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Suggested Citation:"References." Institute of Medicine. 2013. Collecting Sexual Orientation and Gender Identity Data in Electronic Health Records: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/18260.
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References

Bockting, W. O. 1999. From construction to context: Gender through the eyes of the transgendered. SIECUS Report 1(Oct/Nov):3-7.

HHS (U.S. Department of Health and Human Services). 2011. Lesbian, gay, bisexual, and transgender health. http://www.healthypeople.gov/2020/topicsobjectives2020/overview.aspx?topicid=25 (accessed October 29, 2012).

IOM (Institute of Medicine). 2011. The health of lesbian, gay, bisexual, and transgender people: Building a foundation for better understanding. Washington, DC: The National Academies Press.

The Joint Commission. 2011. Advancing effective communication, cultural competence, and patient-and family-centered care for the lesbian, gay, bisexual, and transgender (LGBT) community: A field guide. Oak Brook, IL: The Joint Commission. http://LGBTFieldGuide.pdf (accessed October 29, 2012).

Physicians for Human Rights. 2003. The right to equal treatment. http://www.paeaonline.org/index.php?ht=a/GetDocumentAction/i/135605 (accessed October 24, 2012).

Ryan, C., D. Huebner, R. M. Diaz, and J. Sanchez. 2009. Family rejection as a predictor of negative health outcomes in white and Latino lesbian, gay, and bisexual young adults. Pediatrics 123(1):346-352.

Suggested Citation:"References." Institute of Medicine. 2013. Collecting Sexual Orientation and Gender Identity Data in Electronic Health Records: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/18260.
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Suggested Citation:"References." Institute of Medicine. 2013. Collecting Sexual Orientation and Gender Identity Data in Electronic Health Records: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/18260.
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Page 53
Suggested Citation:"References." Institute of Medicine. 2013. Collecting Sexual Orientation and Gender Identity Data in Electronic Health Records: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/18260.
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Page 54
Next: Appendix A: Workshop Agenda »
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Collecting Sexual Orientation and Gender Identity Data in Electronic Health Records: Workshop Summary reviews the statement of task set to the committee which required them to collect sexual orientation and gender identity data in electronic health records. This report summarizes the invited presentations and facilitated discussions about current practices around sexual orientation and gender identity data collection, the challenges in collecting these data, and ways in which these challenges can be overcome.

Areas of focus for the workshop include the clinical rationale behind collecting these data, standardized questions that can be used to collect these data, mechanisms for supporting providers and patients in the collection of these data, technical specifications involved in creating standards for sexual orientation and gender identity data collection and exchange, and policy considerations related to the health information technology (HIT) Meaningful Use process being overseen by the Department of Health and Human Services. This report summarizes the workshop agenda, select invited speakers and discussants, and moderate the discussions. Invited participants will include lesbian, gay, bisexual, and transgender (LGBT) health care consumer advocates, providers with experience working with LGBT populations, HIT vendors and other HIT specialists, health care administrators, and policy makers.

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