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The Safety of The Directly Acting Antiviral Treatment For Hepatitis C Virus According To The Egyptian National
Ahmed Farouk Alaarag1, Ahmed Mohamed Hamam2, Osama Ahmed Amin3
1Department of Cardiology Tanta University, EG.
Insights
Directly acting antiviral agents for hepatitis C virus are safe for patients with midrange heart function. Treatment showed no adverse cardiovascular effects and improved insulin resistance.
Area of Science:
- Cardiology
- Hepatology
- Pharmacology
Background:
- The Egyptian National Committee of Viral Hepatitis leads global hepatitis C virus (HCV) management.
- Limited data exists on the cardiovascular effects of new directly acting antiviral agents (DAAs).
Purpose of the Study:
- To assess the cardiovascular safety of DAAs in HCV patients with midrange left ventricular ejection fraction (LVEF).
Main Methods:
- A multicenter study of 400 HCV patients (LVEF 40-49%) treated with Sofosbuvir/Daclatasvir (Group I) or Sofosbuvir/Daclatasvir/Ribavirin (Group II).
- Evaluations included cardiac function, biomarkers (BNP), metabolic profiles, and Holter monitoring before and after treatment.
Main Results:
- No significant changes in cardiac function (NYHA Class, LVEF, BNP) or heart rate variability were observed.
- DAA treatment did not induce bradycardia or non-sustained ventricular tachycardia.
- Improved insulin resistance and decreased glucose/insulin levels were noted; HDL/LDL increased in Group II.
Conclusions:
- DAA regimens are safe for HCV patients with NYHA Class I/II and midrange LVEF (40-49%).
- HCV clearance with DAAs leads to beneficial metabolic changes, including improved insulin resistance.
Background:
The Egyptian National Committee of Viral Hepatitis program is the leading national hepatitis C virus (HCV) management program globally. However, limited data is available about the effect of the new directly acting antiviral agents on the cardiovascular system.
Objectives:
Our study aimed to assess the safety of the relatively new directly acting antiviral agents approved by the National Health Committee in Egypt to treat patients infected with hepatitis C virus who have midrange left ventricular ejection fraction.
Methods:
This multicenter study included 400 successive patients with an ejection fraction (40-49%) from May 2017 to December 2019. We classified them into two groups: Group I (Child A), who received Sofosbuvir and Daclatasvir for twelve weeks, and Group II (Child B), who received Sofosbuvir, Daclatasvir, and Ribavirin for twelve weeks. Patients were evaluated for their symptoms, ejection fraction, brain natriuretic peptide, lipid profile, fasting blood glucose, fasting insulin, Homeostatic Model Assessment of Insulin Resistance levels, and Holter monitoring (just before the start of treatment and within three days after completing therapy).
Results:
We found New York Heart Association Class, ejection fraction, brain natriuretic peptide, premature ventricular contractions burden, as well as highest and lowest heart rate did not show a statistically significant difference in both groups after treatment. The treatment did not cause bradycardia or non-sustained ventricular tachycardia. Fasting blood glucose and fasting insulin levels declined, with improved insulin resistance after treatment in both groups. Both low and high-density lipoprotein cholesterol increased after treatment in Group II.
Conclusions:
Both regimens of directly acting antiviral agents used in Egypt to treat chronic hepatitis C virus infection are safe in patients with New York Heart Association Class I and II with midrange left ventricular ejection fraction (40-49%). There are beneficial metabolic changes following HCV clearance as an improvement of insulin resistance.
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