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Return to: Laboratory Content Modules

Development Only

The PCC Wiki Content is used only for development of IHE PCC Content. The Normative content of the PCC Technical Framework and the current supplements can be found at http://www.ihe.net/Technical_Framework/index.cfm#PCC

Trial.gif Laboratory Report Data Processing Entry

At least one Lab Report Data Processing Entry shall be present. The <entry> SHALL contain a single <act> sub-element. This <act> is hereafter referred to as the Specimen Act.

The figure below shows how the information for this element is coded, and further constraints are provided in the following sections.


See Templates using Laboratory Report Data Processing Entry

Laboratory Report Data Processing Entry Example
<entry typeCode="DRIV">
  <templateId root=""/>
  <act classCode="ACT" moodCode="EVN">
    <statusCode code="completed"/>

<templateId root=""/>

The <templateId> element identifies this <entry> as a Laboratory Report Data Processing Entry. The templateId SHALL be recorded as shown above, root="".

<act classCode="ACT" moodCode="EVN"/>

There shall be one Act sub-element. This <act> is hereafter referred to as the Specimen Act. This sub-element uses the following modules conforming to the following requirements. These modules, when present, shall be recorded as <entryRelationship> elements under the Specimen Act.

Modules unique to the document body
Sub-Element Opt Description R2 Notification Organizer R2 Notifiable Condition R2 Case Identifier R2 Outbreak Identifier R2 Specimen Collection R2 Specimen Received R2 Laboratory Battery Organizer R2 Laboratory Isolate Organizer R Laboratory Observation O Annotation Comment (PCC)

Modules with counterparts in the cda header
Sub-Element Opt Description R2 Non-Human Subject R2 Human Patient with Non-Human Subject O Laboratory Result Verifier O Laboratory Performer