Giris ve Amaç: Genotip 1b ile infekte kronik hepatit C?li hastalar, tedaviye yaniti en düsük olan hasta grubunu olustururlar. Ülkemizde de en sik genotip 1b ile infeksiyon görülmektedir. Yapilan çalismalarda genotip 1b ile infekte kronik hepatit C?li hastalarin tedavisi sonrasi kalici viral yanit orani %45-55 arasinda degismektedir. Çalismamizin amaci, genotip 1b ile infekte kronik hepatit C hastalarinda tedaviye uyum, sik hasta takibi ve ilaç yan etkileriyle mücadelenin kalici viral yanit üzerine olan etkisini degerlendirmektir. Gereç ve Yöntem: Çalismaya yas ortalamasi 48,48 ± 10,54 olan, 17?si kadin 4?ü erkek toplam 21 genotip 1b ile infekte kronik hepatit C hastasi alinmistir. Hastalara 48 haftalik peginterferon alfa-2a ve ribavirin tedavisi uygulanmistir. Ilaçlara bagli yan etki gelisen hastalar, siki takibe alinarak mümkün oldugunca ilaç dozu azaltilmamaya çalisilmistir. Doz azaltimi gerekse bile bu mümkün oldugunca minimum düzeyde yapilarak her firsatta tekrar eski doza yükseltilmeye çalisilmistir. Bulgular: Çalisma grubumuzda; erken virolojik yanit %95,2, tedavi sonu yanit %85,7, kalici viral yanit %80,9 olarak saptanmistir. Sonuç; kronik hepatit C?de tedaviye yaniti en düsük olan genotip 1b ile infekte hastalarda tedaviye uyum, sik hasta takibi ve ilaç yan etkileriyle mücadelenin tedaviye yaniti artiracagini düsünmekteyiz.
Background and Aim: Chronic hepatitis C patients who infected with genotype 1b consist the patient group which has the lowest response to therapy. Infection with genotype 1b is the most prevalent in our country. In several studies, the post-therapeutic sustained viral response rate of the chronic hepatitis C patients, infected with genotype 1b, is 45-55 %. Our study was done to evaluate the effect of compliance, frequent follow-up, struggle with drug side effects to sustained viral response in chronic hepatitis C infected with genotype1b. 21 chronic hepatitis C patients (17 female, 4 male) infected with genotype 1b were taken in this study. Material and Method: Peginterferon alpha-2a and ribavirin combination therapy was given to all patients for 48 weeks. Patients who experienced drug side effect were taken in close follow-up avoiding dose reductions as much as possible. When necessary, dose reductions were done as in minimal levels, then doses were increased to normal levels as soon as possible. Results: In our study group, early virological response was 95,2%, end of treatment response was 85,7% and sustained viral response was 80,9%. Conclusion: According to our results, we think that compliance, frequeny follow-up and struggle with drug side-effects will improve the therapy response in patient infected with genotype 1b which has the lowest response in chronic hepatitis C.