Efficacy and tolerability of pegylated-interferon alpha-2a in hemodialysis patients with chronic hepatitis C
dc.contributor.author | Kokoglu, OF | |
dc.contributor.author | Uçmak, H | |
dc.contributor.author | Hosoglu, S | |
dc.contributor.author | Cetinkaya, A | |
dc.contributor.author | Kantarceken, B | |
dc.contributor.author | Buyukbese, MA | |
dc.contributor.author | Isik, IO | |
dc.date.accessioned | 2024-04-24T17:11:32Z | |
dc.date.available | 2024-04-24T17:11:32Z | |
dc.date.issued | 2006 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | Background and Aim: Hepatitis C virus (HCV) is prevalent in hemodialysis (HD) patients. These patients experience more side-effects with antiviral treatment. The aim of the present study was to evaluate the efficacy and tolerability of pegylated interferon (PEG-IFN) alpha-2a in chronic hemodialysis patients with chronic hepatitis C. Methods: Twenty-five patients were included into the study. All of the patients were interferon naive, anti-HCV antibodies positive and polymerase chain reaction HCV-RNA positive. Twelve of the patients received PEG-IFN alpha-2a at a dose of 135 mu g weekly for 48 weeks (Group 1). The remaining 13 patients who received no specific treatment were used as controls (Group 2). The patients were prospectively followed up for a period of 18 months. Biochemical and virological responses were evaluated at the end of the study period (end-of-treatment response) and 6 months after the completion of therapy (sustained response). Results: Virological end-of-treatment response was observed in 10 patients (83.4%) in Group 1 and one patient (7.7%) in Group 2 (P < 0.001). Sustained virological response was observed in nine patients (75%) in Group 1 and one patient (7.7%) in Group 2 (P < 0.001). Alanine aminotransferase (ALT) levels were initially increased in seven patients in Group 1 and normalized in five of these patients at the end of the treatment and sustained biochemical response was 71.4%. In contrast, ALT levels in Group 2 were initially high in five patients and normalized in two of them (40%) at the end of the 48 weeks. Even if most of the patients experienced several side-effects (anemia 75%, fatigue 58.3%, thrombocytopenia 33.3% and leukopenia 33.3%), they did not impose the discontinuation of the treatment. Conclusion: The present study showed that PEG-IFN alpha-2a for 48 weeks is efficacious and well tolerated in hemodialysis patients with HCV. (C) 2005 Blackwell Publishing Asia Pty Ltd. | en_US |
dc.identifier.doi | 10.1111/j.1440-1746.2005.04008.x | |
dc.identifier.endpage | 580 | en_US |
dc.identifier.issn | 0815-9319 | |
dc.identifier.issn | 1440-1746 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 16638102 | |
dc.identifier.scopus | 2-s2.0-33645034186 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 575 | en_US |
dc.identifier.uri | https://doi.org/10.1111/j.1440-1746.2005.04008.x | |
dc.identifier.uri | https://hdl.handle.net/11468/17588 | |
dc.identifier.volume | 21 | en_US |
dc.identifier.wos | WOS:000236035300015 | |
dc.identifier.wosquality | Q3 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.relation.ispartof | Journal of Gastroenterology and Hepatology | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Chronic Hepatitis C | en_US |
dc.subject | Chronic Renal Failure | en_US |
dc.subject | Dialysis | en_US |
dc.subject | Pegylated Interferon | en_US |
dc.subject | Tolerability | en_US |
dc.title | Efficacy and tolerability of pegylated-interferon alpha-2a in hemodialysis patients with chronic hepatitis C | en_US |
dc.title | Efficacy and tolerability of pegylated-interferon alpha-2a in hemodialysis patients with chronic hepatitis C | |
dc.type | Article | en_US |