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首页> 外文期刊>Acta gastro-enterologica Belgica >The disease burden of hepatitis C in Belgium: Development of a realistic disease control strategy
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The disease burden of hepatitis C in Belgium: Development of a realistic disease control strategy

机译:比利时丙型肝炎的疾病负担:制定切实可行的疾病控制策略

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Background: Novel direct antiviral agents (DAAs) will become available soon with higher sustained viral response (SVR), fewer side-effects and higher compliance. Our aim was to evaluate different realistic strategies to control the projected increase in HCVrelated disease burden in Belgium. Methods: Based on literature review, expert opinions and historical assumptions, HCV-disease progression and mortality in Belgium was modeled to 2030. Strategies exploring the impact of increased treatment, treatment delay, and treatment restrictions were developed. Results: Although the overall HCV prevalence is decreasing in Belgium, the burden of advanced stage HCV, including cirrhosis and hepatocellular carcinoma (HCC), is expected to increase under current treatment and cure rates. By increasing SVR to 90% from 2016 onward and the number of treated cases (from 710 to 2,050), in 2030 the cases with cirrhosis, decompensated cirrhosis and HCC would be significantly lower than in 2013. This strategy was found most efficient when applied to F2-F4 cases. To obtain comparable outcomes with F0-F4 cases, 3,490 patients should be treated. A two year delayed access to the DAAs increased HCV related morbidity and mortality by 15% relative to our strategy. Conclusions: Considering the evolving burden of HCV disease and the need for efficacious usage of healthcare resources, primary application of new DAAs in Belgium should focus on patients with significant and advanced fibrosis (F2-F4), providing these new drugs without delay upon availability and increasing access to therapy.
机译:背景:新型直接抗病毒药物(DAA)即将面世,具有更高的持续病毒应答(SVR),更少的副作用和更高的依从性。我们的目标是评估不同的现实策略,以控制比利时HCV相关疾病负担的预计增加。方法:基于文献综述,专家意见和历史假设,对比利时的HCV疾病进展和死亡率进行了建模,直至2030年。制定了探索增加治疗,治疗延迟和治疗限制的影响的策略。结果:尽管比利时的总体HCV患病率正在降低,但在目前的治疗和治愈率下,包括肝硬化和肝细胞癌(HCC)在内的晚期HCV的负担预计将增加。通过将SVR从2016年开始增加至90%,治疗病例数(从710增至2,050),到2030年,肝硬化,代偿性肝硬化和HCC的病例将大大低于2013年。该策略被发现最有效F2-F4案件。为了获得与F0-F4病例相当的结果,应治疗3,490例患者。相较于我们的策略,延迟使用DAA两年将HCV相关的发病率和死亡率提高了15%。结论:考虑到HCV疾病不断发展的负担和有效利用医疗资源的需求,比利时新的DAA的主要应用应侧重于患有严重和晚期纤维化(F2-F4)的患者,提供这些新药物时应不延迟可用性和增加获得治疗的机会。

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