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Efficacy of new direct acting antiviral-DAA (sofosbuvir) therapy in the management of rheumatological extrahepatic manifestations of HCV / Shaimaa Ahmed Saad ; Supervised Amira Abdelsabour Shahin , Hania Salah Zayed , Mohamed Said Abdelaziz

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Shaimaa Ahmed Saad , 2016Description: 189 P. : facsimiles ; 25cmOther title:
  • دراسة فاعلية وأمان استخدام العقار الجديد لعلاج فيروس س (سوفوسبوفير) في حالات الأعراض الروماتيزمية لمرضى فيروس س [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Rheumatology and Rehabilitation Summary: Background: The HCV epidemic is particularly devastating in Egypt as Egypt has the highest HCV prevalence in the world (14.7%). According to Health Issues Survey in 2015; 7% of Egyptians are chronic active hepatitis C patients. Chronic HCV infection primarily affects the liver with an array of extrahepatic manifestations, involving different organ systems leading to the concept of systemic HCV infection these manifestations include autoimmune phenomena and frank autoimmune and/or rheumatic diseases and may dominate its course. Objectives: This study aimed to assess the efficacy and safety of the new Direct Acting Antiviral drug Sofosbuvir in management of HCV related rheumatologic extrahepatic manifestations Arthropathy and Vasculitis. Patients and Methods: Thirty HCV patients with rheumatologic extrahepatic manifestation were included in this study. They received Sofosbuvir-based therapy as dual or triple regimen (Group A). The data of fifteen patients received the standard combined Peg-Interferon and RBV (Group B) were included as controls. The prospective data of the patients and the retrospective data of the controls were considered for analysis at baseline, at the end of treatment, 12weeks and 24weeks after termination of treatment.Results: On comparing the four visits in Group A with the four visits in Group B, statistically significant difference was found in VAS and in TJC and in modified DAS28 in all visits (P<0.05), however the difference in FAS between both groups in all visits was statistically insignificant. There was a statistically significant improvement in BVAS 2003(P<0.05) in the four visits
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.32.M.Sc.2016.Sh.E (Browse shelf(Opens below)) Not for loan 01010110070485000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.32.M.Sc.2016.Sh.E (Browse shelf(Opens below)) 70485.CD Not for loan 01020110070485000

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Rheumatology and Rehabilitation

Background: The HCV epidemic is particularly devastating in Egypt as Egypt has the highest HCV prevalence in the world (14.7%). According to Health Issues Survey in 2015; 7% of Egyptians are chronic active hepatitis C patients. Chronic HCV infection primarily affects the liver with an array of extrahepatic manifestations, involving different organ systems leading to the concept of systemic HCV infection these manifestations include autoimmune phenomena and frank autoimmune and/or rheumatic diseases and may dominate its course. Objectives: This study aimed to assess the efficacy and safety of the new Direct Acting Antiviral drug Sofosbuvir in management of HCV related rheumatologic extrahepatic manifestations Arthropathy and Vasculitis. Patients and Methods: Thirty HCV patients with rheumatologic extrahepatic manifestation were included in this study. They received Sofosbuvir-based therapy as dual or triple regimen (Group A). The data of fifteen patients received the standard combined Peg-Interferon and RBV (Group B) were included as controls. The prospective data of the patients and the retrospective data of the controls were considered for analysis at baseline, at the end of treatment, 12weeks and 24weeks after termination of treatment.Results: On comparing the four visits in Group A with the four visits in Group B, statistically significant difference was found in VAS and in TJC and in modified DAS28 in all visits (P<0.05), however the difference in FAS between both groups in all visits was statistically insignificant. There was a statistically significant improvement in BVAS 2003(P<0.05) in the four visits

Issued also as CD

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