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Frequencies and causes of ABO-incompatible red cell transfusions in France, Germany and the United Kingdom.

作者信息

Mirrione-Savin Aline, Aghili Pour Hengameh, Swarbrick Nicola, Müller Susanne, Bacquet Caroline, Malard Lucile, Murphy Michael F, Richard Pascale, Davies Jennifer, Rowley Megan, Poles Debbi, Sandid Imad, Funk Markus B, Narayan Shruthi, Tiberghien Pierre, Schäfer Richard

机构信息

Etablissement Français du Sang PACA Corse, Marseille, France.

Division Safety of Biomedicines and Diagnostics, Paul-Ehrlich-Institut, Federal Institute for Vaccines and Biomedicines, Langen, Germany.

出版信息

Br J Haematol. 2025 Feb;206(2):726-734. doi: 10.1111/bjh.19848. Epub 2024 Oct 30.

Abstract

Prevention of ABO-incompatible red cell transfusions (ABO-it) requires accurate donor and patient identification and correct application of processes for transfusion safety. In France and Germany, a bedside identity check and ABO compatibility test are performed. In the UK, an identity check, often structured as a bedside checklist, is performed with or without electronic patient identification (ePID). To compare the efficacy of ABO-it bedside preventive measures, frequencies and causes of ABO-it between 2013 and 2022 were investigated in all three countries. Despite differing bedside safety measures, similar average ABO-it frequencies were observed in France (0.19 [SD:0.09]/100 000 issued red cell units) and in the UK (0.28 [SD:0.17]/100 000), whereas a higher frequency (0.71 [SD:0.23]/100 000) was observed in Germany which has similar bedside safety measures to France. ABO-it resulted mostly from erroneous patient identification and transfusion of a red cell unit intended for another patient. In France and Germany, all ABO-it were associated with incorrectly performed identity check and ABO compatibility test. In the UK, most ABO-it were associated with incorrectly performed identity checks. Current measures to prevent ABO-it are not fully effective. Further development and implementation of effective patient identification systems, including electronic information systems, across the entire transfusion process, should be considered.

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