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A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
Published on: May 10, 2022
Decision analysis model for hepatitis B prophylaxis one year after liver transplantation
Sammy Saab1, Maggie Y Ham, Michael A Stone
1Department of Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA. ssaab@mednet.ucla.edu
Prophylaxis with lamivudine and adefovir is more cost-effective than hepatitis B immunoglobulin (HBIG) and lamivudine for liver transplant recipients. This strategy offers significant cost savings and supports its use as first-line therapy for preventing hepatitis B recurrence.
Area of Science:
- Hepatology and Transplantation
- Pharmacoeconomics
- Virology
Background:
- Hepatitis B immunoglobulin (HBIG) and lamivudine is the current standard for preventing hepatitis B recurrence post-liver transplant, with recurrence rates between 0-11%.
- Emerging data indicate adefovir's efficacy in managing recurrent hepatitis B infections.
- Hepatitis B recurrence remains a significant concern in liver transplant recipients, necessitating optimized prophylactic strategies.
Purpose of the Study:
- To compare the pharmacoeconomic outcomes of two hepatitis B prophylaxis strategies in liver transplant recipients one year post-transplantation.
- To evaluate the cost-effectiveness of using lamivudine and adefovir as a first-line strategy versus HBIG and lamivudine with later adefovir addition for hepatitis B prophylaxis.
Main Methods:
- A Markov decision analysis model was employed to simulate costs and outcomes over 10 years.
- Strategy 1: Prophylaxis with lamivudine and adefovir.
- Strategy 2: Prophylaxis with intramuscular HBIG and lamivudine, with adefovir added for recurrent cases; subsequent treatment failure managed with tenofovir and entecavir.
Main Results:
- After 10 years, lamivudine and HBIG treatment resulted in a 16.8% hepatitis B recurrence rate.
- Strategy 1 (lamivudine and adefovir) incurred medical costs of $151,819, while Strategy 2 incurred $166,246, yielding a cost saving of $14,427 with Strategy 1.
- Sensitivity analysis indicated the model's highest sensitivity to adefovir and HBIG costs and hepatitis B virus recurrence rates.
Conclusions:
- The lamivudine and adefovir strategy provides significant cost savings compared to the standard HBIG and lamivudine regimen.
- This pharmacoeconomic analysis supports the use of lamivudine and adefovir as a preferred first-line therapy for hepatitis B prophylaxis in liver transplant recipients.
- Optimizing prophylaxis strategies is crucial for improving long-term outcomes and reducing healthcare costs in liver transplantation.
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