학술논문

The selection and preparation of red cell components for intrauterine transfusion: A national survey.
Document Type
Article
Source
Vox Sanguinis. Mar2024, Vol. 119 Issue 3, p265-271. 7p.
Subject
*ERYTHROCYTES
*CELL anatomy
*HOSPITAL laboratories
*BLOOD banks
*FETAL death
Language
ISSN
0042-9007
Abstract
Background and Objectives: The practice regarding the selection and preparation of red blood cells (RBCs) for intrauterine transfusion (IUT) is variable reflecting historical practice and expert opinion rather than evidence‐based recommendations. The aim of this survey was to assess Canadian hospital blood bank practice with respect to red cell IUT. Materials and Methods: A survey was sent to nine hospital laboratories known to perform red cell IUT. Questions regarding component selection, processing, foetal pre‐transfusion testing, transfusion administration, documentation and traceability were assessed. Results: The median annual number of IUTs performed in Canada was 109 (interquartile range, 103–118). RBC selection criteria included allogeneic, Cytomegalovirus seronegative, irradiated, fresh units with most sites preferentially providing HbS negative, group O, RhD negative, Kell negative and units lacking the corresponding maternal antibody without extended matching to the maternal phenotype. Red cell processing varied with respect to target haematocrit, use of saline reconstitution (n = 4), use of an automated procedure for red cell concentration (n = 1) and incorporation of a wash step (n = 2). Foetal pre‐transfusion testing uniformly included haemoglobin measurement, but additional serologic testing varied. A variety of strategies were used to link the IUT event to the neonate post‐delivery, including the creation of a unique foetal blood bank identifier at three sites. Conclusion: This survey reviews current practice and highlights the need for standardized national guidelines regarding the selection and preparation of RBCs for IUT. This study has prompted a re‐examination of priorities for RBC selection for IUT and highlighted strategies for transfusion traceability in this unique setting. [ABSTRACT FROM AUTHOR]