Chen Gang, Liu Hong, Hu Zong-Qiang, Bai Jian-Hua, Liu Qi-Yu, Zhao Ying-Peng, Gan Xue-Mei, Wang Fan, Wang Dong-Dong, Ma Lin-Jie, Li Li
aGanmei Hospital Affiliated to Kunming Medical University bThe First Affiliated Hospital of Kunming Medical University, Yunnan, People's Republic of China.
Eur J Gastroenterol Hepatol. 2015 Aug;27(8):901-6. doi: 10.1097/MEG.0000000000000388.
Liver transplantation significantly increases recurrence of hepatitis B virus (HBV) among high-risk patients. Hepatitis B immunoglobulin (HBIG) and antiviral nucleotide analogues are effective prophylaxis reagents in preventing HBV recurrence. However, HBV recurrence still occurs with these treatments.
To explore a more cost-effective prophylaxis protocol in patients after liver transplantation, we treated patients with an initial high dose of 10 000 IU HBIG during the anhepatic phase and a second high dose of HBIG at an optimal time point during surgery. The patients were treated with the traditional European protocol as a control, in which one dose of 10 000 IU HBIG was infused during the anhepatic phase and multiple doses of 10 000 IU HBIG were administered daily for 1 week after liver transplantation.
There were two mortalities among 50 patients treated with the new protocol and nine mortalities among 52 patients treated with the European protocol within 3 years after liver transplantation. The new prophylaxis method markedly improved the 3-year survival without HBV recurrence in 50 treated patients. However, there were five recurrences in 52 patients treated with the European protocol. High-risk factors such as HBV DNA+, positive hepatitis B e antigen, and hepatocellular carcinoma were all detected among five patients with HBV recurrence. The suppressed HBV recurrence was associated with significantly lower serum alanine aminotransferase and aspartate aminotransferase in the new protocol-treated patients tested at 1 month and 1 week after liver surgery compared with those treated with the European protocol.
Infusion of two high doses of HBIG during surgery in combination with entecavir significantly prevented HBV recurrence and improved the 3-year survival after liver transplantation.
肝移植显著增加了高危患者中乙型肝炎病毒(HBV)的复发率。乙型肝炎免疫球蛋白(HBIG)和抗病毒核苷酸类似物是预防HBV复发的有效预防试剂。然而,采用这些治疗方法仍会发生HBV复发。
为了探索一种更具成本效益的肝移植术后患者预防方案,我们在无肝期对患者给予初始高剂量10000IU的HBIG,并在手术期间的最佳时间点给予第二剂高剂量HBIG。将患者采用传统欧洲方案治疗作为对照,即在无肝期输注一剂10000IU的HBIG,并在肝移植术后每天给予多剂10000IU的HBIG,持续1周。
采用新方案治疗的50例患者中有2例死亡,采用欧洲方案治疗的52例患者在肝移植术后3年内有9例死亡。新的预防方法显著提高了50例接受治疗患者无HBV复发的3年生存率。然而,采用欧洲方案治疗的52例患者中有5例复发。在5例HBV复发患者中均检测到HBV DNA阳性、乙肝e抗原阳性和肝细胞癌等高风险因素。与采用欧洲方案治疗的患者相比,在肝移植术后1个月和1周检测时,采用新方案治疗的患者中,HBV复发受到抑制且血清丙氨酸氨基转移酶和天冬氨酸氨基转移酶显著降低。
手术期间输注两剂高剂量HBIG联合恩替卡韦可显著预防HBV复发,并提高肝移植术后的3年生存率。