EN ISO 12967-3:2020

Health informatics - Service Architecture (HISA) - Part 3: Computational viewpoint (ISO 12967-3:2020)

This document specifies the fundamental characteristics of the computational model implemented by a specific architectural layer of the information system (i.e. the service architecture) to provide a comprehensive and integrated interface to the common enterprise information and to support the fundamental business processes of the healthcare organization, as defined in ISO 12967‑1. The computational model is specified without any explicit or implicit assumption about the physical technologies, tools or solutions to adopt for its physical implementation in the various target scenarios. The specification is nevertheless formal, complete and non-ambiguous enough to allow implementers to derive an efficient design of the system in the specific technological environment which will be selected for the physical implementation.
The computational model specified in this document provides the basis for ensuring consistency between different engineering and technology specifications (including programming languages and communication mechanisms) since they are intended to be consistent with the same computational object model. This consistency allows open inter-working and portability of components in the resulting implementation.
This document does not aim at representing a fixed, complete, specification of all possible interfaces that might be necessary for any requirement of any healthcare enterprise. It specifies only a set of characteristics — in terms of overall organization and individual computational objects, identified as fundamental and common to all healthcare organizations, and that are satisfied by the computational model implemented by the service architecture.
Preserving consistency with the provisions of this document, physical implementations of the computational model specified in this document can allow extensions in order to support additional and local requirements. Extensions can include both the definition of additional properties of the objects of the computational model specified in this document and the implementation of entirely new objects.
Also, the computational model specified in this document can be extendable over time according to the evolution of the applicable standardization initiatives, in accordance to the methodology defined in ISO 12967‑1:2020, Clause 7, which identifies a set of healthcare common information services, describing the requirements behind them and the methodology through which they will be used.
The information services specified in this document are only the minimal set identifiable according to the identified requirements of the healthcare enterprise, and constituting the service architecture (i.e. the integration platform) to serve as the basis for healthcare applications, e.g. EHR or patient administration.

Medizinische Informatik - Servicearchitektur - Teil 3: Verarbeitungssicht (ISO 12967-3:2020)

Informatique de santé - Architecture de service - Partie 3: Point de vue informatique (ISO 12967-3:2020)

Le présent document spécifie les caractéristiques fondamentales du modèle de traitement mis en place par une couche architecturale spécifique du système d'informations (c'est-à-dire l'architecture de service) pour assurer une interface cohérente et intégrée aux données d'entreprise communes et prendre en charge les processus métier fondamentaux de l'organisme de santé, tel que défini dans l'ISO 12967-1. Le modèle de traitement est spécifié sans émettre d'hypothèse explicite ou implicite sur les technologies physiques, les outils ou les solutions à adopter pour sa mise en œuvre physique dans le cadre des différents scénarios cible. La spécification n'en est pas moins formelle, exhaustive et sans ambiguïté, afin de permettre aux implémenteurs de prévoir une conception efficace du système dans l'environnement technologique spécifique sélectionné pour sa mise en œuvre physique.
Le modèle de traitement spécifié dans le présent document fournit la base permettant de garantir la cohérence des différentes spécifications d'ingénierie et de technologie (notamment des langages de programmation et des mécanismes de communication) étant donné qu'elles sont censées être conformes au même modèle d'objet de traitement. Cette cohérence permet de garantir l'interfonctionnement ouvert et la portabilité des composants dans la mise en place finale.
Le présent document n'a pas pour objet d'être une représentation fixe et exhaustive de toutes les interfaces possibles susceptibles d'être nécessaires aux exigences d'une entreprise de santé. Il spécifie simplement un ensemble de caractéristiques (en termes d'objets organisationnels globaux et de traitement individuels) identifiées comme étant essentielles et communes à tous les organismes de santé et que le modèle de traitement mis en place par l'architecture de service doit satisfaire.
Tout en préservant la cohérence avec les dispositions du présent document, les mises en place physiques du modèle de traitement spécifié dans le présent document peuvent permettre des extensions afin de répondre à des exigences supplémentaires et locales. Les extensions peuvent inclure aussi bien la définition de propriétés supplémentaires d'objets du modèle de traitement spécifié dans le présent document que la mise en œuvre d'objets totalement nouveaux.
De même, le modèle de traitement spécifié dans le présent document peut être étendu dans le temps en fonction de l'évolution des initiatives de normalisation applicables, conformément à la méthodologie définie dans l'ISO 12967-1:2020, Article 7, qui identifie un ensemble de services d'informations communs au domaine de la santé, en décrivant les exigences sous-jacentes et la méthodologie en fonction de laquelle ils seront utilisés.
Les services d'informations spécifiés dans le présent document ne correspondent qu'au plus petit ensemble de services d'informations identifiable en fonction des exigences identifiées de l'entreprise de santé et constituant l'architecture de service (c'est-à-dire la plateforme d'intégration) servant de base aux applications de santé, par exemple DIS ou administration des patients.

Zdravstvena informatika - Arhitektura storitve - 3. del: Računalniški vidik (ISO 12967-3:2020)

General Information

• Status: Published
• Publication Date: 17-Nov-2020
• Withdrawal Date: 30-May-2021
• ICS: 35.240.80 - IT applications in health care technology
• Technical Committee: CEN/TC 251 - Medical informatics
• Drafting Committee: CEN/TC 251/WG 1 - Information models
• Current Stage: 6060 - Definitive text made available (DAV) - Publishing
• Start Date: 18-Nov-2020
• Completion Date: 18-Nov-2020
• Ref Project: SIST EN ISO 12967-3:2021 - Health informatics - Service Architecture (HISA) - Part 3: Computational viewpoint (ISO 12967-3:2020)

Relations

• Replaces: EN ISO 12967-3:2011 - Health informatics - Service architecture - Part 3: Computational viewpoint (ISO 12967-3:2009)
• Effective Date: 06-Apr-2016

Standards Content (Sample)

SLOVENSKI STANDARD
01-januar-2021
Nadomešča:
SIST EN ISO 12967-3:2011
Zdravstvena informatika - Arhitektura storitve - 3. del: Računalniški vidik (ISO
12967-3:2020)
Health informatics - Service Architecture (HISA) - Part 3: Computational viewpoint (ISO
12967-3:2020)
Medizinische Informatik - Servicearchitektur - Teil 3: Verarbeitungssicht (ISO 12967-
3:2020)
Informatique de santé - Architecture de service - Partie 3: Point de vue informatique (ISO
12967-3:2020)
Ta slovenski standard je istoveten z: EN ISO 12967-3:2020
ICS:
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EN ISO 12967-3
EUROPEAN STANDARD
NORME EUROPÉENNE
November 2020
EUROPÄISCHE NORM
ICS 35.240.80 Supersedes EN ISO 12967-3:2011
English Version
Health informatics - Service Architecture (HISA) - Part 3:
Computational viewpoint (ISO 12967-3:2020)
Informatique de santé - Architecture de service - Partie Medizinische Informatik - Servicearchitektur - Teil 3:
3: Point de vue informatique (ISO 12967-3:2020) Verarbeitungssicht (ISO 12967-3:2020)
This European Standard was approved by CEN on 11 June 2020.

CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this
European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references
concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN
member.
This European Standard exists in three official versions (English, French, German). A version in any other language made by
translation under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management
Centre has the same status as the official versions.

CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway,
Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and
United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2020 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 12967-3:2020 E
worldwide for CEN national Members.

Contents Page
European foreword . 3

European foreword
This document (EN ISO 12967-3:2020) has been prepared by Technical Committee ISO/TC 215 "Health
informatics" in collaboration with Technical Committee CEN/TC 251 “Health informatics” the
secretariat of which is held by NEN.
This European Standard shall be given the status of a national standard, either by publication of an
identical text or by endorsement, at the latest by May 2021, and conflicting national standards shall be
withdrawn at the latest by May 2021.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN shall not be held responsible for identifying any or all such patent rights.
This document supersedes EN ISO 12967-3:2011.
According to the CEN-CENELEC Internal Regulations, the national standards organizations of the
following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria,
Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland,
Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Republic of
North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the
United Kingdom.
Endorsement notice
The text of ISO 12967-3:2020 has been approved by CEN as EN ISO 12967-3:2020 without any
modification.
INTERNATIONAL ISO
STANDARD 12967-3
Second edition
2020-11
Health informatics — Service
architecture (HISA) —
Part 3:
Computational viewpoint
Informatique de santé — Architecture de service —
Partie 3: Point de vue informatique
Reference number
ISO 12967-3:2020(E)
©
ISO 2020
ISO 12967-3:2020(E)
© ISO 2020
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: [phone]
Email: [e-mail]
Website: www.iso.org
Published in Switzerland
ii © ISO 2020 – All rights reserved

ISO 12967-3:2020(E)
Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 2
4 Abbreviated terms . 2
5 Methodological principles . 2
5.1 General . 2
5.2 Clusters of objects . 2
5.3 Computational language . 3
5.4 The computational objects and interfaces . 4
5.5 Interactions . 5
6 General characteristics of the model . 6
6.1 The two types of computational objects for handling the information . 6
6.2 The ‘basic’ information services . 6
6.2.1 General requirements . 6
6.2.2 ‘Add’ basic information services . 7
6.2.3 "Update" basic information services . 8
6.2.4 "Delete" basic information services .10
6.2.5 "Detail" basic information services .12
6.2.6 "List" basic information services .13
6.3 General-purpose interface .15
6.3.1 General.15
6.3.2 List of information services .16
6.3.3 Behavioural specifications .16
6.4 The eHealth business-related interfaces supporting the workflow computational
objects . .17
6.4.1 General.17
6.4.2 eHealth business-related services managing healthcare workflows .17
6.4.3 Interfaces supporting the “Subject of care workflow” .17
6.4.4 Interfaces supporting the “Healthcare information workflow” .19
6.4.5 Interfaces supporting the “Activity management workflow” .21
6.4.6 Behavioural specifications, common to the eHealth business-related services .23
6.5 Common requirements of the interfaces .24
6.5.1 Interface documentation and organization .24
6.5.2 Naming criteria .24
6.5.3 Data types .25
6.5.4 Structure and organization of the interfaces .25
Annex A (informative) Example of services.27
Annex B (informative) HISA and FHIR® .29
Bibliography .33
ISO 12967-3:2020(E)
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 standar
...