Reevaluation of the medical necessity of washed red blood cell transfusion in chronically transfused adults.

allergic transfusion reaction blood component processing sickle cell disease thalassemia washing

Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
21 Dec 2023
Historique:
revised: 05 12 2023
received: 18 11 2023
accepted: 07 12 2023
medline: 22 12 2023
pubmed: 22 12 2023
entrez: 22 12 2023
Statut: aheadofprint

Résumé

Washing red blood cell (RBC) units mitigates severe allergic transfusion reactions. However, washing reduces the time to expiration and the effective dose. Automated washing is time- and labor-intensive. A shortage of cell processor tubing sets prompted review of medical necessity for washed RBC for patients previously thought to require washing. A single-center, retrospective study investigated discontinuing wash RBC protocols in chronically transfused adults. In select patients with prior requirements for washing, due to a history of allergic transfusion reactions, trials of unwashed transfusions were performed. Patient demographic, clinical, laboratory, and transfusion data were compiled. The per-unit washing cost was the sum of the tubing set, saline, and technical labor costs. Fifteen patients (median age 34 years interquartile range [IQR] 23-53 years, 46.7% female) were evaluated. These patients had been transfused with a median of 531 washed RBC units (IQR 244-1066) per patient over 12 years (IQR 5-18 years), most commonly for recurrent, non-severe allergic reactions. There were no transfusion reactions with unwashed RBCs aside from one patient with one episode of pruritus and another with recurrent pruritus, which was typical even with washed RBC. We decreased the mean number of washed RBC units per month by 72.9% (104 ± 10 vs. 28.2 ± 25.2; p < .0001) and saved US $100.25 per RBC unit. Washing of RBCs may be safely reconsidered in chronically transfused patients without a history of anaphylaxis. Washing should be implemented judiciously due to potential lack of necessity and logistical/operational challenges.

Sections du résumé

BACKGROUND BACKGROUND
Washing red blood cell (RBC) units mitigates severe allergic transfusion reactions. However, washing reduces the time to expiration and the effective dose. Automated washing is time- and labor-intensive. A shortage of cell processor tubing sets prompted review of medical necessity for washed RBC for patients previously thought to require washing.
STUDY DESIGN AND METHODS METHODS
A single-center, retrospective study investigated discontinuing wash RBC protocols in chronically transfused adults. In select patients with prior requirements for washing, due to a history of allergic transfusion reactions, trials of unwashed transfusions were performed. Patient demographic, clinical, laboratory, and transfusion data were compiled. The per-unit washing cost was the sum of the tubing set, saline, and technical labor costs.
RESULTS RESULTS
Fifteen patients (median age 34 years interquartile range [IQR] 23-53 years, 46.7% female) were evaluated. These patients had been transfused with a median of 531 washed RBC units (IQR 244-1066) per patient over 12 years (IQR 5-18 years), most commonly for recurrent, non-severe allergic reactions. There were no transfusion reactions with unwashed RBCs aside from one patient with one episode of pruritus and another with recurrent pruritus, which was typical even with washed RBC. We decreased the mean number of washed RBC units per month by 72.9% (104 ± 10 vs. 28.2 ± 25.2; p < .0001) and saved US $100.25 per RBC unit.
CONCLUSION CONCLUSIONS
Washing of RBCs may be safely reconsidered in chronically transfused patients without a history of anaphylaxis. Washing should be implemented judiciously due to potential lack of necessity and logistical/operational challenges.

Identifiants

pubmed: 38130071
doi: 10.1111/trf.17690
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023 AABB.

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Auteurs

Tait Huso (T)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Kristen Buban (K)

Division of Transfusion Medicine, Johns Hopkins Hospital, Baltimore, Maryland, USA.

Tayler A Van Denakker (TA)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Department of Pathology and Laboratory Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Kathy Haddaway (K)

Division of Transfusion Medicine, Johns Hopkins Hospital, Baltimore, Maryland, USA.

Heather Smetana (H)

Division of Transfusion Medicine, Johns Hopkins Hospital, Baltimore, Maryland, USA.

Christi Marshall (C)

Division of Transfusion Medicine, Johns Hopkins Hospital, Baltimore, Maryland, USA.

Herleen Rai (H)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Paul M Ness (PM)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Evan M Bloch (EM)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Aaron A R Tobian (AAR)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Elizabeth P Crowe (EP)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Classifications MeSH