Health Informatics — Terminology resource map quality measures (MapQual)

This document provides quality requirements for producing a quality map between terminological systems. This document establishes measures which can be used to assess the quality and utility of a map between terminological resources in order to determine the types and levels of measure required for common use cases in healthcare. NOTE Examples of such cases include conformity assessment.

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Status
Published
Publication Date
17-Jun-2019
Current Stage
9599 - Withdrawal of International Standard
Start Date
28-May-2025
Completion Date
31-May-2025
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ISO/TS 21564:2019 - Health Informatics — Terminology resource map quality measures (MapQual) Released:6/18/2019
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Technical specification
ISO/TS 21564:2019 - Health Informatics -- Terminology resource map quality measures (MapQual)
English language
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TECHNICAL ISO/TS
SPECIFICATION 21564
First edition
2019-06
Health Informatics — Terminology
resource map quality measures
(MapQual)
Reference number
©
ISO 2019
© ISO 2019
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Fax: +41 22 749 09 47
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2019 – All rights reserved

Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Determinants of map quality . 4
4.1 General . 4
4.2 Terminological resource capacity . 4
4.2.1 General. 4
4.2.2 Determinant 1: Common categorial structure . 4
4.2.3 Determinant 2: Shared semantic domain . 5
4.2.4 Determinant 3: Language and translation . 6
4.3 Equivalence of individual maps . 7
4.3.1 General. 7
4.3.2 Determinant 4: Equivalence identification/Publication . 7
4.3.3 Determinant 5: Equivalence assessment . 7
4.3.4 Determinant 6: Map set outliers . 8
4.4 Building a map set . 9
4.4.1 Map development process . 9
4.4.2 Determinant 7: Clear documentation of the purpose of the map . 9
4.4.3 Determinant 8: Currency of the map . 9
4.4.4 Determinant 9: Business arrangements .10
4.4.5 Determinant 10: Methodology documentation .10
4.4.6 Validation .11
4.4.7 Determinant 13: Decision making — Consensus building process .12
4.4.8 Determinant 14: Tools used to develop or maintain the map .13
4.4.9 Determinant 15: Workforce .14
4.5 Map governance and maintenance .16
4.5.1 Determinant 16: Governance .16
4.5.2 Determinant 17: Map maintenance .16
5 Using map quality determinants .17
5.1 Required determinants .17
5.2 Level of quality .17
5.2.1 Step 1: Establish map quality requirement .17
5.2.2 Step 2: Assess map against requirement .17
5.2.3 Step 3: Calculate the score and actions required .17
6 Use cases .18
6.1 General .18
6.2 Determining requirements for a purpose . .18
6.2.1 General.18
6.3 Direct patient care use case .19
6.3.1 General.19
6.3.2 Direct patient care level of conformance required and rationale .19
6.4 Administrative, financial or service planning use case .20
6.4.1 General.20
6.5 Administrative, financial or service planning level of conformance required and
rationale .21
6.6 Other use cases .22
Annex A (informative) Example of map quality evaluation .23
Bibliography .24
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out
through ISO technical committees. Each member body interested in a subject for which a technical
committee has been established has the right to be represented on that committee. International
organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of
electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of
any patent rights identified during the development of the document will be in the Introduction and/or
on the ISO list of patent declarations received (see www .iso .org/patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO's adherence to the
World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see www .iso
.org/iso/foreword .html.
This document was prepared by Technical Committee ISO/TC 215, Health Informatics.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www .iso .org/members .html.
iv © ISO 2019 – All rights reserved

Introduction
0.1  General
Healthcare organizations and software vendors are increasingly using maps to convert data from one
code system to another code system. In the past, data in health information systems was largely used
for organizations’ administrative planning and decision making. Data captured in Electronic Health
Records (EHR) systems for patient care has a significant impact on patient safety. The use of this data
as the source of data for other purposes and for information exchange in clinical care through the use of
information technology is an emerging problem. Where that data is translated through maps from one
code system to another, the safety and quality issues associated with data use can be significant. The
increasing use of maps is costly.
The objective of this work is to support the definition of quality requirements for map sets to
a) establish standard quality conformance requirements for a map for a purpose,
b) assess the quality of a map for a purpose,
c) guide decision makers in map project requirements and processes, and
d) establish pathways to improvement.
Maps are widely used but the quality of these maps cannot be accurately and consistently assessed and
compared against their intended use. It is not currently possible for decision makers to assess whether
a map will be worth the cost of building and whether the scope and map processes will deliver a map
which is able to meet the intended business case.
[1]
This document is based upon ISO/TR 12300 . Some terminological resources are so different in their
content and purpose that they will never map closely to a resource designed and structured differently.
Therefore, the decision maker might need to consider whether to map at all or to move to a new
terminological resource.
Quality measures consider a wide range of requirements and processes relevant to the creation and
maintenance of data maps and their use (including manual and tool-based mapping), as well as for the
map sets delivered as a result of using that process.
0.2  Stakeholders and audience
This document is focused on the needs of
a) implementers and software vendors developing and implementing maps sets,
b) health information and data managers developing and using maps sets,
c) data users such as researchers, government, decision makers, and
d) developers of map sets including all in mapping teams including terminologists, coders, clinical
users, epidemiologists and statisticians, project managers.
Additionally, the target audience for this document might include
— procurement officers who establish requirements of map product capacity and quality, or
— decision makers to determine and assess resources needed in projects and services associated with
map produce, maintenance or use.
0.3  Challenges of mapping
Healthcare organizations and software vendors are i
...


TECHNICAL ISO/TS
SPECIFICATION 21564
First edition
2019-06
Health Informatics — Terminology
resource map quality measures
(MapQual)
Reference number
©
ISO 2019
© ISO 2019
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Fax: +41 22 749 09 47
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2019 – All rights reserved

Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Determinants of map quality . 4
4.1 General . 4
4.2 Terminological resource capacity . 4
4.2.1 General. 4
4.2.2 Determinant 1: Common categorial structure . 4
4.2.3 Determinant 2: Shared semantic domain . 5
4.2.4 Determinant 3: Language and translation . 6
4.3 Equivalence of individual maps . 7
4.3.1 General. 7
4.3.2 Determinant 4: Equivalence identification/Publication . 7
4.3.3 Determinant 5: Equivalence assessment . 7
4.3.4 Determinant 6: Map set outliers . 8
4.4 Building a map set . 9
4.4.1 Map development process . 9
4.4.2 Determinant 7: Clear documentation of the purpose of the map . 9
4.4.3 Determinant 8: Currency of the map . 9
4.4.4 Determinant 9: Business arrangements .10
4.4.5 Determinant 10: Methodology documentation .10
4.4.6 Validation .11
4.4.7 Determinant 13: Decision making — Consensus building process .12
4.4.8 Determinant 14: Tools used to develop or maintain the map .13
4.4.9 Determinant 15: Workforce .14
4.5 Map governance and maintenance .16
4.5.1 Determinant 16: Governance .16
4.5.2 Determinant 17: Map maintenance .16
5 Using map quality determinants .17
5.1 Required determinants .17
5.2 Level of quality .17
5.2.1 Step 1: Establish map quality requirement .17
5.2.2 Step 2: Assess map against requirement .17
5.2.3 Step 3: Calculate the score and actions required .17
6 Use cases .18
6.1 General .18
6.2 Determining requirements for a purpose . .18
6.2.1 General.18
6.3 Direct patient care use case .19
6.3.1 General.19
6.3.2 Direct patient care level of conformance required and rationale .19
6.4 Administrative, financial or service planning use case .20
6.4.1 General.20
6.5 Administrative, financial or service planning level of conformance required and
rationale .21
6.6 Other use cases .22
Annex A (informative) Example of map quality evaluation .23
Bibliography .24
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out
through ISO technical committees. Each member body interested in a subject for which a technical
committee has been established has the right to be represented on that committee. International
organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of
electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of
any patent rights identified during the development of the document will be in the Introduction and/or
on the ISO list of patent declarations received (see www .iso .org/patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO's adherence to the
World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see www .iso
.org/iso/foreword .html.
This document was prepared by Technical Committee ISO/TC 215, Health Informatics.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www .iso .org/members .html.
iv © ISO 2019 – All rights reserved

Introduction
0.1  General
Healthcare organizations and software vendors are increasingly using maps to convert data from one
code system to another code system. In the past, data in health information systems was largely used
for organizations’ administrative planning and decision making. Data captured in Electronic Health
Records (EHR) systems for patient care has a significant impact on patient safety. The use of this data
as the source of data for other purposes and for information exchange in clinical care through the use of
information technology is an emerging problem. Where that data is translated through maps from one
code system to another, the safety and quality issues associated with data use can be significant. The
increasing use of maps is costly.
The objective of this work is to support the definition of quality requirements for map sets to
a) establish standard quality conformance requirements for a map for a purpose,
b) assess the quality of a map for a purpose,
c) guide decision makers in map project requirements and processes, and
d) establish pathways to improvement.
Maps are widely used but the quality of these maps cannot be accurately and consistently assessed and
compared against their intended use. It is not currently possible for decision makers to assess whether
a map will be worth the cost of building and whether the scope and map processes will deliver a map
which is able to meet the intended business case.
[1]
This document is based upon ISO/TR 12300 . Some terminological resources are so different in their
content and purpose that they will never map closely to a resource designed and structured differently.
Therefore, the decision maker might need to consider whether to map at all or to move to a new
terminological resource.
Quality measures consider a wide range of requirements and processes relevant to the creation and
maintenance of data maps and their use (including manual and tool-based mapping), as well as for the
map sets delivered as a result of using that process.
0.2  Stakeholders and audience
This document is focused on the needs of
a) implementers and software vendors developing and implementing maps sets,
b) health information and data managers developing and using maps sets,
c) data users such as researchers, government, decision makers, and
d) developers of map sets including all in mapping teams including terminologists, coders, clinical
users, epidemiologists and statisticians, project managers.
Additionally, the target audience for this document might include
— procurement officers who establish requirements of map product capacity and quality, or
— decision makers to determine and assess resources needed in projects and services associated with
map produce, maintenance or use.
0.3  Challenges of mapping
Healthcare organizations and software vendors are i
...

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