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Veterans health administration hepatitis B testing and treatment with anti-CD20 antibody administration.

dc.contributor.author Hunt, CM
dc.coverage.spatial United States
dc.date.accessioned 2016-05-01T22:27:19Z
dc.date.issued 2016-05-21
dc.identifier http://www.ncbi.nlm.nih.gov/pubmed/27217704
dc.identifier.uri https://hdl.handle.net/10161/11950
dc.description.abstract AIM: To evaluate pretreatment hepatitis B virus (HBV) testing, vaccination, and antiviral treatment rates in Veterans Affairs patients receiving anti-CD20 Ab for quality improvement. METHODS: We performed a retrospective cohort study using a national repository of Veterans Health Administration (VHA) electronic health record data. We identified all patients receiving anti-CD20 Ab treatment (2002-2014). We ascertained patient demographics, laboratory results, HBV vaccination status (from vaccination records), pharmacy data, and vital status. The high risk period for HBV reactivation is during anti-CD20 Ab treatment and 12 mo follow up. Therefore, we analyzed those who were followed to death or for at least 12 mo after completing anti-CD20 Ab. Pretreatment serologic tests were used to categorize chronic HBV (hepatitis B surface antigen positive or HBsAg+), past HBV (HBsAg-, hepatitis B core antibody positive or HBcAb+), resolved HBV (HBsAg-, HBcAb+, hepatitis B surface antibody positive or HBsAb+), likely prior vaccination (isolated HBsAb+), HBV negative (HBsAg-, HBcAb-), or unknown. Acute hepatitis B was defined by the appearance of HBsAg+ in the high risk period in patients who were pretreatment HBV negative. We assessed HBV antiviral treatment and the incidence of hepatitis, liver failure, and death during the high risk period. Cumulative hepatitis, liver failure, and death after anti-CD20 Ab initiation were compared by HBV disease categories and differences compared using the χ(2) test. Mean time to hepatitis peak alanine aminotransferase, liver failure, and death relative to anti-CD20 Ab administration and follow-up were also compared by HBV disease group. RESULTS: Among 19304 VHA patients who received anti-CD20 Ab, 10224 (53%) had pretreatment HBsAg testing during the study period, with 49% and 43% tested for HBsAg and HBcAb, respectively within 6 mo pretreatment in 2014. Of those tested, 2% (167/10224) had chronic HBV, 4% (326/7903) past HBV, 5% (427/8110) resolved HBV, 8% (628/8110) likely prior HBV vaccination, and 76% (6022/7903) were HBV negative. In those with chronic HBV infection, ≤ 37% received HBV antiviral treatment during the high risk period while 21% to 23% of those with past or resolved HBV, respectively, received HBV antiviral treatment. During and 12 mo after anti-CD20 Ab, the rate of hepatitis was significantly greater in those HBV positive vs negative (P = 0.001). The mortality rate was 35%-40% in chronic or past hepatitis B and 26%-31% in hepatitis B negative. In those pretreatment HBV negative, 16 (0.3%) developed acute hepatitis B of 4947 tested during anti-CD20Ab treatment and follow-up. CONCLUSION: While HBV testing of Veterans has increased prior to anti-CD20 Ab, few HBV+ patients received HBV antivirals, suggesting electronic health record algorithms may enhance health outcomes.
dc.language eng
dc.publisher Baishideng Publishing Group Co. Limited
dc.relation.ispartof World J Gastroenterol
dc.relation.isversionof 10.3748/wjg.v22.i19.4732
dc.subject Anti-CD20 antibody
dc.subject Chemotherapy
dc.subject Hepatitis B
dc.subject Hepatitis B antivirals
dc.subject Hepatitis B reactivation
dc.subject Lymphoma
dc.subject Rituximab
dc.subject Vaccination
dc.subject Veteran
dc.title Veterans health administration hepatitis B testing and treatment with anti-CD20 antibody administration.
dc.type Journal article
duke.contributor.id Hunt, CM|0096086
pubs.author-url http://www.ncbi.nlm.nih.gov/pubmed/27217704
pubs.begin-page 4732
pubs.end-page 4740
pubs.issue 19
pubs.organisational-group Clinical Science Departments
pubs.organisational-group Duke
pubs.organisational-group Duke Cancer Institute
pubs.organisational-group Institutes and Centers
pubs.organisational-group Medicine
pubs.organisational-group Medicine, Gastroenterology
pubs.organisational-group Medicine, Medical Oncology
pubs.organisational-group School of Medicine
pubs.publication-status Published
pubs.volume 22
dc.identifier.eissn 2219-2840
duke.contributor.orcid Hunt, CM|0000-0002-6874-8889


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