BS EN ISO 21549-6-2008 Health informatics - Patient healthcard data - Administrative data《健康信息学 病人医疗卡数据 管理数据》.pdf
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1、BRITISH STANDARDBS EN ISO 21549-6:2008Health informatics Patient healthcard data Part 6: Administrative dataICS 35.240.80g49g50g3g38g50g51g60g44g49g42g3g58g44g55g43g50g56g55g3g37g54g44g3g51g40g53g48g44g54g54g44g50g49g3g40g59g38g40g51g55g3g36g54g3g51g40g53g48g44g55g55g40g39g3g37g60g3g38g50g51g60g53g4
2、4g42g43g55g3g47g36g58BS EN ISO 21549-6:2008This British Standard was published under the authority of the Standards Policy and Strategy Committee on 30 May 2008 BSI 2008ISBN 978 0 580 55978 5National forewordThis British Standard is the UK implementation of EN ISO 21549-6:2008. The UK participation
3、in its preparation was entrusted to Technical Committee IST/35, Health informatics.A list of 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
4、correct application.Compliance with a British Standard cannot confer immunity from legal obligations.Amendments/corrigenda issued since publicationDate CommentsEUROPEAN STANDARDNORME EUROPENNEEUROPISCHE NORMEN ISO 21549-6April 2008ICS 35.240.80English VersionHealth informatics - Patient healthcard d
5、ata - Part 6:Administrative data (ISO 21549-6:2008)Informatique de sant - Donnes relatives aux cartes desant des patients - Partie 6: Donnes administratives (ISO21549-6:2008)Medizinische Informatik - Patientendaten auf Karten imGesundheitswesen - Teil 6: Verwaltungsdaten (ISO 21549-6:2008)This Europ
6、ean Standard was approved by CEN on 14 March 2008.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 references concer
7、ning such nationalstandards may be obtained on application to the CEN 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 translationunder the responsibility of a CEN member into its own la
8、nguage and notified to the CEN Management Centre has the same status as theofficial versions.CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland,France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Lu
9、xembourg, Malta, Netherlands, Norway, Poland, Portugal,Romania, 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 2008 CEN All righ
10、ts of exploitation in any form and by any means reservedworldwide for CEN national Members.Ref. No. EN ISO 21549-6:2008: EForeword This document (EN ISO 21549-6:2008) has been prepared by Technical Committee ISO/TC 215 “Health informatics“ in collaboration with Technical Committee CEN/TC 251 “Health
11、 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 October 2008, and conflicting national standards shall be withdrawn at the latest by October
12、2008. Attention is drawn to the possibility that some of the 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. According to the CEN/CENELEC Internal Regulations, the national standards organi
13、zations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Rom
14、ania, Slovakia, Slovenia, Spain, Sweden, Switzerland and the United Kingdom. Endorsement notice The text of ISO 21549-6:2008 has been approved by CEN as a EN ISO 21549-6:2008 without any modification. BS EN ISO 21549-6:2008iii Introduction With a more mobile population, greater healthcare delivery i
15、n the community and at patients homes, together with a growing demand for improved quality of ambulatory care, portable information systems and stores have increasingly been developed and used. Such devices are used for tasks ranging from identification, through portable medical record files, and on
16、 to patient-transportable monitoring systems. The functions of such devices are to carry and to transmit person-identifiable information between themselves and other systems; therefore, during their operational lifetime they may share information with many technologically different systems which dif
17、fer greatly in their functions and capabilities. Healthcare administration increasingly relies upon similar automated identification systems. For instance prescriptions may be automated and data exchange carried out at a number of sites using patient transportable computer readable devices. Healthca
18、re funding institutions and providers are increasingly involved in cross-region care, where reimbursement may require automated data exchange between dissimilar healthcare systems. Administrative data objects may require linkage to external parties responsible for their own domains which are not wit
19、hin the scope of this part of ISO 21549. For instance, cross-border reimbursement of healthcare services are usually regulated by law and intergovernmental agreements which are not subject to standardization. The advent of remotely accessible data bases and support systems has led to the development
20、 and use of “Healthcare Person” identification devices that are also able to perform security functions and transmit digital signatures to remote systems via networks. With the growing use of data cards for practical everyday healthcare delivery, the need has arisen for a standardized data format fo
21、r interchange. The person-related data carried by a data card can be categorised in three broad types: identification (of the device itself and the individual to whom the data it carries relates), administrative and clinical. It is important to realise that a given healthcare data card “de facto” ha
22、s to contain device data and identification data and may in addition contain administrative, clinical, medication and linkage data. Device data are defined to include: identification of the device itself; identification of the functions and functioning capabilities of the device. Identification data
23、 can include: unique identification of the device holder (and not information of other persons!). Administrative data can include: complementary person(s) related data; identification of the funding of healthcare, whether public or private, and their relationships, i.e. insurer(s), contract(s) and p
24、olicy(ies) or types of benefits; identification of other persons as a part of the insurance contract (e.g. a family contract); other data (distinguishable from clinical data) that are necessary for the purpose of healthcare delivery. BS EN ISO 21549-6:2008ivClinical data may include: items that prov
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