Effectiveness and safety of narlaprevir in real clinical practice of chronic hepatitis C

Objective: to analyze the efficacy and safety of using direct antiviral action drug narlaprevir/ritonavir in combination with the prolonged alpha-interferon and ribavirin drugs in the conditions of day-time hospitals of St. Petersburg and. Novgorod.Materials and methods: The study included. 35 patie...

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Main Authors: V. V. Basina, S. E. Kalach, N. V. Tyurenkova, M. E. Semenova, E. Yu. Yushina, E. G. Gordievskaya, R. A. Ganchenko, Е. V. Esaulenko
Format: Article
Language:Russian
Published: Journal Infectology 2019-12-01
Series:Žurnal Infektologii
Subjects:
Online Access:https://journal.niidi.ru/jofin/article/view/963
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spelling doaj-5cd4b2ae126f45efacaf5c25ecff5e162021-08-02T08:43:24ZrusJournal InfectologyŽurnal Infektologii 2072-67322019-12-01114657110.22625/2072-6732-2019-11-4-65-71763Effectiveness and safety of narlaprevir in real clinical practice of chronic hepatitis CV. V. Basina0S. E. Kalach1N. V. Tyurenkova2M. E. Semenova3E. Yu. Yushina4E. G. Gordievskaya5R. A. Ganchenko6Е. V. Esaulenko7Saint-Petersburg State Pediatric Medical UniversityNovgorod regional infectious diseases hospitalClinical Infectious hospital named after S.P. BotkinClinical Infectious hospital named after S.P. BotkinClinical Infectious hospital named after S.P. BotkinChildren's Infectious Diseases Hospital № 3Saint-Petersburg State Pediatric Medical UniversitySaint-Petersburg State Pediatric Medical University; Clinical Infectious hospital named after S.P. BotkinObjective: to analyze the efficacy and safety of using direct antiviral action drug narlaprevir/ritonavir in combination with the prolonged alpha-interferon and ribavirin drugs in the conditions of day-time hospitals of St. Petersburg and. Novgorod.Materials and methods: The study included. 35 patients with CHC of the 1st genotype. For treating these patients, a three-component regimen was used, which included the use of narlaprevir/ritonavir in combination, with peg-interferon and ribavirin.Results: among all patients included, in the study, a sustained, virological response was noted, in 85,7%. Early virological response was observed, in 91,3% cases. The recurrence rate was observed, in 10% patients. In 3 patients, therapy was interrupted, for the following reasons: due to inefficiency, the development of serious adverse events, and on its own initiative.Conclusion: the data obtained, demonstrate high, virological and. clinical efficacy and. safety of narlaprevir in combination with peg-interferon and ribavirin, in the treatment of chronic viral hepatitis C.https://journal.niidi.ru/jofin/article/view/963antiviral therapynarlaprevirchronic hepatitis c1 genotype
collection DOAJ
language Russian
format Article
sources DOAJ
author V. V. Basina
S. E. Kalach
N. V. Tyurenkova
M. E. Semenova
E. Yu. Yushina
E. G. Gordievskaya
R. A. Ganchenko
Е. V. Esaulenko
spellingShingle V. V. Basina
S. E. Kalach
N. V. Tyurenkova
M. E. Semenova
E. Yu. Yushina
E. G. Gordievskaya
R. A. Ganchenko
Е. V. Esaulenko
Effectiveness and safety of narlaprevir in real clinical practice of chronic hepatitis C
Žurnal Infektologii
antiviral therapy
narlaprevir
chronic hepatitis c
1 genotype
author_facet V. V. Basina
S. E. Kalach
N. V. Tyurenkova
M. E. Semenova
E. Yu. Yushina
E. G. Gordievskaya
R. A. Ganchenko
Е. V. Esaulenko
author_sort V. V. Basina
title Effectiveness and safety of narlaprevir in real clinical practice of chronic hepatitis C
title_short Effectiveness and safety of narlaprevir in real clinical practice of chronic hepatitis C
title_full Effectiveness and safety of narlaprevir in real clinical practice of chronic hepatitis C
title_fullStr Effectiveness and safety of narlaprevir in real clinical practice of chronic hepatitis C
title_full_unstemmed Effectiveness and safety of narlaprevir in real clinical practice of chronic hepatitis C
title_sort effectiveness and safety of narlaprevir in real clinical practice of chronic hepatitis c
publisher Journal Infectology
series Žurnal Infektologii
issn 2072-6732
publishDate 2019-12-01
description Objective: to analyze the efficacy and safety of using direct antiviral action drug narlaprevir/ritonavir in combination with the prolonged alpha-interferon and ribavirin drugs in the conditions of day-time hospitals of St. Petersburg and. Novgorod.Materials and methods: The study included. 35 patients with CHC of the 1st genotype. For treating these patients, a three-component regimen was used, which included the use of narlaprevir/ritonavir in combination, with peg-interferon and ribavirin.Results: among all patients included, in the study, a sustained, virological response was noted, in 85,7%. Early virological response was observed, in 91,3% cases. The recurrence rate was observed, in 10% patients. In 3 patients, therapy was interrupted, for the following reasons: due to inefficiency, the development of serious adverse events, and on its own initiative.Conclusion: the data obtained, demonstrate high, virological and. clinical efficacy and. safety of narlaprevir in combination with peg-interferon and ribavirin, in the treatment of chronic viral hepatitis C.
topic antiviral therapy
narlaprevir
chronic hepatitis c
1 genotype
url https://journal.niidi.ru/jofin/article/view/963
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