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العنوان
DIRECTLY ACTING ANTI-VIRAL DRUGS
AND ITS METABOLIC SIDE EFFECTS IN
PATIENTS WITH chrONIC HCV /
المؤلف
Abdallah,Abdallah Mohamed.
هيئة الاعداد
باحث / Abdallah Mohamed Abdallah
مشرف / Mohamed Marei Makhlouf
مشرف / Moataz Mohamed Said
مشرف / Khaled Amr Zaki
تاريخ النشر
2017
عدد الصفحات
126p.;
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الطب الباطني
تاريخ الإجازة
1/1/2017
مكان الإجازة
جامعة عين شمس - كلية الطب - باطنة عامة
الفهرس
Only 14 pages are availabe for public view

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from 126

Abstract

HCV infection is a major cause of liver cirrhosis, (HCC)
and end-stage liver disease. The development of an interferonfree,
all-oral treatment regimen represents an important
advance. We evaluated daclatasvir (an HCV NS5A replication
complex inhibitor) plus sofosbuvir (a nucleotide analogue HCV
NS5B polymerase inhibitor) with or without Ribavirin in
chronic HCV patients.
Results
Sustained virological response (12 weeks ) after end of
the treatment in more than 90% of patients , Liver function
parameters including albumin, bilirubin, and prothrombin time
and liver enzymes Ast , Alt improved in the majority of
patients during and after the end of therapy ,but there is
significant increase in urea level , serum creatinin and HbA1C.
There is significant decrease in LDL and mild increase in
TG level.
Conclusion
Once-daily oral daclatasvir plus sofosbuvir with or
without Ribavirin was associated with high rates of sustained
virologic response among patients infected with HCV ,
including chronic cirrhotic patients and relapsers , successful
treatment associated with Improvement of liver function parameters in the majority of patients , Increase in urea level,
serum creatinin and HbA1C.
There is significant decrease in LDL and mild increase in
TG level.
Recommendations
 To avoid side effects of DAAs on patients, they have to
restrict diet and continue medical treatment of diabetes
with follow up RBS.
 During treatment, patient must follow up renal function
to avoid the side effects of drug.
 Good monitoring for hyperlipidemia to avoid ischemic
heart disease..