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Effect of Chronic Hepatitis C Virus Treatment by Combination Therapy on Cardiovascular System
Reda Biomy1, Mohamed Abdelshafy2, Ahmed Abdelmonem2
1Faculty of Medicine, Kafrelsheikh University, Kafr El-Sheikh, Egypt.
Insights
Direct-acting antiviral agents (DAAs) for hepatitis C virus (HCV) showed no significant cardiovascular effects in Egyptian patients. This study confirms the safety of DAAs in managing HCV, even with high prevalence.
Area of Science:
- Hepatology
- Cardiology
- Virology
Background:
- Hepatitis C virus (HCV) infection poses a significant public health challenge in Egypt.
- Direct-acting antiviral agents (DAAs) offer a promising treatment for HCV.
Purpose of the Study:
- To evaluate the cardiovascular impact of DAAs in patients with HCV.
- To assess potential cardiac adverse events associated with DAA therapy.
Main Methods:
- 170 HCV patients received either triple (pegylated interferon alfa, sofosbuvir, ribavirin) or dual (sofosbuvir, simeprevir) DAA therapy.
- Cardiovascular assessments included medical history, clinical exams, ECG, echo-Doppler, and lab tests over 6-12 months.
- Primary endpoint was the occurrence of major cardiovascular events.
Main Results:
- No major cardiovascular events were observed in either treatment group.
- No significant changes in ECG parameters (ST-T wave, arrhythmias, QT interval) were noted.
- Echocardiographic parameters, including regional wall motion, systolic, and diastolic functions, remained stable.
Conclusions:
- Combined oral DAAs, with or without interferon, do not significantly impact the cardiovascular system in HCV patients.
- DAA therapy is safe concerning cardiovascular effects in this patient population.
- Further research may explore long-term cardiovascular outcomes.
Background:
The prevalence of hepatitis C virus (HCV) in Egypt is quite high, and the combined oral direct-acting antiviral agents (DAAs) may have impressive results.
Objective:
To assess the cardiovascular effects of DAAs in patients with HCV.
Methods:
A total of 170 patients with HCV were divided into 2 groups: first group (100 patients) received triple combination therapy (pegylated interferon alfa, sofosbuvir, and ribavirin, whereas the second group (70 patients) received dual combination therapy (sofosbuvir and simeprevir). Group 1 patients were followed up for 1 year more than 3 visits, whereas group 2 patients were followed up for 6 months more than 2 visits; and the end point of the study was the development of a major cardiovascular event (eg, congestive heart failure, echocardiographic evidence of left ventricular dysfunction, occurrence of significant arrhythmias, or acute coronary syndrome). The following parameters were accomplished: medical history and clinical examination, electrocardiogram, echo-Doppler study, and laboratory investigations.
Results:
No significant differences were found between the 2 study groups regarding demographic criteria. None of the both group patients had developed any major cardiac event. No significant changes were observed regarding ST-T wave abnormalities, arrhythmias, or QT interval. None of the both group patients developed echocardiographic regional wall motion abnormalities at baseline or at study end. Systolic function parameters showed minute nonsignificant changes over study visits. Diastolic function parameters showed nonsignificant changes between baseline and 6-month and 12-month visits.
Conclusions:
The DAAs used in combination regimen with interferon or used orally in combination do not significantly affect the cardio-vascular system.
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