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The European Committee for Standardization is one of three European Standardization Organizations (together with CENELEC and ETSI) that have been officially recognized by the European Union and by the European Free Trade Association (EFTA) as being responsible for developing and defining voluntary standards at European level.

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Reference CEN/TR 15253:2005
Title Health informatics - Quality of service requirements for health information interchange
Work Item Number 00251122
Abstract/Scope This document is concerned with QoS as it applies to interactions between components of distributed healthcare IT systems. The scope is not limited to network infrastructures; it includes the QoS requirements of information storage and processing IT systems. The related areas of security and financial cost considerations are not within the primary scope of the document, although they are considered briefly. Of course, an informatics system with a high QoS does not guarantee a high standard of healthcare in terms of clinical outcomes or patient care. The quality of healthcare delivered to patients (the ultimate "users") depends upon a number of external factors such as the experience and competence of the healthcare professional(s) or institution(s) involved. Potential QoS characteristics for the total healthcare delivery process such as mortality rate, clinical outcome, etc. are therefore not within the scope of this report. The report contains no provisions to avoid the incorporation of bad or dangerous practice into healthcare IT systems. It is possible to circumvent good clinical practice with technical solutions which may cause bad practice. This vital issue is not covered by this report. To take an example scenario: A patient consults a doctor, who takes a blood sample and arranges to see the patient again in two weeks. a) A "good" practice doctor sees and reviews the blood test result as soon as it comes back from the laboratory and then files it if no action is required. b) A "bad" practice doctor sees and reviews the blood test results only when he reviews the patient's case on the patient's next visit. This case is not defensible if the patient has a preventable adverse event and takes legal action (source: MPS Casebook Summer 1997). The healthcare information system put into the medical practice in electronic form could build-in either practice (a) or practice (b). This report does not consider the clinical quality assurance mechanism fo
Status
Published
Reference Document
date of Availability (DAV) 2005-12-07
ICS 35.240.80 - IT applications in health care technology
A-Deviation(s)  
Special National Condition(s)  

Legal

Directive(s)  
Mandate(s)  
Citation in OJEU  

Implementation Dates

date of Ratification (DOR) (1) 2005-11-13
date of Availability (DAV) (2) 2005-12-07
date of Announcement (DOA) (3)
date of Publication (DOP) (4)
date of Withdrawal (DOW) (5)

Relations

Supersedes  
Superseded by  
Normative reference (6)  
Sales Points

(1) Date of ratification (dor) date when the Technical Board notes the approval of an EN (and HD for CENELEC), from which time the standard may be said to be approved


(2) Date of availability (dav) date when the definitive text in the official language versions of an approved CEN/CENELEC publication is distributed by the Central Secretariat


(3) Date of announcement (doa) latest date by which the existence of an EN (and HD for CENELEC), a TS or a CWA has to be announced at national level


(4) Date of publication (dop) latest date by which an EN has to be implemented at national level by publication of an identical national standard or by endorsement


(5) Date of withdrawal (dow) latest date by which national standards conflicting with an EN (and HD for CENELEC) have to be withdrawn


(6) This list of normative references is purely indicative. The only official list of normative reference is the list of the published standard.


In the case of undated standard, a link to the last dated version is provided.


In the case of series, a link to each standard identified in the series is provided.


We also invite you to check (via the website) whether corrigenda and/or amendments shall be read in conjunction with the main standard.

 

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