Initial Treatment and Management of Hepatitis B
For patients diagnosed with chronic hepatitis B, the initial treatment should be entecavir or tenofovir, which are the preferred first-line agents due to their high potency and high barrier to resistance. 1, 2
Patient Assessment and Treatment Criteria
When to Treat
- Treatment is indicated for patients with HBV DNA ≥2,000 IU/mL, elevated ALT and/or at least moderate histological lesions 1
- All patients with cirrhosis and detectable HBV DNA should receive treatment, regardless of ALT levels 1
- For HBeAg-positive patients:
- For HBeAg-negative patients:
Initial Monitoring (Before Treatment)
- Complete serological profile: HBsAg, HBeAg, anti-HBe, HBV DNA quantification 1
- Liver function tests including ALT, AST, bilirubin, albumin, prothrombin time 3
- Assessment of liver fibrosis (biopsy or non-invasive methods like transient elastography) 2
- HIV testing should be offered to all patients prior to initiating therapy 4
Treatment Options
First-Line Agents
Nucleos(t)ide analogues (NAs) with high genetic barrier to resistance:
- Entecavir (0.5-1mg daily) - preferred for treatment-naïve patients 3, 2
- Tenofovir disoproxil fumarate (TDF) (300mg daily) - preferred for all patients, including those with lamivudine resistance 3, 2
- Tenofovir alafenamide fumarate (TAF) - preferred for patients with renal dysfunction or bone disease 1
Peginterferon alfa-2a:
Not Recommended as First-Line
- Lamivudine - high resistance rates (up to 70% after 5 years) 3, 2
- Adefovir - inferior efficacy and resistance profiles compared to tenofovir 3, 4
- Telbivudine - intermediate rate of resistance 3
Treatment Duration and Monitoring
Duration
- Long-term, potentially indefinite treatment is typically required with NAs 1
- For patients on peginterferon alfa-2a, treatment duration is 48 weeks 3
- For patients on NAs who achieve HBeAg seroconversion, consider continuing treatment for at least 6-12 months after confirmation 3
Monitoring During Treatment
- Check HBV DNA and ALT levels at baseline and every 3-6 months during therapy 2
- For patients on tenofovir, monitor renal function regularly due to potential nephrotoxicity 2
- For patients on peginterferon, monitor for side effects and perform complete blood count regularly 3
Special Populations
Pregnant Women
- Tenofovir is the preferred agent during pregnancy to prevent mother-to-child transmission 1
- Consider antiviral therapy in the third trimester for mothers with high viral load 1
Patients with Renal Dysfunction
- Entecavir or TAF are preferred for patients with renal dysfunction 1
- For patients on adefovir with renal impairment, dose adjustment is required based on creatinine clearance 4
Immunosuppressed Patients
- Prophylactic antiviral therapy should be initiated before or simultaneously with immunosuppressive therapy 3
- Continue anti-HBV prophylaxis during immunosuppressive therapy and for at least 6 months after completion (12 months for anti-CD20 therapies) 3
Common Pitfalls and Caveats
- Do not discontinue treatment prematurely - severe acute exacerbations of hepatitis may occur in patients who discontinue therapy 4
- Do not use lamivudine as first-line therapy due to high resistance rates 3, 2
- Do not assume patients with normal ALT don't need treatment - they can still have significant liver disease 3
- Do not delay antiviral therapy in patients with decompensated cirrhosis 1
- Do not use entecavir in patients with prior lamivudine exposure as they may have resistance mutations 3
By following these evidence-based guidelines for the initial treatment and management of hepatitis B, clinicians can help prevent disease progression and improve long-term outcomes for patients with this chronic infection.