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本文引用的文献

1
Asian-Pacific consensus statement on the management of chronic hepatitis B: a 2012 update.《亚太地区慢性乙型肝炎管理共识声明:2012年更新版》
Hepatol Int. 2012 Jun;6(3):531-61. doi: 10.1007/s12072-012-9365-4. Epub 2012 May 17.
2
Relationship between level of hepatitis B virus DNA and liver disease: a population-based study of hepatitis B e antigen-negative persons with hepatitis B.乙型肝炎病毒DNA水平与肝脏疾病的关系:一项基于人群的乙肝e抗原阴性乙肝患者研究。
Clin Gastroenterol Hepatol. 2014 Apr;12(4):701-6.e1-3. doi: 10.1016/j.cgh.2013.09.005. Epub 2013 Sep 11.
3
Expert recommendations on the application of interferon for chronic hepatitis B.关于慢性乙型肝炎应用干扰素的专家建议。
J Dig Dis. 2013 Dec;14(12):626-37. doi: 10.1111/1751-2980.12096.
4
The current status of combination therapy of chronic hepatitis B.慢性乙型肝炎联合治疗的现状
Eur Rev Med Pharmacol Sci. 2013;17(15):2023-31.
5
Complexity and diversity of hepatitis B virus quasispecies: correlation with long-term entecavir antiviral efficacy.乙型肝炎病毒准种的复杂性和多样性:与长期恩替卡韦抗病毒疗效的相关性。
Antiviral Res. 2013 Sep;99(3):312-7. doi: 10.1016/j.antiviral.2013.06.020. Epub 2013 Jul 4.
6
Serum HBV DNA level at week 12 is superior to viral response at week 24 in predicting long-term treatment outcome of telbivudine for chronic hepatitis B patients.在预测替比夫定治疗慢性乙型肝炎患者的长期治疗结局方面,第 12 周的血清 HBV DNA 水平优于第 24 周的病毒应答。
Chin Med J (Engl). 2013 Jun;126(12):2333-6.
7
Quantitative hepatitis B surface antigen titres in Chinese chronic hepatitis B patients over 4 years of entecavir treatment.恩替卡韦治疗4年以上的中国慢性乙型肝炎患者的乙肝表面抗原定量滴度
Antivir Ther. 2013;18(8):955-65. doi: 10.3851/IMP2579. Epub 2013 May 2.
8
Patient adherence to antiviral treatment for chronic hepatitis B and C: a systematic review.患者对慢性乙型肝炎和丙型肝炎抗病毒治疗的依从性:系统评价。
Ann Hepatol. 2013 May-Jun;12(3):380-91.
9
Extended treatment with peginterferon α-2a in combination with lamivudine or adefovir for 96 weeks yields high rates of HBeAg and HBsAg seroconversion.延长聚乙二醇干扰素α-2a 联合拉米夫定或阿德福韦酯治疗 96 周可获得较高的 HBeAg 和 HBsAg 血清学转换率。
J Dig Dis. 2013 Aug;14(8):446-50. doi: 10.1111/1751-2980.12065.
10
A different look at the management of chronic hepatitis B in a resource-constrained country.资源有限国家慢性乙型肝炎管理的别样视角。
J Viral Hepat. 2013 Apr;20 Suppl 1:1. doi: 10.1111/jvh.12056.

慢性乙型肝炎治疗的优化疗法。

Optimization therapy for the treatment of chronic hepatitis B.

作者信息

Chen En-Qiang, Tang Hong

机构信息

En-Qiang Chen, Hong Tang, Center of Infectious Diseases, West China Hospital of Sichuan University, Chengdu 610041, Sichuan Province, China.

出版信息

World J Gastroenterol. 2014 May 21;20(19):5730-6. doi: 10.3748/wjg.v20.i19.5730.

DOI:10.3748/wjg.v20.i19.5730
PMID:24914334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4024783/
Abstract

Chronic hepatitis B (CHB) is currently medically managed with either interferon-alpha or one of the five nucleos(t)ide analogs. However, there are still a large number of CHB patients whose response to the above therapies remains less than satisfactory, and their incomplete or non-response to antiviral therapies has plagued clinicians worldwide. In recent years, a newly proposed optimization therapy has provided us with a new approach to solve this problem. The key points in this optimization therapy are to initiate antiviral therapy with an appropriate agent at the correct time point, and to adjust treatments in patients with poor early responses by adding a second agent or switching to another more potent agent. In this review, we summarize recent developments in optimization therapy for the treatment of CHB, and provide an outlook for future research in this field.

摘要

慢性乙型肝炎(CHB)目前的医学治疗方法是使用α干扰素或五种核苷(酸)类似物之一。然而,仍有大量CHB患者对上述治疗的反应不尽人意,他们对抗病毒治疗的不完全反应或无反应一直困扰着全球的临床医生。近年来,新提出的优化治疗为我们解决这一问题提供了新方法。这种优化治疗的关键点是在正确的时间点用合适的药物启动抗病毒治疗,并通过添加第二种药物或换用另一种更有效的药物来调整早期反应不佳患者的治疗方案。在本综述中,我们总结了CHB治疗优化疗法的最新进展,并对该领域未来的研究进行了展望。