dc.contributor.author | Besisik, F | |
dc.contributor.author | Kaymakoglu, S | |
dc.contributor.author | Demir, K | |
dc.contributor.author | Poturoglu, S | |
dc.contributor.author | Danalioglu, A | |
dc.contributor.author | Bozaci, M | |
dc.contributor.author | Cakaloglu, Y | |
dc.contributor.author | Karaca, C | |
dc.contributor.author | Okten, A | |
dc.contributor.author | Badur, S | |
dc.date.accessioned | 2021-03-05T13:19:25Z | |
dc.date.available | 2021-03-05T13:19:25Z | |
dc.date.issued | 2005 | |
dc.identifier.citation | Kaymakoglu S., Karaca C., Demir K., Poturoglu S., Danalioglu A., Badur S., Bozaci M., Besisik F., Cakaloglu Y., Okten A., "Alpha interferon and ribavirin combination therapy of chronic hepatitis D", ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, cilt.49, ss.1135-1138, 2005 | |
dc.identifier.issn | 0066-4804 | |
dc.identifier.other | av_b1a99e77-31ef-4943-a1ee-ee4b1a9e5657 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/118360 | |
dc.identifier.uri | https://doi.org/10.1128/aac.49.3.1135-1138.2005 | |
dc.description.abstract | The success of alpha interferon (IFN-alpha) monotherapy for the treatment of chronic hepatitis D is very limited. In this study, the efficacy of IFN-alpha and ribavirin combination therapy for chronic hepatitis D was investigated. Nineteen patients (15 males; mean age +/- standard deviation, 36.8 +/- 12.8 years) with chronic hepatitis D who were treated with IFN-alpha2b (10 million U, three times/week, subcutaneously) and ribavirin (1,000 to 1,200 mg/day, orally) for 24 months were studied. All patients had compensated liver disease (15 were precirrhotic), elevated transaminase levels, and hepatitis D virus RNA positivity at baseline. Genotypic analyses revealed hepatitis D virus genotype I and hepatitis B virus genotype D. All patients completed the 24 months of treatment and at least 6 months (7 to 19 months) of a follow-up period. Biochemical responses were observed in eight patients (42.1%) at the end of treatment and in seven patients (36.8%) at the end of follow-up. Eight patients (42.1%) at the end of treatment and four patients (21%) at the end of follow-up had virological responses. In conclusion, combination treatment of IFN-alpha and ribavirin for chronic hepatitis D is not able to induce virological responses at a sufficient rate, despite its partial effectiveness in improving biochemical responses, and is not superior to IFN-alpha monotherapy. | |
dc.language.iso | eng | |
dc.subject | Eczacılık | |
dc.subject | Mikrobiyoloji | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.subject | FARMAKOLOJİ VE ECZACILIK | |
dc.subject | Farmakoloji ve Toksikoloji | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Temel Eczacılık Bilimleri | |
dc.subject | Yaşam Bilimleri | |
dc.subject | Temel Bilimler | |
dc.title | Alpha interferon and ribavirin combination therapy of chronic hepatitis D | |
dc.type | Makale | |
dc.relation.journal | ANTIMICROBIAL AGENTS AND CHEMOTHERAPY | |
dc.contributor.department | , , | |
dc.identifier.volume | 49 | |
dc.identifier.issue | 3 | |
dc.identifier.startpage | 1135 | |
dc.identifier.endpage | 1138 | |
dc.contributor.firstauthorID | 174517 | |