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Joint United Kingdom (UK) Blood Transfusion and Tissue Transplantation Services Professional Advisory Committee
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Guidelines for the Blood
Transfusion Services in the UK
Updates
1: Introduction
2. Quality in blood and tissue establishments and hospital blood banks
3: Care and selection of whole blood and component donors (including donors of pre-deposit autologous blood)
4: Premises and quality assurance at blood donor sessions
5: Collection of a blood or component donation
6: Evaluation and manufacture of blood components
7: Specifications for blood components
8: Evaluation of novel blood components, production processes and blood packs: generic protocols
9: Microbiology tests for donors and donations: general specifications for laboratory test procedures
10: Investigation of suspected transfusion-transmitted infection
11: Reagent manufacture
12: Donation testing (red cell immunohaematology)
13: Patient testing (red cell immunohaematology)
14: Guidelines for the use of DNA/PCR techniques in Blood Establishments
15: Molecular typing for red cell antigens
16: HLA typing and HLA serology
17: Granulocyte immunology
18: Platelet immunology
19: Tissue banking: general principles
20: Tissue banking: selection of donors
21: Tissue banking: tissue retrieval and processing
22: Haemopoietic progenitor cells
23: Specification for the uniform labelling of blood, blood components and blood donor samples
24: Specification for the uniform labelling of human tissue products using ISBT 128
25: Standards for electronic data interchange within the UK Blood Transfusion Services
26: Specification for blood pack base labels
27: Specification for labelling consumables used in therapeutic product production
A1: NIBSC standards available from MHRA
A2: ISBT 128 check character calculation
A3: Provisional Components
A4: Redundant Components
A5: Blood Components for Contingency Use
A6: Advanced Therapy Medicinal Products (ATMPs)
A7: Requirements for the timing of testing for HPCs
Donor Selection
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Donor Selection Guidelines
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XMRV
Whole Blood and Components
A-Z Search
Updates
Drug Index
Preliminaries
Introduction
Document and Change Control
General Principles
Medication
Inspection of the Donor
Use of Alphabetical Listing
Appendices
Appendix 1 - Estimated Blood Volume for Female donors (after Nadler) by height and weight
Appendix 2 - Table of Immunisations
Appendix 3 - Maximum permitted ECV for component donors
Appendix 4 - Management of post donation illness
Source Files
XMRV
Discretionary
Donors who have been tested positive for XMRV, accept.
Additional Information
As there is no evidence that XMRV is implicated in human disease, a positive test is not a bar to blood donation.
Reason for change
This is a new entry.
Update Information
This entry was last updated in:
DSG-WB Edition 203, Release 10 Issue 01