Difference between revisions of "Registry CDEs"
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[[CIC|Return to Main CIC page]] | [[CIC|Return to Main CIC page]] | ||
| − | ==Welcome to the | + | ==Welcome to the Common Clinical Registry Framework CDEs Wiki!== |
| − | + | The Common Clinical Registry Framework (CCRF) project is part of Clinical Interoperability Council (CIC) Work Group | |
| − | '''Registry | + | '''Registry CDEs Project Need:''' <br> |
| − | (to be | + | This project will identify and define, where not already defined, and harmonize a set of common clinical data elements (CDEs) that are generalizable across most clinical registries. For the purposes of this project, by CDEs we mean clinical data elements that are expected to be used in most registries. Data that are generally collected regardless of the type of patient or clinical care provided e.g., demographics, history, immunizations, vital signs, smoking status. This set of CDEs will not contain data that are mostly specific to medical specialties e.g., cardiology data. For more information see the Project Scope Statement. |
'''Project Participants''' <br> | '''Project Participants''' <br> | ||
| − | + | Facilitator: Seth Blumenthal <br> | |
| + | Modeling facilitator: AbdulMalik Shakir <br> | ||
| + | Publishing facilitator: Amy Nordo <br> | ||
| + | Vocabulary facilitators: Rob Hausam, Susan Matney, Sarah Ryan <br> | ||
| + | Domain expert representatives: James Tcheng, Chrystal Price <br> | ||
| + | Business requirement analysts: Laura Heermann Langford, Julia Skapik, Anita Walden <br> | ||
==CCRF Meeting Minutes== | ==CCRF Meeting Minutes== | ||
==CCRF CDEs Draft== | ==CCRF CDEs Draft== | ||
| − | [[Media: | + | [[Media:HL7_CCRF_CDEs_draft_set_2018_10_2.xlsx|CDEs draft spec sheet, October 2, 2018 (version date)]] <br> |
==Project Documentation== | ==Project Documentation== | ||
| − | [[Media:HL7_PSS_- | + | [[Media:HL7_PSS_-_CCRF_CDEs_2018_10_2.docx|CDEs project scope statement, October 2, 2018 (version date)]] <br> |
| + | [[Media:HL7_CCRF_CDEs_vetting_letter_2018_10_2.docx|CDEs October 2018 vetting letter]] <br> | ||
Latest revision as of 13:50, 2 October 2018
Contents
Welcome to the Common Clinical Registry Framework CDEs Wiki!
The Common Clinical Registry Framework (CCRF) project is part of Clinical Interoperability Council (CIC) Work Group
Registry CDEs Project Need:
This project will identify and define, where not already defined, and harmonize a set of common clinical data elements (CDEs) that are generalizable across most clinical registries. For the purposes of this project, by CDEs we mean clinical data elements that are expected to be used in most registries. Data that are generally collected regardless of the type of patient or clinical care provided e.g., demographics, history, immunizations, vital signs, smoking status. This set of CDEs will not contain data that are mostly specific to medical specialties e.g., cardiology data. For more information see the Project Scope Statement.
Project Participants
Facilitator: Seth Blumenthal
Modeling facilitator: AbdulMalik Shakir
Publishing facilitator: Amy Nordo
Vocabulary facilitators: Rob Hausam, Susan Matney, Sarah Ryan
Domain expert representatives: James Tcheng, Chrystal Price
Business requirement analysts: Laura Heermann Langford, Julia Skapik, Anita Walden
CCRF Meeting Minutes
CCRF CDEs Draft
CDEs draft spec sheet, October 2, 2018 (version date)
Project Documentation
CDEs project scope statement, October 2, 2018 (version date)
CDEs October 2018 vetting letter
