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Preventing Hepatitis B Reactivation During Anti-CD20 Antibody Treatment in the Veterans Health Administration.

Publication ,  Journal Article
Jasmine Bullard, A; Cunningham, FE; Volpp, BD; Lowy, E; Beste, LA; Heron, BB; Geraci, M; Hammond, JM; LaPlant, K; Stave, EA; Turner, MJ ...
Published in: Hepatol Commun
September 2018

Hepatitis B virus (HBV) reactivation may occur with high risk immunosuppression, such as anti-cluster of differentiation (CD)20 antibodies (Abs). Appropriate HBV prophylaxis during anti-CD20 Ab therapy averts hepatitis, chemotherapy disruption, and death. Serologic evidence of prior HBV exposure is present in one in nine veterans in the Veterans Health Administration (VHA). In 2014, most (61%-73%) patients in the VHA who were receiving anti-CD20 Ab treatment underwent HBV testing, yet <20% of eligible patients received HBV antiviral prophylaxis. We aimed to prevent HBV reactivation by increasing HBV testing and antiviral treatment rates among anti-CD20 Ab recipients through prospective interventions. A multidisciplinary team of clinicians, pharmacists, and public health professionals developed comprehensive prevention systems, including national seminars/newsletters/websites; pharmacy criteria for HBV screening/treatment prior to anti-CD20 Ab use; changes to national formulary restrictions to expand HBV prophylaxis prescribing authority; Medication Use Evaluation Tracker to identify omissions; national e-mail alert to all VHA oncology providers detailing specific testing and HBV antiviral treatment needs; and a voluntary electronic medical record "order check" used at interested facilities (n = 11) to automatically assess pretreatment HBV testing and antiviral treatment and only generate a reminder to address deficiencies. Analysis of monthly data from June 2016 through September 2017 among anti-CD20 Ab recipients revealed pre-anti-CD20 Ab treatment HBV testing increased to 91%-96% and appropriate HBV antiviral prophylaxis to 76%-85% nationally following implementation of the intervention. Medical centers using the voluntary electronic medical record order check increased HBV testing rates to 93%-98% and HBV antiviral prophylaxis rates to 99%. Conclusion: Multimodal intervention systems to prevent HBV reactivation among VHA patients receiving anti-CD20 Ab therapies increased national rates of HBV testing to >90% and antiviral prophylaxis to >80%.

Duke Scholars

Published In

Hepatol Commun

DOI

EISSN

2471-254X

Publication Date

September 2018

Volume

2

Issue

9

Start / End Page

1136 / 1146

Location

United States

Related Subject Headings

  • 3202 Clinical sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Jasmine Bullard, A., Cunningham, F. E., Volpp, B. D., Lowy, E., Beste, L. A., Heron, B. B., … Hunt, C. M. (2018). Preventing Hepatitis B Reactivation During Anti-CD20 Antibody Treatment in the Veterans Health Administration. Hepatol Commun, 2(9), 1136–1146. https://doi.org/10.1002/hep4.1238
Jasmine Bullard, A., Francesca E. Cunningham, Bryan D. Volpp, Elliott Lowy, Lauren A. Beste, Bernadette B. Heron, Mark Geraci, et al. “Preventing Hepatitis B Reactivation During Anti-CD20 Antibody Treatment in the Veterans Health Administration.Hepatol Commun 2, no. 9 (September 2018): 1136–46. https://doi.org/10.1002/hep4.1238.
Jasmine Bullard A, Cunningham FE, Volpp BD, Lowy E, Beste LA, Heron BB, et al. Preventing Hepatitis B Reactivation During Anti-CD20 Antibody Treatment in the Veterans Health Administration. Hepatol Commun. 2018 Sep;2(9):1136–46.
Jasmine Bullard, A., et al. “Preventing Hepatitis B Reactivation During Anti-CD20 Antibody Treatment in the Veterans Health Administration.Hepatol Commun, vol. 2, no. 9, Sept. 2018, pp. 1136–46. Pubmed, doi:10.1002/hep4.1238.
Jasmine Bullard A, Cunningham FE, Volpp BD, Lowy E, Beste LA, Heron BB, Geraci M, Hammond JM, LaPlant K, Stave EA, Turner MJ, O’Leary MC, Kelley MJ, Hunt CM. Preventing Hepatitis B Reactivation During Anti-CD20 Antibody Treatment in the Veterans Health Administration. Hepatol Commun. 2018 Sep;2(9):1136–1146.

Published In

Hepatol Commun

DOI

EISSN

2471-254X

Publication Date

September 2018

Volume

2

Issue

9

Start / End Page

1136 / 1146

Location

United States

Related Subject Headings

  • 3202 Clinical sciences