Creating a Learning Health System
Latest Posts
Making FY19 The “Year of Data Quality” for Medicaid
MITRE’s Rebecca Bruno shares perspectives on CMS efforts to achieve Medicaid data quality to improve its oversight functions and provide data to the public that can be used effectively by researchers and stakeholders. For a program that provides health...
Harmonizing Data and Facilitating Its Use Across Entities to Advance the Learning Health Care System
The promises of a learning health system are endless. Intelligent automation could reduce clinician burden. Clinical decision support systems may lead providers and patients to the best treatment option. Major federal initiatives are focused on putting the...
Opportunities to Improve Care Coordination and Patient Engagement Among Medicaid Beneficiaries
Highlighting research presented at the Academy Health Annual Research Meeting (ARM) in June 2018, Rebecca Bruno points in this blog post to solutions for addressing social determinants of health and improving health outcomes and reduced costs of care for...
Who’s using health data from your fitbit and smartphone?
The importance of ethical standards for consumer-generated data use in healthcare was a hot topic at AcademyHealth's recent 2018 Health Datapalooza conference. In this blog post in partnership with AcademyHealth, MITRE’s Jessica Skopac and Susan...
Putting the patient at the center of the healthcare system
Kim Warren highlights four areas where the Centers for Medicare & Medicaid Services and the health industry could have high impact on expanding patient access to data.
Using mobile health assessments to improve outcomes for individuals with chronic neurological conditions
A Datapalooza18 presentation by Elizabeth Brokaw, Michael Fine, and Tony Donadio from MITRE and Sahana Kukke from The Catholic University of America.
Easier Clinical Notes to Improve Care and Research
Greg Quinn and Andrew Quina from MITRE demonstrate in this HIMSS18 presentation an open source application to empower clinicians to author clinical notes while simultaneously enabling low burden collection of structured clinical data.
Democratizing Patient Data: A Story of Patient Empowerment
The most critical member of the care team, the patient, is being left out. Hear insights from this HIMSS18 video presentation by Kristina Sheridan, MS, Principal Investigator and Researcher Patient Empowerment, MITRE, and Kate Sheridan, Student, George Mason University about managing pediatric chronic conditions, the value of patient-generated data, and an update of the patient empowerment research that was inspired by their experience.
Health Information Sharing Maturity Model
In this HIMSS18 presentation Gail Hamilton, MITRE and Thomas Novak, HHS discuss how health interoperability is key for improving care coordination, efficiency, and reducing physician burden.
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