Assessing the risks of haemolysis as an adverse reaction following the transfusion of ABO incompatible plasma-containing components - A scoping review.


Journal

Blood reviews
ISSN: 1532-1681
Titre abrégé: Blood Rev
Pays: England
ID NLM: 8708558

Informations de publication

Date de publication:
11 2022
Historique:
received: 22 02 2022
revised: 30 05 2022
accepted: 05 07 2022
pubmed: 24 7 2022
medline: 26 10 2022
entrez: 23 7 2022
Statut: ppublish

Résumé

Background The limited supply of universal plasma has resulted in transfusion of ABO incompatible plasma to patients. As the need to implement whole blood transfusion in pre-hospitals setting rises, the lowest cut-off for anti-A/anti-B that does not cause haemolysis remains unknown. In this first scoping review, we aimed to determine the lowest ABO titre and volume reported in the literature to cause haemolysis from ABO incompatible plasma transfusions (plasma, platelets, cryoprecipitate, and whole blood). Methods We searched several databases from inception to April 2022, including all study types. Three independent reviewers extracted and reviewed the data. Primary outcome was the anti-A and anti-B titre (measured by IgM or IgG) that resulted in measurable haemolysis following ABO incompatible plasma transfusion. Results We identified 5681 citations, of which 49 studies were eligible, reporting a total of 62 cases (34 adults, 14 children and 14 did not specify age). The methods for antibody measurement and antibody type (IgG or IgM) varied significantly between studies. Component volumes were poorly reported. The most common component responsible for the haemolysis was apheresis platelets followed by pooled platelets and whole blood. Most haemolytic cases reported were due to anti-A. The lowest anti-A titre reported to cause haemolysis (children and adults) was 32 (IgG), while for anti-B it was 512 (IgG and IgM) for adults, 16,384 for paediatrics (IgG and IgM) and 128 (IgM) in cases where the age was not specified. The lowest reported volume associated with haemolysis were 100 ml (adults) and 15 ml (children). Of the 62 15 (24%) died. Conclusion The lowest titre reported to cause haemolysis was an anti-A of 32. ABO mismatch plasma transfusion may be associated with significant mortality. There is a need to agree/standardise methods for ABO titration measurement internationally for plasma components and agree the lowest anti-A/anti-B titre for transfusing ABO mismatched plasma.

Identifiants

pubmed: 35871104
pii: S0268-960X(22)00063-7
doi: 10.1016/j.blre.2022.100989
pii:
doi:

Substances chimiques

ABO Blood-Group System 0
Immunoglobulin G 0
Immunoglobulin M 0

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

100989

Subventions

Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

Copyright © 2022. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest All authors declare no conflict of interests.

Auteurs

Josephine McCullagh (J)

Barts Health NHS Trust, London, United Kingdom; Bolton NHS Foundation Trust, Greater Manchester, United Kingdom. Electronic address: j.mccullagh@nhs.net.

Rebecca Cardigan (R)

Component Development Laboratory, NHS Blood and Transplant, Cambridge, United Kingdom; Department of Haematology, University of Cambridge, United Kingdom.

Susan J Brunskill (SJ)

Systematic Review Initiative, NHS Blood and Transplant, Oxford, United Kingdom.

Tom Bullock (T)

Red Cell Immunohaematology NHS Blood and Transplant, United Kingdom.

Carolyn Doree (C)

Systematic Review Initiative, NHS Blood and Transplant, Oxford, United Kingdom.

Lise Estcourt (L)

Systematic Review Initiative, NHS Blood and Transplant, Oxford, United Kingdom.

Sian Huish (S)

Component Development Laboratory, NHS Blood and Transplant, Cambridge, United Kingdom.

Josie Sandercock (J)

Systematic Review Initiative, NHS Blood and Transplant, Oxford, United Kingdom.

Laura Green (L)

Barts Health NHS Trust, London, United Kingdom; Component Development Laboratory, NHS Blood and Transplant, Cambridge, United Kingdom; Blizard Institute, Queen Mary University of London, London, United Kingdom.

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Classifications MeSH