Difference between revisions of "Specimen Event Tracking"

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'''Actors & Transactions:'''
 
'''Actors & Transactions:'''
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''<Insert an actor-transaction diagram, and or list of Content Definitions>''
 
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'''Documents:'''  
 
'''Documents:'''  
 
Link to current draft document: [https://docs.google.com/viewer?a=v&pid=forums&srcid=MDQ3NDcyMTUyODAxMzMyMzAzNTQBMTY0MjQ4ODk4Njk5ODUzMTMzNTQBd1UtbVFHMHhDUUFKATAuMQFpaGUubmV0AXYy&authuser=0]  
 
Link to current draft document: [https://docs.google.com/viewer?a=v&pid=forums&srcid=MDQ3NDcyMTUyODAxMzMyMzAzNTQBMTY0MjQ4ODk4Njk5ODUzMTMzNTQBd1UtbVFHMHhDUUFKATAuMQFpaGUubmV0AXYy&authuser=0]  
Link to SET matrix with collection of all data elements per use case: NEED TO STILL UPLOAD!!!
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Link to SET matrix with collection of all data elements per use case: https://wiki.ihe.net/index.php/Specimen_Event_Tracking
  
 
'''Underlying Standards:'''
 
'''Underlying Standards:'''

Revision as of 09:48, 13 January 2019

Specimen Event Tracking (SET) defines all use cases and related events relevant to be tracked, when one or more operations involving a specimen occur (i.e., container preparation, collection, movement from one facility to another one, archiving, and so on).that could happen to a specimen.

Summary

The key driver around the SET is to be able to recreate the entire history of the specimen from collection to final disposition. For most recent information on the SET please see: http://wiki.ihe.net/index.php/Pathology_and_Laboratory_Medicine_(PaLM)#Current_Activity Higher level use case categories are: 1) Specimen collecting tracking: this is the starting link of the specimen tracking chain for every SET profile use case. 2) Specimen Inter-Organization transfer: these use cases cover scenarios where specimens have to be transported from an institution to another. 3) Intra-organization testing workflow specimen transfer: this use case analyzes some workflows occurring inside the same institution, where the involved facilities can be physically located in the same building, or physically separated, with an intra-organization inter-facilities transfer. 4) Intra-laboratory IVD testing specimen tracking: this use case is focused on the main tracking events happening during all In Vitro Diagnostics (IVD) testing operations performed on a specimen 5) Specimen biobank transfer: these use cases are related to the transfer of a specimen to a biobank and its future retrieval for further analysis. See also 2.7. 6) Pathology specimen tracking: this class of use cases addresses the tracking of specimens related to Anatomic Pathology testing workflow.

1) A new message type will be proposed for implementation. The main purpose for this message type is that of carrying specimen events tracking information, during all the phases of its clinical lifecycle, as: labeled containers production, collection, movement intra or inter organization/facilities, movement in an analyzer chain, biobanks, and so on. 2) The proposed structure for the new message type shall be able to carry all needed information for all the different types of events. Some of the segments/blocks will be mandatory or not, according to the different types of events that the new message is tracking. All these restricting rules could be directly addressed in IHE Specimen Event Tracking (SET) profile Volume 2 implementation. 3) For tracking purposes, some of the tracking events defined inside the SET profile require a reference to the order (i.e., Placer Order Number) that originated the request for specimens production (Transactions LAB-1 and LAB-2). In order to avoid to add into the new message structure both ORC and OBR segments only for this reason, a field inside the SPM segment has to be found, in order to fulfill these requirement. For this reason, the proposed new message structure will not consider the presence of an ORDER block section.


<Insert a simple graphic that, at a glance, visually summarizes what the profile is about. Do not use an actor/transaction diagram here. Show your graphic to someone for 5 seconds (literally) and ask them what it's about. If what they say hits the main points in your summary paragraph, you have succeeded. E.g. a graphic of a hospital, a clinic, and a lab with patient records moving between them. .>

<See Help - Tips and Tricks for details on inserting an image/graphic.>

Benefits

<If the profile can improve Cost, Safety, Quality or Efficiency then list the specific examples of that benefit (e.g. error reduction, increased throughput) and how they come about (e.g. SWF reduces patient errors due to mistyped demographics at the modality by transfering demographics electronically from the Order Filler). Consider using a bullet list for readability. Such benefits help users and vendors make the business case for the profile. If the profile does not improve any aspect of Cost, Safety, Quality or Efficiency feel free to talk about something else here.>

Details

<A few paragraphs, if appropriate, providing more details (mostly in user-speak, not tech-speak) on what the profile does and how it works.>

<If the user might be familiar with the mechanisms used by the profile, you can mention them here. E.g. Evidence Documents is based on DICOM Structured Report (SR) Templates.>

<If the user might have an appreciation for the problems addressed in the profile, you can mention them here, but keep it short. E.g. Mapping HL7 Order fields to DICOM Modality Worklist attributes can be inconsistent in the marketplace, so Scheduled Workflow provides vendors with more detailed instructions.>

Systems Affected

<List (in user terms) the types of systems they might expect to have implemented actors from this profile, e.g. RIS, PACS, HIS, CAD Workstation, etc. and for each, how it would participate.>

  • EHR-S
  • LIS
  • Lab automation manager
  • ...


Actors & Transactions:


<Insert an actor-transaction diagram, and or list of Content Definitions>

Specification

Profile Status: Final Text <Replace "Final Text" with "Trial Implementation" or "Public Comment" as appropriate.>

Documents: Link to current draft document: [1] Link to SET matrix with collection of all data elements per use case: https://wiki.ihe.net/index.php/Specimen_Event_Tracking

Underlying Standards:

  • HL7 v2 - chapters 7 (for OSM^R26) and 13 (for SSU^U03) HL7
  • ...

See Also

<The following sections can be left out if there is nothing to point to. This is just to show where such information can go.>


Related Profiles

<List profiles this one depends on, profiles that depend on this one, profiles that are synergistic with this one. Start with the name of the other profile as a link and then explain the relationship.>

  • <to be updatedReporting Workflow [RWF] may use Evidence Documents as inputs to the reporting process.>


Consumer Information

The Profile FAQ Template answers typical questions about what the Profile does. <Replace the link with a link to the actual FAQ page for the Profile>

The Profile Purchasing Template describes considerations when purchasing equipment to deploy this Profile. <Replace the link with a link to the actual Purchasing page for the Profile>

Implementer Information

The Profile Implementation Template provides additional information about implementing this Profile in software. <Replace the link with a link to the actual Implementation page for the Profile>

Reference Articles

<List References (good and bad) (with link if possible) to Journal Articles that mention IHE's work (and hopefully include some analysis). Go ahead, Google: IHE <Profile Name> abstract or Google: IHE <Profile Name> and under the "more" select "Scholar". You might be surprised. >

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