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A practical strategy to reduce the risk of passive hemolysis by screening plateletpheresis donors for high‐titer ABO antibodies
Author(s) -
Quillen Karen,
Sheldon Sherry L.,
DanielJohnson Jennifer A.,
LeeStroka A. Hallie,
Flegel Willy A.
Publication year - 2011
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1111/j.1537-2995.2010.02759.x
Subject(s) - plateletpheresis , abo blood group system , titer , medicine , apheresis , antibody , hemolysis , coombs test , antibody titer , immunology , autoanalyzer , serology , autotransfusion , serial dilution , blood transfusion , platelet , pathology , alternative medicine
BACKGROUND: Hemolytic transfusion reactions (HTRs) can occur from ABO‐incompatible platelet (PLT) transfusions. After a series of cases at our institution, a procedure to screen all plateletpheresis donors for high‐titer ABO antibodies was implemented. STUDY DESIGN AND METHODS: Plasma samples from plateletpheresis donors were screened using pooled 0.8% A1 and 0.8% B red blood cells (RBCs) in buffered gel. Dilutions of 1 in 150, 1 in 200, and 1 in 250 were sequentially evaluated. A component testing positive for high‐titer ABO antibodies was restricted to ABO‐identical or group O recipients or washed. RESULTS: At the initial dilution of 1 in 150, half of group O components were labeled as high titer. At the current dilution of 1 in 250, 25% of group O components are labeled as high titer. No PLT‐associated HTR has been reported since screening began. CONCLUSION: Universal screening for high‐titer ABO antibodies in plateletpheresis donors can be implemented efficiently to reduce the risk of HTRs. The cutoff for classifying a unit as high titer depends on the serologic method used and may be customized by the individual facility. Our screening method uses one gel test per donation regardless of blood group and a plasma dilution of 1 in 250 with pooled A1/B RBCs in buffered gel.