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Retrospective observational study of temporal trends and outcomes of hepatitis B screening in patients receiving rituximab

OBJECTIVE: Hepatitis B reactivation (HBr) is strongly associated with rituximab therapy. Guidelines advise hepatitis B screening and use of preventive nucleoside analogue (NA) in patients at risk. In this study, we examined screening trends, post-screening interventions and outcomes in patients rece...

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Detalles Bibliográficos
Autores principales: Haider, Mahnur, Flocco, Gianina, Lopez, Rocio, Carey, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745525/
https://www.ncbi.nlm.nih.gov/pubmed/33323450
http://dx.doi.org/10.1136/bmjopen-2020-043672
Descripción
Sumario:OBJECTIVE: Hepatitis B reactivation (HBr) is strongly associated with rituximab therapy. Guidelines advise hepatitis B screening and use of preventive nucleoside analogue (NA) in patients at risk. In this study, we examined screening trends, post-screening interventions and outcomes in patients receiving rituximab in light of recommendations. DESIGN: Retrospective, observational study. SETTING: Single, tertiary care centre in the USA. PARTICIPANTS: Patients receiving rituximab from January 2005 to December 2017. PRIMARY OUTCOME: Trends of hepatitis B screening prior to initiation of rituximab. SECONDARY OUTCOME: Results of hepatitis B screening, use of preventive NA therapy and HBr incidence. RESULTS: Over 13 years, 2219 patients received rituximab. Screening, with at least hepatitis B core antibody (anti-HBc) prior to the first dose of rituximab, improved from 20% to 97%. Because only 4.5% of patients had a positive anti-HBc, the overall HBr incidence was very low (0.42%). In susceptible patients, the incidence of HBr was 8%. In at-risk patients given preventive NA, 96% remained free of HBr. However, only 23% received a preventive NA and no temporal improvement in compliance was seen. Of those with HBr, 87.5% were hepatitis B surface antigen (HbsAg−)/anti-HBc+. CONCLUSIONS: In those treated with rituximab, we demonstrated near-universal anti-HBc screening. Screening unlinked to preventive NA use, in those who are anti-HBc+, is ineffective in reducing HBr. HBr has a high fatality rate. The majority of cases occurred in those who were HBsAg negative. Efforts are needed to educate providers who use rituximab not only to screen for anti-HBc, but to provide preventive NA to those who test positive.