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CEN

ENV 13730-2:2002

(Main)

Healthcare Informatics - Blood transfusion related messages - Part 2: Production related messages (BTR-PROD)

Healthcare Informatics - Blood transfusion related messages - Part 2: Production related messages (BTR-PROD)

Transfusion of blood [3.10]  and blood components[3.12] to subjects of care[3.56] is a medical activity that is subject to many legal regulations and constraints. Many problems may be encountered during treatment due to immunological conditions, transmitted diseases, sustainability and other difficulties. Mistakes and failures may have serious or even fatal consequences. Minimising human activity through the increased use of data processing and automated messaging will introduce an additional safety mechanism.
This prENV specifies general messages[3.43] for electronic information interchange between computer systems used by healthcare [3.34] parties [3.38] in the blood transfusion [3.18] domain. The content and structure of the messages specified in this prENV have been developed with the aim of optimising the safety of Blood transfusion activity and to facilitate compliance monitoring and secure audit trails [3.4].
This prENV is applicable to Blood transfusion related messages including those for:
- the collection of blood/blood components[3.25] from donor
- manufacturing [3.47]and processing[3.52] of blood components
- classification [3.19]of Blood donations
- dispensing [3.28]of  blood components (to be transfused) to the recipient

Healthcare Informatics - Blood transfusion related messages - Part 2: Production related messages (BTR-PROD)

General Information

Status
Withdrawn
Publication Date
17-Sep-2002
Withdrawal Date
16-Jun-2020
ICS
35.240.80 - IT applications in health care technology
Technical Committee
CEN/TC 251 - Medical informatics
Drafting Committee
CEN/TC 251/WG 1 - Information models
Current Stage
9960 - Withdrawal effective - Withdrawal
Completion Date
17-Jun-2020
Ref Project
SIST ENV 13730-2:2003 - Healthcare Informatics - Blood transfusion related messages - Part 2: Production related messages (BTR-PROD)

Relations

Parent
ENV 13730-1:2001 - Health informatics - Blood transfusion related messages - Part 1: Subject of care related messages
Effective Date
22-Dec-2008

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SLOVENSKI STANDARD
SIST ENV 13730-2:2003
01-oktober-2003
Healthcare Informatics - Blood transfusion related messages - Part 2: Production
related messages (BTR-PROD)
Healthcare Informatics - Blood transfusion related messages - Part 2: Production related
messages (BTR-PROD)
Ta slovenski standard je istoveten z: ENV 13730-2:2002
ICS:
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
SIST ENV 13730-2:2003 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST ENV 13730-2:2003

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SIST ENV 13730-2:2003
EUROPEAN PRESTANDARD
ENV 13730-2
PRÉNORME EUROPÉENNE
EUROPÄISCHE VORNORM
September 2002
ICS 35.240.80
English version
Healthcare Informatics - Blood transfusion related messages -
Part 2: Production related messages (BTR-PROD)
This European Prestandard (ENV) was approved by CEN on 18 October 2001 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 can be converted into a European Standard.
CEN members are required to announce the existence 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 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, Czech Republic, Denmark, Finland, France, Germany, Greece,
Iceland, Ireland, Italy, Luxembourg, Malta, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland and United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: rue de Stassart, 36  B-1050 Brussels
© 2002 CEN All rights of exploitation in any form and by any means reserved Ref. No. ENV 13730-2:2002 E
worldwide for CEN national Members.

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SIST ENV 13730-2:2003
ENV 13730-2:2002 (E)
CONTENTS
FOREWORD .5
INTRODUCTION.6
1 SCOPE.7
2 NORMATIVE REFERENCES.9
3 TERMS, DEFINITIONS AND ABBREVIATIONS.9
4 REQUIREMENTS .17
4.1 GENERAL CONFORMANCE REQUIREMENTS.17
4.2 IMPLEMENTATION RECOMMENDATIONS.17
5 COMMUNICATION ROLES .17
5.1 GENERAL .17
5.1.1 Sending role requirements .17
5.1.2 Receiving role requirements.17
5.2 USE CASE DIAGRAM AND SCENARIOS (GENERAL USE CASE).18
5.3 GROUP 2: MESSAGE SEQUENCES .20
5.3.1 Blood component production message domain .20
6 REQUIREMENTS AND GENERAL MESSAGE DESCRIPTIONS .22
6.1 CONFORMANCE REQUIREMENTS.22
6.2 GENERAL MESSAGE DESCRIPTIONS .22
6.3 BLOOD/BLOOD COMPONENT COLLECTION REQUEST MESSAGE .24
6.3.1 Scope of this message.
...

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