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HBV prophylaxis in chemotherapy

  • moderate risk: HBsAg-positive individuals receieved cytotoxic chemotherapy
  • confirm HBV/HCV profiles prior to administering preventive anti-viral agents for HBV flare-up prophylaxis during chemotherapy.
  • start entecavir concurrently or prior to initiating chemotherapy
    • maintained for at least 6 months after withdrawal of immunosuppression
    • duration of chemotherapy: ___/___/___ to ___/___/___ (estimated)
    • explain adverse effects:
      • headache, fatigue, dizziness, nausea reported in 22% of patients.
  • monitor if HBV reactivation:
    • previously had undetectable HBV DNA detectable HBV DNA
    • 10x to 100x fold increase in HBV DNA
    • HBsAg negative/anti-HBc positive becomes HBsAg positive

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