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    Imaging the dynamics and microstructure of fibrin clot polymerization in cardiac surgical patients using spectrally encoded confocal microscopy

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    Manuscript_AJH_revised_Final.pdf
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    Author
    Tshikudi, Diane M
    Simandoux, Olivier
    Kang, Dongkyun
    Van Cott, Elizabeth M
    Andrawes, Michael N
    Yelin, Dvir
    Nadkarni, Seemantini K
    Affiliation
    College of Optical Sciences and Department of Biomedical Engineering, University of Arizona
    Issue Date
    2021-05-10
    
    Metadata
    Show full item record
    Publisher
    John Wiley and Sons Inc
    Citation
    Tshikudi, D. M., Simandoux, O., Kang, D., Van Cott, E. M., Andrawes, M. N., Yelin, D., & Nadkarni, S. K. (2021). Imaging the dynamics and microstructure of fibrin clot polymerization in cardiac surgical patients using spectrally encoded confocal microscopy. American Journal of Hematology.
    Journal
    American journal of hematology
    Rights
    © 2021 Wiley Periodicals LLC.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    During cardiac surgery with cardiopulmonary bypass (CPB), altered hemostatic balance may disrupt fibrin assembly, predisposing patients to perioperative hemorrhage. We investigated the utility of a novel device termed spectrally-encoded confocal microscopy (SECM) for assessing fibrin clot polymerization following heparin and protamine administration in CPB patients. SECM is a novel, high-speed optical approach to visualize and quantify fibrin clot formation in three dimensions with high spatial resolution (1.0 μm) over a volumetric field-of-view (165 × 4000 × 36 μm). The measurement sensitivity of SECM was first determined using plasma samples from normal subjects spiked with heparin and protamine. Next, SECM was performed in plasma samples from patients on CPB to quantify the extent to which fibrin clot dynamics and microstructure were altered by CPB exposure. In spiked samples, prolonged fibrin time (4.4 ± 1.8 to 49.3 ± 16.8 min, p < 0.001) and diminished fibrin network density (0.079 ± 0.010 to 0.001 ± 0.002 A.U, p < 0.001) with increasing heparin concentration were reported by SECM. Furthermore, fibrin network density was not restored to baseline levels in protamine-treated samples. In CPB patients, SECM reported lower fibrin network density in protaminized samples (0.055 ± 0.01 A.U. [Arbitrary units]) vs baseline values (0.066 ± 0.009 A.U.) (p = 0.03) despite comparable fibrin time (baseline = 6.0 ± 1.3, protamine = 6.4 ± 1.6 min, p = 0.5). In these patients, additional metrics including fibrin heterogeneity, length and straightness were quantified. Note, SECM revealed that following protamine administration with CPB exposure, fibrin clots were more heterogeneous (baseline = 0.11 ± 0.02 A.U, protamine = 0.08 ± 0.01 A.U, p = 0.008) with straighter fibers (baseline = 0.918 ± 0.003A.U, protamine = 0.928 ± 0.0006A.U. p < 0.001). By providing the capability to rapidly visualize and quantify fibrin clot microstructure, SECM could furnish a new approach for assessing clot stability and hemostasis in cardiac surgical patients. © 2021 Wiley Periodicals LLC.
    Note
    12 month embargo; first published: 10 May 2021
    EISSN
    1096-8652
    PubMed ID
    33971046
    DOI
    10.1002/ajh.26217
    Version
    Final accepted manuscript
    ae974a485f413a2113503eed53cd6c53
    10.1002/ajh.26217
    Scopus Count
    Collections
    UA Faculty Publications

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