<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gountas, I.</style></author><author><style face="normal" font="default" size="100%">Sypsa, V</style></author><author><style face="normal" font="default" size="100%">Papatheodoridis, G.</style></author><author><style face="normal" font="default" size="100%">Souliotis, G.</style></author><author><style face="normal" font="default" size="100%">Razavi, H.</style></author><author><style face="normal" font="default" size="100%">Hatzakis, A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Is elimination of HCV possible in a country with low diagnostic rate and moderate HCV prevalence?: The case of Greece</style></title><secondary-title><style face="normal" font="default" size="100%">J Gastroenterol Hepatol</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Journal of gastroenterology and hepatology</style></alt-title><short-title><style face="normal" font="default" size="100%">Journal of gastroenterology and hepatologyJournal of gastroenterology and hepatology</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antiviral Agents/*administration &amp; dosage</style></keyword><keyword><style  face="normal" font="default" size="100%">Disease Eradication</style></keyword><keyword><style  face="normal" font="default" size="100%">Drug Therapy, Combination</style></keyword><keyword><style  face="normal" font="default" size="100%">Greece/epidemiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatitis C/diagnosis/*epidemiology/mortality/*prevention &amp; control</style></keyword><keyword><style  face="normal" font="default" size="100%">Humans</style></keyword><keyword><style  face="normal" font="default" size="100%">Interferon-alpha/administration &amp; dosage</style></keyword><keyword><style  face="normal" font="default" size="100%">Mass Screening</style></keyword><keyword><style  face="normal" font="default" size="100%">Morbidity</style></keyword><keyword><style  face="normal" font="default" size="100%">Polyethylene Glycols/administration &amp; dosage</style></keyword><keyword><style  face="normal" font="default" size="100%">Prevalence</style></keyword><keyword><style  face="normal" font="default" size="100%">Recombinant Proteins/administration &amp; dosage</style></keyword><keyword><style  face="normal" font="default" size="100%">Ribavirin/*administration &amp; dosage</style></keyword><keyword><style  face="normal" font="default" size="100%">Time Factors</style></keyword><keyword><style  face="normal" font="default" size="100%">World Health Organization</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Feb</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">2</style></number><volume><style face="normal" font="default" size="100%">32</style></volume><pages><style face="normal" font="default" size="100%">466-472</style></pages><isbn><style face="normal" font="default" size="100%">1440-1746 (Electronic)0815-9319 (Linking)</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">BACKGROUND AND AIM: The treatment of hepatitis C (HCV) with interferon (IFN)-free direct-acting antivirals (DAAs) is anticipated to change the future burden of disease. The aim of this study is to quantify the impact of IFN-free DAAs on HCV-related morbidity and mortality in Greece under different scenarios concerning treatment coverage and primary prevention, including the proposed by World Health Organization Global Hepatitis Strategy. METHODS: A previously described model was used to project the future disease burden up to 2030 under scenarios, which includes treatment based on the combination of pegylated-IFN with ribavirin (base case) and scenarios using DAAs therapies. RESULTS: Under the base case scenario, an increase in HCV-related morbidity and mortality is predicted in Greece (mortality in 2030: +23.6% compared with 2015). If DAAs are used with the same treatment coverage, the number of hepatocellular carcinoma cases and of liver related deaths are predicted to be lower by 4-7% compared with 2015. Under increased treatment coverage (from 2000 treated/year to approximately 5000/year in 2015-2020 and 2500/year subsequently), morbidity and mortality will decrease by 43-53% in 2030 compared with 2015. To achieve the WHO Global Hepatitis Strategy goals, a total number of 86 500 chronic hepatitis C patients will have to be treated during 2015-2030. CONCLUSIONS: Elimination of HCV in Greece by 2030 necessitates great improvements in primary prevention, implementation of large screening programs and high treatment coverage.</style></abstract><accession-num><style face="normal" font="default" size="100%">27403912</style></accession-num><notes><style face="normal" font="default" size="100%">Gountas, IliasSypsa, VanaPapatheodoridis, GeorgeSouliotis, GeorgeRazavi, HomieHatzakis, AngelosengAustralia2016/07/13 06:00J Gastroenterol Hepatol. 2017 Feb;32(2):466-472. doi: 10.1111/jgh.13485.</style></notes><auth-address><style face="normal" font="default" size="100%">Department of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.Department of Gastroenterology, Medical School, National and Kapodistrian University of Athens, Laiko General Hospital, Athens, Greece.Faculty of Social and Political Sciences, University of Peloponnese, Korinthos, Greece.Center for Disease Analysis, Lafayette, Colorado, USA.</style></auth-address></record></records></xml>