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  1. FHIR Specification Feedback
  2. FHIR-38220

Device Identification Information referenced incorrectly

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    • Icon: Change Request Change Request
    • Resolution: Persuasive with Modification
    • Icon: Highest Highest
    • CodeX™ Radiation Therapy (FHIR)
    • 1.0.0-ballot [deprecated]
    • Cross-Group Projects
    • Treatment Device [deprecated]
      Treatment Device Manufacturer [deprecated]
      Treatment Device Model [deprecated]
    • Hide

      References to devices will be moved out of extensions to use the built-in fields in the ServiceRequest and Procedure profiles.   

      In ServiceRequest, the device reference will use the performer field.
      In Procedures, implantable devices will use focalDevice.manipulated, and treatment devices will use the usedReference field.

      Devices are represented by two distinct profiles.   One of the profiles RadiotherapyTreatmentDevice (a profile of Device) and RadiotherapySeedDevice (a profile of USCoreImplantableDevice).
       
      The latter supports the same UDI requirement (MS) as USCoreImplantableDevice.
      Note:  this iG requires an exception to the requirement of using the USCore Implantable Device as the base for RadiotherapyTreatmentDevice, since the devices here are machines that provide treatment, and are not implanted.

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      References to devices will be moved out of extensions to use the built-in fields in the ServiceRequest and Procedure profiles.    In ServiceRequest, the device reference will use the performer field. In Procedures, implantable devices will use focalDevice.manipulated, and treatment devices will use the usedReference field. Devices are represented by two distinct profiles.   One of the profiles RadiotherapyTreatmentDevice  (a profile of Device) and  RadiotherapySeedDevice (a profile of USCoreImplantableDevice).   The latter supports the same UDI requirement (MS) as USCoreImplantableDevice. Note:  this iG requires an exception to the requirement of using the USCore Implantable Device as the base for RadiotherapyTreatmentDevice , since the devices here are machines that provide treatment, and are not implanted.
    • Saul Kravitz / Martin von Siebenthal : 12-1-5
    • Correction
    • Non-compatible

    Description

      The device resource should be used to convey device identification information instead of extensions.  The device identification information should be mapped to the Procedure.usedReference with Reference (Device)

      If the UDI is available - the value should be in: Device.udiCarrier.carrierHRF 

      If the UDI is not available - the value should support both name and model in the following element: Device.deviceName.value with type = manufacturer-name and another element with type = model-name (please note these values will be available in future FHIR releases. Do not use udi-label-name).

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            Unassigned Unassigned
            marti_velezis Marti Velezis
            Marti Velezis
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              Created:
              Updated:
              Resolved: