In a Real-Life Setting, Direct-Acting Antivirals to People Who Inject Drugs with Chronic Hepatitis C in Turkey
dc.contributor.author | Yıldırım, Figen | |
dc.contributor.author | User, Ulku | |
dc.contributor.author | Sarı, Nagehan Didem | |
dc.contributor.author | Kurtaran, Behice | |
dc.contributor.author | Önlen, Yusuf | |
dc.contributor.author | Senates, Ebubekir | |
dc.contributor.author | Gündüz, Alper | |
dc.date.accessioned | 2024-08-23T16:08:13Z | |
dc.date.available | 2024-08-23T16:08:13Z | |
dc.date.issued | 2022 | en_US |
dc.department | Düzce Üniversitesi | en_US |
dc.description.abstract | Background: People who inject drugs (PWID) should be treated in order to eliminate hepatitis C virus in the world. The aim of this study was to compare direct-acting antivirals treatment of hepatitis C virus for PWID and non-PWID in a real-life setting. Methods: We performed a prospective, non-randomized, observational multicenter cohort study in 37 centers. All patients treated with direct-acting antivirals between April 1, 2017, and February 28, 2019, were included. In total, 2713 patients were included in the study among which 250 were PWID and 2463 were non-PWID. Besides patient characteristics, treatment response, follow-up, and side effects of treatment were also analyzed. Results: Genotype 1a and 3 were more prevalent in PWID-infected patients (20.4% vs 9.9% and 46.8% vs 5.3%). The number of naïve patients was higher in PWID (90.7% vs 60.0%), while the number of patients with cirrhosis was higher in non-PWID (14.1% vs 3.7%). The loss of follow-up was higher in PWID (29.6% vs 13.6%). There was no difference in the sustained virologic response at 12 weeks after treatment (98.3% vs 98.4%), but the end of treatment response was lower in PWID (96.2% vs 99.0%). In addition, the rate of treatment completion was lower in PWID (74% vs 94.4%). Conclusion: Direct-acting antivirals were safe and effective in PWID. Primary measures should be taken to prevent the loss of follow-up and poor adherence in PWID patients in order to achieve World Health Organization’s objective of eliminating viral hepatitis. | en_US |
dc.identifier.doi | 10.5152/tjg.2022.21834 | |
dc.identifier.endpage | 978 | en_US |
dc.identifier.issn | 1300-4948 | |
dc.identifier.issue | 11 | en_US |
dc.identifier.startpage | 971 | en_US |
dc.identifier.trdizinid | 1175267 | en_US |
dc.identifier.uri | https://search.trdizin.gov.tr/tr/yayin/detay/1175267 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12684/15175 | |
dc.identifier.volume | 33 | en_US |
dc.indekslendigikaynak | TR-Dizin | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Turkish Journal of Gastroenterology | en_US |
dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.title | In a Real-Life Setting, Direct-Acting Antivirals to People Who Inject Drugs with Chronic Hepatitis C in Turkey | en_US |
dc.type | Article | en_US |
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