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Treatment Algorithm for Managing Chronic Hepatitis B Virus Infection in the United States: 2021 Update
Paul Martin1, Mindie H Nguyen2, Douglas T Dieterich3
1Division of Digestive Health and Liver Diseases, University of Miami School of Medicine, Miami, Florida.
Insights
This updated algorithm guides chronic hepatitis B (CHB) management, incorporating new treatments like tenofovir alafenamide and evolving understanding of CHB natural history. It addresses the increasing complexity of managing CHB in aging populations with comorbidities.
Area of Science:
- Hepatology and Viral Hepatitis Research
- Liver Disease Management
- Clinical Practice Guidelines
Background:
- Chronic hepatitis B (CHB) is a leading cause of liver cancer and cirrhosis worldwide.
- Despite vaccination efforts, many individuals remain at risk for progressive liver disease.
- The aging CHB patient population presents increased challenges due to comorbidities.
Purpose of the Study:
- To provide an updated clinical algorithm for managing chronic hepatitis B.
- To incorporate recent advancements in antiviral therapy and disease understanding.
- To guide healthcare professionals in the evolving landscape of CHB treatment.
Main Methods:
- Algorithm development based on scientific literature, clinical experience, and expert consensus.
- Inclusion of new antiviral agents such as tenofovir alafenamide.
- Consideration of updated insights into CHB natural history and patient demographics.
Main Results:
- The updated algorithm reflects current best practices for CHB management.
- It incorporates the use of tenofovir alafenamide for its favorable safety profile.
- The algorithm addresses the growing impact of comorbidities in aging CHB patients.
Conclusions:
- This algorithm serves as a practical guide for managing CHB.
- It highlights areas of ongoing debate and future research needs.
- The recommendations aim to optimize patient care amidst evolving therapeutic options.
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.
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