A prospective multicenter observational study assessing incidence and risk factors for acute blood transfusion reactions in dogs.

AHTR FNHTR TACO TRALI dog leukoreduction storage lesion

Journal

Journal of veterinary internal medicine
ISSN: 1939-1676
Titre abrégé: J Vet Intern Med
Pays: United States
ID NLM: 8708660

Informations de publication

Date de publication:
06 Sep 2024
Historique:
received: 29 11 2023
accepted: 01 08 2024
medline: 6 9 2024
pubmed: 6 9 2024
entrez: 6 9 2024
Statut: aheadofprint

Résumé

Reported incidence of blood transfusion reactions (TR) varies greatly. To prospectively evaluate the incidence of acute TRs in dogs receiving allogenic blood products, using consensus definitions, and to assess factors associated with TRs. Dogs (n = 858) administered allogenic blood products (n = 1542) between March and November 2022. Prospective, multicenter surveillance study occurring in referral hospitals in the United States, United Kingdom, and Australia recording TRs in dogs administered blood products as defined by the consensus guidelines published by The Association of Veterinary Hematology and Transfusion Medicine in 2021. The incidence of acute TR was 8.9% (95% CI 7.0-11.1) for packed red blood cells (pRBCs) and 4.5% (95% CI 2.9-6.6) for plasma products. The most frequently reported TRs were febrile nonhemolytic TRs (FNHTR; 4%, 95% CI 2.8-5.5) when administering pRBCs and allergic TRs (3.2%, 95% CI 1.80-5.10) when administering plasma products. A higher dose of pRBC (adjusted odds ratio [aOR] 1.04 [95% CI 1.00-1.08]) was associated with a higher odds of TR. Administration of pRBCs stored for longer than 28 days was associated with higher odds of FNHTR (aOR 4.10 [95% CI 1.58-10.65]) and acute hemolytic TR (AHTR; OR 15.2 [95% CI 3.35-68.70]) when compared with pRBCs stored for 14 days or fewer. Leukoreduction of pRBC was not associated with lower odds of developing a TR (OR 1.47 [95% CI 0.89-2.42]). Clinicians should be mindful of the age and dose of pRBC prescribed to dogs.

Sections du résumé

BACKGROUND BACKGROUND
Reported incidence of blood transfusion reactions (TR) varies greatly.
OBJECTIVE OBJECTIVE
To prospectively evaluate the incidence of acute TRs in dogs receiving allogenic blood products, using consensus definitions, and to assess factors associated with TRs.
ANIMALS METHODS
Dogs (n = 858) administered allogenic blood products (n = 1542) between March and November 2022.
METHODS METHODS
Prospective, multicenter surveillance study occurring in referral hospitals in the United States, United Kingdom, and Australia recording TRs in dogs administered blood products as defined by the consensus guidelines published by The Association of Veterinary Hematology and Transfusion Medicine in 2021.
RESULTS RESULTS
The incidence of acute TR was 8.9% (95% CI 7.0-11.1) for packed red blood cells (pRBCs) and 4.5% (95% CI 2.9-6.6) for plasma products. The most frequently reported TRs were febrile nonhemolytic TRs (FNHTR; 4%, 95% CI 2.8-5.5) when administering pRBCs and allergic TRs (3.2%, 95% CI 1.80-5.10) when administering plasma products. A higher dose of pRBC (adjusted odds ratio [aOR] 1.04 [95% CI 1.00-1.08]) was associated with a higher odds of TR. Administration of pRBCs stored for longer than 28 days was associated with higher odds of FNHTR (aOR 4.10 [95% CI 1.58-10.65]) and acute hemolytic TR (AHTR; OR 15.2 [95% CI 3.35-68.70]) when compared with pRBCs stored for 14 days or fewer. Leukoreduction of pRBC was not associated with lower odds of developing a TR (OR 1.47 [95% CI 0.89-2.42]).
CONCLUSIONS AND CLINICAL IMPORTANCE CONCLUSIONS
Clinicians should be mindful of the age and dose of pRBC prescribed to dogs.

Identifiants

pubmed: 39239720
doi: 10.1111/jvim.17175
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The Author(s). Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC on behalf of American College of Veterinary Internal Medicine.

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Auteurs

Georgina B F Hall (GBF)

Clinical Science and Services, The Royal Veterinary College, London, UK.

Rachael Birkbeck (R)

The Ralph, Marlow, UK.

Benjamin M Brainard (BM)

Department of Small Animal Medicine and Surgery, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.

Fernanda Camacho (F)

Willows Veterinary Centre and Referral Service, Solihull, UK.

Elizabeth B Davidow (EB)

Timberline Veterinary Emergency and Specialty, Seattle, Washington, USA.

Dana N LeVine (DN)

Department of Clinical Sciences, Auburn University College of Veterinary Medicine, Auburn, Alabama, USA.

Andrew Mackin (A)

College of Veterinary Medicine, Mississippi State University, Starkville, Mississippi, USA.

Taylor Moss (T)

Department of Clinical Sciences, Auburn University College of Veterinary Medicine, Auburn, Alabama, USA.

Katherine J Nash (KJ)

School of Veterinary Science, University of Queensland, Gatton, Queensland, Australia.

Giacomo Stanzani (G)

Dick White Referrals, Newmarket, UK.

Daria Starybrat (D)

The Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, UK.

David Q Stoye (DQ)

Oxford School of Public Health, Oxford, UK.

Carolyn Tai (C)

Cummings School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts, USA.

John Thomason (J)

College of Veterinary Medicine, Mississippi State University, Starkville, Mississippi, USA.

Julie M Walker (JM)

Department of Medical Sciences, University of Wisconsin-Madison School of Veterinary Medicine, Madison, Wisconsin, USA.

K Jane Wardrop (KJ)

College of Veterinary Medicine, Washington State University, Pullman, Washington, USA.

Helen Wilson (H)

Langford Vets, University of Bristol, Bristol, UK.

Virginie A Wurlod (VA)

Louisiana State University School of Veterinary Medicine, Baton Rouge, Louisiana, USA.

Karen Humm (K)

Clinical Science and Services, The Royal Veterinary College, London, UK.

Classifications MeSH