Affiliation:
1. Umm-Al-Qura University,Department of Pharmacology and Toxicology,Makkah,Saudi Arabia,
2. The Islamia University of Bahawalpur,Department of Pharmacology,Bahawalpur,Pakistan,
Abstract
Oral interferon-free DAAs (IFN-free DAAs) have proven their clinical and
therapeutic worth in real-life situations by achieving higher sustained virologic
response rates (SVRs >90%) in treated individuals. After their recommendations to be
administered to hepatitis C-infected populations in 2017 more than 5 million hepatitis
C-infected individuals have been treated across the world and the overall health care
burden of active hepatitis C comorbidities and mortalities have been declined from 130
million hepatitis C patients to approximately 71 million. Despite these great
achievements in hepatitis C therapeutics, certain patient-oriented, clinical, and societal
challenges are still prevailing to accept IFN-free DAAs on the large scale clinical,
hospital, and primary health care settings in low and middle-income countries as well
as even in developed nations. High therapy costs, treatment access and monitoring, co infection status of certain vulnerable hepatitis C infected populations, racial disparity,
pre-, and post-therapeutic monitoring, and long-term follow-ups are potential barriers
to consensually implementing uniform treatment algorithms and accessibility to DAAs
regimens worldwide. Furthermore, recurrence of hepatitis C infection, reactivation
risks of co-infections (e.g., HCV/HIV, HCV/HBV or HCV/CKD), minefield risks of
hepatocellular carcinoma (HCC) rebound, and surveillance of hepatitis C liver
transplant recipients which are on treatment with IFN-free DAAs also limit the
administration of these regimens to every hepatitis C infected individual. In this book
chapter, we will explore all these real-world challenges and will discuss/suggest the
strategies to coup them in clinical, hospital, and community settings to improve the
cascades of care and scale-up HCV cure. <br>
Publisher
BENTHAM SCIENCE PUBLISHERS