This wiki has undergone a migration to Confluence found Here
Difference between revisions of "DeviceAlert FHIR Resource Proposal"
Jump to navigation
Jump to search
Line 54: | Line 54: | ||
As a rule, resources should encompass all of these aspects. | As a rule, resources should encompass all of these aspects. | ||
--> | --> | ||
+ | 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== | ==RIM scope== |
Revision as of 18:26, 3 October 2014
Contents
- 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
DeviceAlert
Owning committee name
Contributing or Reviewing Work Groups
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