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Statewide analysis of missed opportunities for human papillomavirus vaccination using vaccine registry data

BACKGROUND: Human papillomavirus (HPV) vaccine 3-dose completion rates among adolescent females in the US are low. Missed opportunities impede HPV vaccination coverage. METHODS: A population-based secondary data analysis of de-identified vaccination and demographic data from the Utah Statewide Immun...

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Autores principales: Kepka, Deanna, Spigarelli, Michael G., Warner, Echo L., Yoneoka, Yukiko, McConnell, Nancy, Balch, Alfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985178/
https://www.ncbi.nlm.nih.gov/pubmed/27540595
http://dx.doi.org/10.1016/j.pvr.2016.06.002
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author Kepka, Deanna
Spigarelli, Michael G.
Warner, Echo L.
Yoneoka, Yukiko
McConnell, Nancy
Balch, Alfred
author_facet Kepka, Deanna
Spigarelli, Michael G.
Warner, Echo L.
Yoneoka, Yukiko
McConnell, Nancy
Balch, Alfred
author_sort Kepka, Deanna
collection PubMed
description BACKGROUND: Human papillomavirus (HPV) vaccine 3-dose completion rates among adolescent females in the US are low. Missed opportunities impede HPV vaccination coverage. METHODS: A population-based secondary data analysis of de-identified vaccination and demographic data from the Utah Statewide Immunization Information System (USIIS) was conducted. Records were included from 25,866 females ages 11–26 years at any time during 2008–2012 who received at least one of the following adolescent vaccinations documented in the USIIS: Tdap (Tetanus, Diphtheria, Pertussis), meningococcal, and/or influenza. A missed opportunity for HPV vaccination was defined as a clinical encounter where the patient received at least one adolescent vaccination, but not a HPV vaccine. RESULTS: Of 47,665 eligible visits, there were 20,911 missed opportunities (43.87%). Age group, race/ethnicity, and rurality were significantly associated with missed opportunity (p<0.0001). In a multivariable mixed-effects logistic regression model that included ethnicity, location and age, as fixed effects and subject as a random effect, Hispanics were less likely to have a missed opportunity than whites OR 0.59 (95% CI: 0.52–0.66), small rural more likely to have a missed opportunity than urban youth OR 1.8 (95% CI: 1.5–2.2), and preteens more likely than teens OR 2.4 (95% CI: 2.2–2.7). CONCLUSION: Missed clinical opportunities are a significant barrier to HPV vaccination among female adolescents. Interventions targeted at providers who serve patient groups with the highest missed opportunities are needed to achieve adequate protection from HPV-associated illnesses. IMPACT: This is one of the first studies to utilize state immunization information system data to assess missed opportunities for HPV vaccination.
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spelling pubmed-49851782017-12-01 Statewide analysis of missed opportunities for human papillomavirus vaccination using vaccine registry data Kepka, Deanna Spigarelli, Michael G. Warner, Echo L. Yoneoka, Yukiko McConnell, Nancy Balch, Alfred Papillomavirus Res Article BACKGROUND: Human papillomavirus (HPV) vaccine 3-dose completion rates among adolescent females in the US are low. Missed opportunities impede HPV vaccination coverage. METHODS: A population-based secondary data analysis of de-identified vaccination and demographic data from the Utah Statewide Immunization Information System (USIIS) was conducted. Records were included from 25,866 females ages 11–26 years at any time during 2008–2012 who received at least one of the following adolescent vaccinations documented in the USIIS: Tdap (Tetanus, Diphtheria, Pertussis), meningococcal, and/or influenza. A missed opportunity for HPV vaccination was defined as a clinical encounter where the patient received at least one adolescent vaccination, but not a HPV vaccine. RESULTS: Of 47,665 eligible visits, there were 20,911 missed opportunities (43.87%). Age group, race/ethnicity, and rurality were significantly associated with missed opportunity (p<0.0001). In a multivariable mixed-effects logistic regression model that included ethnicity, location and age, as fixed effects and subject as a random effect, Hispanics were less likely to have a missed opportunity than whites OR 0.59 (95% CI: 0.52–0.66), small rural more likely to have a missed opportunity than urban youth OR 1.8 (95% CI: 1.5–2.2), and preteens more likely than teens OR 2.4 (95% CI: 2.2–2.7). CONCLUSION: Missed clinical opportunities are a significant barrier to HPV vaccination among female adolescents. Interventions targeted at providers who serve patient groups with the highest missed opportunities are needed to achieve adequate protection from HPV-associated illnesses. IMPACT: This is one of the first studies to utilize state immunization information system data to assess missed opportunities for HPV vaccination. Elsevier 2016-07-01 /pmc/articles/PMC4985178/ /pubmed/27540595 http://dx.doi.org/10.1016/j.pvr.2016.06.002 Text en © 2016 The Authors http://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 Article
Kepka, Deanna
Spigarelli, Michael G.
Warner, Echo L.
Yoneoka, Yukiko
McConnell, Nancy
Balch, Alfred
Statewide analysis of missed opportunities for human papillomavirus vaccination using vaccine registry data
title Statewide analysis of missed opportunities for human papillomavirus vaccination using vaccine registry data
title_full Statewide analysis of missed opportunities for human papillomavirus vaccination using vaccine registry data
title_fullStr Statewide analysis of missed opportunities for human papillomavirus vaccination using vaccine registry data
title_full_unstemmed Statewide analysis of missed opportunities for human papillomavirus vaccination using vaccine registry data
title_short Statewide analysis of missed opportunities for human papillomavirus vaccination using vaccine registry data
title_sort statewide analysis of missed opportunities for human papillomavirus vaccination using vaccine registry data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985178/
https://www.ncbi.nlm.nih.gov/pubmed/27540595
http://dx.doi.org/10.1016/j.pvr.2016.06.002
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