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2
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本文引用的文献

1
Changes of duplex parameters and splenic size in liver transplant recipients during a long period of observation.长期观察肝移植受者的双功参数及脾脏大小变化。
World J Gastroenterol. 2005 Nov 21;11(43):6787-91. doi: 10.3748/wjg.v11.i43.6787.
2
Adefovir-lamivudine combination therapy and hepatitis B viral kinetics.阿德福韦-拉米夫定联合治疗与乙型肝炎病毒动力学
J Hepatol. 2005 Aug;43(2):200-2. doi: 10.1016/j.jhep.2005.05.011.
3
Solid-organ transplantation in HBsAg-negative patients with antibodies to HBV core antigen: low risk of HBV reactivation.乙肝核心抗原抗体阳性的HBsAg阴性患者进行实体器官移植:乙肝再激活风险低
Transplantation. 2005 Jun 15;79(11):1631-3. doi: 10.1097/01.tp.0000163468.80223.74.
4
Prophylaxis of hepatitis B virus recurrence after liver transplantation in carriers of lamivudine-resistant mutants.拉米夫定耐药突变携带者肝移植后乙肝病毒复发的预防
Liver Transpl. 2005 May;11(5):532-8. doi: 10.1002/lt.20393.
5
Viral load at the time of liver transplantation and risk of hepatitis B virus recurrence.肝移植时的病毒载量与乙型肝炎病毒复发风险
Liver Transpl. 2005 Apr;11(4):402-9. doi: 10.1002/lt.20402.
6
Acute liver rejection: accuracy and predictive values of doppler US measurements--initial experience.急性肝排斥反应:多普勒超声测量的准确性及预测价值——初步经验
Radiology. 2005 May;235(2):651-8. doi: 10.1148/radiol.2352040506. Epub 2005 Mar 15.
7
Management of antiviral resistance in patients with chronic hepatitis B.慢性乙型肝炎患者抗病毒耐药性的管理
Antivir Ther. 2004 Oct;9(5):679-93.
8
Fibrosis progression after liver transplantation in patients with recurrent hepatitis C.丙型肝炎复发患者肝移植后的纤维化进展
J Hepatol. 2004 Nov;41(5):830-6. doi: 10.1016/j.jhep.2004.06.029.
9
Hepatitis B and hepatitis C viruses in liver transplantation.
Transplantation. 2004 Oct 15;78(7):955-63. doi: 10.1097/01.tp.0000140927.63952.58.
10
Pilot study of pegylated interferon alfa-2b and ribavirin for recurrent hepatitis C after liver transplantation.聚乙二醇化干扰素α-2b与利巴韦林用于肝移植后复发性丙型肝炎的初步研究。
Transplant Proc. 2003 Dec;35(8):3042-4. doi: 10.1016/j.transproceed.2003.10.083.

肝移植术后复发性病毒性肝炎患者的临床管理

Clinical management of patients with recurrent viral hepatitis after liver transplantation.

作者信息

Caremani M, Tacconi D, Giorni P, Lapini L, Corradini S, Giaccherini R

机构信息

Department of Infectious Diseases, San Donato Hospital, Arezzo, Italy.

出版信息

J Ultrasound. 2007 Mar;10(1):46-52. doi: 10.1016/j.jus.2007.02.001. Epub 2007 Apr 16.

DOI:10.1016/j.jus.2007.02.001
PMID:23396377
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3478672/
Abstract

Liver transplantation is indicated in end-stage chronic viral liver disease, but unless adequate prophylaxis is administered, the patient will in most cases develop recurrent hepatitis B (HBV) and C (HCV) virus infection. Today, patients receiving prophylaxis using nucleoside analogue drugs with or without specific immune globulin drugs in connection with orthotopic liver transplantation for HBV related cirrhosis, present low risk of relapse and high 5-10 year survival rates. Lamivudine was the first drug used in the prophylactic treatment, but this drug has increasingly been combined with or replaced by adefovir due to the low genetic barrier, which causes viral resistance. Most patients develop viral recurrence after orthotopic liver transplantation for HCV related cirrhosis, and in an elevated number of cases, cirrhosis and hepatic insufficiency set in after a few years. Prophylaxis before transplantation and pre-emptive treatment using interferon and ribavirin present numerous side effects resulting in reduction of doses and suspension of therapy, with consequently low sustained virological remission rates and risk of rejection.The treatment is better tolerated by patients with histologically confirmed chronic disease, but also in these patients virological remission rates are low. This pathology requires new therapeutic protocols and/or new drugs in order to obtain better compliance and better responses.

摘要

肝移植适用于终末期慢性病毒性肝病,但除非给予充分的预防措施,否则在大多数情况下患者会发生乙肝(HBV)和丙肝(HCV)病毒复发感染。如今,对于与HBV相关肝硬化的原位肝移植患者,使用核苷类似物药物联合或不联合特异性免疫球蛋白药物进行预防,复发风险较低,5至10年生存率较高。拉米夫定是预防性治疗中使用的第一种药物,但由于其导致病毒耐药的遗传屏障较低,该药物越来越多地与阿德福韦联合使用或被阿德福韦替代。对于与HCV相关肝硬化的原位肝移植患者,大多数会发生病毒复发,而且在相当数量的病例中,几年后会出现肝硬化和肝功能不全。移植前的预防措施以及使用干扰素和利巴韦林的抢先治疗存在诸多副作用,导致剂量减少和治疗中断,因此持续病毒学缓解率较低且有排斥风险。组织学确诊的慢性病患者对该治疗的耐受性较好,但在这些患者中病毒学缓解率也较低。这种病症需要新的治疗方案和/或新药,以便获得更好的依从性和更好的疗效。