Op 7-nov-2007, om 13:03 heeft Rong Chen het volgende geschreven:

> If one chooses the first option one should fill out the criteria  
> each and every time, when writing down a diagnosis. Of course this  
> can be automated by the application that is used. Thing is that the  
> knowledge will be stored locally at application level. My feeling  
> is that your suggestion to use the GuidelineID is in conjunction  
> this option. Point is that if I refer to an external guidelines,  
> data in that guideline isn't 'archetyped' and can't be used for  
> computational purposes. So I have to translated those into an  
> archetype.
>
> Guidelines can be computerized as well. There are published  
> guidelines representation formats, e.g. GLIF for instance and their  
> execution engines. Being rules based and decision trees like,  
> personally I think they are not best modelled as archetypes since  
> archetype model are designed to represent more 'static' clinical  
> content model. In applications, EHRs and guidelines should work  
> hand-in-hand: 1) guidelines need to query EHRs through standardized  
> EHR representation format and query language; 2) EHRs need record  
> what guidelines are used etc.

Thanks, this makes sense to me and thanks for pointing out GLIF. I  
wasn't aware of that organisation.
  Let me check if I understand it: 1) in order to be able to compute  
a diagnoses against a guideline/ protocol (with the aid of a decison  
tree/ decision (support) system) the criteria of this guideline/  
protocol should be stored in a format that is 'readable' by a rule  
based/execution engine (such as GLIF).  So  it becomes possible to  
compute that if symptoms A, B and C are present, that according to  
guideline X, diagnose Y is present.

2) In order to be able to establish the 'quality of a given  
diagnoses' the reference to the  guideline(s)/protocol(s) used should  
be stored in the AT (preferably in the protocol section). So if  
guideline X  is used by a qualified person to come to diagnosis Y,  
this could be re-usable information (for a person who adapted  
guideline X)), while if guideline Z was used one would like to do  
some additional testing (for a person who rejected or is unfamiliair  
with guideline Z)

Is the assumption that, the GuidelineID  in hte CARE_ENTRY class   
(that Sam mentioned) could be used to link (if wanted) the reference  
to the actual computable criteria, correct?

Cheers,

Stef


>
> Cheers,
> Rong
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