Bill
H 293
Overview: H 293, "An act relating to health equity data reporting and registry disclosure requirements", was introduced on February 20, 2025 and is currently in the Committee on Ru
Overview: H 293, "An act relating to health equity data reporting and registry disclosure requirements", was introduced on February 20, 2025 and is currently in the Committee on Rules.
Purpose and Intent: The bill aims to address health disparities by enhancing data collection and reporting requirements related to health equity. It seeks to improve transparency and accountability in the healthcare system.
Key Provisions:
- Requires healthcare providers and facilities to collect and report demographic data, including race, ethnicity, language, disability status, and sexual orientation, for all patients.
- Establishes a statewide health equity data registry to track and analyze health outcomes and disparities.
- Mandates the disclosure of health equity data in public reports and on provider and facility websites.
- Directs the Department of Health to develop guidelines and provide technical assistance to support data collection and reporting.
Affected Parties and Impacts:
- Healthcare providers, facilities, and systems would be required to comply with the new data collection and reporting requirements.
- Patients and the general public would have increased access to information on health equity and disparities.
- Policymakers and researchers would have improved data to inform efforts to address health inequities.
Procedural and Timeline Considerations:
The bill is currently in the Committee on Rules, where it will undergo further review and consideration before potentially moving to a vote in the legislature.
Compiled from official sources — confirm details with the bill’s official record.
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