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HITEQ RESOURCES & EVENTS
Office of the National Coordinator for Health IT (ONC’s) Cures Act Final Rule Webinar
Office of the National Coordinator for Health IT (ONC’s) Cures Act Final Rule Webinar

Office of the National Coordinator for Health IT (ONC’s) Cures Act Final Rule Webinar

HHS recently released the Office of the National Coordinator for Health IT (ONC’s) Cures Act Final Rule that will help give patients safe, secure access to their health data, spur innovation, and address industry-wide information blocking practices. The final rule implements interoperability provisions of the bipartisan 21st Century Cures Act and promotes patient access to their health record. Putting patients in charge of their health records is a key piece of patient control in health care, and patient control is at the center of our work toward a value-based health care system. View the webinar recording and slides below for information on the final rule. We also have a website dedicated to the final rule with overview information and detailed fact sheets. This website will continue to be updated on a regular basis with additional resources. 

Colorectal Cancer Screening and Risk Assessment Workflow and Documentation Guide for Health Center NextGen Users
Colorectal Cancer Screening and Risk Assessment Workflow and Documentation Guide for Health Center NextGen Users

Colorectal Cancer Screening and Risk Assessment Workflow and Documentation Guide for Health Center NextGen Users

This Guide provides focused documentation to assist users of NextGen software to improve the process of assessing, documenting, tracking, and following up on colorectal cancer screening. The Guide gives particular attention to assessment of personal and family risk and the tracking and follow-up of screening results that are not addressed in the standard NextGen guidance documents. This work aims to improve health center compliance with HRSA Uniform Data Systems (UDS) colorectal cancer screening (CRCS) through the development and implementation of workflows that produce accurate and reliable structured data and enable proactive outreach and timely follow-up with patients due for CRCS or follow-up testing. This optimization enables health centers to harness broader evidence-based strategies to improve CRCS compliance, and ultimately, health outcomes.

Role of Centers for AIDS Research and Federally Qualified Health Centers (CFAR-FQHC) Partnerships in the Ending the HIV Epidemic (EHE) Initiative
Role of Centers for AIDS Research and Federally Qualified Health Centers (CFAR-FQHC) Partnerships in the Ending the HIV Epidemic (EHE) Initiative

Role of Centers for AIDS Research and Federally Qualified Health Centers (CFAR-FQHC) Partnerships in the Ending the HIV Epidemic (EHE) Initiative

This webinar described the Health Resources and Services Administration's (HRSA) Health Center Program and its engagement in Ending the HIV Epidemic (EHE), as well as opportunity for collaboration between Center for AIDS Research (CFAR) programs and health centers to advance the goals of EHE. This webinar described where Federally Qualified Health Centers (FQHCs) are located, how they are funded, and provided a case study of how they have responded to the EHE funding initiative.

The Role of HIEs in Filling Gaps in Interoperability
The Role of HIEs in Filling Gaps in Interoperability

The Role of HIEs in Filling Gaps in Interoperability

Join Drew Ivan, EVP of Product & Strategy for Corepoint Health and Rhapsody, as he welcomed executives from HIEs in California and Maine for an in-depth discussion on topics, including:

  • The current landscape of healthcare interoperability
  • How HIEs filling gaps in healthcare interoperability
  • Where HIEs are headed
  • Joining the conversation was Shaun T. Alfreds, Executive Director and Chief Executive Officer of HealthInfoNet in Maine, and David Kates, Chief Technology Officer of Manifest Medex, California’s largest nonprofit health information network.
Behavioral Health Consent Management
Behavioral Health Consent Management

Behavioral Health Consent Management

Privacy and confidentiality concerns are currently limiting the inclusion of behavioral health data in electronic health information exchange efforts. ONC has provided a number of tools and recommendations to address some of these concerns.

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