<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kondili LA</submitter><funding>Research Project PITER2010</funding><pagination>1814-1825</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5765396</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>66(6)</volume><pubmed_abstract>We evaluated the cost-effectiveness of two alternative direct-acting antiviral (DAA) treatment policies in a real-life cohort of hepatitis C virus-infected patients: policy 1, "universal," treat all patients, regardless of fibrosis stage; policy 2, treat only "prioritized" patients, delay treatment of the remaining patients until reaching stage F3. A liver disease progression Markov model, which used a lifetime horizon and health care system perspective, was applied to the PITER cohort (representative of Italian hepatitis C virus-infected patients in care). Specifically, 8,125 patients naive to DAA treatment, without clinical, sociodemographic, or insurance restrictions, were used to evaluate the policies' cost-effectiveness. The patients' age and fibrosis stage, assumed DAA treatment cost</pubmed_abstract><journal>Hepatology (Baltimore, Md.)</journal><pubmed_title>Modeling cost-effectiveness and health gains of a "universal" versus "prioritized" hepatitis C virus treatment policy in a real-life cohort.</pubmed_title><pmcid>PMC5765396</pmcid><funding_grant_id>RF-2010-2315839</funding_grant_id><pubmed_authors>Russo FP</pubmed_authors><pubmed_authors>Foti G</pubmed_authors><pubmed_authors>Kondili LA</pubmed_authors><pubmed_authors>Coppola C</pubmed_authors><pubmed_authors>Ciancio A</pubmed_authors><pubmed_authors>Rumi MG</pubmed_authors><pubmed_authors>Nardone G</pubmed_authors><pubmed_authors>Vinci M</pubmed_authors><pubmed_authors>Montalto G</pubmed_authors><pubmed_authors>Ferrari C</pubmed_authors><pubmed_authors>Erne EM</pubmed_authors><pubmed_authors>Ruggeri M</pubmed_authors><pubmed_authors>Zuin M</pubmed_authors><pubmed_authors>Craxi A</pubmed_authors><pubmed_authors>Santantonio TA</pubmed_authors><pubmed_authors>Andreone P</pubmed_authors><pubmed_authors>Persico M</pubmed_authors><pubmed_authors>Rolli FR</pubmed_authors><pubmed_authors>Chemello L</pubmed_authors><pubmed_authors>Alberti A</pubmed_authors><pubmed_authors>Verucchi G</pubmed_authors><pubmed_authors>Madonia S</pubmed_authors><pubmed_authors>Romano F</pubmed_authors><pubmed_authors>Rosato S</pubmed_authors><pubmed_authors>Taliani G</pubmed_authors><pubmed_authors>Borgia G</pubmed_authors><pubmed_authors>Puoti M</pubmed_authors><pubmed_authors>Quaranta MG</pubmed_authors><pubmed_authors>Di Leo A</pubmed_authors><pubmed_authors>Massari M</pubmed_authors><pubmed_authors>Blanc P</pubmed_authors><pubmed_authors>Vella S</pubmed_authors><pubmed_authors>Zignego AL</pubmed_authors><pubmed_authors>Gasbarrini A</pubmed_authors><pubmed_authors>PITER Collaborating Group</pubmed_authors><pubmed_authors>Chessa L</pubmed_authors><pubmed_authors>Cicchetti A</pubmed_authors><pubmed_authors>Raimondo G</pubmed_authors><pubmed_authors>Villa E</pubmed_authors><pubmed_authors>Ieluzzi D</pubmed_authors><pubmed_authors>Gaeta GB</pubmed_authors><pubmed_authors>Brunetto MR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Modeling cost-effectiveness and health gains of a "universal" versus "prioritized" hepatitis C virus treatment policy in a real-life cohort.</name><description>We evaluated the cost-effectiveness of two alternative direct-acting antiviral (DAA) treatment policies in a real-life cohort of hepatitis C virus-infected patients: policy 1, "universal," treat all patients, regardless of fibrosis stage; policy 2, treat only "prioritized" patients, delay treatment of the remaining patients until reaching stage F3. A liver disease progression Markov model, which used a lifetime horizon and health care system perspective, was applied to the PITER cohort (representative of Italian hepatitis C virus-infected patients in care). Specifically, 8,125 patients naive to DAA treatment, without clinical, sociodemographic, or insurance restrictions, were used to evaluate the policies' cost-effectiveness. The patients' age and fibrosis stage, assumed DAA treatment cost</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Dec</publication><modification>2025-04-04T11:30:39.855Z</modification><creation>2019-03-27T00:14:54Z</creation></dates><accession>S-EPMC5765396</accession><cross_references><pubmed>28741307</pubmed><doi>10.1002/hep.29399</doi></cross_references></HashMap>