TY - JOUR
T1 - Treatment Algorithm for Managing Chronic Hepatitis B Virus Infection in the United States
T2 - 2021 Update
AU - Martin, Paul
AU - Nguyen, Mindie H.
AU - Dieterich, Douglas T.
AU - Lau, Daryl T.Y.
AU - Janssen, Harry L.A.
AU - Peters, Marion G.
AU - Jacobson, Ira M.
N1 - Publisher Copyright:
© 2022 AGA Institute
PY - 2022/8
Y1 - 2022/8
N2 - Background & Aims: Chronic hepatitis B (CHB) infection remains the most frequent etiology of hepatocellular carcinoma globally as well as a major cause of cirrhosis. Despite vaccination, substantial numbers of persons have already been infected with hepatitis B virus and remain at risk of progressive liver disease. Methods: In 2004, a CHB management algorithm was developed by a panel of North American hepatologists, which was subsequently updated in 2006, 2008, and 2015. Since the most recent version, several developments have altered the management of CHB. Tenofovir alafenamide, with a more favorable safety profile than tenofovir disoproxil fumarate, has been introduced as an initial antiviral choice as well as an alternative for long-term therapy. Quantitation of hepatitis B surface antigen is becoming more widely available in clinical practice, with implications for monitoring response to treatment. Additionally, there has been a shift in how the natural history of CHB is perceived, as newer evidence has challenged the concept that during the immunotolerant phase of infection disease progression is not a concern. Finally, recent analyses indicate that in the United States, the average age of patients with CHB has increased, implying that the presence of comorbidities, including metabolic liver disease, increasing use of biologics associated with aging will increasingly affect disease management. Results: This updated algorithm is intended to serve as a guide to manage CHB while new antiviral strategies are developed. Conclusions: Recommendations have been based on evidence from the scientific literature, when possible, as well as clinical experience and consensus expert opinion. Points of continued debate and areas of research need are also described.
AB - Background & Aims: Chronic hepatitis B (CHB) infection remains the most frequent etiology of hepatocellular carcinoma globally as well as a major cause of cirrhosis. Despite vaccination, substantial numbers of persons have already been infected with hepatitis B virus and remain at risk of progressive liver disease. Methods: In 2004, a CHB management algorithm was developed by a panel of North American hepatologists, which was subsequently updated in 2006, 2008, and 2015. Since the most recent version, several developments have altered the management of CHB. Tenofovir alafenamide, with a more favorable safety profile than tenofovir disoproxil fumarate, has been introduced as an initial antiviral choice as well as an alternative for long-term therapy. Quantitation of hepatitis B surface antigen is becoming more widely available in clinical practice, with implications for monitoring response to treatment. Additionally, there has been a shift in how the natural history of CHB is perceived, as newer evidence has challenged the concept that during the immunotolerant phase of infection disease progression is not a concern. Finally, recent analyses indicate that in the United States, the average age of patients with CHB has increased, implying that the presence of comorbidities, including metabolic liver disease, increasing use of biologics associated with aging will increasingly affect disease management. Results: This updated algorithm is intended to serve as a guide to manage CHB while new antiviral strategies are developed. Conclusions: Recommendations have been based on evidence from the scientific literature, when possible, as well as clinical experience and consensus expert opinion. Points of continued debate and areas of research need are also described.
KW - Coinfection
KW - Entecavir
KW - Peginterferon Alfa
KW - Tenofovir
UR - http://www.scopus.com/inward/record.url?scp=85117723113&partnerID=8YFLogxK
U2 - 10.1016/j.cgh.2021.07.036
DO - 10.1016/j.cgh.2021.07.036
M3 - Article
C2 - 34329775
AN - SCOPUS:85117723113
SN - 1542-3565
VL - 20
SP - 1766
EP - 1775
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
IS - 8
ER -