Preventing hepatitis B reactivation in immunosuppressed patients: is it time to revisit the guidelines?
Preventing hepatitis B reactivation in immunosuppressed patients: is it time to revisit the guidelines?
复制标题
预防免疫抑制患者乙型肝炎再激活:是时候重新审视指南了吗?
DOI:
10.1002/acr.20167
复制
发表时间:
2010
影响因子:
4.7
通讯作者:
Calabrese,Leonard
中科院分区:
文献类型:
--
作者:
Yazdany,Jinoos;Calabrese,Leonard
Hepatitis B virus (HBV) infection remains a serious global health concern. Approximately one third of the world's population has evidence of previous HBV infection, and 350 million people are chronic HBV carriers. 1 In the United States, the rate of new HBV infections has declined by approximately 82% since 1991, when a national strategy to eliminate HBV infection was implemented. 2 The greatest decline has been among those born since 1991, when universal vaccination of children was first recommended. 2 Despite these improvements, HBV remains prevalent in the United States; 800,000 to 1.4 million individuals are estimated to be chronic carriers. 2 Although intravenous drug users and homosexual men are at high risk for chronic HBV, most cases in the United States are in those emigrating from high prevalence areas (eg Asia or Africa), where early life horizontal and vertical transmission is common. 3Reactivation of HBV in immunosuppressed individuals has been well-documented in the literature for several decades. Reactivation can occur either at the cessation of therapy when immune reconstitution occurs, or with prolonged immunosuppression that can result in an accelerated course of HBV infection. 4-6 Most cases occur in individuals with cancer undergoing chemotherapy, where reactivation among HBV positive patients is common (eg> 50% in some lymphoma series) and sometimes fatal. 7-18 In rheumatology, HBV reactivation has been reported with a number of disease modifying anti-rheumatic drugs (DMARDs), although the lack of large studies makes it hard to ascertain the exact risk for most drugs. However, it is increasingly apparent that newer biologic therapies, such as TNF-α inhibitors and rituximab, may pose a significant risk of HBV reactivation. Therefore, it is especially timely to take stock of how rheumatologists approach HBV in clinical practice.