eAppendix. EQUALITY Stakeholder Advisory Board: Selected Feedback
eFigure. Study Design
eTable 1. Patient and Provider Interview Recruitment
eTable 2. Preferences for Sexual Orientation Collection Among Patients and Providers
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Haider AH, Schneider EB, Kodadek LM, et al. Emergency Department Query for Patient-Centered Approaches to Sexual Orientation and Gender Identity : The EQUALITY Study. JAMA Intern Med. 2017;177(6):819–828. doi:10.1001/jamainternmed.2017.0906
How do views about collection of sexual orientation information in the emergency department compare among patients and health care professionals?
In this exploratory, sequential, mixed-methods study of patients and health care professionals, 10.3% of patients reported they would refuse to provide sexual orientation information in the emergency department, whereas 77.8% of health care professionals thought patients would refuse to provide such information when asked in this setting.
Few patients will refuse to provide sexual orientation information in the emergency department setting in contrast to what most emergency department health care professionals think.
The Institute of Medicine and The Joint Commission recommend routine documentation of patients’ sexual orientation in health care settings. Currently, very few health care systems collect these data since patient preferences and health care professionals’ support regarding collection of data about patient sexual orientation are unknown.
To identify the optimal patient-centered approach to collect sexual orientation data in the emergency department (ED) in the Emergency Department Query for Patient-Centered Approaches to Sexual Orientation and Gender Identity study.
Design, Setting, and Participants
An exploratory, sequential, mixed-methods design was used first to evaluate qualitative interviews conducted in the Baltimore, Maryland, and Washington, DC, areas. Fifty-three patients and 26 health care professionals participated in the qualitative interviews. Interviews were followed by a national online survey, in which 1516 (potential) patients (244 lesbian, 289 gay, 179 bisexual, and 804 straight) and 429 ED health care professionals (209 physicians and 220 nurses) participated. Survey participants were recruited using random digit dialing and address-based sampling techniques.
Main Outcomes and Measures
Qualitative interviews were used to obtain the perspectives of patients and health care professionals on sexual orientation data collection, and a quantitative survey was used to gauge patients' and health care professionals' willingness to provide or obtain sexual orientation information.
Mean (SD) age of patient and clinician participants was 49 (16.4) and 51 (9.4) years, respectively. Qualitative interviews suggested that patients were less likely to refuse to provide sexual orientation than providers expected. Nationally, 154 patients (10.3%) reported that they would refuse to provide sexual orientation; however, 333 (77.8%) of all clinicians thought patients would refuse to provide sexual orientation. After adjustment for demographic characteristics, only bisexual patients had increased odds of refusing to provide sexual orientation compared with heterosexual patients (odds ratio, 2.40; 95% CI, 1.26-4.56).
Conclusions and Relevance
Patients and health care professionals have discordant views on routine collection of data on sexual orientation. A minority of patients would refuse to provide sexual orientation. Implementation of a standardized, patient-centered approach for routine collection of sexual orientation data is required on a national scale to help to identify and address health disparities among lesbian, gay, and bisexual populations.
Lesbian, gay, and bisexual (LGB) populations report poorer health1,2 and less access to health insurance and health services3,4 compared with heterosexual populations. Approximately 8 million Americans identify as LGB,5 and, although some inequities have been identified, lack of data on sexual orientation is a major challenge to understanding and addressing LGB health disparities.6 To address this issue, LGB individuals have been identified as a target group for health improvement by Healthy People 2020,7 and the US Department of Health and Human Services and the Institutes of Medicine now recommend routine collection of sexual orientation data in federally funded population health surveys and in electronic health records.7,8 In response, the National Health Interview Survey began collecting sexual orientation data in 2013.9
Obtaining data through population surveys is important for identifying and addressing health disparities; in addition, collecting data in a patient’s electronic health record (EHR) can help clinicians to provide more complete care.10,11 Recently, the Centers for Medicare & Medicaid Services released Meaningful Use Stage 3 guidelines that require all certified EHR systems to have the capacity to record sexual orientation data,12 but very few health systems or hospitals report routinely collecting such data.11 Emergency departments (EDs) are the source of nearly half of inpatient admissions in the United States and the primary point of entry for uninsured and underinsured patients.13 However, few hospital EDs routinely collect sexual orientation information,11 and there are currently no evidence-based methods standards to collect these data in a patient-centered manner. Despite the importance of sexual orientation collection for providing high-quality, patient-centered care and the opportunity to collect a large volume of sexual orientation information for LGB disparities research, routine collection of data on sexual orientation in the ED setting is rare, and optimal patient-centered approaches for collecting this information remain unclear.
There is little known about the effect of sexual orientation data collection on patient outcomes; yet, given the importance of sexual orientation to population health7-9 and clinical care,14-17 the objectives of this study were (1) to understand the willingness to disclose sexual orientation among patients and willingness to collect sexual orientation data among health care professionals and (2) to identify the optimal patient-centered approach to collecting sexual orientation demographic data in the ED. Every year in the United States, there are more than 130 million ED visits,18 so the potential impact of routinely collecting sexual orientation information in that setting is great given the high volume of patients.
The Emergency Department Query for Patient-Centered Approaches to Sexual Orientation and Gender Identity (EQUALITY) study used an exploratory, sequential, mixed-methods design. In the qualitative first phase, in-depth interviews were conducted with a large sample of patients and ED professionals in the Baltimore, Maryland, and Washington, DC, areas. The results from the qualitative phase informed the development of the quantitative second phase of the study, in which a comprehensive national survey of patients and ED professionals was conducted. A stakeholder advisory board (SAB) consisting of nurses, physicians, researchers, and patients, as well as directors of some of the most influential national and local LGBT (lesbian, gay, bisexual, transgender) advocacy organizations provided feedback and guidance in each phase of the study. Given the highly nuanced considerations surrounding interviews and surveying transgender individuals, the SAB agreed that a separate specialized national survey be devoted to this group, with the results reported in a separate article. The SAB members are listed at the end of this article, and selected minutes from SAB meetings can be found in the eAppendix in the Supplement. A visual representation of the study design is found in eFigure 1 in the Supplement, and further details are available.19 This study was approved by the Johns Hopkins and Partners Healthcare Institutional Review Boards. Written informed consent was obtained prior to beginning the interviews, and interview participants received a $35 gift card. The survey participants received $10 for completing the survey.
A purposive sample of participants was recruited for semistructured, in-depth, 1-on-1 interviews. Patient participants were defined as community members with experience seeking emergency medical care; they were recruited through community outreach, flyers, and social media. Organizations at which active patient recruitment occurred included Equality Maryland, Johns Hopkins Lighthouse, BeSure, B’more Outloud, Sistas of the “T,” and Gay, Lesbian, Bisexual, and Transgender Community Center of Baltimore. Patients could express interest in participation through the study website19 or via a telephone hotline established for recruitment purposes. Some patients also heard about the study through friends or SAB members. Individuals 18 years or older were eligible for study inclusion. Recruitment was designed to ensure approximately equal participation of people who identified as lesbian, gay, bisexual, or heterosexual, with variation in age and race/ethnicity within each stratum and an a priori goal of 10 patients per group. Qualitative data analysis occurred simultaneously with interviews, allowing researchers to continue recruiting patients until no new themes emerged. Final enrollment was determined by achievement of thematic saturation. Further details regarding patient and clinician recruitment can be found in eTable 1 in the Supplement.
In this qualitative phase, ED professional participants, including physicians, nurses, and advanced practice clinicians, were recruited from 3 community and 2 academic medical centers in the northeastern United States. Interview recruitment was designed to ensure that a variety of staff roles within the ED setting were included, as well as diversity across age and race/ethnicity. Interviews for patients and clinicians were conducted until the point of thematic saturation was reached.
Semistructured interview guides were developed a priori and were pilot tested with LGB and straight individuals as well as health care professionals. Interview guides were revised after piloting and throughout the interview process to ensure effective exploration of emergent themes. Interview guides focused on experiences with sexual orientation collection in the ED, barriers and facilitators to sexual orientation collection in the ED, and preferred means of sexual orientation collection in the ED. All gender identity data collected from interview participants were collected via the 2-step method.20
Qualitative interviews took place between August 6, 2014, and January 28, 2015. All interviews were conducted in person by 1 of 2 researchers (L.M.K. and R.Y.S.) in a private location, and all interviews were audiorecorded. Interviews lasted between 30 minutes and 2 hours, with most interviews lasting approximately 1 hour. Audio data were deidentified and transcribed verbatim prior to analysis.
Interview data were independently coded by 2 researchers (L.M.K. and R.Y.S.) using the constant comparative method.21 An iterative coding process was utilized to identify themes. Transcribed interviews were entered into Atlas.TI for analysis.22 The research team met regularly to discuss any differences in data analysis and ensure consistency. Themes identified in the interviews were used to develop questions for the national survey.
To obtain a nationally representative sample, an international market research firm was contracted to conduct national surveys of patients and health care professionals. Patient survey participants were recruited through GfK’s KnowledgePanel, and provider survey participants were recruited through GfK’s Physician Consulting Network. The GfK Knowledge Panel is the largest probability-based survey panel in the United States and has been used for research ranging from climate change23 to vaccinations.24,25 GfK recruits members for its KnowledgePanel using random digit dialing and address-based sampling techniques to ensure inclusion of households with landlines, cell phone–only households, and households with and without internet access.26 After recruitment, GfK provides households without internet access a computer and internet access to be able to participate in surveys. Participants were eligible if they were 18 years or older, lived in the United States, and consented to participate in the online survey. For the health care professional survey, only physicians and nurses who worked in the ED were eligible to participate. Surveys took place between March and April 2015.
Survey content solicited information on the importance of sexual orientation collection, barriers, facilitators, risks and benefits to sexual orientation collection, willingness to disclose/collect sexual orientation information, and preferred methods to disclose/collect sexual orientation information. Survey items were multiple choice, Likert scale, or open-ended. SAB provided guidance on survey item inclusion and wording. All survey items were pilot tested prior to quantitative data collection. The final surveys had 53 questions (patients) and 45 questions (professionals).
Survey content also included questions on the importance of gender identity collection, barriers, facilitators, risks, and benefits as both sexual orientation and gender identity would be routinely collected in the clinical setting. However, due to the nuances of collecting gender identity and feedback from our SAB, these data will be reported separately.
Likert scale survey questions were grouped into 3 categories: agree/strongly agree, neutral, and disagree/strongly disagree. Descriptive statistics of survey items were calculated.
To understand the differences among patients who would refuse to report SO, participants were grouped into 2 categories according to responses to the question, “I would refuse to provide SO.” Patient participants who agreed or strongly agreed were categorized as refuse, and patient participants who were neutral, disagreed, or strongly disagreed were categorized as would not refuse. Demographic characteristics of patients who would refuse vs not refuse to provide sexual orientation information in the ED were weighted to be proportionally representative at the level of the US national population using weights specifically provided for this purpose by the survey provider26 and differences calculated using χ2 tests. The market research firm that conducted the survey provided the sample weights, which consisted of an equal-probability base sample with poststratification weighting for demographics and final probability proportional to size weighting for the study sample.26 Using this technique, we were able to approximate associations at the level of the population.
The odds of refusing to provide sexual orientation were calculated using stepwise logistic regression. The primary independent variable was SO, and covariates included in the model were sex, SO, age, educational level, race, marital status, rental status, head of household, work status, and income. All data analyses were completed using Stata, version 13,27 including the survey suite of commands. All tests were 2-sided, and a P value <.05 was considered significant.
Seventy-nine people participated in the qualitative interviews: 53 patient participants and 26 health care professional participants. Among patient participants, 9 lesbian, 12 gay, 12 bisexual, 2 queer, 14 heterosexual, and 4 patients who identified as “other” participated in the interviews, thus achieving recruitment goals for a diverse representation of SO. All participants who identified as lesbian identified as female, and all participants who identified as gay identified as male. All clinician participants identified as straight. Of patient participants, 45% identified as black/African American, 43% as white/Caucasian, 9% as Asian, and 8% as Hispanic. Most clinician participants identified as white/Caucasian. Full demographic data are found in Table 1.
Medical relevance, normalization, and recognition emerged as themes when discussing routine collection of sexual orientation in the ED (Table 2). Although clinicians recognized the importance of disclosure of sexual orientation when medically relevant, most patients believed that sexual orientation was always relevant to the ED health care encounter. Many patients stated that sexual orientation was something their health care professional needed to know, and they were willing to provide these data when asked. For example, a bisexual man commented, “[Sexual orientation], like what I eat and how I exercise and stuff...plays a huge part of you know, treating me.” A heterosexual man explained, “You’ve got to ask the questions to everyone because you don’t know them.”
Lesbian, gay, and bisexual patients recognized the importance of collection of sexual orientation not only for their individual encounters in the ED but also for the societal benefits of recognition and normalization of LGB minorities. Many patients recognized that routine collection of sexual orientation as demographic information facilitates normalization and recognition. A queer female explained what routine collection of sexual orientation suggests: “If you are counted, if you are visible, it is sort of another form of recognition at an institutional level.” A gay male echoed the need for institutional and societal recognition: “If the question becomes standard and I think everybody is pushing for those questions to become standard because there are all sorts of things we don’t know about the community—the more those questions become standard, the less people will be surprised by them.”
Conversely, clinicians valued treating all patients the same and thus often described not needing to know their patients’ SO. One ED nurse explained, “If it affected their medical treatment or if it was related to their reason they came to the ED, then I think that was necessary to ask...but if they come here for a cold or if they come here for a laceration...it’s none of my business.” Similarly, an ED physician assistant stated, “If they come in with a broken toe, then I don’t need to know that they’re a lesbian.” These interviews suggest that, although patients recognize the need for collection of SO, some physicians and nurses may not.
The quantitative patient survey response rate was 70.1%, and the clinician survey response rate was 86.2%. Mean (SD) age of patient and clinician participants was 49 (16.4) and 51 (9.4) years, respectively. Additional demographic data for patients and clinicians are found in Table 3. Results from the national survey confirmed the generalizability of the qualitative findings to the national level.
Data on willingness to provide sexual orientation when routinely collected in the ED are presented in Table 4. Patients and clinicians would be willing to provide or collect sexual orientation if assured of confidentiality (52.1% and 87.0%, respectively) or a private space (84.2% and 88.2%, respectively). Similarly, if sexual orientation is documented the same as other demographic questions (eg, race and education), 749 patients (49.4%) and 275 clinicians (64.1%) would be willing to provide or collect the data. When asked whether they would be offended if sexual orientation data were routinely collected in the ED, 159 (10.7%) of all patients agreed. In contrast, 342 clinicians (79.8%) thought that patients would be offended if asked their sexual orientation in the ED. Similarly, 333 clinicians (77.8%) thought that patients would refuse to provide their sexual orientation in the ED; however, only 154 (10.3%) of all patients reported they would refuse to provide such information during an ED health care encounter.
In population-weighted results, 143 (10.1%) straight, 1 (4.8%), lesbian, 3 (12.0%) gay, and 5 (16.4%) bisexual patients would refuse to provide sexual orientation in the ED (Table 5); in examining between-group variation in refusal, significant differences were found between straight and bisexual individuals (χ2 = 5.82; P = .04), gay and lesbian individuals (χ2 = 8.72; P = .02), and lesbian and bisexual individuals (χ2 = 16.5; P < .001). No significant differences were found for refusal to provide sexual orientation by age, race, educational level, or marital status. In unadjusted logistic regression, bisexual patients had 1.73 times the odds of refusing to provide sexual orientation compared with straight patients (95% CI, 1.01-2.98; P = .048). Patients aged 60 years or older had 2.19 greater odds of refusing to provide sexual orientation information (95% CI, 1.04-4.62; P = .04). After adjustment for other demographic characteristics, only bisexual patients continued to have significantly increased odds of refusing to provide sexual orientation compared with straight patients (odds ratio, 2.40; 95% CI, 1.26-4.56; P = .008).
Both patients and clinicians indicated nonverbal self-report as their preferred method of sexual orientation information collection (eTable 2 in the Supplement). This preference was supported by the qualitative interviews, in which patients identified normalization and recognition as major facilitators of sexual orientation data collection.
The results of this study demonstrate that most Americans are willing to disclose sexual orientation in the ED setting. The nationally representative survey data are supported by in-depth qualitative interviews, which suggest discordance between patient and health care professional views on routine collection of SO; although most clinicians believe that patients will refuse to provide sexual orientation information, few patients reported that they would refuse to provide such information. Routine collection of sexual orientation data from all patients signals normalization of LGB minorities within society, and both patients and clinicians identify nonverbal self-report as the preferred method of collection.
Routine collection of sexual orientation information in the health care setting contributes to normalization of LGB individuals within society28; Healthy People 2010 laid out comprehensive recommendations to support health care, education and training, policy and advocacy, and research targeting LGB populations in multiple sectors, including health care and education.29 Normalizing collection of sexual orientation information for every patient creates a dialogue between patients and health care professionals30 and promotes a welcoming, inclusive environment.31 Whereas there are data to suggest that Asian Americans and Hispanics are more likely to refuse to provide sexual orientation on a public health survey than are non-Hispanic whites,32 our data suggest no racial or ethnic differences in reporting sexual orientation in the clinical setting. Previous research in community health settings shows that patients think it is important for health care professionals to know their sexual orientation and that they are willing to provide such information when asked.33 The present study extends these findings to the ED setting, indicating that few patients will be offended or refuse to participate in routine collection of sexual orientation information.
Our data suggest that bisexual individuals are more likely to refuse to provide sexual orientation than are straight individuals, which is in line with previous research.34 Prior research indicates that bisexual individuals experience higher levels of identity confusion35 and disclosure events later36 than lesbian and gay individuals, thus potentially contributing to refusal to disclose sexual orientation in the ED setting. In addition, bisexual individuals have been documented to experience double discrimination, in which both heterosexual and lesbian/gay individuals report higher levels of binegative attitudes than bisexual individuals37; thus, bisexual individuals may be less willing to report sexual orientation to fit into those communities without stigma.
Our findings also indicate that lesbian women are less likely to refuse to provide sexual orientation information than are gay men. Evidence on disclosure of sexual orientation to health care professionals among lesbian vs gay individuals is mixed,38,39 and some researchers theorize that disclosure is more related to sexual identity development than to fear of discrimination.40 Although not statistically significant, our data also suggest that lesbian women are less likely to refuse to provide sexual orientation than are straight individuals. Previous research indicates that LGB individuals think that it is more important to collect sexual orientation information routinely compared with straight individuals33; thus, lesbians may be less likely to refuse to provide sexual orientation than straight individuals.
One of the most striking results of this study is the contradictory views of willingness to provide sexual orientation information between patients and clinicians. Given that federal regulations are moving toward requiring hospitals to collect sexual orientation data,12,41,42 identifying the preferred way to obtain this information among both patients and clinicians is crucial. It is clear that sexual orientation information needs to be asked of every patient, and this study identifies patient preferences for methods of collection. We believe that the next step will be testing different potential approaches for data collection. A trial aimed at doing this is presently under way as part of the EQUALITY study.
Findings from this trial will be especially pertinent as health centers around the country prepare for routine collection of sexual orientation information. Effective implementation of sexual orientation collection will require careful examination of confidentiality, standardization of collection, method of data collection, and cultural competency and training.43 The implementation of Meaningful Use Stage 3 guidelines will mean that any hospital system using a certified EHR will have the capacity to record sexual orientation data,12 thus easing routine collection. Many EDs and hospitals are moving away from paper-based records, providing an opportunity to incorporate electronic tablets into patient care that integrate directly with the EHR. Thus, when a patient registers for care, they could provide sexual orientation as part of demographic information on an electronic tablet, which populates into the EHR that the clinical team uses.
By not routinely asking patients for their sexual orientation information, clinicians may be alienating approximately 3% to 10% of the US population.9 In fact, the importance of normalization and equality for the LGB community44 was a central tenet in the US Supreme Court decision legalizing gay marriage. It appears that society is ready for change in practice to promote such normalization and inclusion of LGB patients. A key component to support changing practice toward routine sexual orientation data collection will be education and training of nurses, physicians, and other staff; several health and LGBT organizations are already leading the way with resources and trainings for this purpose.45
This study has several limitations. First, the qualitative interview sample was from only 1 region of the United States; however, the interviews informed the development of the survey, which confirmed the interview themes in a large, national survey sample. In addition, SAB members provided valuable feedback on both interview and survey questions and results. Second, there is an inability to easily compare patient and clinician survey results with statistical tests owing to differing sampling weights. Finally, the study was unable to discern how patients respond when actively asked sexual orientation information in the clinical setting.
This study also has a number of strengths. To our knowledge, this is the first study to compare patients’ and clinicians’ views of routine collection of sexual orientation information. In addition, both the interview and survey samples contain participants of varying age, race, and ethnicity, and the survey participants live in all regions of the United States, thus contributing to the generalizability of the results. Finally, the mixed methods design provides robust data that could not be captured by qualitative or quantitative methods alone.
Routine collection of data on sexual orientation is important not only for individual patients but also for normalization of LGB individuals within the broader society. This research shows that patients are willing to be asked for such information, are not likely to take offense, and prefer nonverbal collection methods. Routine collection of sexual orientation information in health care is on the horizon46,47 and is necessary to improve health disparities and clinical care for LGB patients. Identifying patient-centered ways to collect this information is imperative to create a welcoming and inclusive environment for all patients.
Accepted for Publication: February 27, 2017.
Corresponding Author: Adil H. Haider, MD, MPH, Center for Surgery and Public Health, Harvard Medical School, Harvard T. H. Chan School of Public Health, One Brigham Circle, 1620 Tremont St, Ste 4-020, Boston, MA 02120 (firstname.lastname@example.org).
Published Online: April 24, 2017. doi:10.1001/jamainternmed.2017.0906
Author Contributions: Dr Haider had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Study concept and design: Haider, Kodadek, Snyder, Vail, German, Peterson, Lau.
Acquisition, analysis, or interpretation of data: Schneider, Kodadek, Adler, Ranjit, Torain, Shields, Schuur, German, Peterson, Lau.
Drafting of the manuscript: Adler.
Critical revision of the manuscript for important intellectual content: Haider, Schneider, Kodadek, Ranjit, Snyder, Schuur, Vail, German, Peterson, Lau.
Statistical analysis: Schneider, Adler, Ranjit, Shields.
Obtained funding: Haider, German, Peterson, Lau.
Administrative, technical, or material support: Adler, Ranjit, Torain, Schuur, German, Peterson.
Supervision: Haider, Schneider, German, Peterson, Lau.
Conflict of Interest Disclosures: Dr Haider is the principal investigator on Health Services grant HU0001-11-1-0023 from the Department of Defense through the Henry M. Jackson Foundation and is a cofounder and equity holder in Patient Doctor Technologies Incorporated, which owns and operates the website http://www.doctella.com. Mr Lau is supported by the Institute for Excellence in Education Berkheimer Faculty Education Scholar Grant contract CE-12-11-4489 from the Patient Centered Outcomes Research Institute (PCORI) and grant 1R01HS024547 from the Agency for Healthcare Research and Quality. No other conflicts were reported.
Funding/Support: This research was funded by PCORI (contract AD-1306-03980).
Role of the Funder/Sponsor: PCORI had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Disclaimer: The views presented in this publication are solely the responsibility of the authors and do not necessarily represent the views of PCORI, its board of governors, or its methodology committee.
Additional Contributions: The Stakeholder Advisory Board members include Adrian Sandra Dobs, MD, MHS (Johns Hopkins Clinical Research Network), Asa Keiswetter, MS, RN, ACRN (Baltimore County Department of Health), Baligh Yehia, MD, MPP, MSHP (Penn Medicine Program for Lesbian, Gay, Bisexual, Transgender [LGBT] Health), Barbara Warren, PsyD, LMHC (LGBT Programs and Policies, Office for Diversity and Inclusion of Mount Sinai Health System), Carl J. Streed Jr, MD (Johns Hopkins Bayview Medical Center), Carlisle Harvey Sr (Greater Baltimore Human Immunodeficiency Virus Health Services Planning Council), Carlton Ray Smith, BA (Baltimore Black Pride), Cheri Charmaine Wilson, MA, MHS, CPHQ (Culture-Quality-Collaborative and Clearview Organizational Assessments-360, Johns Hopkins Bloomberg School of Public Health), Daniel Brotman, MD (Hospitalist Program, Johns Hopkins Hospital), Edward J. Callahan, PhD, MA (University of California, Davis School of Medicine), Emma Elizabeth McGinty, PhD, MS (Johns Hopkins Bloomberg School of Public Health), Harvey J. Makadon, MD (National LGBT Health Education Center, The Fenway Institute), Hilary Meyer, JD (National Programs at Services & Advocacy for GLBT Elders), Ignatius Bau, JD (Institute of Medicine Workshop on Collection of Sexual Orientation and Gender Identity in Electronic Health Records), Jane E. Hill, MPH (Johns Hopkins Hospital Department of Patient Relations), Jean-Michel Brevelle (Maryland Department of Health and Mental Hygiene), Kellan Baker, MPH, MA (LGBT Research and Communications Project, Center for American Progress), Mara Keisling, BA (National Center for Transgender Equality), Monica Stevens Yorkman (Sistas of the “T”), Paula Neira, JD, BSN (Department of Emergency Nursing, Johns Hopkins Hospital), Robert Espinoza, MPP (Public Policy and Communications, Services & Advocacy for GLBT Elders), Shane Snowdon, MA (LGBT Health & Aging Program of Human Rights Campaign), Tonia Poteat, PhD, MPH, PA-C (Johns Hopkins Bloomberg School of Public Health), Vann Michael Millhouse (Black Transmen, Inc), and Paul Howard Krieger, MD (Mount Sinai Beth Israel Medical Center). The board members receive financial compensation.