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Over the last 30 years, efforts to prevent new HIV infections among gay and bisexual men have been guided by paradigms that hold individuals responsible for their health behaviors. HIV Care in the United States addresses existing gaps in the collection, analysis, and integration of data on the care and treatment experiences of people living with HIV/AIDS (PLWHA).

These approaches, rooted primarily in social-cognitive frameworks (Halkitis, 2010b), have resulted in maintaining new infections in the United States at a steady state for the last decade (Centers for Disease Control and Prevention [CDC], 2011b). Psychosocial issues among gay and non-gay-identifying HIV-seropositive African American and Latino MSM. This report identifies critical data and indicators related to continuous HIV care and access to supportive services, assesses the impact of the NHAS and the ACA on improvements in HIV care, and identifies public and private data systems that capture the data needed to estimate these indicators.

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