Collecting Sexual Orientation and Gender Identity Data in Electronic Health Records - Workshop Summary
||December 20, 2012
Note: Proceedings contain the opinion of the presenters, but do NOT reflect the conclusions of the Health and Medicine Division or the National Academies. Learn more about the differences between Reports and Proceedings.
In 2011, the 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. One of the recommendations in this report was that 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. These data are essential because demographics provide the foundation for understanding any population’s status and needs.
As the next step in exploring this recommendation, the IOM held a workshop on October 12, 2012, on collecting sexual orientation and gender identity data in electronic health records. This document summarizes the workshop.