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  4. Hepatitis B reactivation: diagnosis and management
 
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Hepatitis B reactivation: diagnosis and management

Journal
Expert Review of Gastroenterology and Hepatology
Journal Volume
14
Journal Issue
7
Pages
565-578
Date Issued
2020
Author(s)
SHANG-CHIN HUANG  
HUNG-CHIH YANG  
JIA-HORNG KAO  
DOI
10.1080/17474124.2020.1774364
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85086922675&doi=10.1080%2f17474124.2020.1774364&partnerID=40&md5=2a11a0b4bb96d947c47d6230db1470ff
https://scholars.lib.ntu.edu.tw/handle/123456789/570827
Abstract
Introduction: Hepatitis B virus (HBV) reactivation can be induced by treatments that attenuate the immunological control over HBV, leading to increased morbidity and mortality. The risk of HBV reactivation is determined by host immunity, viral factors, and the type and dose of treatments. Nevertheless, the risk of HBV reactivation for a growing number of novel therapies remains uncertain and needs to be carefully examined. Identification of patients at risk and administration of prophylactic antiviral agents are critical to prevent HBV reactivation. Early diagnosis and initiation of antiviral treatment are the keys to avoid devastating outcomes. Area covered: We summarized the latest evidence and recommendations for risk stratification, early diagnosis, prophylaxis, and management of HBV reactivation. Expert opinion: Universal screening, adequate prophylaxis, and close monitoring are essential for the prevention of HBV reactivation. Risk stratification of patients at risk with appropriate antiviral prophylaxis can prevent HBV reactivation effectively. Several emerging biomarkers have been proved to help determine the risk precisely. Early detection and timely administration of antiviral agents are crucial for management. Further studies on the precision of risk stratification as well as the optimal duration of prophylaxis and treatment are needed to establish an individualized strategy. ? 2020 Informa UK Limited, trading as Taylor & Francis Group.
SDGs

[SDGs]SDG3

Other Subjects
afatinib; anthracycline; antivirus agent; bortezomib; CD20 antibody; circular DNA; complementary DNA; covalently closed circular DNA; cytotoxic agent; dasatinib; direct antiviral agent; entecavir; erlotinib; gefitinib; glucocorticoid; imatinib; infliximab; nilotinib; osimertinib; prednisolone; programmed death 1 receptor; protein tyrosine kinase inhibitor; secukinumab; tenofovir alafenamide; tenofovir disoproxil; tocilizumab; tumor necrosis factor inhibitor; unclassified drug; antivirus agent; circular DNA; immunosuppressive agent; virus DNA; antiviral therapy; B lymphocyte; cost effectiveness analysis; disease exacerbation; early diagnosis; hematopoietic stem cell transplantation; hepatitis B; Hepatitis B virus; human; immunization; immunoprophylaxis; infection control; infection prevention; infection risk; liver failure; nonhuman; patient monitoring; pregnancy; Review; risk assessment; screening test; treatment duration; virus reactivation; blood; chronic hepatitis B; drug effect; hepatitis B; Hepatitis B virus; isolation and purification; physiology; virus activation; Antiviral Agents; DNA, Circular; DNA, Viral; Hepatitis B; Hepatitis B virus; Hepatitis B, Chronic; Humans; Immunosuppressive Agents; Risk Assessment; Virus Activation
Publisher
Taylor and Francis Ltd
Type
review

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

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開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

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