Collection of Data on Sex, Sexual Orientation, and Gender Identity by U.S. Public Health Data and Monitoring Systems, 2015–2018

We aimed to assess Centers for Disease Control and Prevention (CDC) data systems on the extent of data collection on sex, sexual orientation, and gender identity as well as on age and race/ethnicity. Between March and September 2019, we searched 11 federal websites to identify CDC-supported or -led...

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Autores principales: Alissa C. Kress, Asia Asberry, Julio Dicent Taillepierre, Michelle M. Johns, Pattie Tucker, Ana Penman-Aguilar
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/2e5e99f4a86e4d0299d029cf10ca383d
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spelling oai:doaj.org-article:2e5e99f4a86e4d0299d029cf10ca383d2021-11-25T17:51:51ZCollection of Data on Sex, Sexual Orientation, and Gender Identity by U.S. Public Health Data and Monitoring Systems, 2015–201810.3390/ijerph1822121891660-46011661-7827https://doaj.org/article/2e5e99f4a86e4d0299d029cf10ca383d2021-11-01T00:00:00Zhttps://www.mdpi.com/1660-4601/18/22/12189https://doaj.org/toc/1661-7827https://doaj.org/toc/1660-4601We aimed to assess Centers for Disease Control and Prevention (CDC) data systems on the extent of data collection on sex, sexual orientation, and gender identity as well as on age and race/ethnicity. Between March and September 2019, we searched 11 federal websites to identify CDC-supported or -led U.S. data systems active between 2015 and 2018. We searched the systems’ website, documentation, and publications for evidence of data collection on sex, sexual orientation, gender identity, age, and race/ethnicity. We categorized each system by type (disease notification, periodic prevalence survey, registry/vital record, or multiple sources). We provide descriptive statistics of characteristics of the identified systems. Most (94.1%) systems we assessed collected data on sex. All systems collected data on age, and approximately 80% collected data on race/ethnicity. Only 17.7% collected data on sexual orientation and 5.9% on gender identity. Periodic prevalence surveys were the most common system type for collecting all the variables we assessed. While most U.S. public health data and monitoring systems collect data disaggregated by sex, age, and race/ethnicity, far fewer do so for sexual orientation or gender identity. Standards and examples exist to aid efforts to collect and report these vitally important data. Additionally important is increasing accessibility and appropriately tailored dissemination of reports of these data to public health professionals and other collaborators.Alissa C. KressAsia AsberryJulio Dicent TaillepierreMichelle M. JohnsPattie TuckerAna Penman-AguilarMDPI AGarticlewomen’s healthsexual and gender minoritiesdata collectionMedicineRENInternational Journal of Environmental Research and Public Health, Vol 18, Iss 12189, p 12189 (2021)
institution DOAJ
collection DOAJ
language EN
topic women’s health
sexual and gender minorities
data collection
Medicine
R
spellingShingle women’s health
sexual and gender minorities
data collection
Medicine
R
Alissa C. Kress
Asia Asberry
Julio Dicent Taillepierre
Michelle M. Johns
Pattie Tucker
Ana Penman-Aguilar
Collection of Data on Sex, Sexual Orientation, and Gender Identity by U.S. Public Health Data and Monitoring Systems, 2015–2018
description We aimed to assess Centers for Disease Control and Prevention (CDC) data systems on the extent of data collection on sex, sexual orientation, and gender identity as well as on age and race/ethnicity. Between March and September 2019, we searched 11 federal websites to identify CDC-supported or -led U.S. data systems active between 2015 and 2018. We searched the systems’ website, documentation, and publications for evidence of data collection on sex, sexual orientation, gender identity, age, and race/ethnicity. We categorized each system by type (disease notification, periodic prevalence survey, registry/vital record, or multiple sources). We provide descriptive statistics of characteristics of the identified systems. Most (94.1%) systems we assessed collected data on sex. All systems collected data on age, and approximately 80% collected data on race/ethnicity. Only 17.7% collected data on sexual orientation and 5.9% on gender identity. Periodic prevalence surveys were the most common system type for collecting all the variables we assessed. While most U.S. public health data and monitoring systems collect data disaggregated by sex, age, and race/ethnicity, far fewer do so for sexual orientation or gender identity. Standards and examples exist to aid efforts to collect and report these vitally important data. Additionally important is increasing accessibility and appropriately tailored dissemination of reports of these data to public health professionals and other collaborators.
format article
author Alissa C. Kress
Asia Asberry
Julio Dicent Taillepierre
Michelle M. Johns
Pattie Tucker
Ana Penman-Aguilar
author_facet Alissa C. Kress
Asia Asberry
Julio Dicent Taillepierre
Michelle M. Johns
Pattie Tucker
Ana Penman-Aguilar
author_sort Alissa C. Kress
title Collection of Data on Sex, Sexual Orientation, and Gender Identity by U.S. Public Health Data and Monitoring Systems, 2015–2018
title_short Collection of Data on Sex, Sexual Orientation, and Gender Identity by U.S. Public Health Data and Monitoring Systems, 2015–2018
title_full Collection of Data on Sex, Sexual Orientation, and Gender Identity by U.S. Public Health Data and Monitoring Systems, 2015–2018
title_fullStr Collection of Data on Sex, Sexual Orientation, and Gender Identity by U.S. Public Health Data and Monitoring Systems, 2015–2018
title_full_unstemmed Collection of Data on Sex, Sexual Orientation, and Gender Identity by U.S. Public Health Data and Monitoring Systems, 2015–2018
title_sort collection of data on sex, sexual orientation, and gender identity by u.s. public health data and monitoring systems, 2015–2018
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/2e5e99f4a86e4d0299d029cf10ca383d
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