- From: Kashyap, Vipul <VKASHYAP1@PARTNERS.ORG>
- Date: Wed, 6 Dec 2006 10:15:59 -0500
- To: "Forsberg, Kerstin L" <Kerstin.L.Forsberg@astrazeneca.com>, <public-semweb-lifesci@w3.org>
Received on Wednesday, 6 December 2006 15:16:58 UTC
Hi Chimezie, I have just briefly looked through the introduction to your Problem Oriented Medical Record ontology and I find it very interesting. In the same way as HL7 RIM Acts has a "ontological failings" in mixing up the "concept of the action of recording clinical information and the phenomena being described by such recordings", CDISC (Clinical Data Interchange Standards Consortium) fundamental Observations has a similar problem. [VK] This reminds me of a discussion I had with Dan Russler and similar to the above sentiment, the design choices seem to be between one of the following: 1. Modeling the action of recording a clinical information; or ordering a drug; or making a diagnosis, ... 2. Modeling the information required for performing the action; and the information as a result of the outcome of the action... The argument appears to be that the use case in requires metrics such as cost and efficiency of hospital operations. etc. That said, one still needs to differentiate the two and chances are you may want to model (2) as opposed to (1) It will be great if Kerstin can point us to the "use cases" and metrics in the Pharma context which would drive the modeling efforts. Cheers, ---Vipul
Received on Wednesday, 6 December 2006 15:16:58 UTC