A cross-sectional study of prevalence, distribution, cause, and impact of blood product recalls in the United States.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
28 04 2020
Historique:
received: 23 09 2019
accepted: 10 03 2020
entrez: 29 4 2020
pubmed: 29 4 2020
medline: 15 5 2021
Statut: ppublish

Résumé

Defective blood products that are recalled because of safety or potency deviations can trigger adverse health events and constrict the nation's blood supply chain. However, the underlying characteristics and impact of blood product recalls are not fully understood. In this study, we identified 4700 recall events, 7 reasons for recall, and 144 346 units affected by recalls. Using geospatial mapping of the newly defined county-level recall event density, we discovered hot spots with high prevalence and likelihood of blood product recall events. Distribution patterns and distribution distances of recalled blood products vary significantly between product types. Blood plasma is the most recalled product (87 980 units), and leukocyte-reduced products (34 230 units) are recalled in larger numbers than non-leukocyte-reduced products (8076 units). Donor-related reasons (92 382 units) and sterility deviations (22 408 units) are the major cause of blood product recalls. Monetary loss resulting from blood product recalls is estimated to be $17.9 million, and economic sensitivity tests show that donor-related reasons and sterility deviations contribute most to the overall monetary burden. A total of 2.8 million days was required to resolve recall events, and probabilistic survival time analysis shows that sterility deviations and contamination took longer to resolve because of their systemic effect on blood collection and processing. Our studies demonstrate that better donor screening procedures, rigorous sterility requirements, improved containment methods, and mitigation of recall events in high-prevalence regions will enable a more robust blood supply chain.

Identifiants

pubmed: 32343797
pii: S2473-9529(20)31369-0
doi: 10.1182/bloodadvances.2019001024
pmc: PMC7189286
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1780-1791

Informations de copyright

© 2020 by The American Society of Hematology.

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Auteurs

Ibrahim Alqemlas (I)

Master of Biotechnology Program and.

Sneha Shankar (S)

Master of Biotechnology Program and.

Winode Handagama (W)

Master of Biotechnology Program and.

P Arthur Felse (PA)

Master of Biotechnology Program and.
Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL.

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Classifications MeSH