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▼a Alper, Joe,
▼e author. |
| 245 | 10 |
▼a Collecting sexual orientation and gender identity data in electronic health records :
▼b workshop summary /
▼c Joe Alper, Monica N. Feit, and Jon Q. Sanders, rapporteurs ; Board on the Health of Select Populations, Institute of Medicine of the National Academies. |
| 264 | 1 |
▼a Washington, D.C. :
▼b National Academies Press,
▼c [2013] |
| 300 | |
▼a 1 online resource (1 PDF file (xiv, 73 pages)) :
▼b illustrations. |
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▼a Title from PDF t.p. |
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▼a Includes bibliographical references. |
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▼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. |
| 520 | 3 |
▼a 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. |
| 536 | |
▼a This activity by the National Academy of Sciences was supported in part by the National Institutes of Health under Contract Number HHSN263201200074I, with additional support from The California Endowment under grant number 20121371, and the California HealthCare Foundation, based in Oakland, California, under grant number 17133. |
| 588 | |
▼a Description based on version viewed: Oct. 26, 2013. |
| 650 | 12 |
▼a Data Collection
▼x standards
▼z United States
▼v Congresses. |
| 650 | 12 |
▼a Electronic Health Records
▼x standards
▼z United States
▼v Congresses. |
| 650 | 22 |
▼a Gender Identity
▼z United States
▼v Congresses. |
| 650 | 22 |
▼a Sexuality
▼z United States
▼v Congresses. |
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▼a Medical records
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▼x Data processing
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▼a Medical records
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▼z United States
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| 650 | 0 |
▼a Medical records
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▼z United States
▼v Congresses. |
| 650 | 0 |
▼a Gender identity
▼z United States
▼v Congresses. |
| 650 | 0 |
▼a Sexual orientation
▼z United States
▼v Congresses. |
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▼a Electronic books. |
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▼a Feit, Monica N.,
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▼a Sanders, Jon Q.,
▼e author. |
| 710 | 2 |
▼a Institute of Medicine (U.S.).
▼b Board on the Health of Select Populations,
▼e sponsoring body. |
| 711 | 2 |
▼a Collecting Sexual Orientation and Gender Identity Data in Electronic Health Records (Workshop)
▼d (2012:
▼c Washington, D.C.) |
| 776 | 08 |
▼i Print version:
▼t Collecting sexual orientation and gender identity data in electronic health records : workshop summary.
▼d Washington, District of Columbia : National Academies Press, [2013]
▼h xiv, 73 pages ; 23 cm
▼z 9780309268042
▼w (OCoLC)828139253
▼w (DLC) 10863774 |
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