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Volume 35, Issue 1, Pages 19-23 (August 2006)


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Comparative sensitivity of solid phase versus PEG enhancement assays for detection and identification of RBC antibodies

Denis M. DwyreCorresponding Author Informationemail address, Yasuko Erickson, Mary Heintz, Charlene Elbert, Ronald G. Strauss

Received 24 November 2005; received in revised form 25 January 2006; accepted 13 February 2006.

Abstract 

Blood banks require a sensitive, specific, and efficient method to detect clinically significant RBC antibodies. Solid phase antibody screening methods are popular due to high sensitivity and automation. However, the high degree of reactivity detects “false positive” antibodies of questionable clinical significance leading to additional testing. We studied positive rates of Capture-R vs. PEG methods and categorized RBC antibodies identified by initial test results of 33,564 consecutive samples by Capture-R method. Capture-R was positive in 1084/33,564 (3.2%) of samples. Using PEG as our “gold standard”, PEG confirmed true positivity (i.e., ⩾1 cell reacting) in 710 Capture-R positive samples (65.5%); 374 Capture-R positive samples (34.5%) did not react in PEG (i.e., false positives). Of the 710 samples with true positivity, only 510 showed clinically significant alloantibodies. Using PEG as our “gold standard”, only 2/3 of reactions by Capture-R were considered true positives. Because of ease and automation, Capture-R is popular as a screening test, but a more specific method may be helpful in order to identify truly significant alloantibodies.

Department of Pathology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA 52242, United States

Corresponding Author InformationCorresponding author. Present address: Department of Pathology, University of California Davis Medical Center, 4400 V street, Sacramento, CA 95817, United States. Tel.: +1 916 734 2525; fax: +1 916 734 2560.

PII: S1473-0502(06)00086-3

doi:10.1016/j.transci.2006.02.002


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