HHS Office For Civil Rights Issues Report on National HIV/AIDS Compliance Review Initiative

Cross-posted from AIDS.gov, originally authored by Jocelyn Samuels.
 

To be free of discrimination on the basis of HIV status is both a human and a civil right. Vigorous enforcement of the Americans with Disabilities Act, . . . the Rehabilitation Act, and other civil rights laws is vital to establishing an environment where people will feel safe in getting tested and seeking treatment. 

—National HIV/AIDS Strategy for the United States

Since 2010, the HHS Office for Civil Rights (OCR) has been proud to serve as a member of the National HIV/AIDS Strategy (NHAS) Implementation Group. As a federal law enforcement agency, OCR is committed to responding to the National HIV/AIDS Strategy’s call for vigorous enforcement of our Nation’s civil rights laws.

Today, we are pleased to release a report on our National HIV/AIDS Compliance Review Initiative [PDF 534 KB]. This important Initiative was initiated in 2014 and 2015, when OCR conducted coordinated compliance reviews at 12 hospitals – one hospital in each of the 12 cities most impacted by HIV/AIDS:  Atlanta, GA; Baltimore, MD; Chicago, IL; Dallas, TX; Houston, TX; Los Angeles, CA; Miami, FL; New York City, NY; Philadelphia, PA; San Francisco, CA; San Juan, PR; and Washington, DC.  Focusing on HIV testing, prevention and treatment services, the compliance reviews examined the ways in which each hospital ensures:  (1) equal access for HIV-positive individuals to programs and services; (2) meaningful access for limited English proficient (LEP) individuals; and (3) the privacy and security of individuals’ health information and their rights with regard to that information.

OCR evaluated each hospital’s policies and practices and found that all of the hospitals under review had implemented some policies and practices to promote equal access and protect health information.  In addition, many of the hospitals had implemented evidence-based interventions to increase the number of newly diagnosed individuals entering or retained in care.  However, OCR also found that in some of the hospitals, there were opportunities for improvement; OCR provided those hospitals with technical assistance.  Today’s report summarizes OCR’s findings and identifies steps that hospitals and other health care providers must take to protect the civil rights and health information privacy of people living with HIV/AIDS.  For example, hospitals and other health care providers (“covered entities”) must:

• Adopt and post Notices and Nondiscrimination Statements which explain that the covered entity does not discriminate on the basis of race, color, national origin, sex, age, or disability, including HIV status;
• Designate Civil Rights Coordinators to establish and implement grievance procedures for patients and consumers;
• Provide auxiliary aids and services to ensure effective communication for individuals with disabilities;
• Take reasonable steps to provide meaningful access to each LEP individual eligible to be served or likely to be encountered in the covered entity’s health programs or activities.  Reasonable steps may include:  (1) the provision of qualified interpreters to LEP individuals when oral interpretation is required to provide meaningful access; and (2) the provision of qualified translators to translate written documents or web content.
• Ensure that such language assistance services are provided free of charge, are accurate and timely, and protect the privacy and independence of LEP individuals. Covered entities, with limited exceptions, are prohibited from allowing children, family members or friends of the patient to serve as interpreters.
• Designate HIPAA Privacy and Security Officials responsible for developing and implementing policies and procedures to protect health information;
• Provide a Notice of Privacy Practices that describes how individuals’ medical information may be used and disclosed and how they can get access to this information;
• Develop and implement policies and procedures regarding individuals’ right to inspect and obtain a copy of their medical records, both in paper and electronic form;
• Evaluate the potential risks and weaknesses to keeping electronic health information confidential, secure, and available and apply sufficient security measures to protect the information; and
• Establish policies and procedures to ensure a notice of a health information breach is provided to affected individuals when needed, to OCR, and to the media (if necessary).

ADDITIONAL OCR ACTIVITY IN SUPPORT OF THE NATIONAL HIV/AIDS STRATEGY

Over the five-year period from FY 2010 to FY2015, OCR opened 145 matters to provide public education and address allegations that people living with HIV suffered violations of their civil rights or health information privacy.

Of particular note, in 2013, OCR launched its Information is Powerful Medicine national campaign, which encourages those living with HIV to be proactive in their medical care.  The campaign explains individuals’ health information privacy rights, including how individuals can monitor and access a copy of their medical records.  The campaign reaches African American men who have sex with men and was featured at Black gay pride events in Atlanta, Chicago, New York City, Oakland and Washington, DC, as well as at the U.S. Conference on AIDS in New Orleans.  To download and share the Information Is Powerful Medicine brochure, poster and/or web banners with others who might find the information useful, visit aids.gov/privacy.

FOR more INFORMATION

• For additional information on OCR’s work on HIV/AIDS issues, visit:  www.hhs.gov/civil-rights/for-individuals/special-topics/HIV/index.html.   
• To file a civil rights or health information privacy complaint with OCR, visit:  http://www.hhs.gov/ocr/filing-with-ocr/index.html.

Jocelyn Samuels is Director of the Office for Civil Rights at the U.S. Department of Health and Human Services.