Cargando…

Safety of 4-valent human papillomavirus vaccine in males: a large observational post-marketing study

The 4-valent human papillomavirus (HPV) vaccine (4vHPV vaccine), Gardasil®, is indicated for the prevention of several HPV-related diseases. The objective was to assess the safety of 4vHPV vaccine administered to males as part of routine care. The study used a US health insurance claims database, an...

Descripción completa

Detalles Bibliográficos
Autores principales: Amend, Kandace L., Turnbull, Bruce, Zhou, Li, Marks, Morgan A., Velicer, Christine, Saddier, Patricia, Seeger, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481146/
https://www.ncbi.nlm.nih.gov/pubmed/35714277
http://dx.doi.org/10.1080/21645515.2022.2073750
_version_ 1784791198362238976
author Amend, Kandace L.
Turnbull, Bruce
Zhou, Li
Marks, Morgan A.
Velicer, Christine
Saddier, Patricia
Seeger, John D.
author_facet Amend, Kandace L.
Turnbull, Bruce
Zhou, Li
Marks, Morgan A.
Velicer, Christine
Saddier, Patricia
Seeger, John D.
author_sort Amend, Kandace L.
collection PubMed
description The 4-valent human papillomavirus (HPV) vaccine (4vHPV vaccine), Gardasil®, is indicated for the prevention of several HPV-related diseases. The objective was to assess the safety of 4vHPV vaccine administered to males as part of routine care. The study used a US health insurance claims database, and included males, age 9 to 26 years, who initiated 4vHPV between October 2009 and December 2016. General safety outcomes were identified using ICD diagnosis codes associated with emergency room visits and hospitalizations in the claims database in risk periods (Days 1–60 and Days 1–14 following vaccine administration) and self-comparison periods (Days 91–150 and 91–104 for the Days 1–60 and Days 1–14 analysis, respectively). Incidence rates (IRs) and relative rates (RRs) with 95% confidence intervals (CIs) were calculated comparing the risk and self-comparison periods. In this study, 114,035 males initiated 4vHPV vaccine and received 202,737 doses. Using the 60-day time window, 5 outcomes had significantly elevated RRs after accounting for multiple comparisons: ear conditions (RR 1.28, 95% CI 1.03–1.59); otitis media and related conditions (RR 1.65, 95% CI 1.09–2.54); cellulitis and abscess of arm (RR 2.17, 95% CI 1.06–4.72); intracranial injury (RR 1.23, 95% CI 1.01–1.50); and concussion (RR 1.29, 95% CI 1.05–1.59). A higher rate of allergic reactions was noted on the day of 4vHPV vaccine receipt compared to other vaccines (21.07 events per 10,000 doses, 95% CI 18.89–23.44 versus 11.44 per 10,000 doses, 95% CI 9.84–13.22). A higher incidence rate of VTE was observed following vaccination but this association was not significant (RR 2.17, 95% CI 0.35–22.74). The 4vHPV vaccine was associated with same-day allergic reactions as well as ear infections, intracranial injury, cellulitis, and concussion within 2 months after vaccination. While allergic reaction and cellulitis are consistent with the known safety profile of 4vHPV vaccine, the association of the other outcomes were determined by an independent Safety Review Committee to be most likely a result of activities common in adolescent males that coincide with the timing of vaccination and not directly related to vaccination itself. Implications and Contributions: The study results support the general safety of routine immunization with 4vHPV vaccine among males to prevent HPV-related diseases and cancers.
format Online
Article
Text
id pubmed-9481146
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-94811462022-09-17 Safety of 4-valent human papillomavirus vaccine in males: a large observational post-marketing study Amend, Kandace L. Turnbull, Bruce Zhou, Li Marks, Morgan A. Velicer, Christine Saddier, Patricia Seeger, John D. Hum Vaccin Immunother HPV – Research Paper The 4-valent human papillomavirus (HPV) vaccine (4vHPV vaccine), Gardasil®, is indicated for the prevention of several HPV-related diseases. The objective was to assess the safety of 4vHPV vaccine administered to males as part of routine care. The study used a US health insurance claims database, and included males, age 9 to 26 years, who initiated 4vHPV between October 2009 and December 2016. General safety outcomes were identified using ICD diagnosis codes associated with emergency room visits and hospitalizations in the claims database in risk periods (Days 1–60 and Days 1–14 following vaccine administration) and self-comparison periods (Days 91–150 and 91–104 for the Days 1–60 and Days 1–14 analysis, respectively). Incidence rates (IRs) and relative rates (RRs) with 95% confidence intervals (CIs) were calculated comparing the risk and self-comparison periods. In this study, 114,035 males initiated 4vHPV vaccine and received 202,737 doses. Using the 60-day time window, 5 outcomes had significantly elevated RRs after accounting for multiple comparisons: ear conditions (RR 1.28, 95% CI 1.03–1.59); otitis media and related conditions (RR 1.65, 95% CI 1.09–2.54); cellulitis and abscess of arm (RR 2.17, 95% CI 1.06–4.72); intracranial injury (RR 1.23, 95% CI 1.01–1.50); and concussion (RR 1.29, 95% CI 1.05–1.59). A higher rate of allergic reactions was noted on the day of 4vHPV vaccine receipt compared to other vaccines (21.07 events per 10,000 doses, 95% CI 18.89–23.44 versus 11.44 per 10,000 doses, 95% CI 9.84–13.22). A higher incidence rate of VTE was observed following vaccination but this association was not significant (RR 2.17, 95% CI 0.35–22.74). The 4vHPV vaccine was associated with same-day allergic reactions as well as ear infections, intracranial injury, cellulitis, and concussion within 2 months after vaccination. While allergic reaction and cellulitis are consistent with the known safety profile of 4vHPV vaccine, the association of the other outcomes were determined by an independent Safety Review Committee to be most likely a result of activities common in adolescent males that coincide with the timing of vaccination and not directly related to vaccination itself. Implications and Contributions: The study results support the general safety of routine immunization with 4vHPV vaccine among males to prevent HPV-related diseases and cancers. Taylor & Francis 2022-06-17 /pmc/articles/PMC9481146/ /pubmed/35714277 http://dx.doi.org/10.1080/21645515.2022.2073750 Text en © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle HPV – Research Paper
Amend, Kandace L.
Turnbull, Bruce
Zhou, Li
Marks, Morgan A.
Velicer, Christine
Saddier, Patricia
Seeger, John D.
Safety of 4-valent human papillomavirus vaccine in males: a large observational post-marketing study
title Safety of 4-valent human papillomavirus vaccine in males: a large observational post-marketing study
title_full Safety of 4-valent human papillomavirus vaccine in males: a large observational post-marketing study
title_fullStr Safety of 4-valent human papillomavirus vaccine in males: a large observational post-marketing study
title_full_unstemmed Safety of 4-valent human papillomavirus vaccine in males: a large observational post-marketing study
title_short Safety of 4-valent human papillomavirus vaccine in males: a large observational post-marketing study
title_sort safety of 4-valent human papillomavirus vaccine in males: a large observational post-marketing study
topic HPV – Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481146/
https://www.ncbi.nlm.nih.gov/pubmed/35714277
http://dx.doi.org/10.1080/21645515.2022.2073750
work_keys_str_mv AT amendkandacel safetyof4valenthumanpapillomavirusvaccineinmalesalargeobservationalpostmarketingstudy
AT turnbullbruce safetyof4valenthumanpapillomavirusvaccineinmalesalargeobservationalpostmarketingstudy
AT zhouli safetyof4valenthumanpapillomavirusvaccineinmalesalargeobservationalpostmarketingstudy
AT marksmorgana safetyof4valenthumanpapillomavirusvaccineinmalesalargeobservationalpostmarketingstudy
AT velicerchristine safetyof4valenthumanpapillomavirusvaccineinmalesalargeobservationalpostmarketingstudy
AT saddierpatricia safetyof4valenthumanpapillomavirusvaccineinmalesalargeobservationalpostmarketingstudy
AT seegerjohnd safetyof4valenthumanpapillomavirusvaccineinmalesalargeobservationalpostmarketingstudy