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    EN 14822-2-2005 en Health informatics General purpose information components Part 2 Non-clinical《健康信息学 一般用途信息元 第2部分 非门诊的》.pdf

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    EN 14822-2-2005 en Health informatics General purpose information components Part 2 Non-clinical《健康信息学 一般用途信息元 第2部分 非门诊的》.pdf

    1、BRITISH STANDARDBS EN 14822-2:2005Health informatics General purpose information components Part 2: Non-clinicalThe European Standard EN 14822-2:2005 has the status of a British StandardICS 35.240.80g49g50g3g38g50g51g60g44g49g42g3g58g44g55g43g50g56g55g3g37g54g44g3g51g40g53g48g44g54g54g44g50g49g3g40g

    2、59g38g40g51g55g3g36g54g3g51g40g53g48g44g55g55g40g39g3g37g60g3g38g50g51g60g53g44g42g43g55g3g47g36g58BS EN 14822-2:2005This British Standard was published under the authority of the Standards Policy and Strategy Committee on 22 November 2005 BSI 22 November 2005ISBN 0 580 46905 0National forewordThis

    3、British Standard is the official English language version of EN 14822-2:2005. The UK participation in its preparation was entrusted to Technical Committee IST/35, Health informatics, which has the responsibility to: aid enquirers to understand the text; present to the responsible international/Europ

    4、ean committee any enquiries on the interpretation, or proposals for change, and keep UK interests informed; monitor related international and European developments and promulgate them in the UK.A list of organizations represented on this committee can be obtained on request to its secretary.Cross-re

    5、ferencesThe British Standards which implement international or European publications referred to in this document may be found in the BSI Catalogue under the section entitled “International Standards Correspondence Index”, or by using the “Search” facility of the BSI Electronic Catalogue or of Briti

    6、sh Standards Online.This publication does not purport to include all the necessary provisions of a contract. Users are responsible for its correct application.Compliance with a British Standard does not of itself confer immunity from legal obligations.Summary of pagesThis document comprises a front

    7、cover, an inside front cover, the EN title page, pages 2 to 199 and a back cover.The BSI copyright notice displayed in this document indicates when the document was last issued.Amendments issued since publicationAmd. No. Date CommentsEUROPEAN STANDARDNORME EUROPENNEEUROPISCHE NORMEN 14822-2October 2

    8、005ICS 35.240.80English VersionHealth informatics - General purpose information components -Part 2: Non-clinicalInformatique de sant - Unit dinformation dans lesmessages - Partie 2: Non-cliniqueMedizinische Informatik - Allgemein verwendbareInformationskompomenten - Teil 2: NichtklinischeInformation

    9、enThis European Standard was approved by CEN on 16 August 2005.CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this EuropeanStandard the status of a national standard without any alteration. Up-to-date lists and bibliographical refe

    10、rences concerning such nationalstandards may be obtained on application to the Central Secretariat or to any CEN member.This European Standard exists in three official versions (English, French, German). A version in any other language made by translationunder the responsibility of a CEN member into

    11、 its own language and notified to the Central Secretariat has the same status as the officialversions.CEN members are the national standards bodies of Austria, Belgium, Cyprus, Czech Republic, Denmark, Estonia, Finland, France,Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Lux

    12、embourg, Malta, Netherlands, Norway, Poland, Portugal, Slovakia,Slovenia, Spain, Sweden, Switzerland and United Kingdom.EUROPEAN COMMITTEE FOR STANDARDIZATIONCOMIT EUROPEN DE NORMALISATIONEUROPISCHES KOMITEE FR NORMUNGManagement Centre: rue de Stassart, 36 B-1050 Brussels 2005 CEN All rights of expl

    13、oitation in any form and by any means reservedworldwide for CEN national Members.Ref. No. EN 14822-2:2005: EEN 14822-2:2005 (E) 2 Contents Page Foreword 5 Introduction6 1 Scope .7 2 Normative references .7 3 Terms and definitions.7 4 Symbols and abbreviations8 5 Rules governing the use of general pu

    14、rpose information components .9 6 Common Attribute Groups (CAG)11 6.1 Introduction.11 6.2 Entity Name CAG 11 6.2.1 Entity Name .11 6.2.2 Entity Name Part .12 6.3 Postal Address CAG.13 6.3.1 Postal Address13 6.3.2 Postal Address Part14 6.4 Telecom CAG 14 6.4.1 Telecom .14 7 Common Sub-Components15 7.

    15、1 General description 15 7.1.1 Overview15 7.1.2 Context inheritance.16 7.2 Non Healthcare Person Participation 16 7.3 Healthcare Professional Participation.19 7.4 Healthcare Organisation Participation 21 7.5 Device Participation23 7.6 Healthcare Agent Participation 24 8 General Purpose Information C

    16、omponents an overview26 9 General Purpose Information Components 34 9.1 Living Subject GPICs34 9.1.1 Overview (informative) .34 9.1.2 Person35 9.1.3 Language Communication .37 9.1.4 Place of Birth.39 9.1.5 Residence Information .41 9.2 Organisation Related GPICs 43 9.2.1 Overview (informative) .43 9

    17、.2.2 Organisation43 9.2.3 Identified Organisation .46 9.2.4 Organisation Hierarchy 47 9.2.5 Related Organisation49 9.2.6 Contact Person .50 9.3 Subject of Care Identification GPICs.52 9.3.1 Overview (informative) .52 9.3.2 Subject Of Care Identification 52 9.3.3 Identified Living Subject.54 9.3.4 Su

    18、bject Of Care Person Identification .56 9.3.5 Subject Of Care Animal Identification .58 EN 14822-2:2005 (E) 3 9.4 Subject of Care GPICs59 9.4.1 Overview (informative) .59 9.4.2 Subject Of Care .60 9.4.3 Subject Of Care Person63 9.4.4 Patient Standard Information.66 9.4.5 Patient Extended Information

    19、 69 9.4.6 Subject Of Care Animal 72 9.4.7 Subject Of Care Animal Group.75 9.5 Subject of Care Related GPICs 76 9.5.1 Overview (informative) .76 9.5.2 Related Subject Of Care .77 9.5.3 Subject Of Care Related Party .81 9.6 Subject of Care And Related Parties Involvement in Activities GPICs.83 9.6.1 O

    20、verview (informative) .83 9.6.2 Referenced Subject of Care .84 9.6.3 Participating Subject of Care .86 9.6.4 Participating Patient .88 9.6.5 Identified Participating Patient.89 9.6.6 Participating Patient Related Party91 9.6.7 Participating Related Subject of Care .93 9.6.8 Care Service Recipient .9

    21、4 9.6.9 Subject Of Investigation.97 9.7 Healthcare Agent GPICs - General principles.101 9.8 Healthcare Professional GPICs101 9.8.1 Healthcare Professional .101 9.8.2 Identified Healthcare Professional 105 9.8.3 Related Healthcare Professional .107 9.9 Healthcare Organisation GPICs.109 9.9.1 Healthca

    22、re Organisation.109 9.9.2 Identified Healthcare Organisation111 9.9.3 Related Healthcare Organisation.113 9.10 Healthcare Agent GPICs.115 9.10.1 Healthcare Party115 9.10.2 Identified Healthcare Party.116 9.10.3 Healthcare Agent 118 9.10.4 Identified Healthcare Agent120 9.10.5 Related Healthcare Agen

    23、t.122 9.11 Referenced Healthcare Agent GPICs.124 9.11.1 Referenced Healthcare Professional.124 9.11.2 Referenced Healthcare Organisation 125 9.11.3 Referenced Healthcare Device.127 9.11.4 Referenced Healthcare Party .128 9.11.5 Referenced Healthcare Agent 130 9.12 Healthcare Agent Involvement in Act

    24、ivity GPICs .131 9.12.1 Participating Healthcare Professional.131 9.12.2 Identified Participating Professional .133 9.12.3 Participating Healthcare Organisation 134 9.12.4 Identified Participating Organisation.135 9.13 Participating Healthcare Agent GPICs 136 9.13.1 Participating Healthcare Party .1

    25、36 9.13.2 Participating Healthcare Agent 138 9.14 Device GPICs.139 9.14.1 Device 139 9.14.2 Identified Device .141 9.14.3 Related Device 143 9.14.4 Related Identified Device144 9.14.5 Device In Use.146 9.14.6 Identified Device In Use147 9.14.7 Device Parameter148 EN 14822-2:2005 (E) 4 9.15 Location

    26、GPICs .150 9.15.1 Care Location 150 9.15.2 Care Location In Use 152 9.15.3 Geographic Location 154 9.16 Transportation GPICs .156 9.16.1 Living Subject Transportation .156 9.16.2 Non Living Entity Transportation.161 9.16.3 Related Living Subject Transportation164 9.16.4 Related Non Living Entity Tra

    27、nsportation.165 9.17 Financial GPICs.166 9.17.1 Care Cost.166 9.17.2 Authorisation.169 9.17.3 Service Agreement171 10 Structural Vocabularies175 10.1 Entity Vocabularies.175 10.1.1 Entity Class .175 10.1.2 Entity Determiner 176 10.2 Role Vocabularies.176 10.2.1 Role Class176 10.3 Participation Vocab

    28、ularies .181 10.3.1 Participation Type.181 10.3.2 Participation Status 185 10.3.3 Participation Mode185 10.4 Context Control Participation 186 Annex A (informative) Rationale for this document on General Purpose Information Components.188 Annex B (informative) How to read the models189 B.1 Introduct

    29、ion.189 B.2 Associations between classes.189 B.3 Generalisation/Specialisation 190 Annex C (informative) Health Level 7 (HL7) Reference Information Model191 Annex D (informative) Common features of the general purpose information components193 Annex E (informative) Localisation of the general purpos

    30、e information components .195 Bibliography.196 EN 14822-2:2005 (E) 5 Foreword This European Standard (EN 14822-2:2005) has been prepared by 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 sta

    31、ndard, either by publication of an identical text or by endorsement, at the latest by April 2006, and conflicting national standards shall be withdrawn at the latest by April 2006. This is part two of a multipart standard under the heading: Health informatics - General purpose information components

    32、: Part 1: Overview Part 2: Non-clinical Part 3: Clinical This European Standard is definition of a set of non-clinical general purpose information components. IMPORTANT Within this document each of the General Purpose Information Components and various sub-components are provided with identifiers, w

    33、hich are unique only internally within this document. According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany

    34、, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom. EN 14822-2:2005 (E) 6 Introduction Many previous messaging and information structure standards for health have o

    35、verlapping parts with a number of objects being defined in separate documents, sometimes with small variations making implementation of conformant applications more difficult. It therefore makes sense to define a set of general purpose components that can be used for definition of message structures

    36、 for different purposes1. This approach was suggested and approved as a strategy for CEN/TC 251 in the Short Strategic Study on message standards alignment in 1999 examining a set of five European prestandards for messages. This European Standard is aiming to provide such a set of components and has

    37、 been developed jointly with a new European Standard for Service Request and Report messages that is using the components defined herein. Another important background to the development of this European Standard has been the wish for a harmonisation of information models for health developed in Euro

    38、pe and the USA expressed in the collaboration agreement entered March 2000 between CEN/TC 251 and HL7 (Health Level Seven, Ann Arbor. Michigan). The goal was set for a maximum degree of alignment while maintaining their independence and need to serve the business requirements of the respective marke

    39、ts but also to make the results available to ISO for possible international standardization. HL7 have adapted a general strategy similar to CEN/TC 251 using information modelling expressed in UML (Unified Modeling Language) for their new standards and a lot of interaction and information sharing has

    40、 occurred between CEN experts and HL7 in an open spirit of collaboration. This European Standard includes a large number of objects which are technically identical to descriptions in draft documents of HL7, although partly described differently due to the fact that CEN is following the ISO rules for

    41、 drafting and presentation of standards which HL7 is not. CEN wishes to express its gratitude towards HL7 experts for generously sharing their models and other technical outputs with the European expert team. This European Standard contains definition of a set of non-clinical General Purpose Informa

    42、tion Components. 1See Annex A: Rationale for this document on General Purpose Information Components. EN 14822-2:2005 (E) 7 1 Scope This European Standard specifies the definition and structuring of information relating to entities that are commonly encountered in communications with and between cli

    43、nical information computer systems. Within the scope of this European Standard is a description of components and their use. In particular, these components relate to the following sub-domains: Subjects of care: including persons, animals and groups of animals. This sub-domain includes descriptions

    44、of the parameters for the identification of the subjects of care. Subject of care related parties: including next of kin and other persons and organisations related to the subject of care (including other subjects of care). Healthcare agents: including healthcare professionals, organisations and dev

    45、ices. Devices: including descriptions of their settings and use within a particular use event. Locations: of two types: care locations, for example, ward and bed where patient receive inpatient care, a clinic where physiotherapy booked, a nursing home, the patients home etc.; geographic locations: w

    46、hich are non-healthcare specific places that are related to laboratory investigations. For example: kitchens, shop counters, hotel air conditioning systems. Transport: including the transportation of persons (patient, related person), animals, or samples/body parts. Financial: including costs associ

    47、ated with care services, authorisation and service agreements (contracts). 2 Normative references Not applicable. 3 Terms and definitions For the purposes of this European Standard, the following terms and definitions apply. 3.1 care location place, often located within a healthcare organisation, wh

    48、ere healthcare services are provided EXAMPLES Ward, room, bed, GP surgery, clinic, patients home, residential home. 3.2 General Purpose Information Component GPIC commonly useful information component that is a specialisation of classes in an international reference information model which is intend

    49、ed to be used in the specification of an information service for health or of a communication between health information systems. EN 14822-2:2005 (E) 8 3.3 healthcare provision of health related services ENV 13940:2001 - modified NOTE 1 This includes more than performing procedures on subjects of care. It includes also, for example, the management of the information about patients, their health status and their relations within the health care framework. NOTE 2 In this document, the term care may be used as a synonym for health care. 3.4 heal


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