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Longitudinal evaluation of liver stiffness and outcomes in patients with chronic hepatitis C before and after short- and long-term IFN-free antiviral treatment

机译:慢性丙型肝炎患者肝硬化和慢性丙型肝炎患者的肝硬化和结果的纵向评估,短期和长期无论是无动抗病毒治疗

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Background: New direct-acting antiviral drugs can eradicate hepatitis C virus (HCV) infection in over 90% of patients and can even reduce the risk of complications in advanced fibrosis/cirrhosis. The aims of this study were to evaluate (1) changes in fibrosis during and after antiviral treatment and (2) incidence of hepatocarcinoma and mortality in various fibrosis stages. Methods: This is a longitudinal monocentric prospective study. Blood and instrumental examinations were evaluated at baseline, at the end of therapy, and 1 and 2 years following treatment. Results: Two hundred and ninety-six patients with chronic HCV were evaluated, of whom 115 were experienced, 181 were treatment-naive, and 2 had previous hepatocellular carcinoma (HCC) and were therefore excluded from the study. At baseline, stiffness values were 13.46 +/- 9.97 kPa. Out of the 294 HCV patients enrolled, 100 had lymphoproliferative disorders and were evaluated separately. This group of patients showed stiffness values pertaining to the F0-F2 group (mean stiffness values were 6.07 +/- 1.68 kPa). All other patients showed stiffness values pertaining to the F3-F4 group (mean stiffness values were 17.93 +/- 10.23). No statistically significant difference was found between stiffness at baseline compared to the end of treatment (EOT), while significant differences were found between the baseline, 1 year (p = .05), and 2 year follow-ups (p < .01). Significant differences were found between baseline and EOT, as well as 1 and 2 years after the end of treatment (p < .001) in the F3-F4 group. Four out of 140 patients with baseline cirrhosis developed HCC during the post-treatment follow-up, 1 of whom died. Conclusions: Non-invasive methods provide important prognostic information, particularly concerning the observed regression of fibrosis and could be extremely useful for monitoring patients with long life expectancies after direct-acting antiviral treatment.
机译:背景:新的直接作用抗病毒药物可以消除超过90%的患者的丙型肝炎病毒(HCV)感染,甚至可以降低先进纤维化/肝硬化的并发症风险。本研究的目的是评估(1)抗病毒治疗期间和后纤维化的变化,(2)肝癌发生率和各种纤维化阶段的死亡率。方法:这是一个纵向单眼的前瞻性研究。在治疗结束时,在疗法结束时评估血液和仪器检查,并在治疗后1和2年。结果:评价二百九十六患者慢性HCV患者,其中115例经验丰富,181例治疗 - 幼稚,2例肝细胞癌(HCC),因此被排除在研究之外。在基线时,刚度值是13.46 +/- 9.97kPa。在294例HCV患者中,100例患有淋巴抑制性疾病,并单独评估。该组患者显示出与F0-F2组有关的刚度值(平均刚度值为6.07 +/- 1.68kPa)。所有其他患者表现出与F3-F4组有关的刚度值(平均刚度值为17.93 +/- 10.23)。与治疗结束(EOT)相比,基线的刚度之间没有发现统计学意义差异,而基线之间发现了显着差异,1年(p = .05)和2年后续随访(P <.01) 。基线和EOT之间发现显着的差异,以及在F3-F4组的治疗结束后1和2年之间。在治疗后的后续后,140名患有140名基线肝硬化患者的患者,其中1人死亡。结论:非侵入性方法提供重要的预后信息,特别是关于观察到的纤维化回归,并且在直接作用抗病毒治疗后监测寿命预期的患者可能是非常有用的。

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