Procedure for predicting progressing hepatic fibrosis in patients with human immunodeficiency and hepatitis C coinfection
V.V. Maslyakov, M.S. Aristanbekova
«Reaviz» Medical University, 227 Chapaevskaya Str., Samara, 443001, Russian Federation
Our research goal was to develop a system for predicting nature of fibrosis processes in patients infected with HIV and Hepatitis C virus and to assess its efficiency bearing in mind peculiarities of anti-virus therapy applied for treating the infections.
Research was performed on 459 patients with confirmed HIV/viral hepatitis C who had been treated for 1 year at Saratov Regional Center for AIDS Prevention and Elimination. Most patients were males younger than 36. 72–78% patients had 3–4A HIV infection stages. The rest had 4B–C stages. 32% were treated only with sets of anti-retroviruses medications made up of nucleoside and non-nucleoside inhibitors of reverse transcriptase, inhibitors of protease, and inhibitors of integrase in different combinations. 14% patients infected with both HIV and Hepatitis C virus were treated only with antiviral medications aimed for treating hepatitis C and made up of pegylated interferon α and ribavirin or medications with direct effects such as sofosbuvir and daclatasvir. 19% patients were prescribed both antiviral therapy aimed at treating Hepatitis C and anti-retrovirus therapy.
Research results allowed establishing risk criteria for progressing hepatic fibrosis; they included fibro scanning of liver, number of CD3+CD4+ cells in blood, and immune regulatory index. Basing on the research data, we created an integral parameter for assessing quantitative risk criteria that could be used when a patient was examined for the first time or during a short-term observation period.
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