≥ 92% of participants will know important concepts and factors of health equity.
CEUFast, Inc. is accredited as a provider of nursing continuing professional development by the American Nurses Credentialing Center's Commission on Accreditation. ANCC Provider number #P0274.
CEUFast, Inc. is an AOTA Provider of professional development, Course approval ID#10293. This distant learning-independent format is offered at 0.2 CEUs Intermediate, Categories: OT Professional Issues AOTA does not endorse specific course content, products, or clinical procedures. AOTA provider number 9757.
≥ 92% of participants will know important concepts and factors of health equity.
After completing this continuing education course, the participant will be able to complete the following objectives:
It is sometimes easy to forget when surrounded by our own comfortable environment that our languages, culture, ethnicity, etc., can be unfamiliar to someone else and pose a barrier. For example, imagine you are in Norway hiking on a trail. You get separated from your friends and find yourself lost on this difficult trail. While looking for the way to the main parking area, you trip over a log and injure your ankle. Because of this injury, you are unable to walk. During the fall, you break your phone, rendering it useless. Finally, you see people in the distance and start yelling and waving frantically. You begin explaining your situation when you realize no one can understand you. They start speaking to you in a different language and point to your ankle. Though they may understand you are hurt, you cannot be sure. This situation is nerve-wracking, and it is evident that there is a language barrier. At times, our patients may feel exactly like this.
There are seven billion individuals in this world and over 6,00 languages. It is easy to see how quickly language can become a barrier. The population is increasing and becoming more mobile, blurring traditional language, racial, and ethnic lines. Nearly one-third of the United States (US) population has been identified as an ethnic or racial minority. More than 50 countries report that more than 15% of their population is comprised of immigrants (Kaljee & Stanton, 2011). It is important to be cognizant of the many different cultures and backgrounds of our patients and coworkers.
Culture, bias, age, gender, background, sexuality, and much more help to define our identity and beliefs. We are all unique and deserve appreciation and respect for who we are. Healthcare facilities are responsible for employing staff that reflect their service area and the people they serve. They are also responsible for ensuring staff are educated on cultural issues relevant to their service area and beyond.
Every patient deserves an equal opportunity to be healthy, regardless of any factors or circumstances. Obstacles to health include discrimination, bias, poverty, and a lack of access to equitable healthcare (Gómez et al., 2021). Health equity encompasses and requires fundamental awareness and action in culture and organizational structure. This course will focus on culture and individual variables that are important aspects of health equity.
Health equity is an important aspect of providing competent care. So much so that Healthy People 2020 adopted the term health equity for the first time. To eliminate health disparities, promote independence, and reduce mortality, Healthy People 2030 created and adopted five goals to promote and increase health equity (U.S. Department of Health and Human Services, n.d.).
Beyond the goals of health equity, there are also principles of health equity.
To address the people principle, we should be (American Cancer Society [ACS], 2020):
To address the principle concerning places, we should (ACS, 2020):
To address the partnerships principle, we should (ACS, 2020):
Before defining culture and cultural competency, important concepts of health equity, it is important to provide definitions for common words used when discussing culture.
Race- this is a social construct and term that has been used to group or classify individuals. These classifications have been used to identify and often marginalize people across the globe. Our physical appearance, cultural backgrounds, and social factors help classify our race (National Human Genome Research Institute, 2024). According to the US Census Bureau (2022), there are five major races, and they include:
Unfortunately, prejudice and racism are often tied in with racial identity (Charmaraman & Grossman, 2010).
Both race and ethnicity are social constructs tied to an individual's self-concept and lived experience (Charmaraman & Grossman, 2010).
Social determinants of health- non-medical factors that can influence health. Factors include conditions surrounding where individuals are born, where they live, work, and their age (Centers for Disease Control and Prevention [CDC], 2024c). Other factors include climate change, racism, social policies, and political systems (CDC, 2024d).
When thinking of culture, many equate it to race and ethnicity only. Culture also encompasses shared values, how individuals come to understand their history, and similar behaviors and worldviews. Specific components of culture that may be shared include religious and socioeconomic backgrounds and sexual orientations. There can even be cultures within occupations, such as the nursing culture or military culture. Individuals sharing a cultural belief are often organized into groups and identified by age, gender, and common interests.
Cultural competency- Many definitions of cultural competency exist, and it has evolved over the years. Generally, it means a set of values, behaviors, attitudes, and beliefs allowing effective cross-cultural communication. It represents the ability to:
When discussing culture, it is important to highlight and define types of bias, as many people often see, feel, or experience it.
Facts and Bias
IB is unintentional and attributed to the reflexive neurological system that drives the brain's automatic processing function. As such, an individual's feelings, attitudes, and decisions are involuntary, and their subsequent actions may conflict with their stated views (NCC, 2021). Consequently, the effects of IB can be difficult to identify and measure, and actions resulting from it often are challenging to recognize and control. Healthcare literature describes ongoing IB mitigation efforts, including the promotion of provider awareness, participation in continuing education, advancement of policy development, legislation, and institutional changes, and the contribution of research (FitzGerald & Hurst, 2017; NCCC, 2021; Brecher et al., 2019; The Joint Commission, 2020). Learning about IB (later in the course) and how it differs from explicit bias, recognizing types of IB and how provider-client interactions are affected, and embracing strategies to address its impact on practice are approaches toward reducing barriers to equitable care, closing the gap in health disparities between diverse populations, and achieving patient-centered care.
Some of the social and individual forms of racism have foundational issues that can be traced back for generations in the following categories:
Racial and ethnic minority groups have experienced hardships for as long as anyone can remember. The historical roots of American racism can be traced back to before slavery. Slavery was noted in personal journals in 1619 but is believed to have occurred in the 1400s and 1500s. The nation was divided in the Civil War on the topic and the act of owning enslaved individuals. Specific resistance movements include the Underground Railroad, the Montgomery Bus Boycott, the Selma to Montgomery March, and, most recently, the Black Lives Matter movement (Herschthal, 2022). Each of these movements represents a time when underrepresented populations fought for equality, and many had poor healthcare experiences.
There are specific examples of discrimination in healthcare that have left lasting impressions and resulted in defining types and acts of discrimination and racism.
Throughout history, structural racism has resulted in policies and laws that allocate resources in ways that disempower and devalue individuals, resulting in inequitable access to high-quality care.
Here are some examples of laws that were supposed to promote equality but made systemic issues more difficult:
Because of the history of historical racism, underrepresented groups still struggle today. Interpersonal interactions, professional prospects, and quality of life are all affected by the historical roots of racism.
To better understand IB, consider how it contrasts with explicit bias (EB), which is individuals' or institutions' overt expressions of deliberate bias that tend to be recognizable (Jordan, 2018). EB is attributed to the human brain's reflective system devoted to cognitive processing (NCCC, 2021). Consider the following EB example: A neurosurgeon decides to initiate a patient billing policy that excludes the acceptance of patients' insurance and demands full payment at the point of service. Staff posts a sign in the patient waiting room that states, "As of August 1, 2021, this practice does not accept health insurance." The policy openly favors affluent clients over those without financial means, and the inequitable access to care created by it is deliberate, readily identifiable, and measurable.
IB presents challenges in health care when it manifests itself inappropriately and unconsciously contributes to health disparities.
In 2003, the IOM's formative report, Unequal Treatment: Confronting Racial and Ethnic Disparities in Health Care, laid a foundation for exploration into healthcare disparities in the US, including bias toward patients of diverse racial, ethnic, or cultural populations. The report concluded that "bias, stereotyping, prejudice, and clinical uncertainty on the part of health care providers may contribute to racial and ethnic disparities in health care" (IOM, 2003). More recently, FitzGerald and Hurst's (2017) systematic review of 42 articles discussed robust documentation of IB among nurses and physicians and reinforced the negative effects of professional caregivers' IB on vulnerable populations, including "minority ethnic populations, immigrants, socioeconomically challenged individuals, persons with low health literacy, sexual minorities, children, women, elderly, mentally ill, overweight and the disabled." These reports and studies contribute to the evolving body of knowledge about IB in health care through research and provoke thoughts about the effects of IB on health outcomes.
Multidisciplinary health literature indicates that many factors contribute to health disparities, including "quality of healthcare, underlying chronic conditions, structural racism, and IB" (Petersen et al., 2019). Narayan (2019) cites literature that indicates health care providers' IB is associated with "inequitable care and negative effects on patient care including inadequate patient assessments, inappropriate diagnoses and treatment decisions, less time involved in patient care, and patient discharges with insufficient follow-up." Additionally, Saluja and Bryant (2021), suggest that IB can affect provider-patient communication among people of color. The effects may include "subtle racial biases expressed by providers, such as approaching patients with a condescending tone that decreases the likelihood that patients will feel heard and valued by their providers" (Saluja and Bryant, 2021). Variations in therapy options may also occur based on assumptions about clients' treatment adherence capabilities or presumed health issues.
Additionally, IB may negatively impact clinical outcomes and violate patient trust. Penner et al. (2016) found in a study of oncology patients who were African American and their physicians that patients perceived providers high in IB as less supportive and spent less time with their patients than providers low in IB. In turn, patients recognized those attitudes and viewed physicians with high IP as less patient-centered than physicians low in this bias. "The patients also had more difficulty remembering what their physicians told them, had less confidence in their treatment plans, and thought it would be more difficult to follow recommended treatments." These findings on providers' implicit racial bias underscore patients' perceptions of their experiences with providers' IB. However, its overall effects on healthcare quality and health outcomes for diverse populations invite further exploration (Penner et al., 2016).
A cultural assessment is an important part of a patient visit that can bring forth pertinent knowledge and prevent IB. To care for all patients, including culturally diverse patients, providers should increase their assessment skills and provide thoughtful interventions. Making assumptions about a culture or depending on standard knowledge is inappropriate and may create barriers. An inadequate cultural assessment may result from noncompliance and poor health outcomes, ultimately eroding the patient's trust in the healthcare provider (Kaljee & Stanton, 2011).
Culture
Providers should ensure they are evaluating cultural information that is relevant to the patient's care. The provider should ask open-ended questions to allow the patient to express the situation. The provider should also ask about the patient's thoughts on the illness/injury and how it will impact their lives/quality of life; answers to these questions may reveal important cultural perceptions. The situation's outcome will be enhanced by forming a partnership with the patient and alleviating their fears.
Besides a cultural assessment, healthcare providers should participate in IB testing. Surprising to many providers, the level of IB demonstrated by healthcare professionals is understood to be comparable to the general population (FitzGerald & Hurst, 2017). Given the unconscious nature of IB, directly asking providers about their IB through a self-report survey is not recommended. However, two common methods used to assess IB are Implicit Association Testing (IAT) and Assumption Method (AM).
IAT is a computer-generated online testing method that "measures implicit associations between participants' concepts and attitudes across a wide range of domains: race and ethnicity, disability, sexuality, age, gender, religion, and weight." For over 20 years, web-based IAT data has been collected through Project Implicit, a consortium of researchers from Harvard University, the University of Virginia, and the University of Washington to study and promote the understanding of attitudes, stereotypes, and other hidden biases that influence perception, judgment, and action (Project Implicit, n.d.).
AM is a clinical vignette-based testing method that measures differences across participants' responses. The vignettes are designed to be the same except for one variable, such as gender. Inferences are made based on statistically significant responses correlated with the selected feature, such as the patient's gender. An inference is made that "the response is partly due to the result of implicit processes in the subject's decision-making" (FitzGerald & Hurst, 2017).
Priming is another way to measure reactions related to inherent and subconscious attitudes. The Priming Test is designed to measure the strength of the association between two stimuli, or targets and particular attributes, or primes. The targets are comparable categories, and the primes are associated with those categories. The Semantic Priming Test uses words, and the Visual Priming Test uses images. These tests produce a prime (word or image) on a screen for a specific period before the target is shown. The participant is told to focus on separating the targets. The participant will react faster if the target is more associated with the prime (Ocejo, 2024).
Affect Misattribution Procedure (AMP) is another test used to measure and evaluate IB. The AMP presents multiple images that are assigned to two categories. Examples of categories include products, ethnic groups, or people. The second category may be neutral, such as a gray image. Then, an icon is displayed with a character, judged as positive or negative. According to the measurement logic, the effect associated with the image is transferred to the character (Payne et al., 2005).
These are just some examples of common tests used to measure and evaluate IB. There are others; however, they may not be commonly used, and their validity has not been verified.
The social constructs of race, ethnicity, and culture affect identity in many ways. Cultural identity encompasses the distinctiveness of individuals in a community with shared identities and characteristics (Karjalainen, 2020). Self-perception and self-conception are significant components of cultural identity tied to ethnicity, race, religion, and many other factors.
Unfortunately, with identity comes discrimination for the differences that set us apart. Racial bias, microaggressions, and identity-relevant stressors can, unfortunately, be a part of cultural identity. For many, the formation and modification of identity exist within realms of prejudice and racism. Ethnic and racial discrimination is broadcasted as consistent and unfair treatment within institutions and social structures. Because cultural identity is tied to our very existence, such as school, work, and access to healthcare, the impacts of racism are immeasurable. Racism and discrimination can result in inferiority and a marginalized status, resulting in negative health and quality of life (Yip, 2018).
Because culture, cultural competency, racism, and IB are evident in care, most facilities use a standard tool or model of care to help provide equitable care to all. Madeleine Leininger's theory of cultural care has resulted in the creation of many tools. The foundation of Leininger's theory is based on the idea that each group has important customs and cultural heritage. Leininger's Cultural Care Diversity and Universality Theory and the Sunrise Model arose from this theory. They started the movement of defining cultural care and incorporating concepts of culture within nursing assessment. The Sunrise Model specifically uses components that focus on caring for a patient in a global and multifaceted environment, including characteristics of culture that create an interdependent relationship (Leininger, 2002).
To preserve the cultural atmosphere within the nursing environment, it is crucial that healthcare providers understand these important characteristics and care for each patient individually. From this, transcultural patient care has been created, and several models of transcultural care are used today.
There are six data collection areas within Giger and Davidhizar's Transcultural Assessment Model (2013). This model focuses on the idea that though each culture has different characteristics, they are shared fundamental factors such as (Giger, 2013):
Many areas of care, such as primary, secondary, and tertiary care, utilize the Purnell Model for Cultural Competence. This model is rooted in concepts such as nutrition, social support, communication, development within families, biology, economics, sociology, and anthropology (Purnell, 2002). These many disciplines are conceptualized in this model as a circle; society is depicted as the outer ring, the second ring is community, family represents the third ring, and the inner ring is the person. The twelve domains of the Purnell Model are used as assessment guides and include the following (Purnell, 2002):
This model assumes that healthcare providers all need the same information. The assessment looks at four variables of the individual's functioning, including personal practice, family, health practices, and global society. The model's assumptions include the concept that all cultures have similar core components, but some variations fluctuate with time. This model also assumes that healthcare providers grasp the importance of culture and assess culture while caring for patients.
Another model frequently used is The Process of Cultural Competence in the Delivery of Healthcare Services by Campinha-Bacote (2002). There are five assumptions with this model, including the following:
Our multicultural world is continuously evolving, and this model encompasses the ever-changing and multidirectional roles of culture in our everyday society.
Now that culture has been defined, it is time to review specific cultural and personal variables that may be important to patients.
Religion
Religion denotes shared beliefs and practices. Spirituality encompasses the connection someone feels to something bigger than themselves. It is important to note that individuals with the same religion may possess different practices and beliefs.
It is important to recognize the many different religions that are practiced today. The following list is not all-encompassing, as many other religions and practices exist.
Buddhism- originating in South Asia, this is one of the world's largest religions. In Buddhism, individuals believe that life cycles through a period of suffering and rebirth. The goal is to achieve a state of nirvana, or total enlightenment. Buddhists do not believe in a god or type of deity but believe in supernatural beings that can aid or hinder them on their paths to nirvana (National Geographic Society, 2023). Buddhists also believe in four noble truths, which include the following (Aich, 2013):
Christianity- with over two billion practicing this faith, it is the most widely practiced religion. This religion's center is Jesus Christ and His birth, death, and resurrection. Christians, followers of Christianity, are considered monotheistic, believing in only one God. Christians who believe God sent Jesus to save the world also believe Jesus will return for the Second Coming. This religion is outlined in the Holy Bible (History, 2024a).
The three elements of God include the following:
These three exist as one God and are termed the Holy or Blessed Trinity (Stanford Encyclopedia of Philosophy, 2020).
Hindus also believe in pluralism, which allows for diversity. Those both alike and unlike can connect through unique and varying characteristics with the Divine and on their own. Pluralism allows for increased religious and social freedom (Hindu American Foundation, n.d.).
Islam is the second-largest religion. Like Christianity, it is considered a monotheistic faith, believing in only one God, Allah. Followers of Islam, also known as Muslims, try to live in complete submission to Allah. Muslims follow the Koran, believing there will be a judgment day and that life exists after death (History, 2024b).
There are five pillars to the Islam faith, and they include the following:
Jehovah's Witness- this religion is newer, starting in the 19th century. Jehovah's Witnesses do not believe in the Trinity; they believe Jesus is a separate entity and that the Holy Spirit refers to the power of God. Kingdom Halls serve as a gathering center for Jehovah's Witnesses (Schmalz, 2023). While some of their beliefs are similar to those of Christians, such as living morally by the Bible and aiming to live honestly, they hold unique beliefs and perspectives. For example, Jehovah's Witnesses do not celebrate Christmas or non-religious holidays like birthdays. Jehovah's Witnesses' beliefs also prevent them from receiving blood transfusions (Pavlikova & van Dijk, 2021).
Judaism- this is another older religion that follows monotheism, believing only one God exists. Abraham is the founder of Judaism. Followers of Judaism are referred to as Jews. Jews and rabbis (their spiritual leaders) worship in places called synagogues. Followers of Judaism also follow the sacred text called the Tanakh. The Torah, the first five books of the Tanakh, is more well-known and provides a guideline for Jews to follow (History, 2024c).
Age
There tend to be groups or clusters of people within a cultural group with personal beliefs or characteristics others may not possess. These groups of people share the same cultural beliefs as the group, but each has individual differences, for example, age. Significant differences in physique and development exist between infants, children, adolescents, adults, and aging adults.
Children are impacted by the group's belief about the role of children, with limited communication and cognition. Also, the caregiver's race, ethnicity, and religion may impact the child. The family unit may differ significantly, and culture helps determine the family dynamic's design, roles, and functions (Committee on Family Caregiving for Older Adults et al., 2016).
The aging adult, at times with cognitive limitations and disabilities, must endure the added complications of the group's beliefs about individuals who are aging. The aging adult who is considered a minority will often have poorer health, such as an increase in chronic disease and higher rates of premature death (National Academies of Sciences, Engineering, and Medicine et al., 2017). This subset of the population faces barriers such as ageism, which is prejudice, bias, stereotyping, and discrimination based solely on someone's age (WHO, 2021). Stereotypes include older adults being frail, dependent on others, or unable to contribute to society (Stubbe, 2021).
Disability
Individuals with disabilities have additional experiences and beliefs surrounding their disability, with added complications from the disability, including limitations in cognition, functional abilities, and communication. (Van Herwaarden et al., 2020). Individuals diagnosed with a mental illness will have varying experiences and beliefs about that illness (Snodgrass et al., 2017). Because of the stigma of mental illness, acceptance of treatment may be an obstacle to effective care planning.
With the shift towards diversity and equity, there come barriers to inclusion. Such barriers that patients with disabilities experience include attitudinal barriers, physical barriers, a lack of education, inappropriate education, or organizational and policy barriers.
Attitudinal- Attitudinal barriers are a common and basic type of barrier that can contribute to and lead to the formation of other barriers. Common attitudinal barriers include stereotyping, stigma, discrimination, and prejudice. For example, many individuals tend to assume those with disabilities have a poor quality of life. A disability should not be considered a deficit (CDC, 2024a). Attitudinal barriers further stigma and discrimination and deny others dignity and equal opportunity. Negative attitudes foster a disabling environment and intensify discrimination and other barriers to inclusion.
Physical- Physical barriers also pose a challenge to inclusion, including environmental and structural barriers that prevent access and mobility. Examples of physical barriers include not having a wheelchair ramp or accessible walkways (CDC, 2024a).
Communication- Communication barriers exist for many, including those with disabilities. Disabilities involving reading, writing, hearing, and speaking are more likely to experience communication barriers. Examples of barriers include the following (CDC, 2024a):
Financial- Financial barriers exist for disabled and non-disabled individuals. Financial barriers include a lack of insurance coverage, gaps in insurance coverage that may not cover rehabilitation services, lower income for those who are disabled, confusion, or a lack of information surrounding costs, payments, and insurance coverage. Not only is a lack of transportation a barrier, but so is the cost of transportation (Soltani et al., 2019).
Education can serve as a barrier to inclusion. If education is not inclusive, does not provide information on resources, or introduces bias, it is a barrier to inclusion.
Organizational barriers to inclusion encompass a variety of barriers on administrative, programmatic, and architectural levels. Examples include microaggressions, emotional barriers, jargon, and insensitive behaviors (Abbott & McConkey, 2006).
A policy can implement change. Unfortunately, it can also act as a barrier to inclusivity due to a lack of awareness of laws and regulations, a lack of the ability to enforce them, or a lack of ability to make change. Policy barriers can also include a lack of funding (CDC, 2024a).
Social barriers, often related to social determinants of health, are more likely in those who are disabled. The following are statistics related to social barriers for those who are disabled (CDC, 2024a):
Healthcare barriers exist that can make it more difficult for those with disabilities to get the care they deserve. These barriers include a lack of communication, inconvenient scheduling, insufficient time to care for the patient or explain necessary information, and poor attitudes of providers and staff (CDC, 2024a).
Military
Members of the military often have various beliefs related to the training they had and their warrior status. Examples of beliefs and traits may include hyper-masculine qualities such as stoicism, toughness, assertiveness/aggression, and holding values like self-sacrifice (Shields et al., 2017).
Unfortunately, healthcare is often under-utilized by veterans because they believe that non-military healthcare members are unable to meet their needs due to a lack of understanding of the military experience.
There are many health conditions that military members and veterans are at greater risk of experiencing, such as suicide, infectious diseases, exposure to harmful chemicals, hearing loss, and traumatic brain injuries. They are also at an increased risk of experiencing mental illness, such as anxiety, depression, and post-traumatic stress disorder.
It is pertinent that healthcare providers aim to understand the various branches of the military and what they are likely to experience and move beyond seeing just the physical injuries but the emotional and psychological toll as well (National Academies of Sciences, Engineering, and Medicine et al., 2017).
Mental illness
Culture also influences aspects of mental health and illness. When there is a difference in culture and a healthcare provider does not possess knowledge or awareness of the differing culture, differences become obstacles, and the healthcare provider is less likely to meet the patient's needs (Nair & Adetayo, 2019). Members of racial and ethnic minorities who have a mental illness are:
Cultural barriers for patients with mental illness include the following (Fountain House, 2022; Stubbe, 2021):
Cultural Groups
There are often sub-cultural groups within each culture. For example, there are pockets of health-conscious communities that are vigilant against vaccinations worldwide. Immunizations are often viewed with distrust. It is important to note that individuals within cultures may have differing beliefs due to unique experiences.
Previous nontraditional cultural groups are now increasing in popularity. For example, former nontraditional groups, such as street youth and gay and lesbian youth, are now being recognized as cultural groups. Because of the shared values among these groups, healthcare decisions are sometimes made similarly. Health outcomes may be negatively impacted if healthcare providers do not recognize the patient's identification with these groups (Kaljee & Stanton, 2011).
A safe environment created by healthcare providers is necessary for patients to feel comfortable expressing detailed information about their medical history. Medical records that allow patients to safely identify their sexuality, such as lesbian, gay, bisexual, transgender, queer, and/or questioning (LGBTQ+), can bring awareness to the provider on the potential needs of the patient. The healthcare provider's cultural competency can ameliorate the quality of patient interactions.
Unfortunately, the LGBTQ+ community continues to have negative experiences, especially related to homophobia and unequal healthcare treatment.
The Joint Commission and the IOM have supported the inclusion of gender identity and sexual orientation in electronic medical records (Office of Disease Prevention and Health Promotion, 2022; The Joint Commission, 2011). This information assists with tracking and analyzing health disparities in the LGBTQ+ community.
To help bridge the gap in healthcare disparities that affect the LGBTQ+ community, education on providing culturally competent care is pertinent. Many feel it is necessary and support the inclusion of competencies in curricula that address issues on gender, sexuality, and many other important topics.
Continuing education for all forms of healthcare providers on pertinent LGBTQ+ issues is necessary due to the sparsity of education and literature on issues in this community.
The Healthcare Equality Index (HEI), established in 2007, has been used to designate US healthcare facilities as leaders in LGBTQ+ healthcare equality (Human Rights Campaign, n.d.). Though there is an increased need for diversity in a culturally competent workforce, there is also a lack of resources and abilities to train providers in cultural competence. Cultural competency is a fundamental issue that is necessary to provide appropriate healthcare. It is crucial that healthcare providers champion as patient advocates (Human Rights Campaign, n.d.).
LGBTQ+ encompasses lesbian, gay, bisexual, transgender, and questioning/queer people. It also is commonly used to represent others, such as asexual or intersexual subgroups (Pakianathan et al., 2016).
The nomenclature of the LGBTQ+ community is often changing; it is pertinent that healthcare providers are aware of the newer terms and definitions. The following are definitions of terms (Human Rights Campaign, 2023).
There have been many studies that have documented healthcare disparities that involve the LGBTQ+ communities. For example, research has established that bisexual and lesbian women are less likely to receive preventative cancer screenings, specifically breast, colon, and cervical screenings (Pakianathan et al., 2016).
Other inequalities in healthcare delivery to the LGBTQ+ community include substance use and sexual and mental health. To bridge these inequalities, healthcare providers must be culturally aware and competent (Pakianathan et al., 2016).
Sexual health is defined as mental, physical, and social well-being concerning sexuality. Sexual wellness encompasses individual and positive approaches to sexuality, with the goal of safe and pleasurable experiences that are free of discrimination, coercion, and violence (WHO, n.d.).
Sexual health is intricate to the legal, political, cultural, and socioeconomic fabric that provides context and awareness to the lives of LGBTQ+ members. While more awareness and acceptance have been shed on the LGBTQ+ community, such as the increased prevalence of transgender diagnoses (Ettner et al., 2016), there is still much work to be done. For example, until 1992, homosexuality was equivalent to having a mental illness (Hegazi & Pakianathan, 2018).
There is often fear when disclosing sexual orientation; this can lead to increasing rates of various sexually transmitted diseases, including human immunodeficiency virus (HIV) in men who have sex with men or patients who identify as gay or bisexual; this is especially true in areas where sexuality can be criminalized (Hegazi & Pakianathan, 2018). Even in areas where anti-discrimination legislation exists, members of the LGBTQ+ community may get attacked for public displays of affection. In many places, especially in poorer countries, there are reports of increased bullying and poor access to healthcare (Hegazi & Pakianathan, 2018).
Among the LGBTQ+ community, there are higher rates of depression and anxiety, suicide, and drug and alcohol dependence (Hegazi & Pakianathan, 2018). Men who have sex with men are six times more likely to commit suicide when compared to men who have sex with women (Hegazi & Pakianathan, 2018). There are complex and multifactorial causes for these health disparities among the LGBTQ+ community.
Gender dysphoria is a newer medical term that helps to explain dysphoric symptoms that some individuals experience. As patients who are transgender transition medically and socially, they often experience unique challenges. Providers must remain aware of the need for effective care and appropriate support during their transition. More research is necessary on transgender health and communities.
Most of the literature and research that has been performed has focused on patients who are transitioning from male to female. Due to the stigma and discrimination often faced, there is a greater need for gender affirmation. Because of the specific challenges faced by those who are transgender, they may be more susceptible to certain issues. For example, vaginal atrophy may occur in men who are transgender and who are receiving testosterone therapy; this may make them more susceptible to sexually transmitted diseases, especially HIV.
Compared to heterosexual women, lesbian and bisexual women have a lower incidence of sexually transmitted diseases. Bisexual women are also more likely to have an increased number of sexual partners and experience cervical cancer and chronic pain. Healthcare providers must always assess sexual history appropriately and thoroughly.
Bisexual and lesbian women are more commonly affected by bacterial vaginosis. Human papillomavirus (HPV)-related cancers have been found in females participating in female-to-female transmission of genital HPV where there are instances of cervical neoplasia. Even with this, lesbian and bisexual communities have low rates of cervical cancer screening. Compared to heterosexual men, homosexual men are likely to experience increased rates of HPV-associated anal cancers.
Patients may view healthcare interventions differently based on cultural differences. In 1932, the Tuskegee experiment began under the direction of the Public Health Service and the Tuskegee Institute. The goal of the experiment was to examine the history of syphilis in hopes of justifying interventions among black patients (CDC, 2023b).
Six hundred black men were enrolled in the study without any informed consent being obtained. Patients were being told they needed to be treated for a "bad blood" condition. The study, which was supposed to last six months, lasted 40 years. Even though penicillin was chosen for this disease, the patients enrolled in the Tuskegee experiment did not receive adequate treatment. The Assistant Secretary for Health and Scientific Affairs appointed a panel to review the study in 1972 (CDC, 2023b).
The panel concluded that the study was ethically unjustified and the knowledge gained was not worth the risks the participants were exposed to. The panel review resulted in a class-action lawsuit with an out-of-court settlement. To provide healthcare benefits to the remaining participants and their widows and children, the government created a program for which the CDC eventually became responsible. This unjust experiment led to the creation of the National Research Act, which was signed into law in 1974. Then, the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research was created, which also led to the development of the National Bioethics Advisory Commission in 1995 (CDC, 2023b).
The evil and inexcusable Tuskegee experiment had many negative outcomes. For example, African American patients often chose to avoid any preventative healthcare, especially when healthcare was supported by the federal government. However, with the advancing diverse healthcare workforce, some attitudes among minority groups are changing. However, a lot of work is still necessary. Because of the Tuskegee experiment, new laws on ethics within research have been established, heightening cultural competency awareness.
Medicine and healthcare have shifted from a paternalistic view to one where patients actively participate in their care. Healthcare providers should aim to provide services that align with patient values. Previously, discussing a patient's culture was considered to be taboo. Now, with the evolution of patient care, identifying patients within a cultural group and discussing this has been associated with improved health outcomes and patient trust.
Becoming culturally competent is one of the main strategies used to eliminate healthcare disparities. Cultural competence, known to enhance healthcare practices, is a key aspect of practice and policy.
Different cultures perceive the role of healthcare providers differently. Some view the healthcare provider as a trusted confidant who can provide valuable and necessary advice. Other cultures view the healthcare provider's advice as an intrusion. Healthcare providers must adjust their approach to care based on the patient's background and expectations.
The Agency for Healthcare Research and Quality and the Office of Minority Health of the US Department of Health and Human Services (n.d.) created the National Standards on Culturally Linguistically Appropriate Services (CLAS). These standards are recommendations, mandates, and guidelines for eliminating racial and ethnic health disparities. The idea behind CLAS is that improved communication specific to various racial, social, and ethnic groups would improve health status.
Principal Standard
Governance, Leadership, and Workforce
Engagement, Continuous Improvement, and Accountability
Standards 4-7 must be maintained in health organizations that receive federal funding. Many states now follow this guidance by enacting cultural competency legislation.
Communication is a form of self-concept, and when performed with intention and clarity, it is very effective. Unfortunately, communication can also be harmful and detrimental. It is important to implement communication techniques to avoid misinterpretation or miscommunication.
Cross-cultural communication, also called intercultural communication, involves basic communication elements, including specific language, preparedness, openness, and awareness. Cross-cultural communication promotes inclusion while breaking down cultural barriers. Effective and intentional cross-cultural communication aims to change how language is delivered across various backgrounds (Aririguzoh, 2022).
In healthcare, effective cross-cultural communication can lead to increased cultural competence. Many healthcare providers can use the LEARN model to build cultural competence, enhance communication, and increase the quality of patient care and interactions.
Listen- Assess the patient's understanding of health and disease. Providers should be humble and curious, which promotes foundational trust.
Explain- Convey health perceptions without bias and be open-minded to others' understanding of health based on culture.
Acknowledge- Respect the differences in views, perspectives, and understandings.
Recommend- Propose and develop a care plan through understanding, support, and collaboration.
Negotiate- Incorporate culturally relevant interventions in partnership with the patient (Ladha et al., 2018).
While this model may be very effective, additional steps can be taken to ensure effective communication in certain populations. Specifically, there are steps to take to minimize ageism and promote effective communication with the older adult population. Before encountering the patient, recognize the possibility of transference and countertransference. Misconceptions and assumptions should be avoided. Age-related stigmatizations should be recognized, and it is important to create a welcoming and judgment-free environment where the patient and their family feel comfortable. Proactive engagement should be fostered and supported, and the healthcare provider should provide education that empowers the older adult. The healthcare provider should also utilize techniques that promote patient autonomy, such as requesting permission to speak with the caregiver or family members that are present, ensuring the patient actively participates in their care, and, when possible, allotting extra time during appointments for questions. Healthcare providers must optimize the patient's strengths and resiliencies while providing resources to support the patient (Stubbe, 2021). Beyond these steps, a team-based approach and collaboration with other providers are always recommended.
Now that we have covered the steps to promote effective communication and appropriate services and learned the definition of IB, it is time to discuss how to mitigate IB while promoting culturally competent care.
Healthcare professionals typically intend to provide optimal patient care, but IB may negatively impact their aim. Strategies to disrupt IB, such as promoting self-awareness and participation in formal training, suggest that biases learned earlier in life may be mitigated (FitzGerald et al., 2019). Efforts to define consistent, evidence-based bias reduction strategies are advancing, and evaluation is ongoing. Meanwhile, learning about types of IB and how they may affect health care remains important. Likewise, supporting institutional changes is necessary to sustain meaningful, ongoing mitigation efforts. The literature is rich with resources to mitigate IB, including but not limited to the following topics:
Learning about common types of IB and their unintended effects on health professionals and patients is a strategy for building IB awareness. The following list is not intended to be exhaustive but to present a range of IBs that may influence provider-patient or institutional decisions (Brecher et al., 2019; NCCC, 2021; Haghighi, 2021). Reflect on how your beliefs may confirm or conflict with the examples and how you might be affected in these scenarios:
There are legal standpoints of equality and discrimination that have migrated into healthcare. Based on Title VI of the Civil Rights Act of 1964, federally funded programs do not allow discrimination based on color, race, and nationality (Hegazi & Pakianathan, 2018). Therefore, federally funded healthcare programs have to provide equal care to all. Title VI also mandates equal care for those with limited English-speaking skills. Other title mandates require language assistance (Hegazi & Pakianathan, 2018), including Medicaid, Medicare, and state children's health programs.
Recognizing the need to mitigate IB, address health disparities, and further ensure the quality of care provided by licensed healthcare providers among diverse populations, required IB health provider training is emerging across the US. These laws empower policymakers, healthcare licensure boards, and healthcare settings to positively improve health professionals' IB knowledge to change care systems. Likewise, they present opportunities for data collection to measure IB changes and evaluate patients' health outcomes over time. The following list includes examples of recent legislation to address IB in professional health care:
Specific laws are set to protect certain populations, such as older adults. For example, the Older American Act was passed in 1965 to increase community and social services for older adults. However, since its enaction, several law reauthorizations have been made to provide specific provisions. The reauthorizations include guidance on aging and networking and protections for vulnerable older adults while increasing programs that aim to promote elder abuse screening while preventing its occurrence (Administration for Community Living, 2023). The Elder Justice Act of 2010 addresses neglect, exploitation, and abuse of older adults on a federal level. It also provides guidance on resources for prevention, awareness, and detection (Tilghman, 2013).
There are different ways to promote health equity. Examples include the following (National Institute on Minority Health and Health Disparities, 2024):
Policies, practices, and programs should aim to do the following (CDC, 2024b):
Scenario/situation/patient description
A 66-year-old Hispanic male resides in a rural community. He contacted his primary care provider's office with the following complaints: temperature of 100.2 degrees for three days, headache, body ache, fatigue, and nasal congestion with a runny nose. They underwent a COVID-19 polymerase chain reaction (PCR) test at their local pharmacy yesterday, received their positive test result today, and are anxious to speak to their healthcare provider about treatment.
Intervention/strategies
A telehealth appointment is conducted with their healthcare provider. The patient's condition warrants community-based treatment, and strategies are discussed. The patient specifically asks about medication to cure Covid-19. They had heard about it from a friend and believed many people get it through their local livestock supply store. Their healthcare provider responds that they understand from speaking with other local healthcare professionals that some recommend Ivermectin therapy, which is also available for livestock. The healthcare provider proceeds to write that prescription to be filled at the pharmacy.
Discussion of outcomes
The CDC reports that the US Food and Drug Administration has not authorized using Ivermectin to prevent or treat COVID-19 (CDC, 2021). Likewise, Ivermectin has not been recommended by the National Institutes of Health's COVID-19 Treatment Guidelines Panel for treating COVID-19. The healthcare provider's decision to prescribe this medication appears to be influenced by their IB to conform with their patient's request and some colleagues' anecdotal treatment recommendations. It is not an evidence-based treatment decision. Rather, the treatment decision is consistent with conformity bias, a type of IB.
Strengths and weaknesses of the approach used in the case
Typically, healthcare professionals intend to provide optimal care to all patients, but IB may negatively impact their aim. Conformity bias is an IB associated with the tendency to be influenced by other people's views (Brecher et al., 2019).
Our nation is a vessel for many ethnic nationalities, with many subcultures and healthcare ideas. Healthcare professionals are the caregivers responsible for caring for many patients, including those of different backgrounds and cultures. Cultural competence, a continual process of understanding, learning, and advocating, is essential in healthcare. It is important to identify conflicts and awareness of internal ideas and beliefs. Healthcare providers should seek ways and resources to understand ways to care for a diverse population.
IB is the unconscious and, therefore, the unintentional human tendency to make decisions based on inherent factors rather than evidence. No one is immune, not even healthcare professionals. Recognizing common types of IB by building self-awareness and participating in voluntary or mandatory training are steps health professionals may take to minimize its impact on care. Likewise, state governments' mandates specific to IB in healthcare are embedding training across health professions and care settings into law. More research is needed to measure how IB training may change health providers' short- and long-term beliefs, practices, and patients' perceptions. Ultimately, these steps are intended to minimize IB among healthcare providers, reduce barriers to equitable care, close the gap in health disparities between diverse populations, and meet patients' needs. Minimizing IB and promoting cultural competence will increase health equity for all.
CEUFast, Inc. is committed to furthering diversity, equity, and inclusion (DEI). While reflecting on this course content, CEUFast, Inc. would like you to consider your individual perspective and question your own biases. Remember, implicit bias is a form of bias that impacts our practice as healthcare professionals. Implicit bias occurs when we have automatic prejudices, judgments, and/or a general attitude towards a person or a group of people based on associated stereotypes we have formed over time. These automatic thoughts occur without our conscious knowledge and without our intentional desire to discriminate. The concern with implicit bias is that this can impact our actions and decisions with our workplace leadership, colleagues, and even our patients. While it is our universal goal to treat everyone equally, our implicit biases can influence our interactions, assessments, communication, prioritization, and decision-making concerning patients, which can ultimately adversely impact health outcomes. It is important to keep this in mind in order to intentionally work to self-identify our own risk areas where our implicit biases might influence our behaviors. Together, we can cease perpetuating stereotypes and remind each other to remain mindful to help avoid reacting according to biases that are contrary to our conscious beliefs and values.