ISO/IEEE 11073-10103:2014
Health informatics — Point-of-care medical device communication — Part 10103: Nomenclature — Implantable device, cardiac
ISO/IEEE 11073-10103:2014 extends the base nomenclature provided in IEEE 11073 to support terminology for implantable cardiac devices. Devices within the scope of this nomenclature are implantable devices such as pacemakers, defibrillators, devices for cardiac resynchronization therapy, and implantable cardiac monitors. The discrete terms necessary to convey a clinically relevant summary of the information obtained during a device interrogation are defined in this nomenclature. To improve workflow efficiencies, cardiology and electrophysiology practices require the management of summary interrogation information from all vendor devices and systems in a central system such as an Electronic Health Records (EHR) system or a device clinic management system. To address this requirement, the Implantable Device, Cardiac (IDC) Nomenclature defines a standard-based terminology for device data. The nomenclature facilitates the transfer of data from the vendor proprietary systems to the clinic EHR or device clinic management system.
| Get this standard | Prices exclude GST | |
|---|---|---|
| PDF ( Single user document) |
$141.75 NZD
|
|
| HardCopy |
$194.63 NZD
|
|
| Networkable PDF |
Price varies
|
IEEE Std 11073-10103-2012 Front Cover
Title Page
Notice to users
Laws and regulations
Copyrights
Updating of IEEE documents
Errata
Patents
Introduction
Contents
Important Notice
1. Overview
1.1 Scope
1.2 Purpose
1.3 Audience
1.4 Context
2. Normative references
3. Definitions, acronyms, and abbreviations
3.1 Definitions
3.2 Acronyms and abbreviations
4. Introduction to IEEE 11073 implantable devices cardiac domain
5. Nomenclature requirements
5.1 Overview
5.2 Scope requirements
5.3 Organizational structure requirements
5.4 Semantic requirements
6. Nomenclature structure
6.1 Overview
6.2 Highest level containment nodes
6.2.1 Measurement nodes
6.2.2 Setting nodes
6.2.3 Statistic nodes
6.2.4 Discriminators in containment hierarchy
7. Conformance
7.1 Applicability
7.2 Conformance specification
7.3 Implementation conformance statements (ICSs)
7.4 General ICS
7.5 Mandatory ICS
7.6 Optional ICS
8. Extensibility/versioning
Annex A (normative) Base terms
A.1 Overview
A.2 Version
A.3 Base term attributes
A.3.1 Reference identifier
A.3.2 Display name
A.3.3 Definition
A.3.4 Type
A.3.5 Format
A.3.6 Unit of measure
A.3.7 Enumerator identifier
A.4 Partition details
A.5 Table of base terms
A.6 Table of discriminators
Annex B (informative) Base terms additional properties
B.1 Overview
B.2 Primary key
B.3 O—Optionality
B.4 C—Cardinality
B.5 CC—Co-constraint rules
B.5.1 Table of co-constraint rules
Annex C (normative) Expanded terms with systematic name and codes
C.1 Overview
C.2 Expanded term attributes
C.2.1 Reference identifier
C.2.2 Systematic name
C.2.3 Code
C.3 Expanded terms with systematic name and codes (normative)
Annex D (normative) Enumerations
D.1 Overview
D.2 Enumeration attributes
D.2.1 Enumerator identifier
D.2.2 Enumeration code
D.2.3 Display name
D.2.4 Definition
D.3 Enumerations
Annex E (informative) Vendor enumerations
E.1 Overview
E.2 Enumeration attributes
E.2.1 Enumerator identifier
E.2.2 Enumeration code
E.2.3 Display name
E.2.4 Definition
E.3 Vendor enumerations
E.3.1 Enumerations Biotronik
E.3.2 Enumerations Boston Scientific
E.3.3 Enumerations Medtronic
E.3.4 Enumerations Sorin
E.3.5 Enumerations St. Jude Medical
Annex F (informative) Example report
Annex G (informative) Implementation notes
G.1 Overview
G.2 Identifiers based on the [HIGHLOW] discriminator
G.3 Abnormal flags, null flavors
G.4 Maintaining an episode list
G.5 Identifiers incorporating the [MMM] discriminator (Min, Max, Mean)
G.6 Identifiers with a Null discriminator
G.7 Measurement dates and times (_DTM_[STRTEND])
G.8 Measurement dates and times for episode counts (_COUNT_DTM)
Annex H (informative) Schema and XML for nomenclature
H.1 Description
H.2 Schema
H.3 XML
H.4 XSLT
H.5 XML Discriminators
Annex I (informative) Bibliography
Annex J (informative) IEEE list of participants
Blank Page
Untitled
Keep me up-to-date
Sign up to receive updates when there are changes to this standard
Related Information
Similar Standards
-
BS 30440:2023
Validation framework for the use of artificial intelligence (AI) within healthcare. Specification
-
BS 8684:2024
Technology enabled care. Assessment of user needs and risks, system design, installation and maintenance. Code of practice
-
BS EN 1064:2020
Health informatics. Standard communication protocol. Computer-assisted electrocardiography
-
BS EN 1068:2005
Health informatics. Registration of coding systems
IEEE Std 11073-10103-2012 Front Cover
Title Page
Notice to users
Laws and regulations
Copyrights
Updating of IEEE documents
Errata
Patents
Introduction
Contents
Important Notice
1. Overview
1.1 Scope
1.2 Purpose
1.3 Audience
1.4 Context
2. Normative references
3. Definitions, acronyms, and abbreviations
3.1 Definitions
3.2 Acronyms and abbreviations
4. Introduction to IEEE 11073 implantable devices cardiac domain
5. Nomenclature requirements
5.1 Overview
5.2 Scope requirements
5.3 Organizational structure requirements
5.4 Semantic requirements
6. Nomenclature structure
6.1 Overview
6.2 Highest level containment nodes
6.2.1 Measurement nodes
6.2.2 Setting nodes
6.2.3 Statistic nodes
6.2.4 Discriminators in containment hierarchy
7. Conformance
7.1 Applicability
7.2 Conformance specification
7.3 Implementation conformance statements (ICSs)
7.4 General ICS
7.5 Mandatory ICS
7.6 Optional ICS
8. Extensibility/versioning
Annex A (normative) Base terms
A.1 Overview
A.2 Version
A.3 Base term attributes
A.3.1 Reference identifier
A.3.2 Display name
A.3.3 Definition
A.3.4 Type
A.3.5 Format
A.3.6 Unit of measure
A.3.7 Enumerator identifier
A.4 Partition details
A.5 Table of base terms
A.6 Table of discriminators
Annex B (informative) Base terms additional properties
B.1 Overview
B.2 Primary key
B.3 O—Optionality
B.4 C—Cardinality
B.5 CC—Co-constraint rules
B.5.1 Table of co-constraint rules
Annex C (normative) Expanded terms with systematic name and codes
C.1 Overview
C.2 Expanded term attributes
C.2.1 Reference identifier
C.2.2 Systematic name
C.2.3 Code
C.3 Expanded terms with systematic name and codes (normative)
Annex D (normative) Enumerations
D.1 Overview
D.2 Enumeration attributes
D.2.1 Enumerator identifier
D.2.2 Enumeration code
D.2.3 Display name
D.2.4 Definition
D.3 Enumerations
Annex E (informative) Vendor enumerations
E.1 Overview
E.2 Enumeration attributes
E.2.1 Enumerator identifier
E.2.2 Enumeration code
E.2.3 Display name
E.2.4 Definition
E.3 Vendor enumerations
E.3.1 Enumerations Biotronik
E.3.2 Enumerations Boston Scientific
E.3.3 Enumerations Medtronic
E.3.4 Enumerations Sorin
E.3.5 Enumerations St. Jude Medical
Annex F (informative) Example report
Annex G (informative) Implementation notes
G.1 Overview
G.2 Identifiers based on the [HIGHLOW] discriminator
G.3 Abnormal flags, null flavors
G.4 Maintaining an episode list
G.5 Identifiers incorporating the [MMM] discriminator (Min, Max, Mean)
G.6 Identifiers with a Null discriminator
G.7 Measurement dates and times (_DTM_[STRTEND])
G.8 Measurement dates and times for episode counts (_COUNT_DTM)
Annex H (informative) Schema and XML for nomenclature
H.1 Description
H.2 Schema
H.3 XML
H.4 XSLT
H.5 XML Discriminators
Annex I (informative) Bibliography
Annex J (informative) IEEE list of participants
Blank Page
Untitled