BS DD ENV 12537-1-1998 Medical informatics - Registration of information objects used for EDI in healthcare - The register《医疗信息学 医疗保健EDI 用信息客体登记 登记员》.pdf

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1、DRAFT FOR DEVELOPMENT DD ENV 12537-1:1998 Medical informatics Registration of information objects used for EDI in healthcare Part 1: The Register ICS 11.020; 35.240.70DDENV12537-1:1998 This Draft for Development, having been prepared under the direction of the DISC Board, was publishedunder the auth

2、ority ofthe Standards Board and comes into effect on 15 October 1998 BSI 05-1999 ISBN 0 580 30536 8 National foreword This Draft for Development is the English language version of ENV12537-1:1997. This publication is not to be regarded as a British Standard. It is being issued in the Draft for Devel

3、opment series of publications and is of a provisional nature due to the limited duration of the European prestandard. It should be applied on this provisional basis, so that information and experience of its practical application may be obtained. Comments arising from the use of this Draft for Devel

4、opment are requested so that UK experience can be reported to the European organization responsible for its conversion into a European Standard. A review of this publication will be initiated2years after its publication by the European organization so that a decision can be taken on its status at th

5、e end of its three-year life. The commencement of the review period will be notified by an announcement in Update Standards. According to the replies received by the end of the review period, the responsible BSI Committee will decide whether to support the conversion into a European Standard, to ext

6、end the life of the prestandard or to withdraw it. Comments should be sent in writing to the Secretary of BSI Technical Committee IST/35, Medical informatics, at389 Chiswick High Road, LondonW44AL, giving the document reference and clause number and proposing, where possible, an appropriate revision

7、 of the text. A list of organizations represented on this committee can be obtained on request to its secretary. Cross-references The British Standards which implement international or European publications referred to in this document may be found in the BSI Standards Catalogue under the section en

8、titled “International Standards Correspondence Index”, or by using the “Find” facility of the BSI Standards Electronic Catalogue. Summary of pages This document comprises a front cover, an inside front cover, pages i and ii, theENV title page, pages2 to33 and a back cover. This standard has been upd

9、ated (see copyright date) and may have had amendments incorporated. This will be indicated in the amendment table on the inside front cover. Amendments issued since publication Amd. No. Date CommentsDDENV12537-1:1998 BSI 05-1999 i Contents Page National foreword Inside front cover Foreword 2 Text of

10、 ENV 12537-1 3ii blankEUROPEAN PRESTANDARD PRNORME EUROPENNE EUROPISCHE VORNORM ENV12537-1 March1997 ICS35.240.70 Descriptors: Data processing, information interchange, medecine English version Medical informatics Registration of information objectsused for EDI in healthcare Part 1: TheRegister Info

11、rmatique de sant Enregistrement dobjets dinformation utiliss pour lchange de donnes informatis dans le domaine de la sant Partie 1: Registre Medizinische Informatik Registrierung von Informationsobjekten fr den elektronischen Datenaustausch (EDI) im Gesundheitswesen Teil1: Register This European Pre

12、standard (ENV) was approved by CEN on1997-02-09 as a prospective standard for provisional application. The period of validity of this ENV is limited initially to three years. After two years the members of CEN will be requested to submit their comments, particularly on the question whether the ENV c

13、an be converted into an European Standard (EN). CEN members are required to announce the existance of this ENV in the same way as for an EN and to make the ENV available promptly at national level in an appropriate form. It is permissible to keep conflicting national standards in force (in parallel

14、to the ENV) until the final decision about the possible conversion of the ENV into an EN is reached. CEN members are the national standards bodies of Austria, Belgium, Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Luxembourg, Netherlands, Norway, Portugal, Spain, Sweden, Switze

15、rland and UnitedKingdom. CEN European Committee for Standardization Comit Europen de Normalisation Europisches Komitee fr Normung Central Secretariat: rue de Stassart 36, B-1050 Brussels 1997 Copyright reserved to CEN members Ref. No. ENV12537-1:1997EENV12537-1:1997 BSI 05-1999 2 Foreword This Europ

16、ean Prestandard has been prepared by Technical Committee CEN/TC251 “Medical informatics”, the secretariat of which is held by IBN. According to the CEN/CENELEC Internal Regulations, the national standards organisations of the following countries are bound to announce this European Prestandard: Austr

17、ia, Belgium, Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Luxembourg, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland and the UnitedKingdom. The standard is published in two parts. This part specifies the information to be registered for information objects used in e

18、lectronic data interchange (EDI) in healthcare. Part 2 specifies the procedures for the operation of registration authorities. It incorporates a description of the software required to support the practical application of this European Prestandard. Annex A of this Part is normative. Annex B, Annex C

19、, Annex D, Annex E, Annex F, Annex G are informative. Contents Page Foreword 2 Introduction 3 1 Scope 3 2 Normative references 4 3 Definitions, symbols and abbreviations 4 4 Registration of EDI information objects 4 5 Numeric EDI Information Object Identifier (NOI 5 6 EDI Information Object Name (IO

20、N) 5 7 Definition of EDI Information Objects 6 8 Keywords 6 9 Child EDI information objects 6 10 Formal definition of EDI information objects 7 Annex A (normative) The Register of EDI Information Objects 8 Annex B (informative) Object model of the Register 19 Annex C (informative) Formal specificati

21、on of the Register in ASN.1 26 Annex D (informative) Requirement for registration of EDI information objects 29 Annex E (informative) Naming EDI information objects for registration 31 Annex F (informative) Defining EDI information Objects 31 Annex G (informative) The specification of EDI informatio

22、n objects in a formal language for registration 32 Figure 1 Object Model of the register 20ENV12537-1:1997 BSI 05-1999 3 Introduction The following Introduction wording is also used in Part2. The increased use of data processing and telecommunications capabilities has made possible the interchange o

23、f information in machine readable and machine processable formats. As automated interchange of information in healthcare increases it is essential to provide appropriate data interchange standards. All the methods of electronic data interchange (EDI) currently in use require the division of the info

24、rmation to be interchanged into suitable components, which are then identified in some way so that the receiving system can recognize them and process them appropriately. The components are assembled into messages, each message representing a transaction or being equivalent to a form in paper based

25、working methods. In the context of this European Prestandard a component may range from a data element, which is a unit of data normally considered to be indivisible, through logically associated groups of data elements, to complete messages. All are information objects. The rapid growth in EDI is r

26、esulting in the almost simultaneous development of systems each designed to satisfy the requirements of a particular application area. Unfortunately these uncoordinated developments also result in unnecessary variations in the manner in which information is represented, identified, named and describ

27、ed. The use of identical identifiers and names for different data concepts introduces a serious risk of misunderstanding and confusion when data is exchanged between application areas which have developed independently. In the English language the term “date of delivery”, for example, may represent

28、entirely different concepts for gynaecologists and couriers. This European Prestandard describes a procedure by which the components and messages required to facilitate the use of EDI in support of healthcare may be registered and allocated an internationally unique identifier. This European Prestan

29、dard also specifies how components when registered may be included in a widely available International Register which is so indexed and constructed that those designing EDI messages can ascertain easily whether a component or message which is suitable for their purposes already exists. If it is esta

30、blished that new components or messages are essential the procedures for registration specified in this European Prestandard are designed to encourage their derivation from existing entries with appropriate modifications thus avoiding unnecessary variations in the way similar data concepts are repre

31、sented. Registration will also enable synonyms, i.e. two or more information objects serving an identical function, to be identified. Perhaps most importantly, it will highlight the situations where similar or identical names are in use for EDI information objects which are significantly different i

32、n one or more respects. The procedures specified in this European Prestandard recognize that the development of EDI messages is a dynamic and fast moving process and may involve the use of more than one syntax. They are therefore designed to be syntax independent and also to minimize administrative

33、delay. This European Prestandard is based on work within CENTC251 which uses a domain information model (DIM) as a basis for the design of EDI messages. It also draws on work within ISO. 1 Scope This part of the European Prestandard specifies the information to be registered for information objects

34、used in EDI for the purpose of information interchange related to healthcare. The information objects and the information relating to them are recorded in a way which is designed to be independent of interchange format and to facilitate the use of the information objects to construct implementable m

35、essage specifications. This European Prestandard does not cover the registration of information objects which fall within layers1-7 of the Basic Reference Model of Open Systems Interconnection ISO7498, nor does it specify the data base software, programming languages, file organization, storage medi

36、a, etc., to be used for the establishment and maintenance of the Register. NOTEAlthough the scope of this European Prestandard is confined to EDI in support of healthcare the provisions are intended to be capable of application to EDI universally.ENV12537-1:1997 4 BSI 05-1999 2 Normative references

37、The following standards contain provisions which, through reference in this text, constitute provisions of this European Prestandard. At the time of publication, the editions indicated were valid. All standards are subject to revision, and parties to agreements based on this International Standard a

38、re encouraged to investigate the possibility of applying the most recent editions of the standards indicated below. Members of IEC and ISO maintain registers of currently valid International Standards. ISO 7498:1994, Information Technology Reference ModelPart1: Basic Reference Model. ISO/IEC 8824:19

39、90, Information technology Open Systems Interconnection Specification of Abstract Syntax Notation One (ASN.1). 3 Definitions, symbols and abbreviations For the purposes of this European Prestandard, the following definitions apply. 3.1 information object a well defined piece of information, definiti

40、on or specification which requires a name in order to identify its use in an instance of communication ISO/IEC8824:1990 3.2 object identifier a value (distinguishable from all other such values) which is associated with an information object ISO/IEC8824:1990 3.3 requesting organization an organizati

41、on recognized by a sponsoring authority as having a requirement to register EDI information objects for use in inter-organizational electronic data interchange for the purposes of healthcare 3.4 the Register the register of information objects maintained in accordance with this European Prestandard

42、3.5 Registration Authority (RA) the body responsible for maintaining the Register of information objects and for the issue of Numeric EDI Information Object Identifiers (NOIs) 3.6 sponsoring authority a body recognized in accordance with the requirements of this European Prestandard to receive propo

43、sals for the registration of information objects and to submit applications to the Registration Authority 4 Registration of EDI information objects 4.1 Requirement for registration The requirement for the registration of EDI information objects is discussed in informativeAnnex D and the information

44、to be registered is specified in normative Annex A. 4.2 Provision of information in the Register Electronic Data Interchange Information Objects registered under the provisions of this European Prestandard shall each be assigned a Numeric (EDI) Information Object Identifier (NOI) by the Registration

45、 Authority. The information specified inA.2.16 toA.2.18, andA.2.20 toA.2.25 of Annex A is generated during the process of registration. All the other information specified in Annex A shall be provided by the requesting organization.ENV12537-1:1997 BSI 05-1999 5 4.3 Character set Except as provided i

46、n the following paragraph an entry in the Register shall consist of the following characters only. They constitute the PrintableString specified in ISO/IEC8824 and they have been selected because they are consistently rendered on a wide range of equipment. 4.4 Extending the character set Where it is

47、 required to specify the value of another character string all the characters of the defined character string shall appear in the Register surrounded by the characters “whether they occur in the above set or not. However, it is important to recognize that such characters may not be displayed or prin

48、ted in the same way on all equipment, e.g. and $frequently share the same bit encoding. The possibility of an inconsistent rendering of the Register occurring when it is distributed in machine readable form shall therefore be carefully considered if characters not forming part of the above set are i

49、ncluded in Register entries. 5 Numeric EDI Information Object Identifier (NOI) 5.1 The NOI value The NOI value shall be numeric and have a fixed length of six unsigned digits. It shall conform to the specification ofA.2.1 of normative Annex A. The omission of leading zeros is permitted if the values are used as identifiers for EDI information objects when used to interchange data. 5.2 Assignment of the NOI The NOI values shall be assigned to EDI information objects by the Registration Authority in accordance with the procedure specifi