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首页> 外文期刊>Clinical rheumatology >Hepatitis reactivation in patients with rheumatic diseases after immunosuppressive therapy - A report of long-term follow-up of serial cases and literature review
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Hepatitis reactivation in patients with rheumatic diseases after immunosuppressive therapy - A report of long-term follow-up of serial cases and literature review

机译:免疫抑制治疗后风湿性疾病患者的肝炎再激活-系列病例的长期随访及文献复习报告

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摘要

The aims of this paper are to report hepatitis B virus reactivation in 12 patients with rheumatic disease undergoing immunosuppressive therapy and to evaluate whether pre-emptive antiviral therapy is necessary in patients receiving disease-modifying anti-rheumatic drugs. From January 2008 to March 2012, a total of 12 HBV-infected patients with rheumatic diseases were consecutively enrolled in the long-term follow-up. Liver function, HBV DNA, and serum aminotransferase level were tested during the follow-up. We also reviewed the published reports and summarized the clinical characteristics of HBV reactivation during immunosuppressive therapy in patients with rheumatic diseases the medium duration of follow-up was 41 months (range 16-48). Patients were treated with prednisone, disease-modifying anti-rheumatic drugs (DMARDs) or tumor necrosis factor-alpha-blocking agents (TNFBA). HBV reactivation was only documented in two patients treated with prednisone without pre-emptive antiviral therapy. One hundred patients from literature review were identified as having HBV reactivation; 20.8 % of the patients receiving prednisone experienced HBV reactivation compared to only 4.46 and 9.52 % of patients treated with DMARDs or TNFBA, respectively. This long-term follow-up of serial cases suggests that pre-emptive antiviral therapy should be administered in patients receiving prednisone therapy for rheumatic disease. In contrast, DMARDs and TNFBA are relatively safe to HBV-infected patients with rheumatic diseases. Close monitoring of HBV DNA and ALT levels is necessary in the management of HBV reactivation.
机译:本文的目的是报告12例接受免疫抑制治疗的风湿病患者的乙型肝炎病毒再激活,并评估在接受改变疾病的抗风湿药的患者中是否需要先发制人的抗病毒治疗。从2008年1月到2012年3月,总共12例被风湿病感染的HBV感染患者被连续纳入长期随访。随访期间检测肝功能,HBV DNA和血清氨基转移酶水平。我们还回顾了已发表的报告,总结了风湿性疾病患者免疫抑制治疗期间HBV激活的临床特征,随访时间为41个月(范围16-48)。患者接受泼尼松,可缓解疾病的抗风湿药(DMARD)或肿瘤坏死因子-α阻断剂(TNFBA)的治疗。仅在两名接受泼尼松治疗且未进行先发制人的抗病毒治疗的患者中记录了HBV激活。文献复习中有100例患者被确认具有HBV激活。接受泼尼松治疗的患者中有20.8%经历了HBV的再激活,而接受DMARD或TNFBA治疗的患者分别只有4.46%和9.52%。对一系列病例的长期随访表明,对于风湿性疾病接受泼尼松治疗的患者应进行先发制人的抗病毒治疗。相比之下,DMARDs和TNFBA对风湿性疾病感染HBV的患者相对安全。在管理HBV重新激活过程中,必须密切监测HBV DNA和ALT水平。

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