Search In this Thesis
   Search In this Thesis  
العنوان
Ribavirin Dosing, Anemia, Erythropoietin and
Virological responses in Egyptian chronic
Hepatitis C(CHC) Patients Treated with
Combined PegylatedInterferon
and Ribavirin Therapy /
المؤلف
Berbish, Ahmed Said Ahmed.
هيئة الاعداد
باحث / أحمد سعيد أحمد بربش
مشرف / إمام عبد اللطيف واكد
مشرف / أم كلثوم السيد الحداد
مشرف / هالة هانى سعيد
الموضوع
Internal Medicine.
تاريخ النشر
2019.
عدد الصفحات
213 p. :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
الكبد
الناشر
تاريخ الإجازة
18/8/2019
مكان الإجازة
جامعة المنوفية - معهد الكبد - طب الكبد
الفهرس
Only 14 pages are availabe for public view

from 213

from 213

Abstract

Pegylated interferon plus ribavirin therapy given for 48 weeks is
established as the standard therapy for patients with chronic HCV
infection genotype 4 (AlAshgar et al, 2009) .
Forty-eight weeks of combination therapy in genotype 4 patients
showed response rates at an intermediate level compared to genotypes 2
and 3 (Kamal and Nasser, 2008).
Ribavirin has been shown to increase the initial viral kinetic
response to interferon, thus potentially improving early virological
response and overall efficacy of the treatment for hepatitis C (Herrman et
al, 2003).
Ribavirin induces a dose-dependent hemolytic anemia which is
reversible within 4-8 weeks of drug discontinuation. (Sulkowski et al,
2004).
Anemia-related dose reduction or discontinuance may adversely
affect outcome since it reduces the probability of achieving long-term
sustained viral response (Dieterich andSpivak, 2003).
Reddy et al, (2007) reported that minor ribavirin dose reduction to
manage adverse events do not appear to affect sustained virological
response adversely, unless cumulative exposure is less than 60%.
Increasing evidence now supports the use of recombinant human
erythropoietin to manage anemia in these patients, with the objective of
maintaining the RBV dose (Sherman et al, 2006) .