Evidence map›Paper›PMID 42209419›Full record

ArticleVox sanguinis2026

Short-term temperature excursion does not affect plasma and cryoprecipitate quality.

Kelly M Winter, Rachel G Webb, Eugenia Mazur, Peta M Dennington, Denese C Marks

Abstract read
In one paragraph

Article in Vox sanguinis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kelly M WinterResearch and Development, Australian Red Cross Lifeblood, Alexandria, New South Wales, Australia.ORCID https://orcid.org/0000-0001-8423-3618
Rachel G WebbResearch and Development, Australian Red Cross Lifeblood, Alexandria, New South Wales, Australia.
Eugenia MazurResearch and Development, Australian Red Cross Lifeblood, Alexandria, New South Wales, Australia.
Peta M DenningtonPathology Services, Australian Red Cross Lifeblood, Alexandria, New South Wales, Australia.
Denese C MarksResearch and Development, Australian Red Cross Lifeblood, Alexandria, New South Wales, Australia.ORCID https://orcid.org/0000-0002-3674-6934

Funding

Australian Government
6 · The paper itself

Abstract

BACKGROUND AND

objectivesPlasma and cryoprecipitate are stored below -25°C for optimal preservation of component quality. However, there may be situations in which components are exposed to higher temperatures and therefore discarded. This study aimed to determine the quality of plasma and cryoprecipitate following a short-term temperature excursion to inform a possible shelf life. MATERIALS AND

methodsApheresis and whole blood (WB)-derived fresh frozen plasma (FFP; n = 68 and n = 37, respectively) and cryoprecipitate components (apheresis n = 78 and WB n = 80) that incurred a temperature excursion up to -11°C were returned to -25°C. Coagulation factors were measured at 1 month (baseline), 3 months and 6 months post excursion.

resultsThere were no significant differences in factor VIII (FVIII) concentrations in apheresis- and WB-derived plasma and apheresis-derived cryoprecipitate between 1 month, 3 months and 6 months (p = 0.236, p = 0.249 and p = 0.815, respectively). Activated partial thromboplastin time and prothrombin time increased slightly in plasma over storage but were not significantly different from baseline. Fibrinogen, von Willebrand Factor (VWF), protein C and immunoglobulin G were stable in plasma and cryoprecipitate.

conclusionThe data demonstrate that plasma and cryoprecipitate that incurred a temperature excursion can meet quality control specifications when stored for 6 months post temperature excursion.

Indexed as

Blood PreservationFactor VIIIFibrinogenPlasmaBlood Component RemovalHumansTemperatureTime Factorscryoprecipitate coagulumFactor VIIIFibrinogenplasmaqualityshort termtemperature excursion

Identifiers

PMID42209419
PMCPMC13563467

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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.