A recent perspective suggested that prior evidence from over a decade ago established that a liberal rather than a restrictive blood transfusion strategy results in better outcomes in patients with anemia and either acute myocardial infarction or stable cardiovascular disease. Their premise was that physiological evidence, and a different interpretation of the TRICC trial should have been sufficient to establish clinical practice. They also suggest that a more personalized approach to the administration of transfusions would have been made possible by including a usual care arm in all transfusion trials. In this Counter-Point perspective, we describe how and why two discrete and common blood transfusion thresholds were selected in the TRICC, FOCUS, REALITY, and MINT trials. We explain why a usual-care-arm would have been uninformative. We also propose that we still do not have evidence to provide firm transfusion recommendations in several specific subpopulations of patients including those with stable atherosclerotic coronary artery disease. Finally, we provide our perspective on the state of existing evidence and on the clinical recommendations that should be adopted in practice.
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April 29, 2025
Counterpoint: The Design and Interpretation of Blood Transfusion Randomized Clinical Trials
Clinical Trials & Observations
Jeffrey L Carson,
Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, United States
* Corresponding Author; email: carson@rwjms.rutgers.edu
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Paul C Hebert,
Paul C Hebert
Bruyere Health Research Institute, University of Ottawa, Ottawa, Ontario, Canada
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John H Alexander
John H Alexander
Duke Clinical Research Institute, Duke University Medical Center, Durham, North Carolina, United States
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Blood blood.2025029042.
Article history
Submitted:
March 3, 2025
Revision Received:
April 25, 2025
Accepted:
April 27, 2025
Citation
Jeffrey L Carson, Paul C Hebert, John H Alexander; Counterpoint: The Design and Interpretation of Blood Transfusion Randomized Clinical Trials. Blood 2025; blood.2025029042. doi: https://doi.org/10.1182/blood.2025029042
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