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本文(EN ISO 12967-2-2011 en Health informatics - Service architecture - Part 2 Information viewpoint《医疗信息学 服务体系机构 第2部分 信息观点》.pdf)为本站会员(registerpick115)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

EN ISO 12967-2-2011 en Health informatics - Service architecture - Part 2 Information viewpoint《医疗信息学 服务体系机构 第2部分 信息观点》.pdf

1、raising standards worldwideNO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBSI Standards PublicationBS EN ISO 12967-2:2011Health informatics Service architecturePart 2: Information viewpoint (ISO 12967-2:2009)BS EN ISO 12967-2:2011 BRITISH STANDARDNational forewordThis British

2、Standard is the UK implementation of EN ISO 12967-2:2011. It is identical to ISO 12967-2:2009. It supersedes BS EN 12967-2:2007, which is withdrawn.The UK participation in its preparation was entrusted to T e c h n i c a l C o m m i t t e e I S T / 3 5 , H e a l t h i n f o r m a t i c s .A list of

3、organizations represented on this committee can be obtained on request to its secretary.This publication does not purport to include all the necessary provisions of a contract. Users are responsible for its correct application. BSI 2011 ISBN 978 0 580 72273 8 ICS 35.240.80 Compliance with a British

4、Standard cannot confer immunity from legal obligations.This British Standard was published under the authority of the Standards Policy and Strategy Committee on 30 April 2011.Amendments issued since publicationDate T e x t a f f e c t e dEUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN ISO 12967

5、-2 March 2011 ICS 35.240.80 Supersedes EN 12967-2:2007English Version Health informatics - Service architecture - Part 2: Information viewpoint (ISO 12967-2:2009) Informatique de sant - Architecture de service - Partie 2: Point de vue dinformation (ISO 12967-2:2009) Medizinische Informatik - Service

6、architektur - Teil 2: Informationssicht (ISO 12967-2:2009) This European Standard was approved by CEN on 10 March 2011. 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

7、 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 lan

8、guage 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, Denma

9、rk, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISAT

10、ION EUROPISCHES KOMITEE FR NORMUNG Management Centre: Avenue Marnix 17, B-1000 Brussels 2011 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN ISO 12967-2:2011: EBS EN ISO 12967-2:2011 EN ISO 12967-2:2011 (E) 3 Foreword The text of I

11、SO 12967-2:2009 has been prepared by Technical Committee ISO/TC 215 “Health informatics” of the International Organization for Standardization (ISO) and has been taken over as EN ISO 12967-2:2011 by Technical Committee CEN/TC 251 “Health informatics” the secretariat of which is held by NEN. This Eur

12、opean Standard shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by September 2011, and conflicting national standards shall be withdrawn at the latest by September 2011. Attention is drawn to the possibility that some of th

13、e elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible for identifying any or all such patent rights. This document supersedes EN 12967-2:2007. According to the CEN/CENELEC Internal Regulations, the national standards organizations of the fo

14、llowing 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, Romania, Sl

15、ovakia, Slovenia, Spain, Sweden, Switzerland and the United Kingdom. Endorsement notice The text of ISO 12967-2:2009 has been approved by CEN as a EN ISO 12967-2:2011 without any modification. BS EN ISO 12967-2:2011ISO 12967-2:2009(E) ISO 2009 All rights reserved iiiContents Page Foreword .v Introdu

16、ctionvi 1 Scope1 2 Normative references1 3 Terms and definitions .2 4 Symbols and abbreviations2 5 Methodological principles 2 5.1 Language and notation adopted for the specification of the model (informative).2 5.2 UML Class Diagram notation guidelines and profile (informative) 3 5.3 Clusters of ob

17、jects in the information model.4 5.4 Operational and descriptive information: classifications, knowledge and its instantiation .5 5.5 DataTypes.7 5.6 Organization of the document .8 6 General characteristics of the model 9 6.1 Common structure of each information object: the GenericHisaClass.9 6.2 U

18、ML diagram10 6.3 Specification of Generic HISA Class .11 6.3.1 General .11 6.3.2 Class: Set of structured attributes 11 6.3.3 Class: Set of class specific attributes.11 6.3.4 Class: Set of common attributes .11 6.3.5 Class: Set of system attributes12 6.3.6 Class: Set of version attributes .12 6.3.7

19、Class: Extended attributes .13 6.3.8 Class: State changes 13 6.3.9 Class: Business rules .14 6.3.10 Class: Classification criteria 14 7 The reference information models 15 7.1 Classification objects15 7.1.1 Scope15 7.1.2 UML information model 15 7.1.3 Specification of the individual classes .16 7.2

20、Subject of care objects .19 7.2.1 Scope19 7.2.2 UML information model 19 7.2.3 Specification of the individual classes .20 7.3 Activity management objects.25 7.3.1 Scope25 7.3.2 UML information model 25 7.3.3 Specification of the individual classes .26 7.4 Clinical and health information objects 33

21、7.4.1 Scope33 7.4.2 UML information model 33 7.4.3 Specification of the individual classes .34 7.5 Resource management objects .39 7.5.1 Scope39 7.5.2 UML information model 39 7.5.3 Specification of the individual classes .40 BS EN ISO 12967-2:2011ISO 12967-2:2009(E) iv ISO 2009 All rights reserved7

22、.6 User and authorization objects 45 7.6.1 Scope 45 7.6.2 UML information model.46 7.6.3 Specification of the individual classes47 7.7 Messaging Objects 51 7.7.1 Scope 51 7.7.2 UML information model.52 7.7.3 Specification of the individual classes52 Annex A (informative) Mappings between HISA and GP

23、IC.56 Bibliography 58 BS EN ISO 12967-2:2011ISO 12967-2:2009(E) ISO 2009 All rights reserved vForeword 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 carrie

24、d 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. IS

25、O collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization. International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2. The main task of technical committees is to prepare Internatio

26、nal Standards. Draft International Standards adopted by the technical committees are circulated to the member bodies for voting. Publication as an International Standard requires approval by at least 75 % of the member bodies casting a vote. Attention is drawn to the possibility that some of the ele

27、ments of this document may be the subject of patent rights. ISO shall not be held responsible for identifying any or all such patent rights. ISO 12967-2 was prepared by Technical Committee ISO/TC 215, Health informatics, based on the European Standard EN 12967-2:2007 with minor editorial amendments.

28、 ISO 12967 consists of the following parts, under the general title Health informatics Service architecture: Part 1: Enterprise viewpoint Part 2: Information viewpoint Part 3: Computational viewpoint BS EN ISO 12967-2:2011ISO 12967-2:2009(E) vi ISO 2009 All rights reservedIntroduction This is the se

29、cond part of ISO 12967, a multi-part standard that provides guidance for the description, planning and development of new systems as well as for the integration of existing information systems, both within one enterprise and across different healthcare organizations through an architecture integrati

30、ng the common data and business logic into a specific architectural layer (i.e. the middleware), distinct from individual applications and accessible throughout the whole information system through services, as shown in Figure 1. Middleware of objectsintegrating common data and common business logic

31、ApplicationsScope of the standardFigure 1 Scope The overall architecture is formalized according to ISO/IEC 10746 (all parts) and is therefore structured through the following three viewpoints. a) Enterprise viewpoint: specifies a set of fundamental common requirements at enterprise level with respe

32、ct to the organizational purposes, scopes and policies that must be supported by the information and functionality of the middleware. It also provides guidance on how one individual enterprise (e.g. a regional healthcare authority, a large hospital or any other organization where this model is appli

33、cable) can specify and document additional specific business requirements, with a view to achieving a complete specification, adequate for the characteristics of that enterprise. Enterprise viewpoint is specified in ISO 12967-1. b) Information viewpoint: specifies the fundamental semantics of the in

34、formation model to be implemented by the middleware to integrate the common enterprise data and to support the enterprise requirements formalized in ISO 12967-1. It also provides guidance on how one individual enterprise can extend the standard model with additional concepts needed to support local

35、requirements in terms of information to be put in common. Information viewpoint is specified in this part of ISO 12967. c) Computational viewpoint: specifies the scope and characteristics of the services that must be provided by the middleware for allowing access to the common data as well as the ex

36、ecution of the business logic supporting the enterprise processes identified in the information viewpoint and in ISO 12967-1. It also provides guidance on how one individual enterprise can specify additional services needed to support local specific requirements in terms of common business logic to

37、be implemented. Computational viewpoint is specified in ISO 12967-3. BS EN ISO 12967-2:2011INTERNATIONAL STANDARD ISO 12967-2:2009(E) ISO 2009 All rights reserved 1Health informatics Service architecture Part 2: Information viewpoint 1 Scope This part of ISO 12967 specifies the fundamental character

38、istics of the information model to be implemented by a specific architectural layer (i.e. the middleware) of the information system to provide a comprehensive and integrated storage of the common enterprise data and to support the fundamental business processes of the healthcare organization, as def

39、ined in ISO 12967-1. The information model is specified without any explicit or implicit assumption on the physical technologies, tools or solutions to be adopted for its physical implementation in the various target scenarios. The specification is nevertheless formal, complete and non-ambiguous eno

40、ugh to allow implementers to derive an efficient design of the system in the specific technological environment that will be selected for the physical implementation. This specification does not aim at representing a fixed, complete, specification of all possible data that can be necessary for any r

41、equirement of any healthcare enterprise. It specifies only a set of characteristics, in terms of overall organization and individual information objects, identified as fundamental and common to all healthcare organizations, and that is satisfied by the information model implemented by the middleware

42、. Preserving consistency with the provisions of this part of ISO 12967, physical implementations allow extensions to the standard information model in order to support additional and local requirements. Extensions include both the definition of additional attributes in the objects of the standard mo

43、del, and the implementation of entirely new objects. Also this standard specification is extensible over time according to the evolution of the applicable standardization initiatives. The specification of extensions is carried out according to the methodology defined in ISO 12967-1:2009, Clause 7, “

44、Methodology for extensions”. 2 Normative references The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applie

45、s. ISO/IEC 11404:2007, Information technology General-Purpose Datatypes (GPD) ISO 12967-1:2009, Health informatics Service architecture Part 1: Enterprise viewpoint ISO 12967-3:2009, Health informatics Service architecture Part 3: Computational viewpoint BS EN ISO 12967-2:2011ISO 12967-2:2009(E) 2 I

46、SO 2009 All rights reserved3 Terms and definitions For the purposes of this document, the following terms and definitions apply. 3.1 information object information held by the system about entities of the real world, including the ODP system itself, is represented in an information specification in

47、terms of information objects, their relationships and behaviour 3.2 package cluster of information objects 3.3 middleware enabling technology of enterprise application integration (EAI) describing a piece of software that connects two or more software applications so that they can exchange data 3.4

48、enterprise application integration EAI use of software and computer systems architectural principles to integrate a set of enterprise computer applications 4 Symbols and abbreviations ODP Open Distributed Processing HISA Health Informatics Service Architecture UML Unified Modelling Language GPIC Gen

49、eral Purpose Information Component 5 Methodological principles 5.1 Language and notation adopted for the specification of the model (informative) The objective of the information viewpoint specification is to describe the information relevant for the enterprise to be handled by the middleware. It consists of a formal information model detailing the semantic and syntactic aspects of all data to be managed. The specification is based on an object model, derived from the enterprise viewpoint by properly structuring and aggregating the

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