The AHIMA Advocacy Agenda
Our mission of "empowering people to impact health" is rooted in our founder's belief that great possibilities are achieved when we work together toward a common goal.
At AHIMA, our common goal is to transform health and healthcare by connecting people, systems, and ideas. This transformation starts with the most powerful currency for change in the healthcare ecosystem: health information.
The AHIMA 2023 advocacy agenda will leverage our knowledge and expertise of health data and information to influence the public policy environment for the benefit of individuals, communities, clinicians, and the healthcare workforce. Download our agenda to learn more. To read our policy statements, click each statement’s link within our agenda.
Upcoming Event
2023 AHIMA Advocacy Summit: Register Today
The AHIMA Advocacy Summit is where health leaders and policymakers come together to address important key policy issues related to health data and health information.
You may earn up to 13 CEUs at this two-day event, taking place March 20–21, 2023, in Washington, DC, which includes a Public Policy Institute on March 20. AHIMA members also have an opportunity to advocate for issues impacting the health information profession to their elected officials at our Capitol Hill Day on March 21.
Watch a video message from AHIMA’s Lauren Riplinger, Chief Public Policy and Impact Officer.
Latest Advocacy News
How Do the New EHI Definition and Information Blocking Provisions Impact Your Organization?
By October 6, 2022, actors are expected to adhere to the full scope of EHI per the information blocking final rule, or else risk noncompliance. AHIMA22 attendees will hear directly from the policymakers and others working to implement information blocking and its related provisions at a session moderated by the AHIMA Policy and Government Affairs team.
AHIMA Policy Statements
- Individual Access: Enhance individuals’ electronic, timely, and seamless access to their health information.
- Consumer Engagement: Empower individuals to make better decisions about their own health by using trusted data from traditional and emerging data sources.
- Affordability: Ensure patients have access to timely and accurate information about the cost of healthcare services to make informed care decisions, including information about their expected out-of-pocket costs.
- Privacy: Address privacy and security gaps of HIPAA non-covered entities that collect, access, use, disclose, and maintain electronic health information.
- Cybersecurity and Information Security: Enhance and improve the sharing of cyber threats, risks, and cyber hygiene practices in real-time.
- Behavioral health: Encourage policies that further integrate and coordinate behavioral health information with physical health information.
- Healthcare Reform: Promote the continuity of accurate, timely, and trusted health information regardless of health insurance coverage.
- Data Quality: Advance the completeness, accuracy, and timeliness of health data by influencing the development and maintenance of national and international coding standards.
- Data Integrity: Influence and advance policies that promote the accuracy, consistency, and trustworthiness of health information regardless of its form, origin or application.
- Health Equity: Advocate for the collection, use, and sharing of accurate, unbiased, complete, and standardized health information as an integral part of efforts to reduce and eliminate health disparities and inequities.
- Value-Based Care: Promote new payment and delivery models that leverage accurate, timely, and complete health information—as well as technology—in new and innovative ways.
- Telehealth and Remote Patient Monitoring Technologies: Expand access to care through the use of telehealth and remote patient monitoring technologies, while ensuring the continuity of accurate, timely, and trusted health information and also protecting patient confidentiality, privacy and security.
- Patient Identification: Enhance accurate patient identification to improve patient safety, interoperability, and the appropriate use of workforce resources.
- Integrating Clinical and Administrative Data: Enhance and influence efforts to better integrate clinical and administrative data to improve the patient experience, reduce clinician burden, and potentially reduce costs.
- Interoperability: Champion modern data standards (including application programming interfaces) and related infrastructure to support technical, functional, and semantic interoperability across healthcare.
- Public Health: Advocate for the use of accurate and timely data for public health responses and initiatives while protecting the confidentiality, privacy, and security of an individual’s health information.
- Social Determinants of Health: Promote the collection, access, sharing, and use of social determinants of health (SDoH) to enrich clinical decision making and improve health outcomes, public health, and health inequities in ways that are culturally respectful.
Advocacy & Policy Council
The Advocacy and Policy Council advises our leadership and Board of Directors on critical areas for AHIMA’s strategic engagement in advocacy and public policy that align with our mission and vision.
Living the Pledge
As a health information professional, you understand the cost of patient misidentification. Enter a competition and tell us how you or your organization are living the Naming Policy Pledge.
