Transfusion Medicine Reviews
Volume 24, Issue 2 , Pages 77-124, April 2010

Blood Still Kills: Six Strategies to Further Reduce Allogeneic Blood Transfusion-Related Mortality

  • Eleftherios C. Vamvakas

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Eleftherios C. Vamvakas, MD, PhD, Room 3733, Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, 8700 Beverly Boulevard, Los Angeles, CA 90048.
  • ,
  • Morris A. Blajchman

Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, CA

Department of Pathology and Molecular Medicine, McMaster University, and Canadian Blood Services, Hamilton, Ontario, Canada

After reviewing the relative frequency of the causes of allogeneic blood transfusion-related mortality in the United States today, we present 6 possible strategies for further reducing such transfusion-related mortality. These are (1) avoidance of unnecessary transfusions through the use of evidence-based transfusion guidelines, to reduce potentially fatal (infectious as well as noninfectious) transfusion complications; (2) reduction in the risk of transfusion-related acute lung injury in recipients of platelet transfusions through the use of single-donor platelets collected from male donors, or female donors without a history of pregnancy or who have been shown not to have white blood cell (WBC) antibodies; (3) prevention of hemolytic transfusion reactions through the augmentation of patient identification procedures by the addition of information technologies, as well as through the prevention of additional red blood cell alloantibody formation in patients who are likely to need multiple transfusions in the future; (4) avoidance of pooled blood products (such as pooled whole blood–derived platelets) to reduce the risk of transmission of emerging transfusion-transmitted infections (TTIs) and the residual risk from known TTIs (especially transfusion-associated sepsis [TAS]); (5) WBC reduction of cellular blood components administered in cardiac surgery to prevent the poorly understood increased mortality seen in cardiac surgery patients in association with the receipt of non–WBC-reduced (compared with WBC-reduced) transfusion; and (6) pathogen reduction of platelet and plasma components to prevent the transfusion transmission of most emerging, potentially fatal TTIs and the residual risk of known TTIs (especially TAS).

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PII: S0887-7963(09)00119-9

doi:10.1016/j.tmrv.2009.11.001

Refers to erratum:

  • Erratum

    Eleftherios C. Vamvakas
    Transfusion Medicine Reviews July 2010 (Vol. 24, Issue 3, Page 257)

Transfusion Medicine Reviews
Volume 24, Issue 2 , Pages 77-124, April 2010