纤维扫描在评估慢性乙型和丙型肝炎患者肝脏受累程度中的作用

P. Jyothi, D. Vanisree, D. S. Murty, Kolli Prasanthi
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摘要

慢性肝病(CLD)在世界范围内造成严重的发病率和死亡率,每年约有200万人死亡。大多数慢性肝病包括酒精性肝病、慢性病毒性肝炎(包括乙型和丙型肝炎)、非酒精性脂肪性肝病(NAFLD)和血色素沉着症。其中,乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)感染占肝脏疾病的很大比例,导致从轻微疾病到肝硬化和肝细胞癌(HCC)的肝脏损害。纤维扫描是一种通过测量肝脏硬度来评估肝纤维化的新型无创方法。的目标。本研究旨在了解慢性肝病(CLD)患者血源性病毒病原体(HBV, HCV)的患病率,并评估纤维扫描和肝功能检查(LFT)在评估慢性肝病程度中的作用。材料和方法:本研究包括100名在消化内科就诊的慢性肝病患者。所有慢性肝病病例均采用快速免疫层析法检测乙型肝炎和丙型肝炎病毒感染。同时进行肝功能检查和纤维扫描,按F0 ~ F4分期评估纤维化程度。结果:当筛查血源性病毒病原体时,46%为HBV阳性,10%为HCV阳性,没有HIV阳性。未发现合并感染。HBV被确定为CLD的最典型原因,约占46%,其次是非病毒/非传染性(酒精,代谢,自身免疫性)原因,占44%和10%,CLD的原因是HCV。根据纤维扫描结果,80%的HCV患者和39%的HBV患者处于肝硬化/晚期纤维化阶段。结论:HBV是CLD的主要病因。肝僵硬最近被证明是临床结果的一个很好的预测指标。在病毒性肝炎病例中,纤维扫描将有助于疾病分期和治疗选择的决策过程
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of fibroscan in assessing the extent of liver involvement among chronic hepatitis B and C cases
Chronic liver diseases (CLD) cause significant morbidity and mortality worldwide, accounting for approximately 2 million deaths annually. The majority of CLDs include alcoholic liver disease, chronic viral hepatitis, including hepatitis B and C, non-alcoholic fatty liver disease (NAFLD), and hemochromatosis. Of these, hepatitis B virus (HBV) and hepatitis C virus (HCV) infections account for a substantial proportion of liver diseases which is responsible for liver damage ranging from minor disorders to liver cirrhosis and hepatocellular carcinoma (HCC). Fibroscan is a novel non-invasive method for assessing hepatic fibrosis by measuring liver stiffness. The aim. The present study was conducted to know the prevalence of blood-born viral pathogens (HBV, HCV) among patients with chronic liver diseases (CLD) and also to assess the role of Fibroscan and liver function tests (LFT) in evaluating the extent of chronic liver disease. Material and methods: The present study comprised 100 chronic liver disease patients attending the gastroenterology department. All the chronic liver disease cases were tested for Hepatitis B and Hepatitis C viral infections using a rapid Immunochromatography assay. Simultaneously they were subjected to liver function tests and fibroscan to assess the extent of fibrosis by staging from F0 to F4. Results: When screened for bloodborne viral pathogens, 46 % were HBV positive, 10 % were HCV, and none were HIV positive. No co-infection was detected. HBV was identified as the most typical cause of CLD in about 46 %, followed by non-viral/non-infectious (alcoholic, metabolic, autoimmune) cause in 44 % and 10 %, the cause for CLD was HCV. As per fibroscan results, 80 % of HCV and 39 % of HBV patients were in the stage of cirrhosis/advanced fibrosis. Conclusion: HBV was the predominant cause of CLD. Liver stiffness has recently been shown to be a good predictor of clinical outcomes. A fibroscan will help in the decision-making process in staging the disease and choice of treatment in viral hepatitis cases
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