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
Unlike other infectious diseases and viral infections, the long-term
chronicity of hepatitis C infection could worsen or propagate to irreversible extra hepatic manifestations like decompensated cirrhosis or the development of
hepatocellular carcinoma. The recent real-world clinical data of hepatitis C patients
treated with IFN-free DAAs are still fewer to conclude or decide the best treatment
protocols and guidelines for those who are still awaiting the treatment. However; based
on the clinical data retrieved from the diverse patient cohorts, multicenter and
multinational clinical studies, and pre- and post-therapeutic monitoring of hepatitis C treated patients enable the clinicians, physicians, and health care providers to sketch
consensus treatment guidelines and recommendations for the safe administration of
DAAs in general and vulnerable hepatitis C infected populations. Interestingly and
luckily, the treatment guidelines and recommendations approved by the FDA and CDC
are following and working well in real-world clinical, hospital, and primary health care
centers to manage hepatitis C, infected individuals. Albeit; for certain special
populations like pediatric and pregnant hepatitis C females, we do not have clear
guidelines for DAAs usage and their therapeutic monitoring. Furthermore, certain
DAAs are not recommended in decompensated cirrhotics, in HCV rebound patients,
and in previous treatment failure with a DAAs regimen. In this book chapter, we enlist
updated treatment guidelines and recommendations to treat general as well as special
hepatitis C-infected populations with DAAs and will briefly portray an overview of the
pros and cons of these recommendations in real-world clinical settings.<br>
Publisher
BENTHAM SCIENCE PUBLISHERS
Reference52 articles.
1. Martinez M.A.; Franco S.; Impact of COVID-19 in Liver Disease Progression. Hepatol Commun 2021,5(7),1138-1150
2. Shahid I.; Alzahrani A.R.; Al-Ghamdi S.S.; Alanazi I.M.; Rehman S.; Hassan S.; Hepatitis C Diagnosis: Simplified Solutions, Predictive Barriers, and Future Promises. Diagnostics (Basel, Switzerland). 2021; 11, 7.
3. Boettler T.; Newsome P.N.; Mondelli M.U.; Maticic M.; Cordero E.; Cornberg M.; Berg T.; Care of patients with liver disease during the COVID-19 pandemic: EASL-ESCMID position paper. JHEP Reports 2020,2(3)
4. Yu ML; Chen PJ; Dai CY; Hu TH; Huang CF; Huang YH; Taiwan consensus statement on the management of hepatitis C: Part (II) special populations. Journal of the Formosan Medical Association Taiwan 2020; 119(7): 1135-57.
5. Yeon J.E.; Recent update of the 2017 Korean Association for the Study of the Liver (KASL) treatment guidelines of chronic hepatitis C: Comparison of guidelines from other continents, 2017 AASLD/IDSA and 2016 EASL. Clin Mol Hepatol 2018,24(3),278-293