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Difference between revisions of "Device (QDM)"

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| row1cell1 | Device Recommended
 
| row1cell1 | Device Recommended
| row1cell2 | ProcedureRequest.intent
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| row1cell2 | DeviceRequest.intent
 
| row1cell3 | Procedure Request intent uses the concepts proposal, plan, order, original-order, reflex-order, filler-order, instance-order, option. "Proposal" is most consistent with the ProcedureRequest when applied to clinical decision support (CDS) in which the CDS proposes an action to a provider or to a patient. The QDM concept Recommended addresses expectations a provider gives to a patient. Such recommendations are most consistent with the ProcedureRequest.intent value of "plan" (an intension to ensure something occurs without providing an authorization to act).
 
| row1cell3 | Procedure Request intent uses the concepts proposal, plan, order, original-order, reflex-order, filler-order, instance-order, option. "Proposal" is most consistent with the ProcedureRequest when applied to clinical decision support (CDS) in which the CDS proposes an action to a provider or to a patient. The QDM concept Recommended addresses expectations a provider gives to a patient. Such recommendations are most consistent with the ProcedureRequest.intent value of "plan" (an intension to ensure something occurs without providing an authorization to act).
 
|-
 
|-
 
| row2cell1 | Negation Rationale
 
| row2cell1 | Negation Rationale
| row2cell2 | ProcedureRequest.extension (http://hl7.org/fhir/StructureDefinition/procedurerequest-reasonRefused)
+
| row2cell2 | None
| row2cell3 | QDM matched to QI Core / FHIR
+
| row2cell3 | DeviceRequest resource does not include a reason the device request did not occur. QI Core does have a ProcedureRequest.extension (http://hl7.org/fhir/StructureDefinition/procedurerequest-reasonRefused)
 
|-
 
|-
 
| row2cell1 | Reason
 
| row2cell1 | Reason
| row2cell2 | ProcedureRequest.reasonCode
+
| row2cell2 | DeviceRequest.reasonCode
 
| row2cell3 | QDM matched to QI Core / FHIR
 
| row2cell3 | QDM matched to QI Core / FHIR
 
|-
 
|-
 
| row2cell1 | Author dateTime
 
| row2cell1 | Author dateTime
| row2cell2 | ProcedureRequest.AuthoredOn
+
| row2cell2 | DeviceRequest.AuthoredOn
 
| row2cell3 | Note - ProcedureRequest.occurrence(x) defines a dateTime when the event should occur - not addressed in QDM
 
| row2cell3 | Note - ProcedureRequest.occurrence(x) defines a dateTime when the event should occur - not addressed in QDM
 
|-
 
|-
 
| row2cell1 | Code
 
| row2cell1 | Code
| row2cell2 | ProcedureRequest.code
+
| row2cell2 | DeviceRequest.code
 
| row2cell3 | See also, Observation.category
 
| row2cell3 | See also, Observation.category
 
|-
 
|-
 
| row2cell1 | id
 
| row2cell1 | id
| row2cell2 | ProcedureRequest.id
+
| row2cell2 | DeviceRequest.id
 
| row2cell3 | QDM matched to QI Core / FHIR
 
| row2cell3 | QDM matched to QI Core / FHIR
 
|-
 
|-
 
| row2cell1 | Source
 
| row2cell1 | Source
| row2cell2 | ProcedureRequest.requester
+
| row2cell2 | DeviceRequest.requester
 
| row2cell3 | Author, orderer - note also, ProcedureRequest.requester.agent for device, practitioner or organization who initiated the request; or ProcedureRequest.requester.onBehalfOf  - the organization the device or practitioner was acting on behalf of
 
| row2cell3 | Author, orderer - note also, ProcedureRequest.requester.agent for device, practitioner or organization who initiated the request; or ProcedureRequest.requester.onBehalfOf  - the organization the device or practitioner was acting on behalf of
 
|}
 
|}

Revision as of 21:08, 6 April 2018

Back to Harmonization of Health Quality Information Models Page


This QDM to QI Core Mapping for the QDM Datatype "Device" was updated 3 April 2018 based on discussion in the CQI WG on March 30, 2018.
QDM defines Device as an instrument, apparatus, implement, machine, contrivance, implant, in-vitro reagent, or other similar or related article, including a component part or accessory, intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease and not dependent on being metabolized to achieve any of its primary intended purposes. QDM provides three contexts for expressing devices: Device, Applied; Device, Order; and Device, Recommended.

  1. Note that the current use of the QDM datatype “Device, Applied” usually references the procedure to “apply” the device (i.e., to use for the patient, to use on the patient’s body, or to implant in the patient’s body). Each of these current uses should address the concept using the QDM datatypes, Intervention, Performed, or Procedure, Performed.
  2. The original intent of the QDM datatype “Device, Applied” was to reference the specific device or type of device of concern to the measure. And that reference might be as detailed a providing a device class as referenced in a Unique Device Identifier (UDI). The FHIR Device resource (http://hl7.org/fhir/device.html) does have a metadata element for UDI (http://hl7.org/fhir/device-definitions.html#Device.udi). All device metadata reference inherent qualities of the device. And timing addresses Device.manufactureDate and Device.expirationDate. Therefore, a direct map to the Device resource may not be sufficient or appropriate for the QDM Device, Applied datatype.
  3. The FHIR Resource DeviceUseStatement (http://hl7.org/fhir/deviceusestatement.html) is a more appropriate resource to map QDM Device, Applied. The DeviceUseStatement has a maturity level of 0, so the mapping will need to be updated as the resource is updated. Note: this mapping will need to be reviewed with the QI Core DeviceUseStatement to assure alignment since the current QI Core content does not seem to address the most recent version of DeviceUseStatement.

Device, Applied

QDM Attribute QI Core Metadata Element Comment
Device Applied DeviceUseStatement A record of a device being used by a patient where the record is the result of a report from the patient or another clinician.
Anatomical Approach Site None Not addressed in the Device or DeviceUseStatement resources.
Anatomical Location Site DeviceUseStatement.bodySite Indicates the site on the subject's body where the device was used ( i.e. the target site).
Negation Rationale None A DeviceUseStatement does not address negation since there would be no statement if the device were absent. QDM usage to indicate devices that have not been applied should address negation rationale for the order or the recommendation (i.e., ProcedureRequest.extension (reasonRefused).
Reason DeviceUseStatement.indication Reason or justification for use of the device.
Relevant Period DeviceUseStatement.whenUsed The time period over which the device was used.

Note – the DeviceUseStatement resource also has a metadata element: DeviceUseStatement.timing(x) indicating how often the device was used (may be a period or dateTime).

Author dateTime DeviceUseStatement.recordedOn The time at which the DeviceUseStatement was made/recorded.
Code DeviceUseStatement.device

Device.udi.deviceIdentifier

DeviceUseStatemtn.device references Device for details of the device used. Device.udi.deviceIdentifier (DI) is a mandatory, fixed portion of a Unique Device Identified (UDI) that identifies the labeler and the specific version or model of a device.
id DeviceUseStatement.id Logical id of this artifact
Source DeviceUseStatement.source Who reported this device was being used by the patient.

Device, Order

QDM Attribute QI Core Metadata Element Comment
Device Order DeviceRequest.intent Procedure Request intent uses the concepts proposal, plan, order, original-order, reflex-order, filler-order, instance-order, option. Constrain to "order" from the intent value set for QDM datatypes with the order context.
Negation Rationale None DeviceRequest resource does not include a reason the device request did not occur. QI Core does have a ProcedureRequest.extension (http://hl7.org/fhir/StructureDefinition/procedurerequest-reasonRefused)
Reason DeviceRequest.reasonCode QDM matched to QI Core / FHIR
Author dateTime DeviceRequest.AuthoredOn Note - ProcedureRequest.occurrence(x) defines a dateTime when the event should occur - not addressed in QDM
Code DeviceRequest.code See also, Observation.category
id DeviceRequest.id QDM matched to QI Core / FHIR
Source DeviceRequest.requester Author, orderer - note also, ProcedureRequest.requester.agent for device, practitioner or organization who initiated the request; or ProcedureRequest.requester.onBehalfOf - the organization the device or practitioner was acting on behalf of

Device, Recommended

QDM Attribute QI Core Metadata Element Comment
Device Recommended DeviceRequest.intent Procedure Request intent uses the concepts proposal, plan, order, original-order, reflex-order, filler-order, instance-order, option. "Proposal" is most consistent with the ProcedureRequest when applied to clinical decision support (CDS) in which the CDS proposes an action to a provider or to a patient. The QDM concept Recommended addresses expectations a provider gives to a patient. Such recommendations are most consistent with the ProcedureRequest.intent value of "plan" (an intension to ensure something occurs without providing an authorization to act).
Negation Rationale None DeviceRequest resource does not include a reason the device request did not occur. QI Core does have a ProcedureRequest.extension (http://hl7.org/fhir/StructureDefinition/procedurerequest-reasonRefused)
Reason DeviceRequest.reasonCode QDM matched to QI Core / FHIR
Author dateTime DeviceRequest.AuthoredOn Note - ProcedureRequest.occurrence(x) defines a dateTime when the event should occur - not addressed in QDM
Code DeviceRequest.code See also, Observation.category
id DeviceRequest.id QDM matched to QI Core / FHIR
Source DeviceRequest.requester Author, orderer - note also, ProcedureRequest.requester.agent for device, practitioner or organization who initiated the request; or ProcedureRequest.requester.onBehalfOf - the organization the device or practitioner was acting on behalf of