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作 者:夏杰[1] 杨占宇[2] 陈佳[1] 廖睿[2] 张南[1] 郭鹏[2] 周吉军[1] 王宇明[1]
机构地区:[1]第三军医大学西南医院全军感染病研究所,重庆400038 [2]第三军医大学西南医院全军肝胆外科研究所,重庆400038
出 处:《中华消化外科杂志》2007年第5期348-351,共4页Chinese Journal of Digestive Surgery
基 金:国家自然科学基金资助项目(No.30471551)
摘 要:目的探讨肝移植术后HBV再感染的预防与诊治。方法回顾性分析1999年8月至2004年12月98例肝移植患者临床资料。其中40例术后采用拉米夫定(lamivudine,LAM)单用方案预防HBV再感染,58例采用LAM+乙型肝炎免疫球蛋白(HBIg)联用方案。对HBV再感染者予以阿德福韦(adefovir,ADV)抗病毒治疗。结果17例肝移植患者出现HBV再感染,其中14例明确存在YMDD变异。术前血清HBVDNA阳性者术后2年HBV再感染率显著高于阴性者(P〈0.05),前者术后采用LAM+HBIg联合预防者其HBV再感染率显著低于单用LAM预防者(P〈0.05),而后者术后LAM单用和LAM+HBIg联用两组之间差异无统计学意义(P〉0.05)。15例HBV再感染者改用ADV治疗后,13例(86.7%)于治疗后1~3个月HBVDNA转阴。结论术前降低血清HBVDNA水平和术后LAM+HBIg联合预防方案能有效降低肝移植术后HBV再感染率。对术前HBVDNA阴性者,术后可选用LAM单药预防方案。ADV能够有效地治疗肝移植术后HBV再感染,抑制HBV变异株的复制。Objective To study the prevention and treatment of HBV reinfection after liver transplantation. Methods A retrospective study was carried out on 98 patients who received orthotopic liver transplantation (OLT) from August 1999 to December 2004. Fifty-two patients were HBV DNA-positive and 46 HBV DNA-negative. All patients were divided into 4 groups: Group A [ HBV DNA-positive patients treated by lamivudine ( LAM), n = 21 ], Group B ( HBV DNA-negative patients treated by LAM, n = 19 ), Group C [ HBV DNA-positive patients treated by LAM + Hepatis B immunoglobulin (HBIG), n =31 ] and Group D (HBV DNA-negative patients treated by LAM + HBIG, n = 27 ). Adefovir dipivoxil (ADV) was administered to those patients who developed LAM-resistant HBV reinfection (YMDD). Results Of all, 17 patients developed HBV reinfection after OLT but 14 of them were identified to be LAM-resistant HBV reinfection. The 2-year HBV reinfection rate was higher in HBV DNA-positive patients than HBV DNA-negative ones ( P 〈 0. 05 ). The 2-year reinfection rate in Group C was significantly lower than that in Group A ( P 〈 O. 05 ), while it showed no statistical difference between Group B and D. Fifteen HBV reinfection patients were given ADV treatment and HBV DNA negative conversion was observed in 13 patients after 1-3 months of treatment. Conclusions The HBV reinfection rate may be decreased by suppressing HBV DNA replication before OLT or applying the LAM + HBIG therapy after OLT. LAM monotherapy is feasible for those patients with HBV DNA negative before OLT. ADV is effective for patients with LAM-resistant HBV by suppressing HBV variant replication.
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