Evidence map›Paper›PMID 41122822›Full record

ArticleTransfusion2025

Evolving TRALI risk across apheresis and whole blood platelet products in the United States: An 18-year American Red Cross hemovigilance analysis.

Pampee P Young, Umesh Singh, Jonathan Webb, Mark R Looney

Abstract read
In one paragraph

Article in Transfusion, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Pampee P YoungMedical and Scientific Affairs, American Red Cross Biomedical Services, Washington, District of Columbia, USA.ORCID https://orcid.org/0000-0001-5313-0376
Umesh SinghMedical and Scientific Affairs, American Red Cross Biomedical Services, Washington, District of Columbia, USA.
Jonathan WebbMedical and Scientific Affairs, American Red Cross Biomedical Services, Washington, District of Columbia, USA.
Mark R LooneySan Francisco, Departments of Medicine and Laboratory Medicine, University of California, San Francisco, California, USA.

Funding

Immunobiology of the normal and injured lungR35HL161241 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARK ROBERTS LOONEY · 2022 to 2026
$4.2M
Immunomodulation by splenic megakaryocytes and platelets in sepsisR01AI165919 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOONEY, MARK ROBERTS · 2022 to 2025
$3.2M
NHLBI NIH HHS R35 HL161241NIAID NIH HHS R01 AI165919
6 · The paper itself

Abstract

backgroundTransfusion-related acute lung injury (TRALI) remains a leading cause of transfusion-associated mortality in the United States. Donor-based mitigation has reduced TRALI risk from plasma and apheresis platelets, but the residual risk associated with whole-blood-derived pooled platelets is not well defined. STUDY DESIGN AND

methodsWe retrospectively analyzed transfusion reactions reported to the American Red Cross (ARC) national hemovigilance program from 1 January 2006 through 31 December 2023. Reactions were adjudicated using Canadian Consensus Conference criteria; definite or highly probable TRALI cases (levels 5-6) were included. Component distribution data served as denominators. Trends were evaluated in relation to two mitigation efforts: male-predominant plasma (2005-2006) and HLA-antibody screening of previously pregnant apheresis-platelet donors (2016).

resultsOver 18 years ARC distributed 92.7 million red blood cells, 23.5 million plasma units, and 17 million platelets-including 0.87 million pooled WB-derived platelets, 11.7 million plasma-suspended apheresis, 1.5 million PAS apheresis, and 2.9 million pathogen-reduced (PR) platelet-additive solution-3 (PAS) apheresis platelets. We identified 393 high-probability TRALI cases. Plasma-associated TRALI declined from 20.0 to <4 cases per million units following male-predominant policies; RBC risk remained stable (0.7-4.3/million). TRALI incidence for whole blood pooled platelets averaged 13.5/million, exceeding plasma-suspended (4.4/million), PAS (0.8/million), and PLT PR PAS (0.5/million) apheresis platelets (p = .002 for differences among apheresis subtypes). Compared to apheresis PLT, the TRALI incidence for whole blood PLTS is increased by about 9-13/million.

conclusionCurrent mitigation strategies, which are not required for whole blood derived platelets in the United States, have substantially reduced TRALI risk from apheresis platelets. If whole blood-pooled platelets production in the United States increases, consideration should be given to the addition of mitigation strategies-such as male-predominant pooling and donor antibody screening-to align their safety profile.

Indexed as

Blood Component RemovalBlood PlateletsBlood SafetyPlateletpheresisPlatelet TransfusionTransfusion-Related Acute Lung InjuryBlood DonorsFemaleHumansMaleRed CrossRetrospective StudiesRisk FactorsUnited Statesdonor screeninghemovigilancepathogen reductionplateletsTRALI

Identifiers

PMID41122822
PMCPMC12704697

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.