Objective:
To address the staffing challenges in cytopathology and improve rapid on-site evaluation (ROSE) processes at Washington University School of Medicine.
Approach:
- Digital ROSE reclaimed an additional workday of diagnostic time per pathologist each week.
- Real-time adequacy assessment prevents repeat biopsies and ensures sufficient tissue for molecular testing.
- Improved slide preparation consistency across sites due to digital archiving.
- Initial resistance from some pathologists regarding technology adoption.
- Dependence on adequate network bandwidth and compliance with security requirements.
Key Findings:
Interpretation:
The integration of digital technology in cytopathology enhances operational efficiency, improves patient care, and expands access to specialized diagnostics.
Limitations:
Conclusion:
The model demonstrates a scalable solution for providing expert cytopathology services across multiple sites, particularly in underserved areas, with potential for future expansion into other diagnostic areas.
Sources:
This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.
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About the Author(s)
Todd Vanden Branden
Todd Vanden Branden is a senior leader and strategist in digital pathology and clinical diagnostics, currently serving as Senior Director at Grundium US. He works closely with pathology laboratories and healthcare organizations to advance the adoption of digital and remote diagnostic workflows, modernizing laboratory practice and improving access to subspecialty expertise. His work focuses on translating emerging technologies into practical, high-impact solutions for routine clinical use.