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Health IT Standards Committee Work Product Health IT Standards Committee A Public Advisory Body on Health Information Technology to the National Coordinator.

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Presentation on theme: "Health IT Standards Committee Work Product Health IT Standards Committee A Public Advisory Body on Health Information Technology to the National Coordinator."— Presentation transcript:

1 Health IT Standards Committee Work Product Health IT Standards Committee A Public Advisory Body on Health Information Technology to the National Coordinator for Health IT Precision Medicine Task Force Leslie Kelly Hall, co-chair Andy Wiesenthal, co-chair May 17, 2016

2 Health IT Standards Committee Work Product Agenda Welcome, Opening Remarks Task Force Background and Charge Considerations Critical Pathways to Interoperability Recommendations Discussion 2

3 Health IT Standards Committee Work Product Precision Medicine Task Force Members 3 MemberOrganization Co-ChairsLeslie Kelly HallHealthwise Andrew M. WiesenthalDeloitte Consulting, LLP MembersGil AlterovitzHarvard Medical School Dixie BakerMartin, Blanck, and Associates Mary BartonNational Committee for Quality Assurance (NCQA) Stanley CrosleyMember, Drinker Biddle & Reath LLP Steven KeatingMIT Media Lab and Mechanical Engineering David McCallie, Jr.Cerner Corporation Matthew MightHarvard University Andrey OstrovskyCare at Hand Ketan ParanjapeIntel Eric RoseIntelligent Medical Objects Joyce SensmeierHealthcare Information and Management Systems Society Federal Ex OfficioJames BreelingVeterans Health Administration (VHA) Teresa Zayas CabanONC Christina HeideHHS / Office for Civil Rights Betsy HumphreysNational Library of Medicine (NLM) Terry RauchDepartment of Defense Mitra RoccaFood and Drug Administration (FDA) Jon WhiteONC Maya UppaluruUnited States Digital Services (USDS)

4 Health IT Standards Committee Work Product ONC Role in Precision Medicine Initiative Accelerate opportunities for innovative collaboration around pilots and testing of standards that support health IT interoperability for research Adopt policies and standards to support privacy and security of cohort participant data Advance standards that support a participant-driven approach to patient data contribution 4

5 Health IT Standards Committee Work Product Task Force Charge Identify opportunities for ONC to support our federal partners’ PMI efforts and related health IT/interoperability challenges, including National Cancer Institute, Food and Drug Administration, National Institutes of Health, and Department of Veterans Affairs. Identify opportunities for ONC to collaborate with industry and pilot the use of standards to enable data donation and patient access through APIs using standards such as FHIR and OAuth 2.0. Identify standards for uses cases to support interoperability of data types that are critical to PMI-type research and prioritize piloting the exchange of those data types based on a phased approach, that would incorporate most structured/coded data first and add additional data types in subsequent pilot phases. 5

6 Health IT Standards Committee Work Product Precision Medicine Task Force Workplan 6 MeetingsTask Friday February 12, 2016 10:00 AM-11:00 AM Progress and status of current initiatives NCI – PMI-Oncology FDA – Precision FDA needs to harmonize data standards Friday February 26, 2016 1:00 PM - 2:30 PM ONC – Computable Consent NIH – Precision Medicine Initiative Progress & Sync for Science pilots Recap and discussion of issues to explore from other agencies Wednesday March 16, 2016 1:00 PM-2:30 PM Department of Veterans Affairs (VA) Department of Defense (DoD) Wednesday March 30, 2016 1:00 PM-2:30 PM Findings and preliminary recommendations Gaps in interoperability use cases - lab data, patient and provider access Wednesday April 13, 2016 1:00 PM-2:30 PM Discuss draft recommendations Tuesday April 19, 2016 9:30 AM to 3:00 PM Joint HIT Committee Meeting Draft Recommendations to Joint Committee Thursday April 21, 2016 1:00 PM-2:30 PM Task Force Meeting to Finalize Recommendations Wednesday, May 11, 2016 1:00 PM - 2:30 PM Task Force Meeting to Finalize Recommendations  Tuesday, May 17, 2016 9:30 AM - 3:00 PM Joint HIT Committee Meeting Final Recommendations to Joint Committee

7 Health IT Standards Committee Work Product Interoperability Pathways Critical to PMI Overarching Questions What data sources are available? What are the known gaps regarding high value data needed for PMI? What efforts could be accelerated to help the work of PMI? Are there areas for which standards could be recommended to promote scalable and repeatable development for PMI? 7

8 Health IT Standards Committee Work Product Interoperability Pathways Critical to PMI Considerations Volume, complexity and new sources of data will necessitate emphasis on access and query based exchange versus the actual transfer of large datasets »Data volume will be beyond that of current EHR ecosystem »PMI data requires consideration of new data sources which bring complexity –Data for care directly from the patient –Genomic and other data from research platforms (e.g., NIH Cohort), laboratories and disease registries –PCORnet and others device data as well PMI (e.g., genetic) data remain uniquely valid over time, therefore, data validity and availability must be persistent over time 8

9 Health IT Standards Committee Work Product Interoperability Pathways Critical to PMI Considerations Data standards should be interoperable by design to accelerate timelines »Requires use of existing standards »Acceleration and coordination of some standards initiatives to support PMI »Acceleration of access patient generated health data (PGHD) »Interoperable design should be informed by ONC’s Interoperability Roadmap, NIH guidance, and others development and procurement 9

10 Health IT Standards Committee Work Product Three Interoperability Pathways Critical to PMI as Discussed by the Task Force 10 HPO’s EHR (labs, meds, etc.) Individual’s EHR Patient Portal (e.g., labs, meds) and PGHD Individual’s App Focus on EHR data first (e.g., labs, meds) 1 NIH PMI Cohort Enable data gathering from other independent non-provider sources NIH PMI Cohort Labs, PBMs, Claims Retail Pharmacies 2 NIH PMI Cohort ProviderPatient Accelerate ability to return an individual participant’s aggregated data from multiple sources, and eventually research results 3 HPO, Patients, Other Sources

11 Health IT Standards Committee Work Product Recommendations Recommendations fell under three main categories A.Interoperability and Data Reciprocity B.Policy Considerations C.Standards and APIs 11

12 Health IT Standards Committee Work Product Recommendations A. Interoperability and Data Reciprocity (1 of 3) ONC should consider the following promote PMI: »Provide the ONC Interoperability Roadmap addendum for PMI »Engage stakeholders to accelerate –Definition of minimum data set and standards for PMI, PGHD and phenotypic data –Include vocabulary where gaps exist using existing standards and efforts »Provide ongoing guidance –Use Technical Expert Panel(s) (TEP) to enhance participant understanding of utilizing various data sources (e.g., validity overlap, provenance) –Roadmap of current efforts that support PMI (e.g., ONC Tech Lab) –Inform the research community on interoperability with EHRs and standards in general (non-regulatory is the bias of the Task Force) 12

13 Health IT Standards Committee Work Product Recommendations A. Interoperability and Data Reciprocity (2 of 3) PMI should consider high value, non-EHR data sources to promote completeness of longitudinal patient information PMI should encourage use of standard APIs (e.g., FHIR) to source data »Meds –History, lack dispensing, adherence data, complete lists of current meds, feedback on efficacy and effectiveness –Potential sources: PBMs, retail pharmacies and physician notes »Labs –Consider challenges in pulling data from commercial and hospital labs –Explore practical differences between lab data in the EHR vs. data directly from the labs to determine which set may have greater fidelity and value »Claims –Determine how claims data enhance understanding of the patient and the sources PMI should consider means of patient mediated data donation to reduce probabilistic matching 13

14 Health IT Standards Committee Work Product Recommendations A. Interoperability and Data Reciprocity (3 of 3) Individual participant’s access to their aggregated PMI data will promote participation, retention and engagement »Data return should offer dynamic, compelling visualizations to promote its use »Patients should have access to computable, raw genetic testing and sequencing data –These data are among the most potentially useful to patients in the long term »Patients will need provider support on the implications of their genetic data PMI should define near term means of access and accelerate individual access »Recommend that patient-facing portals that enable individuals to access all data types (e.g., labs, meds, genomics) »Portals should allow individuals to use apps and APIs based on existing, and emerging standards (e.g., FHIR) »Draw from stakeholders with relevant strengths and experiences (e.g., Open Humans, PatientsLikeMe, Open Notes) 14

15 Health IT Standards Committee Work Product Recommendations B. Policy Considerations (1 of 3) NIH should educate patients and providers of data access rights and uses »Access rights should be consistent with protected health information (PHI) access standards »Consider The Framework for Responsible Sharing of Genomic and Health- Related Data* in developing data exchange principles »Enrollment should include notification of the use of the patient NIH ID –To accommodate results return and future use cases based on Sync 4 Science recommendations, notification should be sent back to EHR with patient consent »NIH direct enrollment should include strong assurance and identify proofing –Equivalent to the current patient portals model –Use direct language –Employ Web Content Accessibility Guidelines (WCAG) accessibility and enrollment 15

16 Health IT Standards Committee Work Product Recommendations B. Policy Considerations (2 of 3) Gathering patient data from a variety of sources will have implications to: »Identity Matching – the Task Force recognizes that significant efforts are underway to support this necessary capability »Consent and Authorization –Inform patients of implications of identifiers used and consent regarding their use –Clarify in consent if it applies to copies of the data –Employ a consent framework that enables new and/or expansive consent as new data needs emerge –HHS Office of Civil Rights (OCR) should confirm if consent is required for a provider to receive access to NIH data when a covered entity enrolls a patient into the cohort »Data access rights –Should apply to genomic and phenotypic information –Use notification to patients and providers when data is harvested 16

17 Health IT Standards Committee Work Product Recommendations B. Policy Considerations (3 of 3) The Task Force recognizes that efforts are underway to address: »Access –Clarification of related policy that would facilitate patient data access and return of research results (e.g., CLIA, HIPAA) –Privacy and security implications of returning an individual’s aggregated data –Options related to types of data patients would like to access / receive »Liability and Consent –Liability issues of working with genomic data with respect to what a researcher is obligated to disclose back to the patient –Granularity of permissions –Patient notification / consent to ongoing, or further, use of data for research 17

18 Health IT Standards Committee Work Product Recommendations C. Standards and APIs (1 of 2) Data Formats »Participants should be constrained to using a specified EHR export format(s) »Data recipients may need to anticipate a certain level of effort to translate data »Consensus-based models can facilitate exchange, models to consider: –Data Access Framework (DAF) and Argonaut –PCORnet, Sentinel, NCI Cloud Pilots and Cancer Genomic Data Commons, Observational Health Data Sciences and Informatics (OHDSI) –Veterans Administration mapping to (OHDSI) Individual Data »For data donation and return to patient use consistent FHIR-based APIs (e.g., Sync 4 Science, Argonaut, SMART) »New FHIR resources may not be needed immediately; an extension of existing resources may help (e.g., existing MU CDEs) »FHIR will become more necessary as it continues to evolve 18

19 Health IT Standards Committee Work Product Recommendations C. Standards and APIs (2 of 2) Data Sources »HPO enrollment on patients’ behalf should include PGHD when possible –Patients will act as an exchange mechanism among their providers and as a data source for data not captured in EHRs –Promote standardization for use of PGHD (e.g., Genetic Alliance) especially in enrollment –Recognize that standards are evolving »EHRs source for: –Episodic and demographic information, labs, meds, histories, etc. –Common Clinical Data Set minimum bar Standards based app and API implementation is recommended to: »Enable patients to connect to EHRs with apps and APIs »Enable patient to mediate exchange of the data (e.g., via CDS) to NIH cohort »Provide ability for reciprocal queries from EHR for patient specific aggregate requests of PGHD 19

20 Health IT Standards Committee Work Product Appendix: Parking Lot Issues 20

21 Health IT Standards Committee Work Product Parking Lot Items for Future Potential Task Force Work Demographic data »Recommendations to improve structured data around race, ethnicity, gender, sexual orientation? »What are the highest priority demographic data types for PMI? Define specific activities or pilots ONC could lead to support and advance progress Patient rights and ownership of genomic pattern data Record locator services and identity management »This work will be executed by the Coordinating Center awardee Genomic data (not for short-term consideration) 21

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