Your browser doesn't support javascript.
loading
Comparison of adefovir dipivoxil and pegylated interferon alpha-2a treatment in chronic hepatitis B patients.
Korkmaz, Pinar; Usluer, Gaye; Ozgunes, Ilhan; Kartal, Elif Doyuk; Erben, Nurettin; Alpat, Saygin Nayman.
Afiliação
  • Korkmaz P; Department of Infectious Diseaes and Clinical Microbiology, Yunus Emre State Hospital, Eskisehir, Turkey.
  • Usluer G; Department of Infectious Diseaes and Clinical Microbiology, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
  • Ozgunes I; Department of Infectious Diseaes and Clinical Microbiology, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
  • Kartal ED; Department of Infectious Diseaes and Clinical Microbiology, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
  • Erben N; Department of Infectious Diseaes and Clinical Microbiology, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
  • Alpat SN; Department of Infectious Diseaes and Clinical Microbiology, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
North Clin Istanb ; 1(1): 26-32, 2014.
Article em En | MEDLINE | ID: mdl-28058298
ABSTRACT

OBJECTIVE:

In this study, we aimed to evaluate the efficacy of pegylated interferon alpha 2a and adefovir dipivoxil treatment in chronic hepatitis B patients.

METHODS:

This study was performed on patients treated for chronic hepatitis B in the Infectious Disease Clinic of Eskisehir Osmangazi University between 01.09.2005 and 31.03.2008. A total of 30 patients aged between 18 and 65 years constituted the study group. One of patient groups received (10 HBeAg negative, 4 HBeAg positive) PEG-IFN alpha 2a at a dose of 180 µg/once a week, whereas the other group (11 HBeAg negative, 5 HBeAg positive) received daily oral doses of 10 mg ADV. Treatment responses were evaluated at week 48.

RESULTS:

Reductions in serum HBV DNA levels at the end of 48 weeks were 4.8 log10 copy/ml and 4.2 log10 copy/ml in HBeAg negative patients who received ADV or PEG-IFN alpha 2a, respectively. Biochemical response rates were 60% and 91% in PEG-IFN alpha 2a and ADV groups, respectively. Among HBeAg positive patients, reductions in serum HBV DNA levels were 3. 2 log10 copy/ml and 4 log10 copy/ml in ADV and PEG-IFN alpha 2a groups, at week 48, respectively. Biochemical response rates were 50% and 40% in PEG-IFN alpha 2a and ADV groups, respectively. No significant difference was determined in biochemical and virological responses in HBeAg positive and negative patients between PEG-IFN alpha 2a and ADV groups, at week 48. When both treatment groups were evaluated for side effects, it was observed that side effects were significantly common in PEG-IFN alpha 2a group.

CONCLUSION:

When we compared PEG-IFN alpha 2a and ADV treatment in both HBeAg positive and negative patients, biochemical and virological response rates at 48 weeks were similar.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: North Clin Istanb Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Turquia

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: North Clin Istanb Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Turquia