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.
Material type:
TextPublisher: Washington, District of Columbia : National Academies Press, [2013]Copyright date: �2013Description: 1 online resource (87 pages) : color illustrationsContent type: - text
- computer
- online resource
- 9780309268059 (e-book)
- 610.285 23
- R864 .A363 2013
Includes bibliographical references (page 53).
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.
Description based on print version record.
Electronic reproduction. Ann Arbor, MI : ProQuest, 2015. Available via World Wide Web. Access may be limited to ProQuest affiliated libraries.
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