Table 1.
Strategies for Testing and Management of HBV During Immunosuppressive Therapy
| Test | Population to Be Screened | Significance of Positive Result | Action |
|---|---|---|---|
| HBsAg | All patients scheduled to receive immunosuppressive therapy | HBV infection | Antiviral prophylaxis indicated |
| Anti‐HBs alone | None | Immunity to HBV | None |
| Anti‐HBc± anti‐HBs | All patients scheduled to receive myeloablative, rituximab, or TNF inhibitor–containing therapy | Exposure to HBV infection | If HBsAg‐positive: as above |
| If HBsAg‐negative: low risk for standard chemotherapy | |||
| If BMT/rituximab/anti‐TNF: monitoring essential; consider antiviral prophylaxis | |||
| HBV DNA | All HBsAg‐positive and anti‐HBc–positive patients | 1. Undetectable | 1. Lamivudine adequate |
| 2. <2,000 IU/mL | 2. Lamivudine adequate | ||
| 3. ≥2,000 IU/mL | 3. Consider agent with higher barrier to resistance |