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一项关于用阿德福韦酯替代乙肝免疫球蛋白联合拉米夫定作为肝移植后乙肝预防措施的随机研究。

A randomized study of adefovir dipivoxil in place of HBIG in combination with lamivudine as post-liver transplantation hepatitis B prophylaxis.

作者信息

Angus Peter W, Patterson Scott J, Strasser Simone I, McCaughan Geoffrey W, Gane Edward

机构信息

Victorian Liver Transplant Unit, Austin Health, Victoria, Australia.

出版信息

Hepatology. 2008 Nov;48(5):1460-6. doi: 10.1002/hep.22524.

Abstract

UNLABELLED

Prior to effective prophylaxis, liver transplantation for hepatitis B virus (HBV)-related disease was frequently complicated by recurrence, which could be severe and rapidly progressive. Combination hepatitis B immunoglobulin (HBIG) and lamivudine prophylaxis reduces this rate of recurrence to <5% at 5 years; however, HBIG administration is costly and inconvenient. We conducted a multicenter randomized study of adefovir dipivoxil substitution for low-dose intramuscular (IM) HBIG in patients without HBV recurrence at least 12 months posttransplantation for HBV-related disease. Thirty-four patients were randomized, 16 to adefovir (1 patient withdrew consent at 3 months and is not considered in the results) and 18 to continue HBIG. All continued lamivudine. Groups were well matched by age, sex, and time since transplantation (median, 4.5 years), and background virological risk for HBV recurrence (30% of patients in the adefovir group, 24% in the HBIG group having detectable HBV DNA at transplantation). All patients were alive at study completion without recurrence. One patient in the adefovir group became hepatitis B surface antigen-positive at 5 months but was persistently HBV DNA undetectable via polymerase chain reaction (sensitivity 14 IU/mL) over the following 20 months. Median creatinine was not significantly changed over the course of the study in either group. One patient in the adefovir group with a background of diabetic and hypertensive nephropathy (baseline creatinine 150 micromol/L) developed increased creatinine leading to dose reduction and ultimately cessation of adefovir at 15 months. Yearly cost of combination adefovir/lamivudine prophylaxis was $8,290 versus $13,718 IM HBIG/lamivudine.

CONCLUSION

Compared with combination HBIG plus lamivudine prophylaxis, combination adefovir plus lamivudine provides equivalent protection against recurrent HBV infection but with better tolerability and less cost.

摘要

未标注

在有效的预防措施出现之前,乙型肝炎病毒(HBV)相关疾病的肝移植常因复发而出现并发症,且复发可能严重且进展迅速。联合使用乙型肝炎免疫球蛋白(HBIG)和拉米夫定预防可将5年复发率降至<5%;然而,注射HBIG成本高且不方便。我们进行了一项多中心随机研究,在因HBV相关疾病接受肝移植至少12个月且无HBV复发的患者中,用阿德福韦酯替代低剂量肌内注射(IM)HBIG。34例患者被随机分组,16例接受阿德福韦酯治疗(1例在3个月时撤回同意,结果中未纳入),18例继续接受HBIG治疗。所有患者均继续使用拉米夫定。两组在年龄、性别和移植后时间(中位数4.5年)以及HBV复发的背景病毒学风险方面匹配良好(阿德福韦酯组30%的患者、HBIG组24%的患者在移植时可检测到HBV DNA)。研究结束时所有患者均存活且无复发。阿德福韦酯组1例患者在5个月时乙型肝炎表面抗原呈阳性,但在随后20个月通过聚合酶链反应(灵敏度14 IU/mL)持续检测不到HBV DNA。两组在研究过程中肌酐中位数均无显著变化。阿德福韦酯组1例有糖尿病和高血压肾病背景(基线肌酐150 μmol/L)的患者肌酐升高,导致剂量减少,最终在15个月时停用阿德福韦酯。阿德福韦酯/拉米夫定联合预防的年成本为8290美元,而肌内注射HBIG/拉米夫定的年成本为13718美元。

结论

与HBIG加 拉米夫定联合预防相比,阿德福韦酯加拉米夫定联合预防对复发性HBV感染提供了同等的保护,但耐受性更好且成本更低。

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