1. Clinical Interoperability Council Working Group (CIC)
HL7 WGM
Madrid, Spain
May 2017
Each Working Group will have 7-10mins to describe what they do and how it impacts the healthcare setting
Name of Working Group
Leadership
Co-Chairs
Mitra Rocca – Food and Drug Administration
Russ Leftwich - InterSystems
Ed Hammond – Duke University
Anita Walden – University of Arkansas Medical Sciences
Facilitators
AbdulMalik Shakir– Shakir Consulting
Modeling
Sarah Ryan- Vocabulary
Amy Nordo–Duke University
Publishing

2. Our Workgroup’s Mission Highlights
Liaison Between the Clinical Community and HL7
Outreach to Clinicians to include their expertise in Standards Development
Promote Interoperability Across Healthcare, Research, Public Health, Quality Improvement and other Health Domains through Consensus Standard Data Elements
This slide is to briefly highlight what problems you are addressing. Your purpose and desired impact on the healthcare community

3. Some of What We Do Benefits to You Standards/Events
Engage Clinicians and Professional Societies in the Standardization of Semantic Content, Definitions and Variables (Fields)
Clinician engagement helps to improve quality use of EHR data for clinical research, registry and public health reporting. Reduces ETL and mapping time from Data Warehouse
CIIC meeting in July –Data Element Harmonization Effort
Therapeutic Area DAMs Standards
Cardiology, Mental Health, Anesthesia
Standardize Data for FDA
Improve Clinical Trial Review process
Therapeutic Area Clinical DAMs
Improve the Usability of EHR Systems
Increase clinician satisfaction, reduce medical errors, missing data or invalid data
EHR Usability Standard and Paper
Identify & Develop Standards for Registries
Reduce burden of submitting data from Clinical setting to a Registry
Common Clinical Registry Framework
Explain here how CIC works with other clinical groups to develop semantic standards.
PEW - Registry Report
CIIC – Harmonization of Data Element Efforts

4. Those who work with submitting data to Registries.
What We Need From You
Why
Those who work with submitting data to Registries.
Those who have registries.
Identify what is not captured in EHR
Challenges in data extraction and submission to Registries, feedback on Use Cases
How to integrate these clinical standards in the organization (cardiology, mental health, anesthesiology…)
To facilitate easier data aggregation and sharing across organizations.
Review on Exercise Physiology Standards
Need to understand the data that is shared with other clinicians. What is captured in the EHR
Feedback on EHR Usability Guidelines
To understand if these guidelines will improve use of EHR and other Clinical system design
This slide is to ask for the type of contribution needed.
Feedback on data exchange challenges, review of use cases, what exercise data elements are capture or will be useful in the EHR

5. CIC Agenda Date and Quarter Topic Tuesday Q1 RCRIM, BRIDG and CIC
- Discuss GAD Ballot reconciliation
- BRIDG Architectural Review process
- Update on RCRIM projects Q2
EHR Usability session Ballot Reconciliation Session Q3
Trauma Discussion Q4
THEMES Project update
Wed Q1
ONC Meeting update – Lamah
Steve Hufnagel
CIMI Discussion
FHIR Adverse Event Resource (RCRIM- HOST)
Patient Registries Planning (CCRF)
Thursday Q1
CIC Business Meeting - Planning for the May 2017 WGM in Madrid
Education Committee meeting – Clinician Education
Open
Patient Registries Planning and Discussion

6. Important Notes: THEMES “Exercise” DAM- Balloted in May
Registry Standards (DAM) –Ballot in May
Trauma CDA– Ballot in May
Working with CIMI to move DAMs into CIMI models then FHIR Resources
Designing Standards for Registries

7. Contact Information
Presenter:
Amy Nordo
Duke
Phone:
CIC Meeting 4th Thursdays 2pm ET
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