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dc.contributor.authorYip, Terry Cheuk-Fungen
dc.contributor.authorGill, Madeleineen
dc.contributor.authorWong, Grace Lai-Hungen
dc.contributor.authorLiu, Kenen
dc.date.accessioned2022-04-28T02:44:45Z
dc.date.available2022-04-28T02:44:45Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/2123/28240
dc.description.abstractThe world has made significant progress in developing novel treatments for COVID-19 since the pandemic began. Some treatments target the patient's dysregulated inflammatory response during COVID-19 infection and may cause hepatitis B reactivation (HBVr) in patients with current or past hepatitis B virus (HBV) infection. This review summarizes the risk and management of HBVr due to different treatments of COVID-19 in patients who have current or past HBV infection. Abnormal liver function tests are common during COVID-19 infection. Current evidence suggests that current or past HBV infection is not associated with an increased risk of liver injury and severe disease in COVID-19 patients. Among patients who received high-dose corticosteroids, various immunosuppressive monoclonal antibodies and inhibitors of Janus kinase, the risk of HBVr exists, especially among those without antiviral prophylaxis. Data, however, remain scarce regarding the specific use of immunosuppressive therapies in COVID-19 patients with HBV infection. Some results are mainly extrapolated from patients receiving the same agents in other diseases. HBVr is a potentially life-threatening event following profound immunosuppression by COVID-19 therapies. Future studies should explore the use of immunosuppressive therapies in COVID-19 patients with HBV infection and the impact of antiviral prophylaxis on the risk of HBVr.en
dc.language.isoenen
dc.rightsOther
dc.subjectCOVID-19en
dc.subjectCoronavirusen
dc.titleManagement of hepatitis B virus reactivation due to treatment of COVID-19en
dc.typeArticleen
dc.identifier.doi10.1007/s12072-022-10306-x
dc.relation.otherFood and Health Bureauen
usyd.facultyFaculty of Medicine and Healthen


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