Literature DB >> 29478339

[Screening, diagnosis, treatment, and follow up of hepatitis C virus related liver disease. National consensus guideline in Hungary from 22 September 2017].

Béla Hunyady1,2, Zsuzsanna Gerlei3, Judit Gervain4, Gábor Horváth5, Gabriella Lengyel6, Alajos Pár2, Zoltán Péter6, László Rókusz7, Ferenc Schneider8, Ferenc Szalay9, István Tornai10, Klára Werling6, Mihály Makara11.   

Abstract

The treatment of hepatitis C is based on a national consensus guideline updated six-monthly according to local availability and affordability of approved therapies through a transparent allocation system in Hungary. This updated guideline incorporates some special new aspects, including recommendations for screening, diagnostics, use and allocation of novel direct acting antiviral agents. The indication of therapy in patients with no contraindication is based on the demonstration of viral replication with consequent inflammation and/or fibrosis in the liver. Non-invasive methods (elastographies and biochemical methods) are preferred for liver fibrosis staging. The budget allocated for these patients is limited. Interferon-based or interferon-free therapies are available for the treatment. Due to their limited success rate as well as to their (sometimes severe) side-effects, the mandatory use of interferon-based therapies as first line treatment can not be accepted from the professional point of view. However, they can be used as optional therapy in treatment-naïve patients with mild disease. As of interferon-free therapies, priority is given to those with urgent need based on a pre-defined scoring system reflecting mainly the stage of the liver disease, but considering also additional factors, i.e., hepatic decompensation, other complications, activity and progression of liver disease, risk of transmission and other special issues. Approved treatments are restricted to the most cost-effective combinations based on the cost per sustained virological response value in different patient categories with consensus amongst treating physicians, the National Health Insurance Fund of Hungary and patients' organizations. Interferon-free treatments and shorter therapy durations are preferred. Orv Hetil. 2018; 159(Suppl 1): 3-23.

Entities:  

Keywords:  direct acting antiviral drug; direkt ható antivirális szer; genotype; genotípus; hepatitis C virus; hepatitis C-vírus; hepatocellular carcinoma; interferon; liver cirrhosis; májrák; májzsugor; polimerázgátló; polymerase inhibitor; protease inhibitor; proteázgátló; replication complex inhibitor; replikációskomplex-gátló; viral hepatitis; vírushepatitis

Mesh:

Substances:

Year:  2018        PMID: 29478339     DOI: 10.1556/650.2018.31003

Source DB:  PubMed          Journal:  Orv Hetil        ISSN: 0030-6002            Impact factor:   0.540


  1 in total

1.  Ombitasvir/paritaprevir/ritonavir + dasabuvir + ribavirin in HCV genotype 1 infected patients who failed previous protease inhibitor therapy.

Authors:  Béla Hunyady; Margit Abonyi; Zsuzsanna Gerlei; Judit Gervain; Gábor Horváth; Viktor Jancsik; Gabriella Lengyel; Erzsébet Makkai; Alajos Pár; Zoltán Péter; Margit Pusztay; Pál Ribiczey; László Rókusz; Christoph Sarrazin; Ferenc Schneider; Simone Susser; Ferenc Szalay; István Tornai; Anna Tusnádi; Eszter Újhelyi; Klára Werling; Mihály Makara
Journal:  Clin Exp Hepatol       Date:  2018-05-25
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.