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Difference between revisions of "DeviceAlert FHIR Resource Proposal"

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Current Version: https://confluence.hl7.org/display/FHIR/DeviceAlert+FHIR+Resource+Proposal<div style="float: left;">[[Image:OpenHotTopic.GIF|35px| ]]</div>
 
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This page documents a [[:category:Pending FHIR Resource Proposal|Pending]] [[:category:FHIR Resource Proposal|FHIR Resource Proposal]]
 
This page documents a [[:category:Pending FHIR Resource Proposal|Pending]] [[:category:FHIR Resource Proposal|FHIR Resource Proposal]]
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As a rule, resources should encompass all of these aspects.
 
As a rule, resources should encompass all of these aspects.
 
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The DeviceAlert resource is used to represent the status of a simple alarm condition check that a medical device is able to detect. It represents a single alarm only, and alarm can be one of the following type:
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*Physiological alarm (for example: Low SpO2)
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*Technical alarm (for example: Fluid line occlusion)
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*Advisory alert (for example: Alarm of undocumented timeout prior to a surgical procedure)
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Note:
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For the initial scope, this DeviceAlert resource is only applicable to the alarm condition produced by any medical device that implements or derives from the ISO/IEEE 11073 standard.
  
 
==RIM scope==
 
==RIM scope==
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* Have the characteristics of high cohesion & low coupling – need to explore whether coupling is good some places, not elsewhere – layers from Bo’s document  
 
* Have the characteristics of high cohesion & low coupling – need to explore whether coupling is good some places, not elsewhere – layers from Bo’s document  
 
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This DeviceAlert resource is solely used to communicate a single alarm that produced by any medical device that implements or derives from the ISO/IEEE 11073 standard. If there is a need to communicate multiple alarms are triggered from the same medical device, refers to the DeviceAlertList profile for a more appropriate usage.
  
 
==Expected implementations==
 
==Expected implementations==
  
 
<!--Key resources are justified by CCDA, for resources not deemed "key", what interest is there by implementers in using this particular resource. Provide named implementations if possible - ideally provide multiple independent implementations. -->
 
<!--Key resources are justified by CCDA, for resources not deemed "key", what interest is there by implementers in using this particular resource. Provide named implementations if possible - ideally provide multiple independent implementations. -->
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*Center for Medical Interoperability will be in collaboration with Dräger Medical to work on the resource definition for the DeviceAlert.
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*Center for Medical Interoperability is going to work on a prototype ACM system around this DeviceAlert resource.
  
 
==Content sources==
 
==Content sources==
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Are there any source specifications that you wish to consult but are concerned about access to or expertise to consider? -->
 
Are there any source specifications that you wish to consult but are concerned about access to or expertise to consider? -->
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*ISO/IEEE 11073
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*IHE PCD Technical Framework (ACM profile, PCD-04)
  
 
==Example Scenarios==
 
==Example Scenarios==
  
 
<!-- Provide a listing of the types of scenarios to be represented in the examples produced for this resource.  They should demonstrate the full scope of the resource and allow exercising of the resources capabilities (full element coverage, inclusion & omission of optional elements, repeating and singleton repeating elements, etc.) -->
 
<!-- Provide a listing of the types of scenarios to be represented in the examples produced for this resource.  They should demonstrate the full scope of the resource and allow exercising of the resources capabilities (full element coverage, inclusion & omission of optional elements, repeating and singleton repeating elements, etc.) -->
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*Low SpO2, a physiological alarm from a patient monitoring device.
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*Fluid line occlusion, a technical alarm from an infusion pump.
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*An advisory alarm of undocumented timeout prior to a surgical procedure.
  
 
==Resource Relationships==
 
==Resource Relationships==
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Reference to resources is really only relevant at the "same or higher level" (Bo – fix this wording)
 
Reference to resources is really only relevant at the "same or higher level" (Bo – fix this wording)
 
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Uses
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*[http://hl7.org/implement/standards/fhir/device.html Device]
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*[http://hl7.org/implement/standards/fhir/patient.html Patient]
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*[http://hl7.org/implement/standards/fhir/location.html Location]
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*[http://hl7.org/implement/standards/fhir/observation.html Observation]
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*[[DeviceComponent]]
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Potentially used by
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*[http://hl7.org/implement/standards/fhir/list.html List] (DeviceAlertList profile)
  
 
==Timelines==
 
==Timelines==
  
 
<!-- Indicate the target date for having the resource complete from a committee perspective and ready for vetting and voting -->
 
<!-- Indicate the target date for having the resource complete from a committee perspective and ready for vetting and voting -->
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*This proposal will not be addressed in the current DSTU cycle.  It is provided as guidance to our intended overall architecture for device communications and will be implemented in the future.
  
 
==gForge Users==
 
==gForge Users==
  
 
<!-- Identify the userids who will require commit access to gForge to maintain the resource.  (Ensure all users have registered for gForge.) -->
 
<!-- Identify the userids who will require commit access to gForge to maintain the resource.  (Ensure all users have registered for gForge.) -->
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TBD

Latest revision as of 15:04, 31 October 2019



DeviceAlert

Owning committee name

Health Care Devices (DEV) WG

Contributing or Reviewing Work Groups

Health Care Devices (DEV) WG

FHIR Resource Development Project Insight ID

TBD

Scope of coverage

The DeviceAlert resource is used to represent the status of a simple alarm condition check that a medical device is able to detect. It represents a single alarm only, and alarm can be one of the following type:

  • Physiological alarm (for example: Low SpO2)
  • Technical alarm (for example: Fluid line occlusion)
  • Advisory alert (for example: Alarm of undocumented timeout prior to a surgical procedure)

Note:

For the initial scope, this DeviceAlert resource is only applicable to the alarm condition produced by any medical device that implements or derives from the ISO/IEEE 11073 standard.

RIM scope

TBD

Resource appropriateness

This DeviceAlert resource is solely used to communicate a single alarm that produced by any medical device that implements or derives from the ISO/IEEE 11073 standard. If there is a need to communicate multiple alarms are triggered from the same medical device, refers to the DeviceAlertList profile for a more appropriate usage.

Expected implementations

  • Center for Medical Interoperability will be in collaboration with Dräger Medical to work on the resource definition for the DeviceAlert.
  • Center for Medical Interoperability is going to work on a prototype ACM system around this DeviceAlert resource.

Content sources

  • ISO/IEEE 11073
  • IHE PCD Technical Framework (ACM profile, PCD-04)

Example Scenarios

  • Low SpO2, a physiological alarm from a patient monitoring device.
  • Fluid line occlusion, a technical alarm from an infusion pump.
  • An advisory alarm of undocumented timeout prior to a surgical procedure.

Resource Relationships

Uses

Potentially used by

  • List (DeviceAlertList profile)

Timelines

  • This proposal will not be addressed in the current DSTU cycle. It is provided as guidance to our intended overall architecture for device communications and will be implemented in the future.

gForge Users

TBD