Digital Pathology
What is Digital Pathology?
Digital pathology incorporates the acquisition, management, sharing and interpretation of pathology information — including slides and data — in a digital environment. Digital slides are created when glass slides are captured with a scanning device, to provide a high-resolution digital image that can be viewed on a computer screen or mobile device.
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Utilizing high-throughput, automated digital pathology scanners, it is possible to capture an entire glass slide, under bright field or fluorescent conditions, at a magnification comparable to a microscope. Digital slides can be shared over networks using specialized digital pathology software applications. Automated image analysis tools can also be applied to assist in the interpretation and quantification of biomarker expression within tissue sections.
The history of digital pathology goes back over 100 years, when specialized equipment was first used to capture images from a microscope onto photographic plates. The concept of telepathology — transmitting microscope images between remote locations — has been around for nearly 50 years. However, it is in the past decade that pathology has begun to undergo a true digital transformation, moving away from analog into an electronic environment.
The rapid progress of whole slide imaging (WSI) technology, along with advances in software applications, LIS / LIMS interfacing, and high-speed networking, have made it possible to fully integrate digital pathology into pathology workflows.
Digital pathology enables pathologists to engage, evaluate, and collaborate rapidly and remotely, with transparency and consistency, thus improving efficiency and productivity. The future of digital pathology could eventually encompass enhanced translational research, computer aided diagnosis (CAD) and personalized medicine.
What are the Benefits of Digital Pathology?
Glass slides aren’t going anywhere, and for good reason. Pathology starts with a collected tissue. Glass slides are necessary, even if they are later transferred to a digital scan. But today’s pathology goes beyond tissue or scans. It’s all about improving quality, productivity and more.
Consider the way today’s pathology is changing:
- There is a workforce shortage of pathologists, with more pathologists retiring than those entering the field
- Digital technology has increased in adoption, delivering improved quality and innovation
Today’s pathology needs new approaches. And when pathologists stop short of adopting digital pathology fully, they miss out on the benefits that cannot be achieved with glass slides.
Digital pathology offers benefits not easily achieved with glass slides alone. Take a look at the many advantages of digital pathology versus microscopy alone.
Digital pathology can improve quality in meaningful ways:
Improved Analysis:
- Algorithms for analyzing slides are objective, accurate and quicker than microscopy
- Rapid access to prior cases
- Data Storage allows for long-term predictive analytics
Reduced Errors:
- Eliminates breakage
- Barcoding reduces risk of misidentification
Better Views:
- Offers live zoomed and multiple angle views
- Ability to measure multiple AOI
- Allows for team annotation of slides
- Provides a dashboard view of data and annotations
One of the biggest benefits of digital pathology is the many ways it improves productivity in the short and long term:
Improved Workflow
- Fosters collaboration
- Central storage enables easy access in streamlined workflow
- Curbs trend toward outsourcing
- Allows for automation, flex work schedules and remote access
Reduced Turnaround Times:
- Faster access to archived digital slides
- Reduces time retrieving, data matching and organizing
- Speeds up access to samples and improves turnaround time versus manual reviews, especially in complex cases
More Innovation:
- Big data allows pathologists to become more specialized
- Allows practices to extend to broader geographies
- Delivers better tools for teaching and training
“Glass slides work fine” is often a way of saying that pathologists can’t justify the investment in digital solutions. But often they don’t consider some of the long-term cost benefits of digitalization, such as:
- It eliminates courier service
- It speeds up workflow
- Travel for peer reviews is reduced
- New business opportunities are opened up through the ability to geographically extend the practice
- Avoid the need for overtime
The 7 Steps to Digital Pathology
Barriers to Adoption of Digital Pathology
“There’s nothing wrong with the microscope.”
“Our Information Systems won’t integrate with other technology.”
“Change is hard.”
These are a few of the concerns pathologists have about digital pathology. But as they learn more, pathologists are finding that their apprehension about going digital is holding them back from reaping significant benefits. They are also discovering that old methods can’t compete against today’s digital solutions.
And even when pathologists realize that digital methods offer increased speed, accuracy, efficiency and collaboration, the evolution can seem daunting.
As industry leaders with the most widely adopted digital pathology solution, we know the challenges of full adoption.
The process of embracing digital pathology can transform an organization.So, it is important to know the steps and how to get started.
| STEPS | KEY COMPONENTS |
|---|---|
| 1. Champion digital pathology |
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| 2. Define needs and goals |
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| 3. Specify infrastructure and Laboratory Information Systems (LIS) needs |
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| 4. Build workflow |
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| 5. Configuration and training |
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| 6. Rollout |
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| 7. Analyze and expand applications |
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What are the future trends for Digital Pathology and I.H.C.?
Digital pathology is increasingly used by large biopharmaceuticals and top clinical research organizations (CROs) to streamline drug development processes in discovery, pre-clinical and clinical trials.
Particular opportunity exists for the potential future use of digital pathology for quantitative analysis of emerging companion diagnostics and novel theranostics. This opportunity may become especially relevant with the advent of assays which are difficult to discern with the human eye, such as multiplex, or markers which exhibit diffuse staining characteristics across multiple cellular compartments of which, for example, only one may be clinically relevant.
The increasing complexity of such assays is driving the development of digital pathology solutions with advanced high-throughput image capture (brightfield, fluorescent or multispectral) coupled with pattern recognition to morphologically identify relevant tissue types and individual cellular compartments followed by the ability to quantify (IHC) intensity of staining.
This is leading to the advent of digital pathology systems that can offer a clinically relevant diagnostic or prognostic score by comparing sample analysis output against a standard curve derived from clinical data. Indeed, much of the untapped potential of digital pathology may be in the potential ability to generate diagnostic or prognostic scores by combining IHC data and images with that of other modalities such as FACS or MALDI-TOF, in an effort to achieve more discrete patient stratification into clinically relevant groups. Rather than replacing IHC, new molecular tests and the integration of digital pathology may offer complementary diagnostic tools for the future.
Digital Pathology Has Already Helped Revolutionize Education
The education sector was one of the earliest adopters of digital pathology, employing it throughout the full spectrum of histopathology learning from undergraduate and post graduate education through to continuous professional development (CPD) and external quality assurance (EQA).
Traditional education using light microscopes and glass slides has many challenges, including access to slides and variable course content, which can be overcome with the use of digital pathology. These include:
- Standardization of course material: With digital pathology, each participant sees the exact same content, as opposed to similar slides cut from the same tissue block, which may or may not exhibit the same morphological and biomarker expression patterns. Standardization of the content ensures that each participant has the same learning opportunities and quality of education. In addition, digital pathology facilitates the inclusion of rare cases in course material as only one digital copy of the slide is required, compared to multiple glass slides for a standard class size.
- Improved Accessibility: Digital pathology facilitates greater access to tissue and slide-based material outside of the laboratory and traditional tutorial times. Users can access their digital course content via the internet on a standard web-browser, via personal computer, tablet, or smartphone devices, giving them the ability to view slides anytime, anywhere. The use of digital pathology to support CPD and EQA schemes helps to reduce circulation turnaround time and costs, as the slides no longer have to be physically shipped from one site to the other, but rather can be efficiently shared with multiple locations simultaneously.
- Improved Learning: Moving from a physical to a digital environment for histopathology education offers many benefits over traditional light microscopy and glass slide teaching methods. Users can view multiple digital slides simultaneously, aligning them side-by-side for improved comparison between different tissue sections and immunohistochemistry (IHC) markers (Figure 6).
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Educators can annotate significant regions of interest, right down to the cellular and sub-cellular level, which cannot be done readily with glass slides (Figure 7). And with specialized digital pathology educational software applications, questions and tutorials can be embedded into the digital slides, providing contextual information and direct links to tissue or cellular features referenced in the questions.
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For Research Use Only. Not for use in diagnostic procedures.
The clinical use claims described in the information supplied have not been cleared or approved by the U.S. FDA or are not available in the United States.
This reference document is presented as a service to health care professionals by Leica Biosystems and has been compiled from available literature. Although every effort has been made to report faithfully the information, Leica Biosystems cannot be held responsible for the correctness. This document is not intended to be, and should not be construed as medical advice. For any use, the product information guides, inserts and operation manuals of the various drugs and devices should be consulted. Leica Biosystems and the editors disclaim any liability arising directly or indirectly from the use of drugs, devices, techniques or procedures described in this reference document.