实用器官移植电子杂志 ›› 2018, Vol. 6 ›› Issue (3): 209-212.DOI: 10.3969/j.issn.2095-5332.2018.03.011

• 论著 • 上一篇    下一篇

HBIG 联合恩替卡韦用于 HBsAg 阳性受者接受 HBsAg 阳性供肾移植的临床观察

邱涛,陈永连,周江桥,陈忠宝,张龙,潘丽娜,周奕文   

  • 出版日期:2018-05-20 发布日期:2021-06-24

The combined HBIG and entecavir were applied into HBsAg positive receiver,which received kidney transplantation from HBsAg positive donor

  • Online:2018-05-20 Published:2021-06-24

摘要:

目的 探讨乙肝免疫球蛋白(HBIG)联合恩替卡韦预防乙肝表面抗原(HBsAg)阳性受 者接受 HBsAg 阳性供肾移植后的疗效。方法 回顾性分析 2015 年 1 月 - 2017 年 8 月的 30 例肾移植病 例的临床资料。其均为 HBsAg 阳性受者接受 HBsAg 阳性供肾,同时在供肾植入前,将 HBIG 400 U 注入 100 ml HTK 保存液中,并经肾动脉灌注入肾脏中,以及术后 HBIG 联合恩替卡韦预防策略。术后随访,评 价移植肾、肝功能,检测乙肝DNA 复制,并分析受者和移植物的存活率。结果 截至 2017 年 10 月,随访 3 ~ 36 个月。受者存活率为 100 %,移植肾存活率为 100 %。术后 3 周时,丙氨酸转氨酶(ALT)为(67±17)U/L, 天 冬 氨 酸 转 氨 酶(AST) 为(53±12)U/L, 血 肌 酐 为(112±67.3)μmol/L, 乙 肝 DNA 为 1×102 ~ 5×108 拷贝 /ml,2 例患者 HBV DNA 拷贝数较前明显增加,1 例患者进展为肝硬化代偿期,无急性肝衰竭 和肝肿瘤发生。结论 HBsAg 阳性受者可接受 HBsAg 阳性供肾,同时利用 HBIG 联合恩替卡韦预防,可有 效控制乙肝短期爆发发生。

Abstract:

Objective To observe the effect of preventing the recurrence of hepatitis B with the combination entecavir and hepatitis B immune globulin(HBIG)in the hepatitis B surface antigen(HBsAg)positive renal transplant receipts,which received the HBsAg positive allograft. Methods The clinical data of 30 cases renal transplant were retrospectively analyzed from January 2015 to August 2017. To prevent outbreak of hepatitis B in the early time,the stategry was that the recipients with HBsAg positive received the allograft with hepatitis B positive. Prior to the transplantation,the 100 ml HTK preservation solution with HBIG 400 U was perfused into the kidney through the renal artery. In addition,entecavir was used for prophylaxis postoperatively. All of them were followed up for 3 to 36 months,the graft function,liver function,HBV DNA,and recipient and graft survival rates were evaluated. Results Up to October 2017,with 6 ~ 36 months follow-up,the one year survival of allograft was 100%. The one year survival of recipients was 100%. Post-transplantation 3 weeks,the liver function was ALT(67±17)U/L,AST(53±12)U/L. Serum creatine was(112±67.3)μmol/L and HBV DNA was 1×102 ~ 5×108 copies/ml. HBV DNA increased significantly for two cases. One patients came to cirrhosis compensatory phase.There was no case with acute liver failure and liver tumor. Conclusion The HBIG plus entecavir in HBsAg positive recipients which received allograft from HBsAg positive donor can effectively prevent outbreak of hepatitis B in short term. The conclusion should be made by large clinical trials in the future.