Dear Colleagues,

I am often asked about the relationship between ISO EN 13606 and openEHR, and I 
note this topic has recently been raised on our lists.

To say straight off, some people imagine there are tensions between these, but 
most of the people active in taking forward 13606 are also active in openEHR, 
and see value in both. I certainly do. Inevitably those close up to this 
subject tend to focus on fine differences, while those further away cannot 
understand what the differences are or why they might be important. If one 
looks at the modest quality and poor consistency of clinical data and the 
limited interoperability of EHR systems today, the differences between openEHR 
and 13606 are really rather slight.

13606 was developed drawing on a long thread of R&D on EHR representations, 
starting from the early 1990's and embodied in two past generations of European 
Standard as well as openEHR's specifications. All of this background work was 
inter-linked through time and people, many of whom contributed to the 
development of the standard, directly or indirectly. 

The priority during the development of the standard - expressed especially by 
the vendors and the health ministry representatives - was to find the simplest 
possible model for communication between heterogeneous EHR systems, whilst 
meeting published requirements including medico-legal requirements e.g. ISO 
18308. The goal was to keep the complexity of the interoperability models low, 
and not to require a large number of information properties that many legacy 
systems might not be capable of providing for export or of safety storing on 
import. As the work migrated from its origins in CEN to ISO, this philosophy 
was endorsed by the broader international community: for example the ISO 
version of Part 1 (2008) is identical to the CEN version (2007).

Archetypes were very much liked, and there was a wish to support the sound use 
of archetypes as promoted by openEHR, but optionally - recognising that 
archetypes will take some years for marketplace penetration, and that EHR 
interoperability has to work in a non-archetyped, a fully archetyped and in a 
transitional mixed economy. We have tried to support these options in 13606. 
When developing ISO 13606 Part 2 we recognised that the then current version of 
ADL would evolve, and also that other representations of archetypes might gain 
favour over time e.g. XML, OWL. That part-standard is therefore deliberately 
called an "Archetype Interchange Specification" - i.e. it is for sharing 
archetypes, not for operationalising them within particular systems. The 
normative parts are the requirements and the UML logical representation, and 
the conformance requirements are to be able to map any physical representation 
of archetypes to this local expression. ADL 1.4 was included as it was then 
stable and implemented within tools (i.e. the paint on it was dry), but with 
optional conformance. (Readers of the standard are invited to go to the openEHR 
Web site for more on archetypes.) It is therefore permitted by the standard to 
use, for example, ADL 1.5. 

Other part of 13606 deal with confidentiality policy interoperability and with 
interface specifications, and some internal vocabularies. (There is a data type 
"inter-regnum" that should be addressed in the near future.)

Some vendors and countries have found 13606 attractive because of its 
stability: since the time line from design to return on investment for EHR 
system products can be many years, an evolving specification is considered by 
some to be a disadvantage. 13606 is considered to be easy on the learning curve 
and potentially well suited to feed a national EHR network that has to federate 
multiple (legacy) systems from multiple vendors. 

openEHR, of course, offers a more detailed and comprehensive EHR reference 
model and other specifications targeted primarily as an EHR system 
architecture.  This suits other use cases and budgets. I won't elaborate on 
openEHR here as you all know it well.

Since both support archetypes, investments in clinical modelling activities by 
health professional bodies or eHealth programmes can be exploited by both kinds 
of specification. This is important since a significant investment is now 
needed, globally, in scaling up archetype development and validation.

When 13606 is revisited over the next few years we will see what experiences 
have been gained across all dimensions of health record interoperability 
globally, in order to identify deficiencies and new priorities for it to meet. 
Since openEHR is also learning hugely as its implementation base grows, I would 
expect the shared learning to result in better alignment between the two 
specifications next time.

However, as I have often made clear, I am strongly resistant to modelling by 
"religion" so I do not like to be drawn yet on how close that alignment might 
be, nor on how close we can align with HL7 CDA - desirable as those alignments 
might be. To me requirements and experience are everything! I would like to see 
all of our representations for EHRs (including those developed by HL7) more 
transparently and robustly mapped to evidenced requirements.  If we do all work 
to the same requirements, our differences will surely evaporate.

Thanks to all of you on the lists for enriching our understanding of what is 
needed of the EHR and for sharing your experiences along our common journey of 
learning. 

With best wishes,

Dipak
________________________________________________________
Dipak Kalra
Clinical Professor of Health Informatics
Director, Centre for Health Informatics and Multiprofessional Education
University College London
Holborn Union Building, Highgate Hill, London N19 5LW
Honorary Consultant, The Whittington Hospital NHS Trust, London

Phone: +44-20-7288-5966






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