehta, Rajiv, Kabrawala, Mayank, Nandwani, Subhash, Tekriwal, Rini, Nandaniya, Payal, Shah, Mrunal, Bhayani, Vishwa |
| Zdroj: |
Indian Journal of Gastroenterology; Nov2016, Vol. 35 Issue 6, p459-464, 6p |
| Abstrakt: |
Background: The safety and efficacy of sofosbuvir-based treatment (sofosbuvir and ribavirin with or without pegylated interferon-α) for hepatitis C virus (HCV) infection has been established in clinical trials. However, there is limited data regarding safety and efficacy of sofosbuvir-based treatment for HCV infection in a 'real-life' cohort. We describe our experience with sofosbuvir-based treatment for HCV infection in a real-life cohort. Methods: This was a prospective, nonrandomized and observational study at a tertiary care centre in Surat, India. The primary end-point was proportion of the study patients who achieved a sustained virological response 12 weeks after cessation of treatment (SVR 12). Secondary end-points of the study include SVR 4, virological relapse and appearance of adverse events. Results: A total of 107 patients with chronic HCV who received sofosbuvir-based treatment were included in the study. During study period, two patients died due to severity of liver complications. Hence, overall rate of SVR 4 and SVR 12 was 98.1 % ( n = 103/105) and 94.3 % ( n = 99/105), respectively. Among 67 patients with HCV genotype-3 infection, the SVR 12 rate was 92.5 % ( n = 62/67), and among 38 patients with HCV genotype-1 infection, the rate of SVR 12 was 97.4 % ( n=37/38). A total of 32 (29.9 %) patients reported adverse events during the course of sofosbuvir-based treatment. None of the patient discontinued treatment due to adverse event. Conclusions: Sofosbuvir-based treatment is safe and efficacious in clinical practice in Indian patients with HCV genotype-1 and genotype-3 infection. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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