DeviceAlert FHIR Resource Proposal
- 1 DeviceAlert
- 1.1 Owning committee name
- 1.2 Contributing or Reviewing Work Groups
- 1.3 FHIR Resource Development Project Insight ID
- 1.4 Scope of coverage
- 1.5 RIM scope
- 1.6 Resource appropriateness
- 1.7 Expected implementations
- 1.8 Content sources
- 1.9 Example Scenarios
- 1.10 Resource Relationships
- 1.11 Timelines
- 1.12 gForge Users
Owning committee name
Contributing or Reviewing Work Groups
FHIR Resource Development Project Insight ID
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.
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.
- 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.
- ISO/IEEE 11073
- IHE PCD Technical Framework (ACM profile, PCD-04)
- 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.
- List (DeviceAlertList profile)