NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Better hemostatic profiles of never-frozen liquid plasma compared with thawed fresh frozen plasma.

Author(s): Matijevic N, Wang YW, Cotton BA, Hartwell E, Barbeau JM, Wade CE, Holcomb JB

Publication: J Trauma Acute Care Surg, 2013, Vol. 74, Page 84-90; discussion 90-1

PubMed ID: 23271081 PubMed Review Paper? No

Purpose of Paper

The purpose of this study was to determine the effects of refrigeration, freezing, and subjecting plasma to a freeze-thaw cycle after refrigeration on TEG, thrombogram, plt counts, PMPs, clotting factors, and coagulation inhibitors. Frozen plasma was thawed in a 37 degrees C water bath, analyzed immediately and again after 5 days at 2-6 degrees C. Fresh plasma was refrigerated and analyzed at all time-points, and an additional aliquot was taken at each timepoint and was frozen and thawed once before analysis.

Conclusion of Paper

Plt counts, endogenous thrombin potential (ETP) and clotting capacity were higher in fresh plasma than in plasma that was frozen, but PMPs contents were comparable between the two types of specimens. Refrigerated storage of plasma led to decreases in the plt counts, ETP, clotting capacity, factor V, factor VIII and free protein S, and led to increases in PMPs, activated partial thromboplastin time (APTT), prothrombin time (PT), factor VII, factor XII and von Willebrand factor levels. Both thrombograms and TEG showed a gradual decrease during refrigerated storage of plasma in some specimens, but an initial decrease followed by an increase was observed in other specimens. In addition, subjecting refrigerated plasma to a single freeze-thaw cycle, after 0-26 days of refrigeration, decreased the plt count and decreased the TEG-maximum amplitude compared to plasma refrigerated for the same duration, but never frozen.

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of refrigeration, freezing, and subjecting plasma to a freeze-thaw cycle after refrigeration on TEG, thrombogram, plt counts, PMPs, clotting factors, and coagulation inhibitors. Frozen plasma was thawed in a 37 degrees C water bath, analyzed immediately and again after 5 days at 2-6 degrees C. Fresh plasma was refrigerated and analyzed at all time-points, and an additional aliquot was taken at each timepoint and was frozen and thawed once before analysis.

    Summary of Findings:

    The plt count was 10.8 fold higher in fresh plasma than in plasma that was frozen (p<0.0001), but after 26 days of refrigerated storage the plt count was not significantly different from that in plasma that was frozen and analyzed immediately after thawing or 5 days later. PMPs were comparable in fresh and frozen plasma on day 0, but they were higher in plasma that was refrigerated for 26 days than in plasma that was frozen, thawed, and refrigerated for 5 days before analysis (p<0.001). The thrombogram revealed that ETP was higher in fresh than frozen plasma on day 0, but it declined by 16% during 26 days of refrigerated storage and was comparable to levels in frozen plasma. Thrombogram tracings revealed that plasma either showed a gradual decrease in homeostatic potential throughout the refrigerated storage or decreased initially and then rebounded. Initially fresh plasma had significantly higher maximum amplitude, shear elastic module strength, and total thrombus generation than frozen plasma, but the capacity of plasma to clot decreased with refrigerated storage, such that, after 26 days, values were comparable to those in frozen plasma that had been thawed and refrigerated for 5 days before analysis. Similar to the thrombograms, some TEG showed a gradual decrease during refrigerated storage of plasma, while others showed an initial decrease followed by an increase during storage. Most clotting factors, fibrinogen and coagulation inhibitors remained within 88% of values measured in fresh plasma during the 26 days of refrigerated storage, but APTT, PT, factor VII, factor XII and von Willebrand factor levels increased, and factor V, factor VIII and free protein S decreased by day 26 of storage. Subjecting refrigerated plasma, after 0-26 days of refrigeration, to a single freeze-thaw cycle decreased the plt count by up to 50% (p<0.001), and decreased the TEG-maximum amplitude compared to plasma refrigerated for the same duration, but never frozen

    Biospecimens
    Preservative Types
    • None (Fresh)
    • Other Preservative
    • Frozen
    Diagnoses:
    • Normal
    Platform:
    AnalyteTechnology Platform
    Cell count/volume Flow cytometry
    Protein Hematology/ auto analyzer
    Morphology Hematology/ auto analyzer
    Glycoprotein Hematology/ auto analyzer
    Peptide Hematology/ auto analyzer
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Storage Freeze/thaw cycling 0 cycles
    1 cycle
    Storage Storage duration 0 days
    5 days
    10 days
    15 days
    20 days
    26 days
    Biospecimen Preservation Type of fixation/preservation Frozen
    None (fresh)
    Refrigeration

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