| Literature DB >> 29478340 |
Gábor Horváth1, Zsuzsanna Gerlei2, Judit Gervain3, Gabriella Lengyel4, Mihály Makara5, Alajos Pár6, László Rókusz7, Ferenc Szalay8, István Tornai9, Klára Werling4, Béla Hunyady6,10.
Abstract
Diagnosis and treatment of hepatitis B virus (HBV) and hepatitis D virus infection mean for the patient to be able to maintain working capacity, to increase quality of life, to prevent cancer, and to prolong life expectancy, while the society benefits from eliminating the chances of further transmission of the viruses, and decreasing the overall costs of serious complications. The guideline delineates the treatment algorithms from 22 September 2017 set by a consensus meeting of physicians involved in the treatment of these diseases. The prevalence of HBV infection in the Hungarian general population is 0,5-0,7%. The indications of treatment are based upon viral examinations (including viral nucleic acid determination), determinations of disease activity and stage (including biochemical, pathologic, and/or non-invasive methods), and excluding contraindications. To avoid unnecessary side effects and for a cost-effective approach, the guideline stresses the importance of quick and detailed virologic evaluations, the applicability of transient elastography as an acceptable alternative of liver biopsy in this regard as well as the relevance of appropriate consistent follow-up schedule for viral response during therapy. The first choice of therapy in chronic HBV infection can be pegylated interferon for 48 weeks or continuous entecavir or tenofovir therapy. The latter two must be continued for at least 12 months after hepatitis B surface antigen seroconversion. Lamivudine is no longer the first choice; patients currently taking lamivudine must switch if the response is inadequate. Appropriate treatment of patients taking immunosuppressive medications is highly recommended. Pegylated interferon based therapy is recommended for the treatment of concomitant hepatitis D infection. Orv Hetil. 2018; 159(Suppl 1): 24-37.Entities:
Keywords: adefovir; cirrhosis; entecavir; hepatitis B virus; hepatitis B-vírus; hepatitis D virus; hepatitis D-vírus; interferon; lamivudin; lamivudine; liver cancer; májrák; májzsugor; pegilált interferon; pegylated interferon; tenofovir; viral hepatitis; vírushepatitis
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Year: 2018 PMID: 29478340 DOI: 10.1556/650.2018.31004
Source DB: PubMed Journal: Orv Hetil ISSN: 0030-6002 Impact factor: 0.540