Fixation on Histology: A New Approach to Bladder Cancer Detection

Written based on the research article published in the Journal of Histotechnology

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Fixation on Histology: Understanding the Tools of Embedding

Written based on the NSH Webinar: Embedding Basics & Troubleshooting

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Fixation on Histology: The High Cost of Johne’s Disease

Written based on the NSH Webinar Jonesing For Johne’s - AFB Control Tissue

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Fixation on Histology: Top 5 Traits of a Great Histotechnologist

Written by: Connie Wildeman, Director of Education, NSH

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In this episode, NSH Director Education, Connie Wildeman, sat down with Olivia Hoppe and Olivia Mouch, both Application Support Specialists with Milestone Medical, to discuss their unique roads to histology. The also discuss important traits of a histotech - no matter the background. Whether you looking to hire a tech or trying to determine if you could be a good tech, this podcast provides great insights into your histology lab future!

Special thanks to Milestone Medical for supporting this episode.

Fixation on Histology: Are Multiple GMS-Stained Levels Needed? Not Necessarily, According to Study

Written based on the article "Multiple levels of Gomori methenamine silver (GMS) stains do not improve diagnostic yield in esophageal biopsies" published in the Journal of Histotechnology

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Fixation on Histology: NSH Was Doing Distance Learning Before It Was Cool — Here’s Why It Still Works

Written by: Connie Wildeman, MPA, Director of Education at NSH

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Title: Histological Whole Slide Scanning Reproducibility Study

Authors: Hannah Benton, BSa, Tomoe Shiomi, MS, HTL(ASCP)CM, CT(IAC)CM, Fatma Farooqi, BSc, HTL(ASCP), Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC and Luis Chiriboga, PhD, HT(ASCP)QIHC

Abstract: Whole slide imaging (WSI) is an increasingly versatile method for capturing and sharing high-resolution digital images of stained histological slides. These images can be used for a variety of applications, including clinical diagnosis, pathology review, and image analysis. While many whole slide scanners exist with varying features tailored to different use cases, a critical factor across all platforms is the accuracy and reproducibility of the scanned images. To investigate scan consistency over time, a control slide was prepared using a tissue microarray stained with Hematoxylin and Eosin (H&E). Ink dots were applied to the slide to define a consistent scanning region. The slide was scanned 77 times over six months using an Aperio AT2 whole slide scanner at 40x magnification.Image analysis was performed using HALO software by Indica Labs. Both the entire scan area and individual tissue punches were analyzed to assess total stained area and stain intensity, quantified by optical density (OD) for both hematoxylin and eosin. A linear regression model was applied to data from all individual punches and the full scan region. Additionally, a two-way ANOVA was conducted to compare OD values of hematoxylin and eosin between the first 10 scans and the last 10 scans. Key findings were that hematoxylin showed a statistically significant decline in both stained areas and OD over time, while eosin demonstrated a statistically significant increase in stained area, but a decrease in OD. These results suggest potential degradation of staining quality or imaging consistency over time. Possible contributing factors include slide bleaching, light source variability, annotation region size, or other imaging conditions. These will be the focus of future investigations to better understand and control variability in longitudinal slide scanning studies.