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

被引:0
|
作者
Tshikudi, Diane M. [1 ]
Simandoux, Olivier [1 ]
Kang, Dongkyun [1 ,2 ,3 ]
Van Cott, Elizabeth M. [4 ]
Andrawes, Michael N. [5 ]
Yelin, Dvir [6 ]
Nadkarni, Seemantini K. [1 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Wellman Ctr Photomed, Boston, MA 02115 USA
[2] Univ Arizona, Coll Opt Sci, Tucson, AZ USA
[3] Univ Arizona, Dept Biomed Engn, Tucson, AZ USA
[4] Harvard Med Sch, Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02115 USA
[5] Harvard Med Sch, Massachusetts Gen Hosp, Dept Anesthesia Crit Care & Pain Med, Boston, MA 02115 USA
[6] Technion Israel Inst Technol, Fac Biomed Engn, Haifa, Israel
基金
美国国家卫生研究院;
关键词
PLASMA; HEMOSTASIS; MANAGEMENT; ACTIVATION; IMPACT;
D O I
10.1002/ajh.26217
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 mu m) over a volumetric field-of-view (165 x 4000 x 36 mu m). 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.
引用
收藏
页码:968 / 978
页数:11
相关论文
共 21 条
  • [1] Imaging of Caenorhabditis elegans by spectrally encoded confocal microscopy
    Rashtchian, Sadaf
    Youssef, Khaled
    Rezaei, Pouya
    Tabatabaei, Nima
    2020 IEEE PHOTONICS CONFERENCE (IPC), 2020,
  • [2] In Vivo Cellular Imaging with Spectrally Encoded Confocal Microscopy
    Kang, D.
    2017 CONFERENCE ON LASERS AND ELECTRO-OPTICS (CLEO), 2017,
  • [3] Flow cytometry using spectrally encoded confocal microscopy
    Golan, Lior
    Yelin, Dvir
    OPTICS LETTERS, 2010, 35 (13) : 2218 - 2220
  • [4] Comprehensive imaging of gastroesophageal biopsy samples by spectrally encoded confocal microscopy
    Kang, DongKyun
    Suter, Melissa J.
    Boudoux, Caroline
    Yoo, Hongki
    Yachimski, Patrick S.
    Puricelli, William P.
    Nishioka, Norman S.
    Mino-Kenudson, Mari
    Lauwers, Gregory Y.
    Bouma, Brett E.
    Tearney, Guillermo J.
    GASTROINTESTINAL ENDOSCOPY, 2010, 71 (01) : 35 - 43
  • [5] Combined spectrally encoded confocal microscopy and optical frequency domain imaging system
    Kang, DongKyun
    Suter, Melissa J.
    Boudoux, Caroline
    Yachimski, Patrick S.
    Bouma, Brett E.
    Nishioka, Norman S.
    Tearney, Guillermo J.
    ENDOSCOPIC MICROSCOPY IV, 2009, 7172
  • [6] Spectrally encoded slit confocal microscopy using a wavelength-swept laser
    Kim, Soocheol
    Hwang, Jaehyun
    Heo, Jung
    Ryu, Suho
    Lee, Donghak
    Kim, Sang-Hoon
    Oh, Seung Jae
    Joo, Chulmin
    JOURNAL OF BIOMEDICAL OPTICS, 2015, 20 (03)
  • [7] Co-registered spectrally encoded confocal microscopy and optical frequency domain imaging system
    Kang, D. K.
    Suter, M. J.
    Boudoux, C.
    Yachimski, P. S.
    Puricelli, W. P.
    Nishioka, N. S.
    Mino-Kenudson, M.
    Lauwers, G. Y.
    Bouma, B. E.
    Tearney, G. J.
    JOURNAL OF MICROSCOPY, 2010, 239 (02) : 87 - 91
  • [8] Spectrally encoded quantitative phase imaging microscopy using 2-μm fiber laser
    Soni, Niraj Kumar
    Ul Alam, Sabir
    Shi, Jiawei
    Wong, Kenneth K. Y.
    2021 CONFERENCE ON LASERS AND ELECTRO-OPTICS (CLEO), 2021,
  • [9] 2D Spectrally Encoded Confocal Microscopy and its Application for Simultaneous Imaging and Laser Surgery with a Single Fiber Probe
    Tsia, Kevin K.
    Goda, Keisuke
    Jalali, Bahram
    2009 CONFERENCE ON LASERS AND ELECTRO-OPTICS AND QUANTUM ELECTRONICS AND LASER SCIENCE CONFERENCE (CLEO/QELS 2009), VOLS 1-5, 2009, : 337 - 338
  • [10] In vivo imaging of the bronchial wall microstructure using fibered confocal fluorescence microscopy
    Thiberville, Luc
    Moreno-Swirc, Sophie
    Vercauteren, Tom
    Peltier, Eric
    Cave, Charlotte
    Heckly, Genevieve Bourg
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 175 (01) : 22 - 31