Bronchoscopic Fibered Confocal Fluorescence Microscopy Image Characteristics and Pathologic Correlations

被引:21
|
作者
Filner, Joshua J. [1 ]
Bonura, Eric J. [2 ]
Lau, Stephanie T. [2 ]
Abounasr, Khader K. [2 ]
Naidich, David [2 ]
Morice, Rodolfo C. [3 ]
Eapen, George A. [3 ]
Jimenez, Carlos A. [3 ]
Casal, Roberto F. [3 ]
Ost, David [3 ]
机构
[1] Kaiser Permanente Oregon, Portland, OR USA
[2] NYU, Sch Med, New York, NY 10003 USA
[3] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
bronchoscopy; diagnostic imaging; image interpretation; computer assisted; microscopy; confocal tomography; optical coherence;
D O I
10.1097/LBR.0b013e318203da1c
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Fibered confocal fluorescence microscopy (FCFM) is a new imaging modality in bronchoscopy. The purpose of this study was to assess FCFM reliability, interpretation, and to make image-pathologic correlations. Methods: Twenty-six patients underwent FCFM. A validation set was used to determine image characteristics and interobserver reliability. Each patient underwent bronchoscopy using a standardized protocol. The images were evaluated by 4 observers based on brightness, fiber thickness, and alveolar cellularity. Image characteristics showing good interobserver agreement were tested to see if they were related to smoking status. Subsequently, 18 consecutive patients underwent FCFM and biopsy to correlate images with pathology. The blinded reviewers were asked to distinguish between controls and patients with pathologically proven disease. Results: Interobserver agreement for image brightness, as measured by intraclass correlation coefficients (ICCs), ranged from 0.48 to 0.92 (P < 0.001) and varied by location. ICCs for image brightness were high, ranging from 0.53 to 0.99 (P < 0.001). Agreement for fiber thickness was poor for respiratory bronchioles (ICC 0.12, P < 0.05) and fair for alveoli (ICC range, 0.37 to 0.42, P < 0.001). The intraobserver (ICC range, 0.69 to 0.91, P < 0.001) and intrapatient (ICC 0.65 to 0.84, P < 0.001) reliability were excellent. Computer image interpretation showed excellent agreement with humans (ICC 0.62 to 0.99, P < 0.001). Smoking was inversely associated with respiratory bronchiole brightness (P < 0.001). In FCFM-pathologic correlation, FCFM could distinguish normal from diseased tissue; however, specific diseases could not be distinguished from other diseases. Conclusion: FCFM shows a high degree of image reliability and can detect changes in the respiratory bronchioles because of smoking and other diseases, but whether it can discriminate among diseases requires additional study.
引用
收藏
页码:23 / 30
页数:8
相关论文
共 50 条
  • [41] The fluorescence characteristics of furfurylated wood studied by fluorescence spectroscopy and confocal laser scanning microscopy
    Thygesen, L. G.
    Barsberg, S.
    Venas, T. M.
    WOOD SCIENCE AND TECHNOLOGY, 2010, 44 (01) : 51 - 65
  • [42] Image characteristics of mast cell tumors on reflection confocal microscopy
    Song, Yuantao
    Rong, Meixiang
    Bi, Tiantian
    Li, Qinfeng
    ASIAN JOURNAL OF SURGERY, 2025, 48 (03) : 1955 - 1956
  • [43] The fluorescence characteristics of furfurylated wood studied by fluorescence spectroscopy and confocal laser scanning microscopy
    L. G. Thygesen
    S. Barsberg
    T. M. Venås
    Wood Science and Technology, 2010, 44 : 51 - 65
  • [44] Confocal in vivo microscopy, confocal laser scanning and fluorescence microscopy in keratoconus
    Somodi, S
    Hahnel, C
    Slowik, C
    Richter, A
    Guthoff, R
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1996, 37 (03) : 4686 - 4686
  • [45] Magnetic targeting of rhodamine-labeled superparamagnetic liposomes to solid tumors: In vivo tracking by fibered confocal fluorescence microscopy
    Martina, Marie-Sophie
    Fortin, Jean-Paul
    Fournier, Laure
    Menager, Christine
    Gazeau, Florence
    Clement, Olivier
    Lesieur, Sylviane
    MOLECULAR IMAGING, 2007, 6 (02): : 140 - 146
  • [46] Functional Fibered Confocal Microscopy: A Promising Tool for Assessing Tendon Regeneration
    Snedeker, Jess G.
    Ben Arav, Ayelet
    Zilberman, Yoram
    Pelled, Gadi
    Gazit, Dan
    TISSUE ENGINEERING PART C-METHODS, 2009, 15 (03) : 485 - 491
  • [47] Reflectance confocal microscopy characteristics of eight cases of pustular eruptions and histopathological correlations
    Debarbieux, Sebastien
    Depaepe, Lauriane
    Poulalhon, Nicolas
    Dalle, Stephane
    Balme, Brigitte
    Thomas, Luc
    SKIN RESEARCH AND TECHNOLOGY, 2013, 19 (01) : E444 - E452
  • [48] Fibered confocal spectroscopy and multicolor imaging system for in vivo fluorescence analysis
    Jean, Florence
    Bourg-Heckly, Genevieve
    Viellerobe, Bertrand
    OPTICS EXPRESS, 2007, 15 (07): : 4008 - 4017
  • [49] Application of avalanche photodiodes to confocal and confocal fluorescence microscopy
    Brown, TG
    Kreger, ST
    THREE-DIMENSIONAL MICROSCOPY: IMAGE ACQUISITION AND PROCESSING III, 1996, 2655 : 68 - 78
  • [50] 3-DIMENSIONAL IMAGE-RESTORATION IN FLUORESCENCE CONFOCAL SCANNING MICROSCOPY
    BERTERO, M
    BOCCACCI, P
    BRAKENHOFF, GJ
    MALFANTI, F
    VANDERVOORT, HTM
    OPTICAL STORAGE AND SCANNING TECHNOLOGY, 1989, 1139 : 86 - 91