Collecting sexual orientation and gender identity data in electronic health records: workshop summary
Gespeichert in:
| 1. Verfasser: | |
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| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Washington, D.C.
National Academies Press
[2013]
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| Schlagworte: | |
| Online-Zugang: | FAW01 FAW02 Volltext |
| Beschreibung: | Title from PDF t.p Description based on version viewed: Oct. 26, 2013 |
| Beschreibung: | 1 online resource (1 PDF file (xiv, 73 pages)) illustrations |
| ISBN: | 0309268044 0309268052 9780309268042 9780309268059 |
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| 505 | 8 | |a Introduction and overview -- Clinical rationale for collecting sexual orientation and gender identity data -- Federal perspective on the use of electronic health records to collect sexual orientation and gender indentity data -- Existing data collection practices in clinical settings -- Developing and implementing questions for collecting data on sexual orientation and gender identity -- Closing remarks | |
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| contents | In 2011, the Institute of Medicine (IOM) released the report The Health of Lesbian, Gay, Bisexual, and Transgender People: Building a Foundation for Better Understanding, the first comprehensive compilation of what is known about the health of each of these groups at different stages of life. This report also outlined an agenda for the research and data collection necessary to form a fuller understanding of this subject. One of the recommendations in this report was that, provided that privacy concerns could be adequately addressed, information on patients' sexual orientation and gender identity should be collected in electronic health records, just as information on race and ethnicity is routinely collected. Such data are essential because demographics provide the foundation for understanding any population's status and needs. This recommendation recognized that the possible discomfort on the part of health care workers asking questions about sexual orientation and gender identity, a lack of knowledge by providers about how to elicit this information, and some hesitancy on the part of patients to disclose this information may be barriers to the collection of meaningful data on sexual orientation and gender identity Introduction and overview -- Clinical rationale for collecting sexual orientation and gender identity data -- Federal perspective on the use of electronic health records to collect sexual orientation and gender indentity data -- Existing data collection practices in clinical settings -- Developing and implementing questions for collecting data on sexual orientation and gender identity -- Closing remarks |
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| spelling | Alper, Joe Verfasser aut Collecting sexual orientation and gender identity data in electronic health records workshop summary Joe Alper, Monica N. Feit, and Jon Q. Sanders, rapporteurs ; Board on the Health of Select Populations, Institute of Medicine of the National Academies Washington, D.C. National Academies Press [2013] 1 online resource (1 PDF file (xiv, 73 pages)) illustrations txt rdacontent c rdamedia cr rdacarrier Title from PDF t.p Description based on version viewed: Oct. 26, 2013 In 2011, the Institute of Medicine (IOM) released the report The Health of Lesbian, Gay, Bisexual, and Transgender People: Building a Foundation for Better Understanding, the first comprehensive compilation of what is known about the health of each of these groups at different stages of life. This report also outlined an agenda for the research and data collection necessary to form a fuller understanding of this subject. One of the recommendations in this report was that, provided that privacy concerns could be adequately addressed, information on patients' sexual orientation and gender identity should be collected in electronic health records, just as information on race and ethnicity is routinely collected. Such data are essential because demographics provide the foundation for understanding any population's status and needs. This recommendation recognized that the possible discomfort on the part of health care workers asking questions about sexual orientation and gender identity, a lack of knowledge by providers about how to elicit this information, and some hesitancy on the part of patients to disclose this information may be barriers to the collection of meaningful data on sexual orientation and gender identity Introduction and overview -- Clinical rationale for collecting sexual orientation and gender identity data -- Federal perspective on the use of electronic health records to collect sexual orientation and gender indentity data -- Existing data collection practices in clinical settings -- Developing and implementing questions for collecting data on sexual orientation and gender identity -- Closing remarks Data Collection / standards / United States / Congresses Electronic Health Records / standards / United States / Congresses Gender Identity / United States / Congresses Sexuality / United States / Congresses HEALTH & FITNESS / Holism bisacsh HEALTH & FITNESS / Reference bisacsh MEDICAL / Alternative Medicine bisacsh MEDICAL / Atlases bisacsh MEDICAL / Essays bisacsh MEDICAL / Family & General Practice bisacsh MEDICAL / Holistic Medicine bisacsh MEDICAL / Osteopathy bisacsh Datenverarbeitung Medizin Politik Medical records United States Data processing Congresses Medical records Government policy United States Congresses Medical records Standards United States Congresses Gender identity United States Congresses Sexual orientation United States Congresses USA (DE-588)1071861417 Konferenzschrift gnd-content Feit, Monica N. Sonstige oth Sanders, Jon Q. Sonstige oth Institute of Medicine (U.S.) Board on the Health of Select Populations Sonstige oth Collecting Sexual Orientation and Gender Identity Data in Electronic Health Records (Workshop) <2012, Washington, D.C.> Sonstige oth Erscheint auch als Druck-Ausgabe Collecting sexual orientation and gender identity data in electronic health records : workshop summary http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=867621 Aggregator Volltext |
| spellingShingle | Alper, Joe Collecting sexual orientation and gender identity data in electronic health records workshop summary In 2011, the Institute of Medicine (IOM) released the report The Health of Lesbian, Gay, Bisexual, and Transgender People: Building a Foundation for Better Understanding, the first comprehensive compilation of what is known about the health of each of these groups at different stages of life. This report also outlined an agenda for the research and data collection necessary to form a fuller understanding of this subject. One of the recommendations in this report was that, provided that privacy concerns could be adequately addressed, information on patients' sexual orientation and gender identity should be collected in electronic health records, just as information on race and ethnicity is routinely collected. Such data are essential because demographics provide the foundation for understanding any population's status and needs. This recommendation recognized that the possible discomfort on the part of health care workers asking questions about sexual orientation and gender identity, a lack of knowledge by providers about how to elicit this information, and some hesitancy on the part of patients to disclose this information may be barriers to the collection of meaningful data on sexual orientation and gender identity Introduction and overview -- Clinical rationale for collecting sexual orientation and gender identity data -- Federal perspective on the use of electronic health records to collect sexual orientation and gender indentity data -- Existing data collection practices in clinical settings -- Developing and implementing questions for collecting data on sexual orientation and gender identity -- Closing remarks Data Collection / standards / United States / Congresses Electronic Health Records / standards / United States / Congresses Gender Identity / United States / Congresses Sexuality / United States / Congresses HEALTH & FITNESS / Holism bisacsh HEALTH & FITNESS / Reference bisacsh MEDICAL / Alternative Medicine bisacsh MEDICAL / Atlases bisacsh MEDICAL / Essays bisacsh MEDICAL / Family & General Practice bisacsh MEDICAL / Holistic Medicine bisacsh MEDICAL / Osteopathy bisacsh Datenverarbeitung Medizin Politik Medical records United States Data processing Congresses Medical records Government policy United States Congresses Medical records Standards United States Congresses Gender identity United States Congresses Sexual orientation United States Congresses |
| subject_GND | (DE-588)1071861417 |
| title | Collecting sexual orientation and gender identity data in electronic health records workshop summary |
| title_auth | Collecting sexual orientation and gender identity data in electronic health records workshop summary |
| title_exact_search | Collecting sexual orientation and gender identity data in electronic health records workshop summary |
| title_full | Collecting sexual orientation and gender identity data in electronic health records workshop summary Joe Alper, Monica N. Feit, and Jon Q. Sanders, rapporteurs ; Board on the Health of Select Populations, Institute of Medicine of the National Academies |
| title_fullStr | Collecting sexual orientation and gender identity data in electronic health records workshop summary Joe Alper, Monica N. Feit, and Jon Q. Sanders, rapporteurs ; Board on the Health of Select Populations, Institute of Medicine of the National Academies |
| title_full_unstemmed | Collecting sexual orientation and gender identity data in electronic health records workshop summary Joe Alper, Monica N. Feit, and Jon Q. Sanders, rapporteurs ; Board on the Health of Select Populations, Institute of Medicine of the National Academies |
| title_short | Collecting sexual orientation and gender identity data in electronic health records |
| title_sort | collecting sexual orientation and gender identity data in electronic health records workshop summary |
| title_sub | workshop summary |
| topic | Data Collection / standards / United States / Congresses Electronic Health Records / standards / United States / Congresses Gender Identity / United States / Congresses Sexuality / United States / Congresses HEALTH & FITNESS / Holism bisacsh HEALTH & FITNESS / Reference bisacsh MEDICAL / Alternative Medicine bisacsh MEDICAL / Atlases bisacsh MEDICAL / Essays bisacsh MEDICAL / Family & General Practice bisacsh MEDICAL / Holistic Medicine bisacsh MEDICAL / Osteopathy bisacsh Datenverarbeitung Medizin Politik Medical records United States Data processing Congresses Medical records Government policy United States Congresses Medical records Standards United States Congresses Gender identity United States Congresses Sexual orientation United States Congresses |
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