Evolution of patients with chronic hepatitis C infection with advanced fibrosis or cirrhosis cured with direct-acting antivirals. Long-term follow-up.

Autor: Badia Aranda E; Servicio de Aparato Digestivo, Hospital Universitario de Burgos, Burgos, España. Electronic address: esterbadara@gmail.com., Fernández Marcos C; Servicio de Aparato Digestivo, Hospital Universitario de Burgos, Burgos, España., Puebla Maestu A; Servicio de Aparato Digestivo, Hospital Universitario de Burgos, Burgos, España., Gozalo Marín V; Servicio de Aparato Digestivo, Hospital Universitario de Burgos, Burgos, España., Vinuesa Campo R; Servicio de Aparato Digestivo, Hospital Universitario de Burgos, Burgos, España., Calvo Simal S; Servicio de Aparato Digestivo, Hospital Universitario de Burgos, Burgos, España., Gómez Camarero J; Servicio de Aparato Digestivo, Hospital Universitario de Burgos, Burgos, España.
Jazyk: English; Spanish; Castilian
Zdroj: Gastroenterologia y hepatologia [Gastroenterol Hepatol] 2022 Dec; Vol. 45 (10), pp. 767-779. Date of Electronic Publication: 2022 Feb 18.
DOI: 10.1016/j.gastrohep.2022.02.002
Abstrakt: Aims: To analyze laboratory parameters, clinical and fibrosis evolution in F3-F4 patients cured with direct-acting antivirals (DAA).
Patients and Methods: Unicenteric, observational and prospective study. All F3-F4 hepatitis C patients cured with DAA from 01/11/2014 to 31/08/2019 were included. A basal visit (BV) was performed and at 12 weeks (12w), 1, 2, 3 and 4 years after treatment. Demographic and laboratory variables, fibrosis measured by non-invasive tests, indirect markers of portal hypertension, the presence of esophageal varices, cirrhosis decompensation and hepatoceullar carcinoma were collected.
Results: 169 patients were treated: 123 (72.8%) men, age 57.5±12 years; 117 (69.2%) with cirrhosis, 99 (84.6%) ChildA. 96,4% achieved SVR. The study was conducted for a median follow-up of 46.14 (2.89-62.55) months. It was observed a significant increase in platelets [155×10 3 /μL (BV); 163×10 3 /μL (12w)], cholesterol [158mg/dL (BV); 179mg/dL (12w)] and albumin [4.16g/dL (BV); 4.34g/dL (12w)] and a significant decrease in ALT [82UI/L (BV); 23UI/L (12w], AST [69UI/L (BV); 26UI/L (12w)], GGT [118UI/L (BV); 48UI/L (12w)] and bilirrubin [0.9mg/dL (BV); 0.7mg/dL (12w)]. Fibrosis also improved early in follow-up, both by serological methods and Fibroscan [19.9kPa (BV); 14.8kPa (12w; P<.05]. 8.1% of compensated cirrhosis patients had some decompensation. 4.5% developed esophageal varices. Nine patients (5.52%) had de novo hepatocellular carcinoma; 6 (3.68%) had hepatoceullar carcinoma in BV and 40% had a recurrence. During follow-up mortality was 9.2%.
Conclusions: There is an improvement in laboratory parameters and fibrosis measured by non-invasive methods in F3-F4 patients cured with DAA. However, the risk of decompensation and the incidence/recurrence of hepatocellular carcinoma still remain, so there is a need to follow these patients.
(Copyright © 2022 Elsevier España, S.L.U. All rights reserved.)
Databáze: MEDLINE