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HL7 Version 3 Process and Tools - Charlie McCay
12 December 2003 Introduction to HL7 Charlie McCay
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Charlie McCay Interest in Clear and Testable specifications
Co-Chair HL7 XML Special Interest Group Chair HL7UK Technical Committee XML input to these specifications: RACPC+PROFESS – CEN data-sets GP2GP – early adopter for HL7V3 ETP – Electronic Transfer of Prescriptions Pilot DMSP Clinical pathways (HL7v3)
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How HL7 works HL7.org and HL7UK… Products… Organisation… Meetings…
Ballots…
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HL7.org and HL7UK Membership organisations
Both aim to provide standards that support Clinical Information System Interoperability HL7UK does this in a UK context
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Products Specifications Methods for developing specifications
V2, V3, CDA, Arden, CCOW, … Informative, Normative or Reference Methods for developing specifications MDF, HDF, …
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Organisation ANSI, ISO, CEN TCs, SIGs and others
Technical Committees Special Interest Groups HL7.org, and the affiliates
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HL7.org Meetings Working Group Meetings Harmonisation Conference calls
Three meetings a year, 400 attendees Committee work and tutorials Harmonisation Three times a year, 20 attendees Conference calls Mailing lists
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HL7UK meetings 6 technical meetings a year, 20-30 attendees
Networking Reporting on UK HL7 projects Planning UK activity in HL7.org detailed review UK conference HC200x Stand and demonstrations
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Ballots Central and Affiliate Committee and Membership
Joining ballot pools, and meaning of votes Resolution of negatives
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Semantics and Technology
“Semantics” is the definition of the data items that are permitted in the message “Technology” is what is used to transmit that meaning between systems Hl7v3 is semantics, XML is technology
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Skills Reuse XML used for more than just EDI
Component interfaces User interface Printed Document formatting Temporary and persistent Data storage Semantics are not just used in interfaces Reporting engines System architecture Requirements gathering
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Training and Skills EDI needs experienced developers
XML skills can be developed elsewhere Parser writing Not need widely in Clinical applications Error prone EDI can become a trap for good developers
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Validation at Source Schemas, DTDs, and black boxes
Keep your own dirty laundry Avoid doing free testing for other suppliers Identify who is responsible for errors Machine readable specifications Taken further in V3
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Are the Schemas normative
Do I have to use the Schema?… What is normative is the definition of the set of valid instances DTD / Schema used for: Description Validation Validation takes time Diagnostic and runtime validation
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Is Schema validation enough?
No – Rules the schema does not check Co-occurrence constraints Contingencies on facts beyond the message Orchestration of the messages No – Schema validators get better
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Tools Visio Tools Schema generator Message Viewer – xClinView
Message Documentation Editor Schema processors, rsXMLtest XML IDE -- XML Spy
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