ENV 13730-1:2001

Health informatics - Blood transfusion related messages - Part 1: Subject of care related messages

The domain of the blood transfusion related messages includes:-the collection of blood from donor; -preparation; - qualification; -dispensing of Blood components (to be transfused) to the recipient. Transfusion of blood and Blood components to patients is a medical activity that is subject to many legal instructions, regulations and constraints. Immunological conditions transmitted diseases; sustainability and other difficulties due to the fact that the treatment involves many problems, including those cause this. Mistakes and failures may have serious or even fatal consequences.

Zdravstvena informatika – Sporočila v zvezi s krvno transfuzijo – 1. del: Vsebina sporočil v zvezi z oskrbo

General Information

• Status: Withdrawn
• Publication Date: 11-Dec-2001
• 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 13730-1:2003 - Health informatics - Blood transfusion related messages - Part 1: Subject of care related messages

Relations

• Child: ENV 13730-2:2002 - Healthcare Informatics - Blood transfusion related messages - Part 2: Production related messages (BTR-PROD)
• Effective Date: 22-Dec-2008

Standards Content (Sample)

SLOVENSKI STANDARD
SIST ENV 13730-1:2003
01-oktober-2003
=GUDYVWYHQDLQIRUPDWLND±6SRURþLODY]YH]LVNUYQRWUDQVIX]LMR±GHO9VHELQD
VSRURþLOY]YH]L]RVNUER
Health informatics - Blood transfusion related messages - Part 1: Subject of care related
messages
Ta slovenski standard je istoveten z: ENV 13730-1:2001
ICS:
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
SIST ENV 13730-1:2003 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST ENV 13730-1:2003

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SIST ENV 13730-1:2003
EUROPEAN PRESTANDARD
ENV 13730-1
PRÉNORME EUROPÉENNE
EUROPÄISCHE VORNORM
December 2001
ICS 35.240.80
English version
Health informatics - Blood transfusion related messages - Part
1: Subject of care related messages
This European Prestandard (ENV) was approved by CEN on 19 October 2000 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, 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
© 2001 CEN All rights of exploitation in any form and by any means reserved Ref. No. ENV 13730-1:2001 E
worldwide for CEN national Members.

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SIST ENV 13730-1:2003
ENV 13730-1:2001(E)
CONTENTS
FOREWORD .5
INTRODUCTION .6
1SCOPE.7
2 NORMATIVE REFERENCES .9
3 NORMATIVE DEFINITIONS AND ABBREVIATIONS .10
4 REQUIREMENTS .17
4.1 General conformance requirements .17
4.2 Implementation recommendations .18
5 COMMUNICATION ROLES .18
5.1 General.18
5.1.1 Sending role requirements.18
5.1.2 Receiving role requirements.18
5.2 Use case diagram and scenarios (General use case).18
5.3 Group 1: Message sequences.20
5.3.1 Testing activities (activities concerned with the testing of subjects of care and blood products)
(including serological and compatibility testing) (See ENV 1613) .20
5.3.2 Transfusion activities (directly concerned with transfusion of Blood components to subjects of
care) 21
6 REQUIREMENTS AND GENERAL MESSAGE DESCRIPTIONS .22
6.1 Conformance requireme
...