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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
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Guidelines for the Blood Transfusion Services
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10.4: Investigation of possible bacterial TTI
Welcome
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
10.1:
General considerations
10.2:
Assessment of validity of the possible diagnosis of TTI
10.3:
Non-bacterial TTI: identification of possible infectious donations
10.4:
Investigation of possible bacterial TTI
10.5:
Closing TTI investigations
10.6:
Look-back investigations
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
Download as PDF
10.4: Investigation of possible bacterial TTI
Refer to Chapter 9, section 9.8 for details of laboratory investigations.
Last updated 13/02/2023