Deformable Registration in Radiation Oncology: Difference between revisions

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==Summary==
==Summary==
''<Describe the profile in about a paragraph using user-oriented language.  Focus on what it accomplishes for a user (i.e. the Use Cases). Don't get into how it works, leave that to the Details section.>''
The DRRO Profile defines the content necessary for exchanging DICOM Deformable Spatial
 
Registration (DSR) objects between radiation oncology systems. In addition to defining the data
 
required to accomplish deformable image registration, it provides requirements on data elements
''<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.  .>''
so that DSR objects can be appropriately handled by radiation oncology systems that test to this
 
profile.
''<See [[Help:Contents#Tips_.26_Tricks| Help - Tips and Tricks]] for details on inserting an image/graphic.>''


==Benefits==
==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.>''
The DRRO profile allows a single system to calculate the DSR and then share that information with other radiation oncology systems. This improves consistency of image
registration and presentation, and facilitates recalculation and addition of dose arrays through the phases of patient treatment.


==Details==
==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==
==Systems Affected==
* ''Contouring Systems.''
* ''Contouring Systems''
* ''Treatment Planning Systems (TPS)''
* ''Treatment Planning Systems (TPS)''
* ''Plan/Dose Review Systems''
* ''Plan/Dose Review Systems''
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'''Underlying Standards:'''
'''Underlying Standards:'''
* [http://dicom.nema.org DICOM]
* [http://dicom.nema.org DICOM]
==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'''
'''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.>''
* [[Multimodality Image Registration for Radiation Oncology-III| MultiModality Image Registration (MMRO-III)]]
 
* ''[[Reporting Workflow]] [RWF] may use Evidence Documents as inputs to the reporting process.''
* ''[[Simple Image & Numeric Reports]] [SINR] may include data copied from Evidence Documents.''
* ''[[Cross-enterprise Document Sharing for Imaging]] [XDS-I] can be used to share Evidence Documents between sites over a network.''
* ''[[Portable Data for Imaging]] [PDI] can store Evidence Documents on media such as CDs.''
* ''[[Import Reconciliation Workflow]] [IRWF] can fix patient ids, etc. of Evidence Documents when importing.''
 


'''Consumer Information'''
'''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 [[DRRO FAQ]] answers typical questions about what the Profile does.


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>''
* The [[DRRO Purchasing]] describes considerations when purchasing equipment to deploy this Profile.


'''Implementer Information'''
'''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>''
* The [[DRRO Implementation]] provides additional information about implementing this Profile in software.


'''Reference Articles'''
'''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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[[Category:RO Profile]]
[[Category:RO Profile]]
[[Category:DICOM]]
[[Category:DICOM]]
[[Category:RO todo]]

Latest revision as of 13:52, 30 July 2025

Summary

The DRRO Profile defines the content necessary for exchanging DICOM Deformable Spatial Registration (DSR) objects between radiation oncology systems. In addition to defining the data required to accomplish deformable image registration, it provides requirements on data elements so that DSR objects can be appropriately handled by radiation oncology systems that test to this profile.

Benefits

The DRRO profile allows a single system to calculate the DSR and then share that information with other radiation oncology systems. This improves consistency of image registration and presentation, and facilitates recalculation and addition of dose arrays through the phases of patient treatment.

Details

Systems Affected

  • Contouring Systems
  • Treatment Planning Systems (TPS)
  • Plan/Dose Review Systems

Actors & Transactions:

Specification

Profile Status: Trial Implementation

Documents:

Underlying Standards:


Related Profiles

Consumer Information

  • The DRRO FAQ answers typical questions about what the Profile does.
  • The DRRO Purchasing describes considerations when purchasing equipment to deploy this Profile.

Implementer Information

  • The DRRO Implementation provides additional information about implementing this Profile in software.

Reference Articles


This page is based on the Profile Overview Template