How do we ensure a safe ABO recheck process?

• Published in: Transfusion 2023, Vol.63 (10), p.1789-1796
• Main Authors: Stephens, Laura D, Allen, Elizabeth S, Bloch, Evan M, Crowe, Elizabeth P, Campbell-Lee, Sally A, Booth, Garrett S, Kopko, Patricia
• Format: Report
• Language: English
• ISSN: 1537-2995
• DOI: 10.1111/trf.17530

BACKGROUNDCollecting a patient's blood in a correctly labeled pretransfusion specimen tube is essential for accurate ABO typing and safe transfusion. Noncompliance with specimen collection procedures can lead to wrong blood in tube (WBIT) incidents with potentially fatal consequences. Recent WBIT events inspired the investigation of how various institutions currently reduce the risk of these errors and ensure accurate ABO typing of patient samples. MATERIALS AND METHODSThis article describes the techniques employed at various institutions across the United States to mitigate the risk of misidentified pretransfusion patient specimens. Details and considerations for each of these measures are provided. RESULTSSeveral institutions require the order for an ABO confirmation specimen, if indicated, to be generated from the transfusion medicine (TM) laboratory. Others issue a dedicated collection tube that is available exclusively from the TM service. Many institutions employ barcoding for electronic positive patient identification. Some use a combination of these strategies, depending on the locations or service lines from which the specimens are collected. CONCLUSIONThe description of various WBIT mitigation strategies will inform TM services on practices that may be effective at their respective institutions. Irrespective of the method(s) utilized, institutions should continue to monitor and mitigate specimen misidentification errors to promote sustained safe transfusion practices.