Direct-Acting Antiviral Treatment in Albanian Patients With Chronic Hepatitis C and Advanced Liver Fibrosis
- PMID: 36540321
- PMCID: PMC9759809
- DOI: 10.7759/cureus.32646
Direct-Acting Antiviral Treatment in Albanian Patients With Chronic Hepatitis C and Advanced Liver Fibrosis
Abstract
Background Treating chronic hepatitis C (CHC) with direct-acting antiviral (DAA) is very effective at clearing the infection. In Albania treatment with DAA is limited to patients with liver stiffness F3-F4, and with other co-infections. The objective of this study was to evaluate the efficacy of DAA in Albanian patients with genotypes 1-5, who mostly suffer from advanced liver fibrosis. Material and Methods This is a retrospective study carried out at the University Hospital Center "Mother Teresa", Tirana, during 2014-2019, including treatment-naïve and treatment-experienced patients with genotypes 1-5. All patients were evaluated with elastography and most of them were F3-F4. The primary endpoint involved the patients achieving SVR-12, or undetectable hepatitis C virus/ribonucleic acid (HCV RNA) 12 weeks after the end of treatment. In patients without a genotype, we have used a pangenotypic regimen. Results This study included 207 patients with a mean age of 48.9 ± 13.1 years, 56% male and 44% female; 152 (73%) were genotype 1, 24 were (11.5%) genotype 2, nine were (4.3%) genotype 3, 14 were (6.7%) genotype 4, one was (0.4%) genotype 5, and seven (3.8%) unassigned genotypes. The sustained virologic response (SVR) percentage according to genotype is discussed in the article. The overall SVR score of all the patients in our study was >93%. According to elastography, 127 (66%) were F3-F4, and 80 (38.6%) were F1-F2. Conclusion Treatment with DAA proved to be very effective in our patients; most of them had advanced liver fibrosis as well as compensated or decompensated liver cirrhosis. The overall SVR score of the patients in our study was >93%. Our country needs to treat all patients with chronic hepatitis C without limitations to attain the WHO objective of eradicating this disease by 2030.
Keywords: antiviral; chronic hepatitis c; elastography; genotype; liver cirrhosis.
Copyright © 2022, Cuko et al.
Conflict of interest statement
The authors have declared that no competing interests exist.
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References
-
- Global prevalence and genotype distribution of hepatitis C virus infection in 2015: a modelling study. Polaris Observatory HCV Collaborators. Lancet Gastroenterol Hepatol. 2017;2:161–176. - PubMed
-
- Hepatitis C virus prevalence and level of intervention required to achieve the WHO targets for elimination in the European Union by 2030: a modelling study. European Union HCV Collaborators. Lancet Gastroenterol Hepatol. 2017;2:325–336. - PubMed
-
- Efficacy and safety of glecaprevir/pibrentasvir in renally impaired patients with chronic HCV infection. Lawitz E, Flisiak R, Abunimeh M, et al. Liver Int. 2020;40:1032–1041. - PubMed
-
- Real-world efficacy and safety of pangenotypic direct-acting antivirals against hepatitis C virus infection. Scotto R, Buonomo AR, Moriello NS, et al. Rev Recent Clin Trials. 2019;14:173–182. - PubMed
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