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Role of assessing liver fibrosis in management of chronic hepatitis C virus infection

机译:评估肝纤维化在慢性丙型肝炎病毒感染管理中的作用

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Fibrosis progression is common in hepatitis C. Both host and viral factors influence its natural history. Liver fibrosis is a key predictive factor for advanced disease including endpoints such as liver failure, cirrhosis and hepatocellular carcinoma (HCC). METAVIR fibrosis stages F3-F4 have been considered as the threshold for antiviral therapy. However, this aspect is controversial after the advent of new directacting antivirals (DAAs) because they show an excellent efficacy and safety profile. Moreover, in the DAA era, fibrosis stage seems not to be a predictive factor of a sustained virological response (SVR). Viral eradication decreases liver damage by improving the inflammation, as well as by regressing fibrosis irrespective of the treatment regimen. Non-invasive methods are useful in the assessment of liver fibrosis, replacing liver biopsy in clinical practice; but their usefulness for monitoring fibrosis after SVR needs to be demonstrated. Fibrosis regression has been demonstrated after the eradication of hepatitis C virus infection and is associated with a lower risk of hepatic cirrhosis and liver cancer. However, patients showing advanced fibrosis and cirrhosis must be followed-up after SVR, as risks of portal hypertension and HCC remain. (C) 2016 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
机译:纤维化进展在丙型肝炎中很常见。宿主和病毒因素都会影响其自然病史。肝纤维化是晚期疾病(包括肝衰竭,肝硬化和肝细胞癌(HCC))终点的关键预测因素。 METAVIR纤维化F3-F4期已被视为抗病毒治疗的门槛。但是,在新的直接作用抗病毒药物(DAA)出现之后,这一方面引起了争议,因为它们显示出出色的功效和安全性。此外,在DAA时代,纤维化阶段似乎并不是持续病毒学应答(SVR)的预测因素。与治疗方案无关,病毒根除可通过改善炎症以及使纤维化消退来减少肝脏损害。非侵入性方法可用于评估肝纤维化,在临床实践中可代替肝活检。但需要证明它们在SVR后监测纤维化的有用性。消灭丙型肝炎病毒感染后已证明纤维化消退,并伴有较低的肝硬化和肝癌风险。然而,由于门静脉高压症和肝癌的风险仍然存在,显示SVR后必须随访显示晚期纤维化和肝硬化的患者。 (C)2016欧洲临床微生物学和传染病学会。由Elsevier Ltd.出版。保留所有权利。

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