Table 7.

Proposed strategies to reduce transfusion-associated septic risk.

Abbreviations: NAT, nucleic acid test; RBCs, red blood cell units. 
  • Reducing risk of blood product contamination:

    1. Improved donor screening.

    2. Improved venepuncture site disinfection.

    3. Removal of first aliquot of donor blood.

  • B. Optimizing blood component processing and storage:

    1. Optimize storage temperature.

    2. Limit storage time.

    3. Universal leukocyte reduction.

  • C. Reduce recipient exposure to blood donors:

    1. Optimize transfusion indications.

    2. Reduce transfusion triggers for RBCs and platelets.

    3. Increase use of apheresis-derived products.

  • Pretransfusion bacterial detection:

    1. Visual inspection of components before issue.

    2. Direct staining for bacteria.

    3. Bacterial ribosomal assays.

    4. Assays for bacterial endotoxin.

    5. NAT for bacterial DNA.

    6. Measure CO2 production by bacteria.

    7. Measure O2 consumption by bacteria.

    8. Direct bacterial culture (manual or automated).

  • Implement pathogen reduction methodology when available.

 
Abbreviations: NAT, nucleic acid test; RBCs, red blood cell units. 
  • Reducing risk of blood product contamination:

    1. Improved donor screening.

    2. Improved venepuncture site disinfection.

    3. Removal of first aliquot of donor blood.

  • B. Optimizing blood component processing and storage:

    1. Optimize storage temperature.

    2. Limit storage time.

    3. Universal leukocyte reduction.

  • C. Reduce recipient exposure to blood donors:

    1. Optimize transfusion indications.

    2. Reduce transfusion triggers for RBCs and platelets.

    3. Increase use of apheresis-derived products.

  • Pretransfusion bacterial detection:

    1. Visual inspection of components before issue.

    2. Direct staining for bacteria.

    3. Bacterial ribosomal assays.

    4. Assays for bacterial endotoxin.

    5. NAT for bacterial DNA.

    6. Measure CO2 production by bacteria.

    7. Measure O2 consumption by bacteria.

    8. Direct bacterial culture (manual or automated).

  • Implement pathogen reduction methodology when available.

 
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