ABO incompatibile graft management in pediatric transplantation

Adriana Balduzzi, Halvard Bönig, Andrea Jarisch, Tiago Nava, Marc Ansari, Alessandro Cattoni, Giulia Prunotto, Giovanna Lucchini, Gergely Krivan, Toni Matic, Krzyzstof Kalwak, Akif Yesilipek, Marianne Ifversen, Peter Svec, Jochen Buechner, Kim Vettenranta, Roland Meisel, Anita Lawitschka, Christina Peters, Brenda GibsonArnaud Dalissier, Selim Corbacioglu, André Willasch, Jean-Hugues Dalle, Peter Bader, EBMT Pediatric Diseases Working Party

5 Citationer (Scopus)

Abstract

Up to 40% of donor-recipient pairs in SCT have some degree of ABO incompatibility, which may cause severe complications. The aim of this study was to describe available options and survey current practices by means of a questionnaire circulated within the EBMT Pediatric Diseases Working Party investigators. Major ABO incompatibility (donor's RBCs have antigens missing on the recipient's cell surface, towards which the recipient has circulating isohemagglutinins) requires most frequently an intervention in case of bone marrow grafts, as immediate or delayed hemolysis, delayed erythropoiesis and pure red cell aplasia may occur. RBC depletion from the graft (82%), recipient plasma-exchange (14%) were the most common practices, according to the survey. Graft manipulation is rarely needed in mobilized peripheral blood grafts. In case of minor incompatible grafts (donor has isohemagglutinins directed against recipient RBC antigens), isohemagglutinin depletion from the graft by plasma reduction/centrifugation may be considered, but acute tolerability of minor incompatible grafts is rarely an issue. According to the survey, minor ABO incompatibility was either managed by means of plasma removal from the graft, especially when isohemagglutinin titer was above a certain threshold, or led to no intervention at all (41%). Advantages and disadvantages of each method are discussed.

OriginalsprogEngelsk
TidsskriftBone Marrow Transplantation
Vol/bind56
Udgave nummer1
Sider (fra-til)84-90
Antal sider7
ISSN0268-3369
DOI
StatusUdgivet - jan. 2021

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