Scimp openEHR CKM workshop 2015
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Transcript of Scimp openEHR CKM workshop 2015
Dr Ian McNicollSCIMP
NHS England Code4HealthCo-chair openEHRHANDIHealth CIC
openEHR:the wider picture
HSCIChave adopted openEHR as primary ‘clinical content standards methodology’
acquiring a separate ‘English CKM’
developing archetypes for
PRSB Discharge summary
GPOC-R / GP2GP
Allergies, Blood pressure, Document metadata
http://www.infostandards.org/
documents/data-structures-v1-0-richard-
kavanagh-pptx.pptx
Professional Records Standards Body
Professional Records Standard Body (4-country)
adopting NHS Scotland / GP2GP medication archetypes
Relationship with HSCIC
HSCIC (largely) fund PRSB
PRSB commission work from HSCIC
NHS England NHS Code4Health/Open source program
Using EHRScape engine for SME / clinical training
Supporting openEHR-based ‘Open platform’ approach
OPENeP
HANDIHealth / Integration Pioneers
part share ‘UK CKM’ licence
SMARTPlatformsPluggable Webapp
API
HL7 FHIR Clinical Content
Exchange NHS API
‘inVivo’Datastore
API
Detailed Clinical Content Development
Clinical leadership PRSB
Terminology Centre
HSCIC
NonopenEHR systems
Archetype+ SNOMED Clinical Content definitions
Apps developers
OPENePopen-source HEPMA solution built on openEHR back-end
will use NHS Scotland medication archetypes for discharge and reconciliation
considering tendering for Scottish HEPMA framework
Archetypes into production
Archetypes are computable
can define clinical aspects of message / interface structures
SCI-XML - ECS, SCI-GW
openEHR
HL7 FHIR (clinical content)
can define data storage schema for openEHR systems
new content can be stored and queried immediately
open standard -> multiple providers
Traditional standards development
Clinical stakeholders engage through top-down governance
Committee-based
Late vendor engagement
Fixed review cycles
Unclear / unresponsive change request mechanism
Are ‘Standards’ necessary?
http://www.woodcote-consulting.com/
farwell-to-ruthless-standardisation/
http://coiera.com/
2013/11/01/are-standards-necessary/
Clinically-led standards development
Clinical content service
Clinical stakeholders, vendors engage directly with clinically-led content service
Continual dialogue with all stakeholders via web-based collaborative tooling
No fixed review cycles
On-demand change request directly to clinical content service
PRSB has high-level governance role