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The Quadruple Aim
Quadruple Aim

A Conceptual Framework

Improving the U.S. health care system requires four aims: improving the experience of care, improving the health of populations, reducing per capita costs and improving care team well-being. HITEQ Center resources seek to provide content and direction aligned with the goals of the Quadruple Aim

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Overview

Data monitoring, from the highest level down to the patient level is critical to identifying trends, gaining insights, and communicating transparently with staff and stakeholders. Data monitoring approaches such as dashboarding are used to display data in a simple and intuitive way, allowing a snapshot of performance on selected measures to see changes or areas for improvement. Business intelligence systems such as population health management analytics allows for the monitoring of the health of a whole patient population, stratified by various characteristics, thereby supporting care planning, resource allocation, and training opportunities. Resources in this section include tools to begin dashboarding, considerations for taking the next step with population health management and guidance on how to navigate the many factors of any data monitoring approach.

Monitoring and Communicating with Data
Event date: 3/11/2020 3:00 PM - 4:00 PM Export event
Office of the National Coordinator for Health IT (ONC’s) Cures Act Final Rule Webinar
Alyssa Carlisle
/ Categories: Health Information Exchange, Privacy and Security, HealthITGov, Webinars, Archived

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

March 2020 Webinar from ONC

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. 
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Resource Links

Acknowledgements

This resource collection was compiled by the HITEQ Center staff with guidance from HITEQ Advisory Committee members and collaborators of the HITEQ Center.