Efficacy and Safety of Combination Therapy of Natural Human Interferon Beta and Ribavirin in Chronic Hepatitis C Patients with Genotype 1b and High Virus Load
| العنوان: | Efficacy and Safety of Combination Therapy of Natural Human Interferon Beta and Ribavirin in Chronic Hepatitis C Patients with Genotype 1b and High Virus Load |
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| المؤلفون: | Kenji Ikeda, Norio Akuta, Yusuke Kawamura, Miharu Hirakawa, Hiromitsu Kumada, Satoshi Saito, Fumitaka Suzuki, Hitomi Sezaki, Yasuji Arase, Hiromi Yatsuji, Yoshiyuki Suzuki, Mariko Kobayashi, Tetsuya Hosaka, Masahiro Kobayashi |
| المصدر: | Internal Medicine. 49:957-963 |
| بيانات النشر: | Japanese Society of Internal Medicine, 2010. |
| سنة النشر: | 2010 |
| مصطلحات موضوعية: | Adult, Male, medicine.medical_specialty, Genotype, Combination therapy, Hepacivirus, Hepatitis C virus, medicine.disease_cause, Gastroenterology, Cohort Studies, chemistry.chemical_compound, Internal medicine, Ribavirin, Internal Medicine, medicine, Humans, Adverse effect, Retrospective Studies, biology, business.industry, Hazard ratio, virus diseases, Retrospective cohort study, Interferon-beta, General Medicine, Exanthema, Hepatitis C, Chronic, Middle Aged, Viral Load, biology.organism_classification, Recombinant Proteins, digestive system diseases, Treatment Outcome, chemistry, Immunology, Drug Therapy, Combination, Female, business, Viral load |
| الوصف: | The aim of this study was to evaluate the efficacy of combination therapy of natural human interferon-beta and ribavirin in patients infected with hepatitis C virus (HCV) genotype 1b.Inclusion criteria were HCV-genotype 1b, serum HCV RNA level ofor=100 KIU/ml before the initiation of treatment. A total of 40 patients were enrolled in this retrospective cohort study. The treatment period of combination therapy was 48 weeks. Nonparametric procedures were employed for the analysis of background features of the patients with SVR and without SVR. A p value of0.05 was considered to indicate a significant difference.Of the 40 study patients, ten had mental disorders before the initiation of combination therapy. One of the patients stopped the treatment due to exacerbation of depression and another patient stopped due to a skin rash. Three patients suspended the therapy due to an insufficient response of positive serum HCV RNA at 24 weeks after the initiation of treatment. Thus, 34 patients completed combination therapy. Fifteen had sustained virological response (SVR). The SVR rate in patients who showed negative HCV RNA 8 weeks after the initiation of combination therapy was 86.7% (13/15). On the other hand, the SVR rate in patients who showed positive HCV RNA at 8 weeks was 8% (2/25) (p.001). Continuous period of negative serum HCV RNA was 33.1 weeks in SVR groups, and 12.5 weeks in non-SVR groups (p.001).The combination therapy of IFN-beta and ribavirin is a possible therapy selection for patients with type C hepatitis of genotype 1b and high virus load. |
| تدمد: | 1349-7235 0918-2918 |
| URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a09299bc1384e4c7fe9f5ea078b472a2 https://doi.org/10.2169/internalmedicine.49.3232 |
| حقوق: | OPEN |
| رقم الأكسشن: | edsair.doi.dedup.....a09299bc1384e4c7fe9f5ea078b472a2 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 13497235 09182918 |
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