Difference between revisions of "Product TD"
(New page: =Product Brief - Therapeutic Devices Domain= __TOC__ back to Main_Page<br/>back to Product_List ==Product Name - HL7 V3:Implantable Device Cardiac - Follow-up Device Summary, Relea...) |
|||
| Line 26: | Line 26: | ||
===Description=== | ===Description=== | ||
In simple terms, we have a message model for describing an Observation of an interrogator at a physical location who is performing an interrogation of a therapeutic medical device (bound to a patient) using identifiable interrogation equipment. | In simple terms, we have a message model for describing an Observation of an interrogator at a physical location who is performing an interrogation of a therapeutic medical device (bound to a patient) using identifiable interrogation equipment. | ||
| − | + | ||
===Business Case (Intended Use, Customers)=== | ===Business Case (Intended Use, Customers)=== | ||
| − | + | To enable a standardized device report format to be used across the (Implantable Device Cardiac) IDC sector.<br/> | |
| + | Users: IDC industry and cardiologists/cardiac technicians. | ||
===Benefits=== | ===Benefits=== | ||
| − | + | Enables a standardized device report format to be used across the IDC sector, thereby improving access to care by patients, and business opportunites to the IDC industry and cardiologists/cardiac technicians. | |
===Implementations/ Case Studies (Actual Users)=== | ===Implementations/ Case Studies (Actual Users)=== | ||
| − | + | IHE Connectathon 2010 | |
===Resources=== | ===Resources=== | ||
| Line 47: | Line 48: | ||
====Presentations==== | ====Presentations==== | ||
| − | * | + | *--> |
===Relationship to/ Dependencies on, other standards=== | ===Relationship to/ Dependencies on, other standards=== | ||
| − | + | Uses IEEE 11073-10103 standardised IDC terminology | |
===Links to current projects in development=== | ===Links to current projects in development=== | ||
*none | *none | ||
Latest revision as of 19:49, 13 November 2009
Product Brief - Therapeutic Devices Domain
Contents
- 1 Product Brief - Therapeutic Devices Domain
- 1.1 Product Name - HL7 V3:Implantable Device Cardiac - Follow-up Device Summary, Release 1
- 1.1.1 Topics
- 1.1.2 Standard Category
- 1.1.3 Integration Paradigm
- 1.1.4 Type
- 1.1.5 Releases
- 1.1.6 Summary
- 1.1.7 Description
- 1.1.8 Business Case (Intended Use, Customers)
- 1.1.9 Benefits
- 1.1.10 Implementations/ Case Studies (Actual Users)
- 1.1.11 Resources
- 1.1.12 Relationship to/ Dependencies on, other standards
- 1.1.13 Links to current projects in development
- 1.1 Product Name - HL7 V3:Implantable Device Cardiac - Follow-up Device Summary, Release 1
back to Main_Page
back to Product_List
Product Name - HL7 V3:Implantable Device Cardiac - Follow-up Device Summary, Release 1
Topics
- Implantable Cardiac Device
Standard Category
- Health Information Exchange Standards
Integration Paradigm
- Messaging
Type
Normative, ANSI Standard
Releases
- ANSI/HL7 V3 IDC, R1-2006;
- ANSI/HL7 V3 IDC, R2-2007: Implantable Device Cardiac - Follow up summary R2
Summary
The therapeutic devices domain comprises the models, messages, and other artifacts that are needed to support messaging related to therapy delivery and observations made by a medical device.
Currently, the scope has been focused only on implantable cardiac devices (pacemakers, defibrillators, etc.).
This message is related to the follow-up of an Implantable Cardiac Device (pacemaker, defibrillator, etc.) that will contain a subset of device observations, current device therapy settings and device diagnostic information.
Description
In simple terms, we have a message model for describing an Observation of an interrogator at a physical location who is performing an interrogation of a therapeutic medical device (bound to a patient) using identifiable interrogation equipment.
Business Case (Intended Use, Customers)
To enable a standardized device report format to be used across the (Implantable Device Cardiac) IDC sector.
Users: IDC industry and cardiologists/cardiac technicians.
Benefits
Enables a standardized device report format to be used across the IDC sector, thereby improving access to care by patients, and business opportunites to the IDC industry and cardiologists/cardiac technicians.
Implementations/ Case Studies (Actual Users)
IHE Connectathon 2010
Resources
Work Groups
Education
- See more at http://www.hl7.org/implement/training.cfm
Relationship to/ Dependencies on, other standards
Uses IEEE 11073-10103 standardised IDC terminology
Links to current projects in development
- none
