Gateway to Think Tanks
来源类型 | ISSUE BRIEF |
规范类型 | 简报 |
HIV/AIDS Inequality: Structural Barriers to Prevention, Treatment, and Care in Communities of Color | |
Russell Robinson; Aisha C. Moodie-Mills | |
发表日期 | 2012-07-27 |
出版年 | 2012 |
语种 | 英语 |
概述 | Russell Robinson of the University of California, Berkeley Law Working Group on HIV and Inequality and Aisha Moodie-Mills discuss the need for a holistic approach to eliminating racial disparities in HIV/AIDS treatment. |
摘要 | Download this brief (pdf) Read this brief in your web browser (Scribd) For the first time in more than two decades the International AIDS Conference returns to the United States and this week more than 20,000 delegates from nearly 200 countries are in Washington D.C. discussing a wide array of HIV/AIDS related issues, including the troubling racial disparities of our domestic HIV epidemic, specifically:
While the Obama administration has taken steps toward the elimination of these disparities through the National HIV/AIDS Strategy and Implementation Plan, there is still much work to be done. This brief highlights underexplored explanations for these disparities and outlines possible solutions to begin addressing them. Oftentimes, popular culture has offered unfortunately erroneous explanations for the stark racial disparate impact of HIV/ AIDS. The mass media, for example, has suggested that black men “on the down low” infect black women by secretly sleeping with male partners, acting as a bisexual “bridge” between gay and straight communities. But public health scholars have found little support for this theory. Many may assume that black people suffer from greater HIV prevalence because they are considered less sexually responsible than whites. Yet several studies have shown that black women and black men who have sex with men—the two groups most severely impacted by HIV/AIDS—have similar numbers of sexual partners and use condoms as often as their white counterparts. Thus, behavioral risk factors, while important, cannot fully explain the racial disparity. Instead, the racial HIV gap and the racial health gap in general, is strongly correlated with the racial wealth gap, which in turn is the direct outcome of both historical and contemporary processes of segregation in housing, education, employment, and health care as well as racially skewed mass incarceration. In this way, race—as it intersects with poverty, gender, and sexuality among other factors—becomes the embodiment of a multifaceted social exclusion and the rationalization for massive health inequities. The high rates of HIV/AIDS we see among communities of color are not the result of high-risk behavior in these communities, but structural inequalities that make them more likely to come in contact with the disease and less likely to treat it. The racial dimensions of the HIV/AIDS epidemic are best understood in this light. The glaring health inequities revealed by the distribution of HIV/AIDS demonstrate that race is a social index of isolation and impoverishment, disregard, and disempowerment rather than a proxy for divergent sexual attitudes or behaviors—much less genetic traits. Addressing the structural forces that shape the spread of infectious disease—or what the World Health Organization has termed “the social determinants of health”—represents a fundamental and necessary shift from the historic approach to the domestic HIV/ AIDS epidemic. Social determinants are a better predictor of HIV outcomes than risk behaviorsThe social determinants of health—“the conditions in which people are born, grow, live, work and age, including the health system”—weigh more heavily in the cause and course of every leading category of illness than do any attitudinal, behavioral, or genetic determinant. This is the case for heart disease, diabetes, and cancer and it is equally true for the HIV/AIDS epidemic. In fact, the effects of the social determinants of health may be even starker with respect to HIV/AIDS because of its communicable nature. For example, a social determinant like residential segregation influences a community’s access to crucial resources such as housing, education, and health care, and also plays a role in determining with whom, with what frequency, and on what terms people interact with others, both publicly and privately. Similarly, the acute and chronic stress that stems from poverty and experiences of racism, sexism, and other power and resource disparities, can have profound impacts on health outcomes in the case of exposure to HIV/AIDS. Therefore, attempting to combat HIV/AIDS through attitude adjustment and behavior modification alone is incomplete and ineffective. A strictly behavioral focus may also be misleading and increase stigma by implying that individuals’ bad decisions are solely to blame for their poor health outcomes. Raising public awareness about the social, political, and economic conditions that exacerbate HIV/AIDS may combat the racial stereotype that blacks and Latinos suffer from higher HIV/AIDS prevalence because of their irresponsible sexual practices or hyper-homophobic cultures. Governmental entities—international and domestic—have already begun to focus on the social determinants framework. The World Health Organization recommends that we focus on improving daily living conditions; tackling the inequitable distribution of power, money, and resources; and measuring and understanding the impact of interventions, to promote health equity. To this end, the National Institute on Minority Health and Health Disparities, an entity within the U.S. Department of Health and Human Services, has launched the Social Determinants of Health Initiative, which sets out to perform this research. Meanwhile, the Centers for Disease Control and Prevention published a White Paper on the social determinants of health as they relate to inequities in HIV, viral hepatitis, sexually transmitted infections, and tuberculosis in the United States.
This brief builds on the holistic framework promoted by these agencies and further explains the structural forces underlying the stark reality depicted in President Obama’s National HIV/AIDS Strategy. The Obama administration’s efforts have cast an important light on the gross disparities in the distribution of HIV/AIDS in the United States, especially those affecting men who have sex with men, racial and ethnic minorities, youth, and populations of the Northeast and the South. Ultimately, this brief spotlights what the National HIV Strategy recognizes (although the media largely overlooked this development when the president released the strategy): We must move beyond exclusively targeting the so-called risk behaviors of the most vulnerable groups to also address the root causes of those structural inequalities— the distribution of wealth, power, and resources based on real or perceived differences of race, class, gender, sexuality, national origin, and immigration status—that constrain individual and collective agency, generate chronic stress, erode immune system functioning, and block access to effective treatment. In our emphasis on the structural dimensions of HIV disparities, we do not aim to undermine the efficacy of behavioral interventions that have been successful. Rather, our goal is to draw attention to the fact that such interventions alone will never be able to mitigate the harsh racial disparities that HIV statistics depict. By focusing on the structural conditions that perpetuate the high rates of HIV/AIDS among communities of color and the poor in addition to existing behavioral strategies, we can create comprehensive interventions that will yield populationwide results, benefitting racial minorities and others. Building on this insight, this brief identifies key areas related to HIV/AIDS outcomes that are in need of reframing and rethinking if we are to mitigate the epidemic, specifically:
In each case, we offer new directions for research and policy recommendations. Let’s examine each in turn. Residential segregation and housing discriminationGeography is one of the key factors that explain the HIV/AIDS-related disparities we see among racial and ethnic minorities across the United States. The effects of residential segregation and regional disparities combine to raise the prevalence and burden of HIV/AIDS on minority communities. HIV infection rates are so high in some minority-dense urban poverty areas that they are on par with levels seen in Ethiopia and Haiti and meet the United Nations’s definition of a “generalized HIV epidemic.” With the average white person living in a community that is 80 percent white, an average black person living in a community that is more than 50 percent black, and an average Hispanic person living in a community that is 46 percent Hispanic, residential segregation by race and ethnicity remains a reality for many Americans. Americans who live in low-income, predominantly minority neighborhoods are significantly less likely to receive early HIV testing and treatment if they are infected. These differences appear to stem from the deteriorated physical conditions and environmental stressors of these neighborhoods and from their relative remoteness to quality medical testing and health care sites. This segregation condenses a community’s social networks, which ultimately increases the “community viral load”—an aggregation of the individual viral loads across a community. An individual viral load is “an important measurement of the amount of active HIV [in] the blood of someone who is HIV positive,” and reflects the likelihood that an individual will transmit HIV. Therefore, the community viral load is directly correlated with HIV/AIDS risk. A person who engages in an unprotected sexual act with a partner from a distressed neighborhood where the community viral load is relatively high, incurs a much greater chance of contracting HIV than a person who engages in the same sexual act with a person from a more affluent neighborhood with a lower community viral load.29 Just as an individual’s viral load reveals whether the person is receiving HIV therapy and the effectiveness of that therapy, changes in community viral load can indicate effective or ineffective interventions on a broader level. Regional differences in the transmission and treatment of HIV infections also exacerbate racial differences related to HIV/AIDS in this country. As a group, people living in the southern United States are significantly less likely to obtain treatment once infected with HIV, and non-White Southerners may be nearly five times more likely than those in all other regions of the United States, Canada, Australia, and Brazil, to experience serious medical complications once infected. Much of the problem is structural. The persistence of abstinence-only education, failed incarceration policies, and resistance to harm-reduction programs combine to make the risk of acquiring, transmitting, and dying of HIV/AIDS higher in the South than in any other region of the country. Stigma is part of the problem as well. Many residents of the South—particularly regular churchgoers—report that they would delay diagnosis and treatment due to embarrassment about sexually transmitted infections. An emerging line of research has also posited that racially distinctive sexual networks may play a role in increasing exposure to and subsequent infection with HIV. While the media tend to depict men who have sex with men as a threat to black women— either because they reject black women for a “gay lifestyle” or they surreptitiously sleep with women and men on the “down low”—black women and black men who have sex with men have much in common. In particular, they face a dearth of eligible black male partners because of factors such as high unemployment, mass incarceration, and violence and they are constrained to dense sexual networks of disproportionately black partners. As the National Strategy recognizes,39 these patterns, which can be explained by the combination of racial preferences and pervasive residential segregation, may perpetuate and facilitate continued racial disparities in HIV transmission. Studies suggest that nonblack potential romantic partners view both black women and black men who have sex with men as less desirable than whites and other people of color. Whether they prefer black partners or struggle to attract nonblacks, black women and black men who have sex with men often face limited romantic options. These limited options may reduce a person’s leverage in sexual relationships and make it harder to insist on condom use and/or monogamy, which may increase HIV risk. Because experts such as Greg Millett have identified sexual networks as an important possible explanation for racial disparities in HIV transmission, this brief calls for greater funding of innovative research to test this theory. Recommendations
EducationMany HIV prevention and risk-reduction interventions have focused on HIV knowledge, sex education, and the promotion of condom use. Although such policies have effectively decreased sexual risk behaviors, conservatives have often opposed programs such as condom education and distribution. This has led to state and federal support for abstinence and abstinence-only programs. Policies that promote abstinence as the only choice or that withhold important health information place individuals at risk for making unhealthy decisions. Whether or not one prefers abstinence as the solution for unmarried teenagers, the reality is that many young people are sexually active and at risk for HIV/AIDS and other sexually transmitted diseases. In addition, many sex education policies provide a predominantly heterosexual perspective, excluding the health needs of lesbian, gay, bisexual, and transgender adolescents, while indirectly stigmatizing them. Resources, in the form of culturally sensitive information and condoms, must be freely and easily available and offered to all populations but most importantly, to those disproportionately impacted by HIV/AIDS. As the National Strategy notes—“[i]t is important to provide access to a baseline of health education information that is grounded in the benefits of abstinence and delaying or limiting sexual activity, while ensuring that youth who make the decision to be sexually active have the information they need to take steps to protect themselves.” Recommendations
Criminal justiceIncarcerated populations and those under criminal justice supervision (such as parole and probation) represent a large and growing segment of the U.S. population. These groups experience elevated rates of HIV, STIs, and other diseases. Nearly 11 million Americans (who are disproportionately black and Latino) are incarcerated at some point of each year, and an estimated 17 percent of those individuals are living with HIV/ AIDS—a rate substantially higher than that of the general population. Many incarcerated people experience repeated arrests and releases over their lifetimes. Hence, interventions carried out with incarcerated populations have the potential to benefit both the criminal justice system through reduced morbidity and mortality among those for whom government is legally obligated to provide medical care, and the larger society to which incarcerated individuals will return. In-custody transmission of HIV, which can occur through sexual activity, including sexual assault, needle-sharing for drug injection, and tattooing with unsterilized equipment is an important concern. Despite the high risk, less than 1 percent of jails and prisons in the United States make condoms accessible to incarcerated individuals. In the absence of such access, those in custody may engage in unprotected sex or turn to crude methods of protection, such as barriers made from food wrappers or gloves, which are far less effective. In-custody condom distribution has been successfully implemented in most Western European countries and many countries in other parts of the world. Further, although in-custody needle exchange programs have been successfully implemented in a number of international settings, no U.S. prison or jail facilities provide needle exchange. For inmates who are diagnosed with HIV prior to or during custody, continuity of HIV-related treatment post-release is a major concern, as the National HIV Strategy recognizes.63 Both HIV transitional case management programs and collaborations between treatment providers in custody and community settings have the potential to increase the likelihood that HIV-positive people who are released from custody connect to and remain in care. Other strategies, such as releasing those on treatment with 30-days worth of HIV medication, also are promising. Although a few state and local governments and organizations are employing these strategies, they are not sufficiently coordinating their efforts and standards to institutionalize them widely.65 Federal resources to identify model programs and make available the necessary information for replicating them may facilitate more widespread adoption. Particular attention must also be focused on the ongoing impact of incarceration on relationship stability and male-female sex ratios in black and Latino communities.66 The removal of potential and actual sexual partners from society through incarceration has dramatic impacts on the partners and families left behind. Specifically, this removal can condense sexual networks and as a result, increase HIV risk. Further, criminal prosecution has additional dire consequences for individuals, their loved ones, and their communities due to the collateral consequences of conviction such as the termination of government benefits (including housing, food assistance, and financial aid for higher education) that are essential to keeping HIV-positive people in care, difficulty seeking employment due to requirements to disclose prior convictions (and for those convicted of HIV exposure crimes, discussed below, HIV status), and the loss of parental rights. Recommendations
HIV exposure lawsCriminalization under HIV exposure laws is a significant structural factor that deters individuals from accessing HIV testing and perpetuates stigma. As of 2012, 38 states and U.S. territories have laws that specifically criminalize HIV exposure through consensual sex, needle-sharing, or through spitting and biting. Some states do not have HIV-specific laws, but instead utilize general criminal laws like attempted murder or assault, to prosecute HIV-positive people for HIV exposure. A majority of the HIV-specific laws do not differentiate between protected and unprotected sex or require actual transmission of HIV or proof of intent to transmit HIV. Further, they often criminalize conduct that carries little or no risk, such as oral sex. Therefore, the punishment is often grossly disproportionate to the risk/culpability. Moreover, sexual partners of HIV-positive women sometimes use these laws as tools of harassment. Importantly, exposure laws contradict public health messages by putting the full responsibility for HIV prevention solely on the person living with HIV, rather than encouraging all people to ask their sexual partners about their HIV status and to use condoms. In general, a person’s knowledge of his or her HIV-positive status and failure to disclose that status prior to sexual activity with another person is all that is needed for a successful prosecution. This system effectively penalizes HIV-positive people for knowing their HIV status and results in one person’s word placed against another’s as to whether the positive person disclosed his or her status, with the HIV-positive person usually losing. Because people who do not know their HIV status are much more likely to transmit HIV than those who know they are positive, these misguided laws fail to address the root problem. The Obama administration and the United Nations have criticized HIV exposure laws. The U.S. National HIV/AIDS Strategy encourages governments to eliminate or amend such laws to reduce HIV stigma, which is a barrier to testing and leads to poor health outcomes. In a recent hearing hosted by the Global Commission on HIV and the Law in High-Income Countries, U.S. HIV exposure laws were identified by the Global Commissioners as “harm[ing] already marginalized communities facing heightened risk of HIV infection—including migrants, women, MSM, sex workers and people who use drugs.” HIV exposure laws therefore exacerbate the structural forces shaping the HIV epidemic and do not effectively prevent the transmission of HIV. Moreover, HIV transmission laws dangerously feed into this nexus of disparities for blacks and Latinos, conflating the much-needed HIV prevention and care sector with the criminal justice system and often using public health officials as tools of criminalization. Recommendations
ImmigrationImmigrants face complex structural obstacles, which may contribute to their increased vulnerability to illness and a limited range of choices related to their health and well-being. The challenges associated with the migratory process itself are often compounded by having to acclimate to a new environment, lack of documentation, and adjusting to a new language. Several studies demonstrate that foreign-born individuals living in the United States are more likely than those born here to enter into HIV care late, to have low T-cell counts and as a result have a weakened immune system at the time of diagnosis, and to be diagnosed with HIV concurrently with AIDS. Various structural factors explain these patterns. Undocumented immigrants fear “the system,” including the risk that seeking medical help could lead to deportation or other adverse legal consequences. Further, the prospect of HIV disclosure to family members may pose a barrier to diagnosis and treatment. Stigma-management becomes compounded when non-English speakers (often parents) must rely on English-speaking relatives (often their children) to communicate with health care providers. In order to obtain testing or treatment, such immigrants may have to sacrifice a reasonable expectation of medical privacy. People who are known to be HIV-positive may face considerable stigma. The fear of the possibility of domestic violence, for instance, is a strong factor shaping women’s negotiation of access to care, condom use in intimate relationships, and disclosure of an HIV diagnosis. Diversity within immigrant populations also leads to different HIV risk profiles. Diversity of country of origin is one important consideration to develop a better appreciation of specific epidemiological profiles and risk factors across mobile populations. One study, for example, calls for a more consistent recording of country of origin data to help distinguish foreign-born from native-born blacks. In some of the localities lumping both these groups into the category African American could be misleading in crucial ways. The structural barriers facing African Americans may be specifically related to institutionalized racism and poverty, while black immigrants may face these in addition to challenges other immigrants face, such as language barriers. Similarly, researchers must pay attention to diversity among Hispanic groupings in terms of countries of origin as well as mobility, because these characteristics could impact their risk and protective behaviors.96 For instance, Dominicans may negotiate HIV risk and protective behaviors in relationship to the centrality of family reunification as a strategy of immigration among much of this population. By contrast, such negotiations may look quite different for Mexican and Central American emerging immigrant settlements on the East Coast where there tend to be large demographic imbalances between immigrant male presence and largely absent or very small numbers of women. In both cases, men may have sexual activity with partners outside of a primary relationship. Nevertheless, the conditions for risk and protective behaviors among men and women in both populations need to be understood in their distinctness—an important nuance that is often glossed over by relying on terms such as “Hispanic” or “Latino” when describing these populations. Lesbian, gay, bisexual, and transgender immigrants face multiple challenges, which are often rendered invisible by the predominant view of immigrants as heterosexual. Emerging research suggests that sexual minorities access geographical mobility through the resources available through biological families and nonkin relations. This suggests that immigration itself may help immigrants negotiate disclosure, discrimination, and privacy concerns by creating distance between immigrants and their biological families. This separation, however, means that any ongoing support they may need from family abroad will require discretion. Sexual minority immigrant access to HIV prevention or related resources may also require identification and involvement with gay-identified groups, which may or may not appeal to immigrants of various sexual identifications or gender expressions. In addition, the lack of access to federal recognition of their partners or spouses relationships means that family reunification statutes in immigration law do not apply to them. Furthermore, the ongoing need for support from within immigrant communities suggests that migration does not detach these immigrants from the social norms they may seek to escape in the first place. Those living with HIV and migrating to escape stigma may continue to confront stigmatizing views, including within sexual minority communities (based on their immigration status, race/ethnicity, and/or HIV status). The mental health effects of stigma might increase the vulnerability of sexual minority immigrants toward patterns of behavior that put them at increased risk for HIV, such as injection drug use, alcohol consumption, and unprotected anal sex. Women and gender nonconforming people may face the additional challenge of vulnerability to rape and violence. Recommendations
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主题 | LGBTQ Rights |
URL | https://www.americanprogress.org/issues/lgbtq-rights/reports/2012/07/27/11834/hivaids-inequality-structural-barriers-to-prevention-treatment-and-care-in-communities-of-color/ |
来源智库 | Center for American Progress (United States) |
资源类型 | 智库出版物 |
条目标识符 | http://119.78.100.153/handle/2XGU8XDN/435299 |
推荐引用方式 GB/T 7714 | Russell Robinson,Aisha C. Moodie-Mills. HIV/AIDS Inequality: Structural Barriers to Prevention, Treatment, and Care in Communities of Color. 2012. |
条目包含的文件 | 条目无相关文件。 |
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