Table Of Content. EU Optimal Blood Use Project... 2 Summary... 3 Coordinator, Leader contact and partners Outputs... 6

Transcription

1 Table Of Content EU Optimal Blood Use Project... 2 Summary... 3 Coordinator, Leader contact and partners... 4 Institute Of Haematology and Transfusion Medicine... 4 Põhja-Eesti Verekeskus... 4 DRK Blutspendedienst baden Württemberg Hessen ggmbh... 4 NHS Blood and Transplants... 4 Austrian Red Cross... 4 Blood Transfusion Centre of Slovenia (Zavod RS ZA Transfuzijsko Medicino (ZTM))... 4 UNIVERSITY OF MEDICINE AND PHARMACY VICTOR BABES ROMANIA... 4 Agenzia Regionale della Sanità - Regione autonoma Friuli Venezia Giulia... 4 Outputs... 6 Final report - Final report... 6 Interim report 1 - Interim report Interim report 2 - Interim report Manual... 6 Page 1/6

2 EU Optimal Blood Use Project JA GPSD [705038] START DATE: 01/05/2007 END DATE: 01/05/2010 DURATION: 36 month(s) CURRENT STATUS: Finalised PROGRAMME TITLE: First Programme of Community action in the field of public health ( ) PROGRAMME PRIORITY: - CALL: Responding Rapidly And In A Co-Ordinated Fashion To Health Threats (Ht 2006) TOPIC: Safety of blood, tissues and cells, organ EC CONTRIBUTION: EUR KEYWORDS: Blood and Blood components, Blood transfusion, Pilot testing PORTFOLIO: Blood and Blood components Page 2/6

3 SUMMARY General objectives This project will encourage best European practice on the optimal use of blood components and therapeutic practice. Strategic relevance and contribution to the public health programme This project addresses the quality and safety of blood, proposes best practice, and supports European legislation in the field of quality and safety of blood. Methods and means A questionnaire study will be conducted to determine current therapeutic practice. The outcome of the study will be reviewed and will subsequently be used to inform the development of a manual. Expected outcomes period The project will: develop a manual to encourage best European practice on the optimal use of blood components and therapeutic practice; produce a manual containing: methods for monitoring and understanding hospital processes that determine whether or not a patient receives the correct blood component, correctly transfused at the right time; methods for training hospital staff who are essential to safe therapeutic transfusion practice; methods for obtaining, analysing and presenting to clinicians comparative information on the quantities of blood components transfused for similar procedures. Page 3/6

4 COORDINATOR, LEADER CONTACT AND PARTNERS COORDINATOR (Scottish National Blood Transfusion Service) Ellen's Glen Road Liberton, Scotland EH17 7QT Edinburgh United Kingdom Project leader contact Name: HART Merredith Phone: PARTNERS Institute Of Haematology and Transfusion Medicine Country: Poland Põhja-Eesti Verekeskus Country: Estonia DRK Blutspendedienst baden Württemberg Hessen ggmbh Country: Germany Page 4/6

5 NHS Blood and Transplants Country: United Kingdom Austrian Red Cross Country: Austria Blood Transfusion Centre of Slovenia (Zavod RS ZA Transfuzijsko Medicino (ZTM)) Country: Slovenia UNIVERSITY OF MEDICINE AND PHARMACY VICTOR BABES ROMANIA Country: Romania Agenzia Regionale della Sanità - Regione autonoma Friuli Venezia Giulia Country: Italy Page 5/6

6 Powered by TCPDF ( OUTPUTS Final report - Final report Interim report 1 - Interim report 1 Interim report 2 - Interim report 2 Manual Page 6/6