The National Native American AIDS Prevention Center (NNAAPC) realesed the following press release to commend the CDC report that raises awareness of the need to close the gap in treatment disparity, specifically among Native people. The NNAAPC helps organizations that serve Native communities to plan, develop and manage HIV/AIDS prevention, intervention, care and treatment programs.
In 2011, Gardner, et.al. released research findings regarding the state of HIV care and treatment in America, and the gaps that exist in working with those people living with HIV to benefit from modern biomedical and treatment options. Out of all of the individuals with HIV in the U.S. , only 80% are aware of their status, 62% have been linked to care, 41% stay in care, 36% get antiretroviral therapy, and only 28% are able to achieve an undetectable viral load through medication adherence. The disturbing results have been widely disseminated and are now commonly referred to as the “treatment cascade”. The treatment cascade coupled with research demonstrating that viral suppression through medication adherence is one of the most effective HIV prevention strategies available and has changed the face of HIV and AIDS prevention in the America. The current focus is shifting to the importance of biomedical interventions and ensuring that people living with HIV or newly diagnosed are linked to stable systems of care and disease maintenance.
The Centers for Disease Control and Prevention (CDC) released on a supplemental surveillance report in January 2013 titled Monitoring Selected National HIV Prevention and Care Objectives by Using HIV Surveillance Data—United States and 6 U.S. Dependent Areas—2010. This report details important statistics on linkage to care, retention in care and viral suppression—all of which are leading health indicators for people living with HIV and are now indicators of successful prevention and treatment efforts. Data were collected from 14 U.S. jurisdictions (Delaware, District of Columbia, Illinois, Indiana, Iowa, Minnesota, Missouri, Nebraska, New York, North Dakota, California [San Francisco], South Carolina, West Virginia, and Wyoming). This sample, while not encompassing all areas within the U.S., is geographically diverse and includes some very large American Indian, Alaska Native and Native Hawaiian populations.
“The CDC should be applauded for releasing these data during this time of shifting prevention priorities,” said Robert Foley, President/CEO of the National Native American AIDS Prevention Center. “However, the disparity continues to grow and this report should serve as a call to action for all parties working for the health and wellness of American Indian, Alaska Native and Native Hawaiian people. HIV and AIDS in America cannot be eradicated and there is no hope of ‘reaching zero’ if these trends are left unaddressed.”
According to the report, American Indians, Alaska Natives and Native Hawaiians are not accessing or receiving the care and attention that they require to in order to maintain their health after an HIV diagnoses.
·Only 0.4% of American Indian/Alaska Native (AI/AN) and 0.1% of Native Hawaiian individuals (13 years or older) that tested positive for HIV during 2010 were linked to medical care within 3 months after their diagnosis. This is compared to 50.6%, 32.8%, and 11.9% for Black/African Americans, Whites, and Hispanic/Latinos, respectively.
·Only 0.3% of American Indian/Alaska Native (AI/AN) and 0.1% of Native Hawaiian individuals (13 years or older) that were diagnosed with HIV in 2008 had achieved viral suppression by the end of 2009. This is compared to 44.8%, 38.0%, and 13.2% for Black/African Americans, Whites, and Hispanic/Latinos, respectively.
This is an alarming trend. When these statistics are viewed beside the statistics that were released by the CDC in 2012 that stated new HIV infections among AI/AN people increased by 8.7% from 2007 to 2010. It is becoming apparent that changes need to be made and action must be taken in order to meet the needs of Native Americans newly diagnosed and living with HIV.
“Knowing what we know now about how to conduct effective HIV prevention and care, it is shocking to see how few Native people are accessing the care that they need. Hopefully, this report can serve as a call to action,” asserted D’Shane Barnett (Mandan/Arikara), chairman of the National Native American AIDS Prevention Center (NNAAPC). “Governmental organizations and federal decision-makers must pay attention to these trends and realign funding and resources to Native communities in order to ensure that Tribes and Native healthcare systems have the capacity to create and sustain linkage to care programs, that HIV medications are readily available, and that adherence programs and treatment regimens are culturally responsive.”
“Native communities need to examine their internal systems in order to ensure that they have processes and staff in place to work with people who are newly diagnosed to assist them with navigating a potentially confusing systems of care,” stated Mr. Foley. “And there needs to be persistent efforts to combat community-based stigma caused by fear, misinformation, and discrimination. These continue to serve as barriers to people who know they need to access care, but are fearful of the social ramifications of doing so. This report is a new signpost laying out the path that we have to follow.”
The CDC report can be viewed on the CDC website at: http://www.cdc.gov/hiv/surveillance/resources/reports/2010supp_vol18no2/pdf/hssr_vol_18_no_2.pdf#page=1