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. 2014 Oct 21;20(39):14142–14155. doi: 10.3748/wjg.v20.i39.14142

Table 3.

Proposed individualized protocols for prophylaxis of hepatitis B virus recurrence post- liver transplantation, based on risk of recurrence

HBV recurrence risk First 6 mo post-LT Withdrawal of HBIG
High-risk:
Resistant mutations pre-LT HBIG-Light Combination of NAs
HCC at transplant Plus (ETV + TFV)
HDV/HBV co-infection Monotherapy with NA (ETV or TFV)
HIV/HBV co-infection
Non-adherence
Moderate-risk:
HbcAb + donors into HbsAb-recipients HBIG-Light Monotherapy with NA
Early post-LT renal dysfunction requiring Plus (ETV or TFV)
Indentation NA dose adjustment Monotherapy with NA (ETV or TFV)
Low risk:
Undetectable HBV DNA at transplant HBIG-free Monotherapy with NA
HbcAb + donors into HbsAb + recipients Monotherapy with NA (ETV or TFV) (ETV or TFV)
Unknown risk:
HBV naïve donor into HbcAb + recipient None None

Ab: Antibody; ETV: Entecavir; HBIG: Hepatitis B immune globulin; HBc: Hepatitis B core; HBV: Hepatitis B virus; HCC: Hepatocellular carcinoma; HDV: Hepatitis D (delta agent); LT: Liver transplantation; NAs: Nucleotide analogues; TFV: Tenofovir; HIV: Human immunodeficiency virus.