Transfusion of Uncrossmatched Group O Erythrocyte-containing Products Does Not Interfere with Most ABO Typings.


Journal

Anesthesiology
ISSN: 1528-1175
Titre abrégé: Anesthesiology
Pays: United States
ID NLM: 1300217

Informations de publication

Date de publication:
03 2020
Historique:
pubmed: 4 12 2019
medline: 23 6 2020
entrez: 3 12 2019
Statut: ppublish

Résumé

Group O erythrocytes and/or whole blood are used for urgent transfusions in patients of unknown blood type. This study investigated the impact of transfusing increasing numbers of uncrossmatched type O products on the recipient's first in-hospital ABO type. This was a retrospective cohort study. Results of the first ABO type obtained in adult, non-type O recipients (i.e., types A, B, AB) after receiving at least one unit of uncrossmatched type O erythrocyte-containing product(s) for any bleeding etiology were analyzed along with the number of uncrossmatched type O erythrocyte-containing products administered in the prehospital and/or in hospital setting before the first type and screen sample was drawn. There were 10 institutions that contributed a total of 695 patient records. Among patients who received up to 10 uncrossmatched type O erythrocyte-containing products, the median A antigen agglutination strength in A and AB individuals on forward typing (i.e., testing the recipient's erythrocytes for A and/or B antigens) was the maximum (4+), whereas the median B antigen agglutination strength among B and AB recipients of up to 10 units was 3 to 4+. The median agglutination strength on the reverse type (i.e., testing the recipient's plasma for corresponding anti-A and -B antibodies) was very strong, between 3 and 4+, for recipients of up to 10 units of uncrossmatched erythrocyte-containing products. Overall, the ABO type of 665 of 695 (95.7%; 95% CI, 93.9 to 97.0%) of these patients could be accurately determined on the first type and screen sample obtained after transfusion of uncrossmatched type O erythrocyte-containing products. The transfusion of smaller quantities of uncrossmatched type O erythrocyte-containing products, in particular up to 10 units, does not usually interfere with determining the recipient's ABO type. The early collection of a type and screen sample is important.

Sections du résumé

BACKGROUND
Group O erythrocytes and/or whole blood are used for urgent transfusions in patients of unknown blood type. This study investigated the impact of transfusing increasing numbers of uncrossmatched type O products on the recipient's first in-hospital ABO type.
METHODS
This was a retrospective cohort study. Results of the first ABO type obtained in adult, non-type O recipients (i.e., types A, B, AB) after receiving at least one unit of uncrossmatched type O erythrocyte-containing product(s) for any bleeding etiology were analyzed along with the number of uncrossmatched type O erythrocyte-containing products administered in the prehospital and/or in hospital setting before the first type and screen sample was drawn.
RESULTS
There were 10 institutions that contributed a total of 695 patient records. Among patients who received up to 10 uncrossmatched type O erythrocyte-containing products, the median A antigen agglutination strength in A and AB individuals on forward typing (i.e., testing the recipient's erythrocytes for A and/or B antigens) was the maximum (4+), whereas the median B antigen agglutination strength among B and AB recipients of up to 10 units was 3 to 4+. The median agglutination strength on the reverse type (i.e., testing the recipient's plasma for corresponding anti-A and -B antibodies) was very strong, between 3 and 4+, for recipients of up to 10 units of uncrossmatched erythrocyte-containing products. Overall, the ABO type of 665 of 695 (95.7%; 95% CI, 93.9 to 97.0%) of these patients could be accurately determined on the first type and screen sample obtained after transfusion of uncrossmatched type O erythrocyte-containing products.
CONCLUSIONS
The transfusion of smaller quantities of uncrossmatched type O erythrocyte-containing products, in particular up to 10 units, does not usually interfere with determining the recipient's ABO type. The early collection of a type and screen sample is important.

Identifiants

pubmed: 31789634
doi: 10.1097/ALN.0000000000003069
doi:

Substances chimiques

ABO Blood-Group System 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

525-534

Investigateurs

David McKenna (D)
David Stroncek (D)
Mark Fung (M)
Alan Tinmouth (A)
Dana Devine (D)
Rebecca Cardigan (R)
Ralph Vassallo (R)
Marc Germain (M)
JoAnna Reems (J)
Henk Garritsen (H)
Minoko Takanashi (M)
Simon Stanworth (S)
Meghan Delaney (M)
José Cancelas (J)
Pieter van der Meer (PV)
Denese Marks (D)
Claudia Cohn (C)
Beth Shaz (B)
Pierre Tiberghien (P)
Mindy Goldman (M)
John Girdlestone (J)
Shibani Pati (S)
Richard Schäfer (R)
Joseph Yossi Schwartz (JY)
Nancy Dunbar (N)
Monica Pagano (M)
Cynthia So-Osman (C)
Femke Noorman (F)
Torunn Oveland Apelseth (TO)
Tamir Kanias (T)
Moritz Stolla (M)
Emanuele di Angelantonio (ED)
Katja van den Hurk (KVD)
Whitney R Steele (WR)
Christian Erikstrup (C)
Eva-Maria Merz (EM)

Auteurs

Mark H Yazer (MH)

From Vitalant, Pittsburgh, Pennsylvania (M.H.Y., D.J.T.) the Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania (M.H.Y., D.J.T.) the Department of Pediatrics, Division of Critical Care Medicine, Washington University in St Louis, St Louis, Missouri (P.C.S.) the Department of Anesthesiology and Pain Medicine, University of Ottawa, Ottawa, Ontario, Canada (L.D.) Canadian Field Hospital, Canadian Armed Forces, Ottawa, Ontario, Canada (L.D.) the Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts (R.M.K.) the Wing-Kwai and Alice Lee-Tsing Chung Transfusion Service, Department of Pathology and Laboratory Medicine, UCLA Health, Los Angeles, California (R.D., A.Z.) the Department of Laboratory Medicine, University of Washington School of Medicine, Seattle, Washington (J.R.H., E.E.T.) Hemorio, Rio de Janeiro, Brazil (L.A.F.) the Department of Pathology, University of Maryland School of Medicine, Baltimore, Maryland (M.F., J.P.) the Institute of Transfusion Medicine, University of Cologne, University Hospital, Cologne, Germany (B.G.) the Department of Pathology and Laboratory Medicine, Emory University, Atlanta, Georgia (B.J.) National Health Service Blood and Transplant, and Oxford Biomedical Research Centre, Oxford, United Kingdom (J. Staves) the Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, North Carolina (J.S.R.) the Vancouver Coastal Health Authority, Vancouver, British Columbia, Canada (K.R., A.W.S.) the Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota (J. Seheult) the Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada (A.W.S.) the Departments of Surgery and Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania (J. Sperry). Current affiliation: Department of Pathology, University of New Mexico, Albuquerque, New Mexico (J.S.R.).

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