Of course it is bad news in this community if the same principles of 13606 / 
Open EHR are applied in HL7 v3 Patient Care and that it works.

I think the debate of either or standard is the scientific debate of last 
century. The work of this century is to standardise clinical content in small 
discrete archetypes to be used in any IT solution.

Lot of work goes in sorting out the clinical stuff and an appropriate binding 
to vocabulary and determination of appropriate datatypes. See earlier points 
made by Cecil Lynch

Then an agnostic modeling serves very well to facilitate implementation in 
several technical systems, either EHR or message. 

Breakthrugh work in this sence is the linkage of HL7 v2 messages and OpenEHR 
archetype identifiers in the message that specify the clinical content.
This methodology can be used in HL7 v3 messages in a similar way (refer in 
the XML tags to the appropriate archetype / template).
Tooling is underway. Transformation form standard A to B or B to A a piece of 
cake if all hard clinical consensusbuilding and specification has been done. 

Since we have so many ( I envision in the tenth of thousands, even up to 
hundreds of thousands discrete and small molecular archetypes, given 
experiences 
in about a dozen of projects involving clinicians, having dealt with about 
10.000 discrite variables, organised in every possible grouping), the most 
dramatic problem to be solved is the repository of these things called GPICs, 
CMETs, 
archetypes, R-MIM, care information models, detailed clinical models, 
templates. 

It is nice to have a big book of all kinds of requirements for archetypes 
specification such as the Iso 13606-2 archetype language, but if nobody worries 
about the content itself it is waste of time and effort of 10 years of research 
in both CEN / OpenEHR and HL7 v.3
Finding a way to organise, maintain and update archetypes/templates/care 
information models is the real challenge. 

So I think this community should re-read the blog by David More carefully and 
see similar worries that I have given 3 years of submitting content to both 
standards organisations, all acknowledging that it is important and all asap 
ignoring it. 

So what we need is a repository of clinical templates, maintained well, that 
basically ignores the specific technical implementation in either OpenEHR or 
HL7 CDA or v3 messages. We can apply similar systems as the ISO OID registry to 
identify sources and content. 

William Goossen
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