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首页> 外文期刊>Hepatology: Official Journal of the American Association for the Study of Liver Diseases >Discontinuation of oral antivirals in chronic hepatitis B: A systematic review
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Discontinuation of oral antivirals in chronic hepatitis B: A systematic review

机译:慢性乙型肝炎中的口腔抗病毒中断:系统审查

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The possibility of safe discontinuation of therapy with nucleos(t)ide analogues (NAs) remains one of the most controversial topics in the management of chronic hepatitis B. Therefore, we systematically reviewed the existing data on NA discontinuation in this setting and tried to identify factors affecting the probability of posttherapy remission. A literature search was performed in order to identify all published studies including patients who discontinued NAs in virological remission (VR) and were followed for 12 months thereafter. Twenty-five studies with 1716 patients were included. The pooled rates of durable VR remission were 51.4%, 39.3%, and 38.2% at 12, 24, and 36 months, respectively, after NA discontinuation, being relatively higher in initially hepatitis B e antigen (HBeAg)-positive patients (62.5%, 53.4%, 51.5%) than HBeAg-negative patients (43.7%, 31.3%, 30.1%) (P=0.064). The weighted probability of durable biochemical remission was 65.4%, being numerically higher in HBeAg-positive than HBeAg-negative patients (76.2% versus 56.7%, P=0.130). The weighted probability of hepatitis B surface antigen loss was 2.0%. The rates of durable VR did not significantly differ according to the VR definition (hepatitis B virus DNA <200,<2000,<20,000 IU/mL) or duration of on-therapy VR in HBeAg-positive patients, but they were significantly higher in studies with HBeAg-negative patients and on-therapy VR>24 than24 months (VR at 12 months off-NAs: 75.0% versus 35.6%, P=0.005). The weighted probability of durable HBeAg seroconversion was 91.9% and 88.0% at 12 and 24 months, respectively, after NA discontinuation without being affected by the duration of on-therapy VR or consolidation therapy (>6 months in all studies). Conclusion: Durable VR seems to be feasible in a substantial proportion of patients who discontinue long-term NA therapy; on-therapy VR>24 months offers higher chances of off-NA VR in patients with HBeAg-negative chronic hepatitis B. (Hepatology 2016;63:1481-1492)
机译:安全停止治疗的可能性(T)IDE类似物(NAS)仍然是慢性乙型肝炎管理中最有争议的主题之一。因此,我们系统地审查了该环境中NA中断的现有数据,并试图识别影响晚期缓解概率的因素。进行文献搜索,以确定所有已发表的研究,包括在病毒学缓解(VR)中停药的患者,然后持续12个月。包括1716名患者的二十五项研究。在Na停止后,持续耐用VR缓解率的汇集率分别为51.4%,39.3%,38.2%,初始乙型肝炎抗原(HBEAG)阳性患者(62.5%)相对较高,比HBEAG阴性患者53.4%,51.5%(43.7%,31.3%,30.1%)(P = 0.064)。耐用生化缓解的加权概率为65.4%,在HBEAG阳性比HBEAG阴性患者的数量上更高(76.2%,p = 0.130)。乙型肝炎表面抗原损失的加权概率为2.0%。根据VR定义(乙型肝炎病毒DNA <200,<2000,<2000,<2000,<2000,<2000,<2000,<2000,<2000,<20,000 IU / mL)或在HBEAG阳性患者中的持续时间没有显着差异,但它们显着高用HBEAG-Digal患者和治疗VR> 24至24个月的研究(12个月偏离NAs:75.0%,比35.6%,p = 0.005)。在NA停止后,耐用HBEAG血清转化的加权概率分别在12和24个月内分别在12和24个月内,在不受治疗持续时间的持续时间(>所有研究中的6个月)的情况下,分别在12和24个月内为12和24个月。结论:耐用的VR似乎是可行的,在长期NA治疗中停止长期患者;疗法VR> 24个月为HBEAG阴性慢性乙型肝炎患者提供了更高的幼稚越多的机会(肝脏2016; 63:1481-1492)

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