A multicentre, observational study on demographic and disease characteristics of patients seeking care for chronic hepatitis C in Belgium in 2016.

IF 1.5 4区 医学 Q2 Medicine Acta Gastro-Enterologica Belgica Pub Date : 2019-01-01
S Bourgeois, J P Mulkay, L Lasser, G Robaeys, B Bastens, J Delwaide, S Pollet, M Van den Enden
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Abstract

Background and study aims: Direct-acting antivirals provide interferon-free treatments for chronic hepatitis C (CHC) virus infection. In Belgium, in 2016, access to these agents was limited to patients with advanced liver fibrosis stages F3 and F4. This study is the first to describe Belgium's patient population ineligible for interferon-free treatment.

Patients and methods: This was an observational, cross-sectional, multicentre study that enrolled adult patients with CHC ineligible for interferon-free treatment. Patient data recorded at a single visit included demographic data, disease characteristics, comorbidities, co-medications, treatment status, and laboratory data.

Results: Three hundred and three patients from 16 centres in Belgium were included in the statistical analysis. On average, patients were aged 53.5 years and 50.2% were women ; 94.1% had health insurance and 99.0% resided in Belgium. The current hepatitis C virus (HCV) infection was the first infection for 96.0% of patients and the mean time since infection was 20.0 years. Liver fibrosis stage was F0 for 23.7%, F0/F1 or F1 for 38.3%, F1/F2 or F2 for 25.8%, F3 for 7.1%, and F4 for 5.1% of patients ; 28.4% of patients were CHC treatment-experienced. The main reason for ineligibility for interferon-free treatment was lack of reimbursement (84.8%). Other reasons included no treatment urgency or medical decision to wait (27.1%), waiting for future treatment option (8.3%), and no social insurance coverage (3.6%).

Conclusions: This study provides recent data on the CHC patient population and disease characteristics in Belgium that could help medical communities and government agencies manage CHC disease burden.

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2016年比利时慢性丙型肝炎患者人口统计学和疾病特征多中心观察性研究
背景与研究目的:直接作用抗病毒药物为慢性丙型肝炎(CHC)病毒感染提供无干扰素治疗。2016年,在比利时,这些药物仅限F3和F4期晚期肝纤维化患者使用。这项研究首次描述了比利时不符合无干扰素治疗条件的患者群体。患者和方法:这是一项观察性、横断面、多中心研究,纳入了不适合无干扰素治疗的成年CHC患者。单次就诊记录的患者数据包括人口统计数据、疾病特征、合并症、联合用药、治疗状况和实验室数据。结果:来自比利时16个中心的303例患者被纳入统计分析。患者平均年龄53.5岁,女性50.2%;94.1%的人有健康保险,99.0%的人居住在比利时。96.0%的患者首次感染丙型肝炎病毒(HCV),平均感染时间为20.0年。肝纤维化分期为F0的占23.7%,F0/F1或F1的占38.3%,F1/F2或F2的占25.8%,F3的占7.1%,F4的占5.1%;28.4%的患者经历过CHC治疗。无干扰素治疗不合格的主要原因是缺乏报销(84.8%)。其他原因包括没有治疗紧急或医疗决定等待(27.1%),等待未来的治疗方案(8.3%),以及没有社会保险覆盖(3.6%)。结论:本研究提供了比利时CHC患者人群和疾病特征的最新数据,可以帮助医疗界和政府机构管理CHC疾病负担。
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来源期刊
Acta Gastro-Enterologica Belgica
Acta Gastro-Enterologica Belgica 医学-胃肠肝病学
CiteScore
2.80
自引率
20.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: The Journal Acta Gastro-Enterologica Belgica principally publishes peer-reviewed original manuscripts, reviews, letters to editors, book reviews and guidelines in the field of clinical Gastroenterology and Hepatology, including digestive oncology, digestive pathology, as well as nutrition. Pure animal or in vitro work will not be considered for publication in the Journal. Translational research papers (including sections of animal or in vitro work) are considered by the Journal if they have a clear relationship to or relevance for clinical hepato-gastroenterology (screening, disease mechanisms and/or new therapies). Case reports and clinical images will be accepted if they represent an important contribution to the description, the pathogenesis or the treatment of a specific gastroenterology or liver problem. The language of the Journal is English. Papers from any country will be considered for publication. Manuscripts submitted to the Journal should not have been published previously (in English or any other language), nor should they be under consideration for publication elsewhere. Unsolicited papers are peer-reviewed before it is decided whether they should be accepted, rejected, or returned for revision. Manuscripts that do not meet the presentation criteria (as indicated below) will be returned to the authors. Papers that go too far beyond the scope of the journal will be also returned to the authors by the editorial board generally within 2 weeks. The Journal reserves the right to edit the language of papers accepted for publication for clarity and correctness, and to make formal changes to ensure compliance with AGEB’s style. Authors have the opportunity to review such changes in the proofs.
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