ArticleTransfusion2025
In vitro and in vivo evaluation of leukoreduced red blood cells after automated separation of whole blood.
Article in Transfusion, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
19 authors.
Funding
Abstract
backgroundLeukoreduced red blood cells (LR-RBCs) prepared from whole blood (WB) with the Reveos™ Automated Blood Processing System (Reveos System) are required to meet US Food and Drug Administration (FDA) criteria for RBC component in vitro quality and in vivo 24-h RBC recovery after 42-day storage. STUDY DESIGN AND
methodsFor the in vitro study, 65 Reveos-derived LR-RBC units were stored for 42 days in citrate phosphate dextrose (CPD)/Additive Solution Formula 5 (AS-5). Units were evaluated for post-filtration residual white blood cell (rWBC) content, post-filtration RBC recovery, and percent hemolysis at end of storage. In vivo 24-h recovery of 42-day stored autologous Reveos-derived LR-RBCs was determined in 26 healthy participants with standard single (
resultsFor all evaluable units processed in the in vitro study, post-filtration rWBC content was <5 × 10
conclusionThe Reveos System met FDA's criteria for RBC component in vitro quality and in vivo 24-h recovery after 42-day storage.
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