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Increasing the cultural competence of health care providers serving Minnesota's diverse populations
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Common medical issues and cultural concerns of lesbian, gay, bisexual, and transgender patients
In order to provide equitable and effective health care, clinicians need to be able to function effectively within the context of the cultural beliefs, behaviors, and needs of consumers and their communities.
According to the Office of Minority Health, lesbian, gay, bisexual, and transgender (LGBT) people have limited access to health care services and insurance, and face unique health challenges. Inadequate health care and inadequate health insurance often leads to negative health outcomes and life-long health problems for people in the LGBT community.1
Research also suggests that these negative outcomes may be due to a lack of cultural competence in the health care system, which can be expressed in an unwelcoming and negative attitude expressed by staff toward people in this community. Also important for this community, for example, are medical programs that provide insurance coverage for sexual reassignment surgery and hormone therapy.
Unique Health Challenges
Health issues can often go undetected for this population. For example, data show that lesbian and bisexual women receive less routine care than other women, including breast and cervical cancer screening. It is important for LGBT people to feel welcome and comfortable enough to seek care and routine health screenings, and for health care providers to be positive and tolerant of sexual and gender diversity. Providers and staff are encouraged to recognize that gender nonconformity is not a disorder.
Providers also need to know about the illnesses and health issues prevalent among lesbian, gay, bisexual, and transgender people. For example, more than half of new HIV infections in the U.S. each year are found in bisexual men, and HIV prevalence among transgender women is over 25 percent. And, nearly 30 percent of LGBT youth report having been physically abused by family members because of their sexual orientation or gender identity. 2
Health Data Collection: The First Step to Improving Care for LGBT Populations
A 2011 Institute of Medicine report, The Health of Lesbian, Gay, Bisexual, and Transgender People: Building a Foundation for Better Understanding, recommends data collection of gender identity and sexual orientation on federally supported surveys.
The report outlines a research agenda and identifies gaps and opportunities related to LGBT health. It also provides guidance to state Medicaid agencies on financial protections for same-sex couples and rules requiring hospitals to protect patients’ right to choose their own visitors during a hospital stay, including a same-sex domestic partner.
In 2013, the Department of Health and Human Services began collecting data for identification of health issues and reduction of health disparities among lesbian, gay, bi-sexual, and transgender populations. Under Section 4302 of the Affordable Care Act, federally conducted or supported health care or public health programs, activities, or surveys are required to collect and report demographic data related to designated health disparities. Questions about sexual orientation and gender identity will be integrated into the National Health Interview Survey. Many researchers, including the Williams Institute at the University of California Los Angeles and the Center for Population Research in LGBT Health at the Fenway Institute have been working on such data collection for several years.
In addition to demographic data collection, in 2012, the National Coalition for LGBT Health and the Rainbow Access Initiative began offering opportunities for LGBT consumers to tell their personal health care stories. The collection of stories by LGBT consumers who have previously been left out of the health care conversation, will then be available online. Information collected will be used to improve LGBT health care. Contributors are asked to respond to the following questions:
Health Care for the Transgender/Transexual Population
Within the LGBT population, are a variety of individuals often referred to as transgender whose behaviors tend to vary from conventional gender roles—cultural and social norms generally accepted as appropriate for either a man or a woman in an interpersonal relationship.
Transgender can refer to gender identity or self-identification as a woman, man, or both—although not corresponding to the physical sex assigned at birth (based on genitals). Transgender people may consider conventional terms of sexual orientation inadequate to describe them. Rather, they may identify anywhere on a transgender continuum as heterosexual, homosexual, bisexual, pansexual (all sexual identities), polysexual (many sexual identities), or asexual.
In order for health care professionals to understand how to provide the most effective, culturally competent care for transgender people, the World Professional Association for Transgender Health (WPATH) recently released the seventh revised edition of Standards of Care for the Health of Transsexual, Transgender, and Gender Nonconforming People (SOC). SOC was first published in 1979. SOC is viewed as the standard of reference on caring for the transsexual, transgender, and gender nonconforming population and offers detailed clinical guidelines to address the unique needs of children, adolescents, and adults who require psychological, hormonal, or surgical care. SOC Committee Chair Eli Coleman, PhD, is a Professor and Director of the Program in Human Sexuality at the University of Minnesota.
WPATH promotes evidence-based care, education, research, advocacy, public policy, and respect in transgender health. It recognizes that well-being requires a social climate that eliminates prejudice, discrimination, and stigma, and promotes a positive and tolerant society that embraces sexual and gender diversity.4
tel: 952-854-3306 | toll-free: 1-877-STRATIS