Quantification of histochemical stains using whole slide imaging: development of a method and demonstration of its usefulness in laboratory quality control

被引:31
作者
Gray, Allan [1 ]
Wright, Alex [2 ]
Jackson, Pete [1 ]
Hale, Mike [2 ]
Treanor, Darren [1 ,2 ]
机构
[1] Leeds Teaching Hosp NHS Trust, Leeds, W Yorkshire, England
[2] Univ Leeds, Leeds, W Yorkshire, England
基金
英国医学研究理事会;
关键词
SECTION THICKNESS;
D O I
10.1136/jclinpath-2014-202526
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aims Histochemical staining of tissue is a fundamental technique in tissue diagnosis and research, but it suffers from significant variability. Efforts to address this include laboratory quality controls and quality assurance schemes, but these rely on subjective interpretation of stain quality, are laborious and have low reproducibility. We aimed (1) to develop a method for histochemical stain quantification using whole slide imaging and image analysis and (2) to demonstrate its usefulness in measuring staining variation. Methods A method to quantify the individual stain components of histochemical stains on virtual slides was developed. It was evaluated for repeatability and reproducibility, then applied to control sections of an appendix to quantify H&E staining (H/E intensities and H:E ratio) between automated staining machines and to measure differences between six regional diagnostic laboratories. Results The method was validated with <0.5% variation in H: E ratio measurement when using the same scanner for a batch of slides (ie, it was repeatable) but was not highly reproducible between scanners or over time, where variation of 7% was found. Application of the method showed H: E ratios between three staining machines varied from 0.69 to 0.93, H: E ratio variation over time was observed. Interlaboratory comparison demonstrated differences in H: E ratio between regional laboratories from 0.57 to 0.89. Conclusions A simple method using whole slide imaging can be used to quantify and compare histochemical staining. This method could be deployed in routine quality assurance and quality control. Work is needed on whole slide imaging devices to improve reproducibility.
引用
收藏
页码:192 / 199
页数:8
相关论文
共 9 条
  • [1] [Anonymous], 2014, VIRTUAL PATHOLOGY U
  • [2] Badano A, CONSISTENCY ST UNPUB
  • [3] Bancroft J. D., 2006, THEORY PRACTICE HIST
  • [4] A technique for section thickness evaluation for microphotometry and image analysis of sectioned nuclei
    Cabrini, RL
    Folco, A
    Orrea, S
    Savino, MT
    Schwint, AM
    Itoiz, ME
    [J]. ANALYTICAL CELLULAR PATHOLOGY, 1998, 17 (02): : 125 - 130
  • [5] GSCHWENDTNER A, 1995, ANAL CELL PATHOL, V9, P29
  • [6] Little Elizabeth, 2010, PATH VIS 2010 SAN DI
  • [7] Magee D., 2009, PROC OPTICAL TISSUE
  • [8] Toward Routine Use of 3D Histopathology as a Research Tool
    Roberts, Nicholas
    Magee, Derek
    Song, Yi
    Brabazon, Keeran
    Shires, Mike
    Crellin, Doreen
    Orsi, Nicolas M.
    Quirke, Richard
    Quirke, Philip
    Treanor, Darren
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2012, 180 (05) : 1835 - 1842
  • [9] Ruifrok AC, 2001, ANAL QUANT CYTOL, V23, P291