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Empowering Patients. Tools and Initiatives. November 20, 2013. A Quick Review. Meaningful Use Interoperability Patient Generated Data. A Few Statistics . In 2011, 10% of the eligible professionals were awarded MU incentive payments
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Empowering Patients Tools and Initiatives November 20, 2013
A Quick Review Meaningful Use Interoperability Patient Generated Data
A Few Statistics • In 2011, 10% of the eligible professionals were awarded MU incentive payments • In 2012, 31% of the eligible professionals were awarded MU incentive payments • Only 10% of the adult US population currently uses a PHR
Barriers to Full Participation • Lack of full interoperability • Misunderstanding of the value of having a consolidated health record • Insufficient interpretive guides • Lack of visualization tools
“Information superiority – – the state of having access to more types of information and being able to process it quicklyand efficiently – canmean the difference between profit andloss or even life and death.”
How do We Provide Information Superiority? • Simplify Presentation: • Easy to consume • Easy to visualize • Ability to understand metrics and action items intuitively • Targeted to audience • Based on role • Drill-down capability • Interactive • Highlight important data • Identify the purpose of the data
How Can We Deliver It? Health & Wellness Platform • Open source • EHR Independent • Customizable • Patient controlled role-based delegation • Special purpose modules • Chronic conditions • Rare diseases • Diet planning • Recovery tracking
Wish List • BlueButton -- seamless import/export of patient clinical data • OpenInfobutton -- additional information and translation of medical terminology • Billing and Payment Information • Symptom Tracker with graphing function • Medication reminder and compliance tracker • Customizable graphic visualization of vital signs • Appointment scheduling, tracking, and reminders • Personal genetic data
Next Week Ed Fennell: An expert – through personal experience – on getting diagnoses and treatments for rare diseases. An opportunity to take the experiencesof an engaged patient advocate and turn them into real helpfor desperate peoplein collaboration withother OSEHRA members.