ISO TR 14292-2012 Health informatics - Personal health records - Definition scope and context《健康信息学 个人健康档案 定义 范围和内容》.pdf
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1、 ISO 2012 Health informatics Personal health records Definition, scope and context Informatique de sant Dossiers de sant personnels Dfinition, domaine dapplication et contexte TECHNICAL REPORT ISO/TR 14292 First edition 2012-03-15 Reference number ISO/TR 14292:2012(E) ISO/TR 14292:2012(E) ii ISO 201
2、2 All rights reserved COPYRIGHT PROTECTED DOCUMENT ISO 2012 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying and microfilm, without permission in writing from eithe
3、r ISO at the address below or ISOs member body in the country of the requester. ISO copyright office Case postale 56 CH-1211 Geneva 20 Tel. + 41 22 749 01 11 Fax + 41 22 749 09 47 E-mail copyrightiso.org Web www.iso.org Published in Switzerland ISO/TR 14292:2012(E) ISO 2012 All rights reserved iii C
4、ontents Page Foreword iv Introduction v 1 Scope 1 2 Terms and definitions . 1 3 Abbreviations . 5 4 Definition of a PHR 5 4.1 Definition . 5 4.2 Explanation of the definition 5 5 Scope of the PHR 6 5.1 PHR Dimension 1: Scope of the information . 6 5.2 PHR Dimension 2: Control over the information 7
5、5.3 PHR Dimension 3: Data processor . 7 5.4 PHR Dimension 4: Repository auditability . 8 5.5 PHR Dimension 5: Interoperability and communication 8 5.6 PHR Dimension 6: Technical architecture 9 6 Context of the PHR10 6.1 Origins 10 6.2 Engagement with healthcare services .10 Annex A (informative) Pub
6、lished definitions of the PHR .13 Annex B (informative) Relationship of this Technical Report to the HL7 PHR System Functional Model .18 Bibliography .20 ISO/TR 14292:2012(E) Foreword ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO
7、 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, gover
8、nmental 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. International Standards are drafted in accordance with the rules given in the ISO/IEC D
9、irectives, Part 2. The main task of technical committees is to prepare International 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
10、bodies casting a vote. In exceptional circumstances, when a technical committee has collected data of a different kind from that which is normally published as an International Standard (“state of the art”, for example), it may decide by a simple majority vote of its participating members to publish
11、 a Technical Report. A Technical Report is entirely informative in nature and does not have to be reviewed until the data it provides are considered to be no longer valid or useful. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights.
12、ISO shall not be held responsible for identifying any or all such patent rights. ISO/TR 14292 was prepared by Technical Committee ISO/TC 215, Health informatics. iv ISO 2012 All rights reserved ISO/TR 14292:2012(E) Introduction Personal health records (PHRs) are by their very nature hard to define.
13、In order to understand the breadth and depth of PHRs, it might be helpful to consider PHRs and clinical electronic health records (EHRs) as being positioned at two opposing ends of a spectrum of health records (see Figure 1). A PHR could be defined as the direct counterpoint to an EHR, but in practi
14、ce the lines of demarcation are most often not clear, nor desirable, except when viewed in terms of who has control over the health record and the content within it. While EHRs have traditionally been defined as “logical representations of information regarding, or relevant to, the health of a subje
15、ct of care”, they have existed primarily for the purposes of the healthcare organization providing care to an individual. Information from EHRs might be made available to the subject of care or his/her authorized representative, upon request to the clinician who is acting as a steward of the health
16、information. In some countries, this is supported by specific legislation. PHRs are also “logical representations of information regarding, or relevant to, the health of a subject”; however, in the strictest sense, these health records are primarily managed and controlled by the individual who is th
17、e subject of the record, or his/her authorized representative. The individual has rights over the clinical content held within a PHR, including the ability to delegate those rights to others, especially in the case of minors, the elderly or the disabled. The individual, or his/her authorized represe
18、ntative, is the key stakeholder, determining that the content of the PHR is relevant and appropriate. The simplest examples include self-contained mobile phone applications that track a personal diet or exercise history, which are controlled by the individual and accessed only by the individual him
19、or herself. Healthcare organizations and healthcare systems are accountable for the content of the EHRs they control. Individuals have autonomy over records they choose to keep. However, in between these two strict views of an EHR and a PHR is a continuum of person-centric health records, which migh
20、t have varying degrees of information sharing and/or shared control, access and participation by the individual and his/her healthcare professionals. Towards the EHR end of the spectrum, some EHRs provide viewing access or annotation by the individual to some or all of the clinicians EHR notes. Towa
21、rds the PHR end of the spectrum, some PHRs enable individuals to allow varying degrees of participation by authorized clinicians to their health information, from the simple viewing of data to the control of part or all of the PHR. Individual-controlled health record Healthcare provider- controlled
22、health record PHRE HR Information exchange or shared use, under mixed governance models Figure 1 The PHREHR spectrum In the middle of this continuum there exists a growing plethora of person-centric health records that operate under collaborative models, combining content from individuals and health
23、care professionals under agreed terms and conditions, depending on the purpose of the health record. Control of the record might be shared, or parts controlled primarily by either the individual or the healthcare professional with specified permissions being granted to the other party. For example,
24、a shared antenatal record might be either primarily a PHR, under the auspice of the individual, permitting authorized healthcare professionals to contribute content or directly edit part or all of the record itself, or it might be an extension of an organizations EHR, permitting the individual to vi
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