In support of our vision of a world where trusted information transforms health and healthcare by connecting people, systems, and ideas, we’re advocating for legislation and regulations in the following areas.
Consumer Access: Empower the electronic, timely, and seamless access of health information to consumers.
Privacy and Security: Protect consumers by addressing existing privacy and security gaps in the protection of health information held by HIPAA non-covered entities.
Information Sharing: Strengthen health information sharing policies by aligning the 42 CFR Part 2 regulations, which govern confidentiality and the sharing of substance use disorder treatment records under HIPAA. This would allow for the appropriate sharing of substance use disorder treatment records for purposes of treatment, payment, and healthcare operations.
Cybersecurity: Protect consumers by improving information sharing about cyber threats, risks, and cyber hygiene practices in real time.
Patient Identification: Repeal the existing ban on the use of federal funds to promulgate or adopt a unique patient identifier (UPI) to enable the US Department of Health and Human Services (HHS) to identify a national solution to address patient misidentification.
Interoperability: Lead efforts to establish a common set of data standards (including application programming interfaces) and related infrastructure to ensure semantic, technical, and functional interoperability across the healthcare ecosystem.
Integration of Clinical and Administrative Data: Transform and influence efforts to improve the use of new approaches to better integrate clinical and administrative data through data standardization, standardized templates, improvements in technology, and electronic transmission of information.
Medical Coding Standards: Strengthen the quality of healthcare data by influencing the development and maintenance of national and international medical coding standards.
Trusted Health Information: Guide and advance standards-based documentation and documentation integrity best practices to generate reliable and trusted information for care continuity, quality improvement, research, population health, reimbursement, and other purposes.
AHIMA Policy Statements
Integrating Clinical and Administrative Health Data
AHIMA supports the use of policy and other tools to realize the benefits of greater integration of clinical and administrative data, including improved patient experience, decreased administrative costs, reduced provider burden, and improved quality of care and outcomes.
AHIMA supports the accurate identification of patients to enhance patient safety, while also improving interoperability and the appropriate use of workforce resources. Health information professionals have extensive knowledge and expertise to inform and advance public policy that seeks to improve the accuracy of matching patients to their health information.
Health Information held by HIPAA non-covered entities
AHIMA supports the use of policy to address existing privacy, confidentiality, and security gaps in the protection of health information held by Health Insurance Portability and Accountability Act (HIPAA) non-covered entities. Federal privacy and security baseline standards should be developed for the protection of health information held by data holders outside of the scope of HIPAA.
From U.S. Government