Lamivudine monoprophylaxis for liver transplant recipients with non-replicating hepatitis B virus infection

被引:36
|
作者
Yoshida, Hideo
Kato, Tomoaki
Levi, David M.
Regev, Arie
Madariaga, Juan R.
Nishida, Seigo
Martinez, Enrique J.
Schiff, Eugene R.
Omata, Masao
Tzakis, Andreas G.
机构
[1] Univ Miami, Sch Med, Dept Surg, Div Liver GI Transplantat, Miami, FL 33136 USA
[2] Univ Miami, Sch Med, Dept Hepatol, Ctr Liver Dis, Miami, FL USA
[3] Univ Tokyo, Dept Gastroenterol, Tokyo, Japan
关键词
hepatitis B immunoglobulin; hepatitis B virus; lamivudine; liver transplantation; DECOMPENSATED CIRRHOSIS; IMMUNE GLOBULIN; RECURRENCE; PREVENTION; THERAPY; IMMUNOPROPHYLAXIS; MONOTHERAPY; PROPHYLAXIS; MULTICENTER; EFFICACY;
D O I
10.1111/j.1399-0012.2006.00557.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
background: The aim of this study was to evaluate the efficacy of lamivudine (LAM) monoprophylaxis for patients with non-replicating hepatitis B virus (HBV) infection at orthotopic liver transplantation (OLT). Methods: Among 128 liver recipients with HBV infection between 1994 and 2004 transplanted at our institution, 60 had non-replicating HBV infection at the time of OLT. Of those, 26 patients received LAM prophylaxis (monoprophylaxis group) and 34 patients received LAM and hepatitis B immunoglobulin (HBIG) prophylaxis (combination group) after OLT. Results: Median follow-up after OLT was 67 and 54 months, for monoprophylaxis and combination groups respectively. One and five yr patient/graft survival were 96/85% and 96/80% in monoprophylaxis group, and 85/79% and 67/55% in combination group. HBV DNA was re-detected or increased > 10(5) IU/mL in four patients (15%) at 20-29 month in monoprophylaxis group and six (18%) at 4-35 months in combination group. Recurrent hepatitis was seen in two patients (8%) at 27 and 45 months and monoprophylaxis group and three (9%) at 21-35 months in combination group. The rate of recurrence was not statistically different between two groups. Conclusion: LAM monoprophylaxis seemed to be effective for OLT recipients with HBV infection who had non-replicating HBV at transplantation. HBIG administration may play a less valuable role in preventing HBV recurrence in this group of patients.
引用
收藏
页码:166 / 171
页数:6
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