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Transient Hepatitis B Surface Antigenemia Following Immunization with Heplisav-B

OBJECTIVE: To delineate the rate and duration of transient hepatitis B surface antigenemia following Heplisav-B vaccination. PATIENTS AND METHODS: We retrospectively reviewed the medical records of all adult patients who received Heplisav-B vaccination at our institution from January 1, 2019, throug...

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Autores principales: Corsini Campioli, Cristina, Esquer Garrigos, Zerelda, Assi, Mariam, Go, John Raymond, Razonable, Raymund R., Beam, Elena, Yao, Joseph, Cummins, Nathan W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8240146/
https://www.ncbi.nlm.nih.gov/pubmed/34195546
http://dx.doi.org/10.1016/j.mayocpiqo.2020.10.010
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author Corsini Campioli, Cristina
Esquer Garrigos, Zerelda
Assi, Mariam
Go, John Raymond
Razonable, Raymund R.
Beam, Elena
Yao, Joseph
Cummins, Nathan W.
author_facet Corsini Campioli, Cristina
Esquer Garrigos, Zerelda
Assi, Mariam
Go, John Raymond
Razonable, Raymund R.
Beam, Elena
Yao, Joseph
Cummins, Nathan W.
author_sort Corsini Campioli, Cristina
collection PubMed
description OBJECTIVE: To delineate the rate and duration of transient hepatitis B surface antigenemia following Heplisav-B vaccination. PATIENTS AND METHODS: We retrospectively reviewed the medical records of all adult patients who received Heplisav-B vaccination at our institution from January 1, 2019, through March 31, 2020, and who had hepatitis B surface antigen (HBsAg) testing within 30 days following immunization. Patients with laboratory evidence of prior hepatitis B virus infection or immunization were excluded. RESULTS: A total of 39 of 1933 patients were tested for HBsAg within 30 days after completing the Heplisav-B vaccination series; of these 39, only 6 (15.4 %) had a positive HBsAg result. Compared with the patients with negative HBsAg results, those with a positive HBsAg result had a significantly lower body mass index (24.8 kg/m(2) [interquartile range (IQR), 23 to 26.4 kg/m(2)] vs 28.6 kg/m(2) [IQR, 26.4 to 30.6 kg/m(2)]; P=.01) and higher prevalence of chronic kidney disease (2 of 6 [33.3%] vs 2 of 33 [6%]; P=.04). The timing of HBsAg testing after completing the vaccination series in the HBsAg-positive group was significantly earlier compared with that of the HBsAg-negative group (2 days [IQR, 0.43 to 2.25 days) vs 12 days [IQR, 10 to 15 days]; P=.0008). Active hepatitis B infection was excluded in all 6 patients. In the HBsAg-positive group, the median time from the date of Heplisav-B administration to a negative HBsAg test result was 17 days (IQR, 8 to 36 days). CONCLUSION: As with all conventional hepatitis B vaccines, transient hepatitis B surface antigenemia can be observed with Heplisav-B vaccine, particularly in those with chronic kidney disease and low body mass index.
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spelling pubmed-82401462021-06-29 Transient Hepatitis B Surface Antigenemia Following Immunization with Heplisav-B Corsini Campioli, Cristina Esquer Garrigos, Zerelda Assi, Mariam Go, John Raymond Razonable, Raymund R. Beam, Elena Yao, Joseph Cummins, Nathan W. Mayo Clin Proc Innov Qual Outcomes Original Article OBJECTIVE: To delineate the rate and duration of transient hepatitis B surface antigenemia following Heplisav-B vaccination. PATIENTS AND METHODS: We retrospectively reviewed the medical records of all adult patients who received Heplisav-B vaccination at our institution from January 1, 2019, through March 31, 2020, and who had hepatitis B surface antigen (HBsAg) testing within 30 days following immunization. Patients with laboratory evidence of prior hepatitis B virus infection or immunization were excluded. RESULTS: A total of 39 of 1933 patients were tested for HBsAg within 30 days after completing the Heplisav-B vaccination series; of these 39, only 6 (15.4 %) had a positive HBsAg result. Compared with the patients with negative HBsAg results, those with a positive HBsAg result had a significantly lower body mass index (24.8 kg/m(2) [interquartile range (IQR), 23 to 26.4 kg/m(2)] vs 28.6 kg/m(2) [IQR, 26.4 to 30.6 kg/m(2)]; P=.01) and higher prevalence of chronic kidney disease (2 of 6 [33.3%] vs 2 of 33 [6%]; P=.04). The timing of HBsAg testing after completing the vaccination series in the HBsAg-positive group was significantly earlier compared with that of the HBsAg-negative group (2 days [IQR, 0.43 to 2.25 days) vs 12 days [IQR, 10 to 15 days]; P=.0008). Active hepatitis B infection was excluded in all 6 patients. In the HBsAg-positive group, the median time from the date of Heplisav-B administration to a negative HBsAg test result was 17 days (IQR, 8 to 36 days). CONCLUSION: As with all conventional hepatitis B vaccines, transient hepatitis B surface antigenemia can be observed with Heplisav-B vaccine, particularly in those with chronic kidney disease and low body mass index. Elsevier 2021-01-24 /pmc/articles/PMC8240146/ /pubmed/34195546 http://dx.doi.org/10.1016/j.mayocpiqo.2020.10.010 Text en © 2020 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Corsini Campioli, Cristina
Esquer Garrigos, Zerelda
Assi, Mariam
Go, John Raymond
Razonable, Raymund R.
Beam, Elena
Yao, Joseph
Cummins, Nathan W.
Transient Hepatitis B Surface Antigenemia Following Immunization with Heplisav-B
title Transient Hepatitis B Surface Antigenemia Following Immunization with Heplisav-B
title_full Transient Hepatitis B Surface Antigenemia Following Immunization with Heplisav-B
title_fullStr Transient Hepatitis B Surface Antigenemia Following Immunization with Heplisav-B
title_full_unstemmed Transient Hepatitis B Surface Antigenemia Following Immunization with Heplisav-B
title_short Transient Hepatitis B Surface Antigenemia Following Immunization with Heplisav-B
title_sort transient hepatitis b surface antigenemia following immunization with heplisav-b
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8240146/
https://www.ncbi.nlm.nih.gov/pubmed/34195546
http://dx.doi.org/10.1016/j.mayocpiqo.2020.10.010
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