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Henry Ford Hospital: A Gold Standard in Pathology & Laboratory Medicine
Jul 15th, 2011 by alowe

I am in the process of accomplishing one of my new years resolutions to become Black Belt certified in Lean Six Sigma. I am two thirds of the way done. I became certified as a Six Sigma Green Belt in April and Lean certified in June; both with a focus in healthcare.  I am currently in the process of taking my black belt course and working on a project for certification.  These days Lean Six Sigma methods are constantly running through my head and I have applied several methods to my consulting work.

The power of Post-It's and moveable whiteboards!

One of my favorite tools are Post-its and take anywhere, disposable white boards.  I use them on-site with clients and I also use them in my office, ALL over my office.  So in an ongoing effort to immerse myself more in Lean Six Sigma for the lab I turned to one the leaders of Lean Six Sigma in pathology, Henry Ford Hospital.

Dr. Mark Tuthill, Division Head of Pathology Informatics, was kind enough to give me a tour and WOW was I impressed.  Yes.. it was a big WOW! My last blog post was about creating WOWs instead of waiting for them to happen.  This is exactly what Henry Ford’s department for Pathology and Laboratory Medicine has done and continues to do, because striving to improve is never complete!  You know from the moment you enter the department you have walked into a remarkable place.  Placards are prominently displayed with powerful messages including:

Every Life Deserves World-Class Laboratory Service”

Lean Six Sigma is a management philosophy and their department is lead by prominent pathologist Dr. Richard Zarbo, who clearly embraces the power of Lean Six Sigma.  The entire department is involved and committed to continuous improvement; a fact that would make their founder, and the father of Lean, Henry Ford proud.

Here are some of my take-aways from my visit.

  • Silence is golden! Dr. Tuthill brought to my attention, while standing in the gross lab, how quiet everything was. This quite and calm environment continued throughout the AP lab too.  The department has moved away from transcription and voice dictation and developed templates that integrate into their LIS.
  • Process improvement takes time and really is continuous. This is a fundamental of Lean Six Sigma but was reinforced throughout my department tour.  White boards are all over to illustrate how new processes are mapped, monitored, and certain boards engage employees to document defects on an ongoing basis.  Defects, as defined in their publication “Effective Reduction of Process Defects and Waste In Surgical Pathology,” are forms of waste including flaws, imperfections, or deficiencies in specimen processing that required work to be delayed, stopped, or returned to the sender.  Here are some pictures of their whiteboards and process flow charts:

Gross Room: Process Flow Chart

Defect Tracking

  • A very visual environment. Everything, and I mean EVERYTHING was labeled- even gauze.  The department loves 5S and Kanbans and you can tell.  You never have to question where something is, where it should go, or if there is more available.  It’s a straight forward concept but is your lab like that?
  • A foundation for success! Henry Ford has been working hard to prepare their lab and department for their digital future over the past few years (while also reducing costs, improving patient safety, and laboratory efficiency). Their entire process is barcoded from accession to sign-out.  The laboratory uses barcode technology from General Data, and even assigns barcodes to requisition forms that are scanned to eliminate paper in the lab.  The gross lab is set up with a Milestone gross imaging system,  digital cameras are mounted on grossing tables and pathologists microscopes.  The cameras are then connected via a TWAIN interface to PathPacs, their middleware software by Apollo.  PathPacs is integrated with their Sunquest CoPath Plus LIS and allows the pathologist to choose and select images to be in the LIS and reports.

Can you guess their next step for their digital future? Digital Pathology!   With the foundation described above, a Lean Six Sigma culture, and a management team with vision I have no doubt that they will be successful.  Thank you Henry Ford Hospital for your level of excellence, you truly are a gold standard.

The DPA Issues Two White Papers
Nov 3rd, 2010 by alowe

I attended Pathology Visions last week (more on that later…) which is organized by the Digital Pathology Association (DPA).  The DPA released on Tuesday two white papers; 1) Interoperability between Anatomic Pathology Laboratory Information Systems (APLIS) and Digital Pathology Systems and 2) Archival and Retrieval in Digital Pathology Systems.

The white papers are good and provide vendor neutral information to help the digital pathology industry and consumers.  Here are the abstracts and a few of my favorite points from each:

Archival and Retrieval in Digital Pathology Systems

This white paper frames the issues related to Archival and Retrieval of images and associated data as Anatomic Pathology laboratories adopt a digital imaging workflow in a research or clinical setting. This overview also includes a brief discussion of some of the solutions being developed and offered in digital pathology systems (DPS’s).

DPS’s start with creation of a whole slide image and provide an imaging workflow for pathologists by associating the images with a patient and case and furnishing the tools to review the cases digitally. Whole slide images (WSI) are very large and will drive the need for extensive storage and information life cycle management. Customers seek options for fast access to high quality and highly available data, when they use the DPS in a business critical application. Most importantly, since DPS’s are deployed in regulated environments, data reliability, privacy, and security need to be built into the solution and its management process.

Solutions that are being developed and deployed in digital pathology systems are also presented.

Favorite points:

  • WSI are about 10x that of Radiology images.  The white paper talks about an average, compressed image size and the storage and network requirements needed to support a DPS for different size programs.
  • The importance of data integrity, reliability, and audit trails for HIPAA, CLIA, and FDA compliance.
  • An overview of Image Life Cycle Management (ILM) and important decision criteria.

Interoperability between Anatomic Pathology Laboratory Information Systems and Digital Pathology Systems

This white paper offers an overview of the current state of interoperability between Anatomical Pathology Laboratory Information Systems (APLIS’s) and Digital Pathology Systems (DPS’s). This overview also includes a brief discussion of future work that will impact interoperability.

Both systems rely on data from the other to efficiently deliver full digital imaging functionality to the healthcare provider. Anatomic Pathology (AP) departments and patients will benefit most from imaging workflow when there is a high degree of integration of Digital Pathology information within AP workflow. Implementations of such data sharing already exist via interfaces and standard communication protocols between APLIS’s and DPS’s, and work continues on these interface standards to improve the degree to which these systems can be used together.

The current state of interoperability provides Pathologists with access to images and image analysis data from within the APLIS or the DPS. This information is then available to the Patient Report.

Favorite points:

  • In depth analysis and information about digital pathology and the AP Lab workflow
  • Examples of current interoperability implementations between the APLIS and DPS
  • Dealing with network and security issues for outside consultations
  • The importance of barcodes
  • Understanding the difference between compatibility and Interoperability

ADVANCE Article: Putting the Digital Pieces Together
Aug 13th, 2010 by alowe

Below is an article I wrote for ADVANCE for Laboratory Professionals, Perspectives In Pathology.

Putting the Digital Pieces Together

By Amanda Lowe

Digital pathology is often described as the scanning of a glass slide into a whole slide image; yet, it is much more. It is so much more, in fact, that pathologists and laboratory professionals find themselves puzzled with how it will affect their future. As technology progresses, we must start to understand how to put the pieces of it together—from acquisition to integration to data management and interpretation.

Acquisition

Acquisition of a whole slide image from a glass slide is done on a slide scanner, which creates the image necessary for interpretation. Important elements of slide preparation and patient information can make the acquisition process simple or complex.

Slide preparation is a crucial and often overlooked element of digital pathology. Pathologists can handle slide artifacts such as folds and air bubbles under a microscope; slide scanners are not always as forgiving. Also, staining has to be perfected, not only for scanning but for accurate interpretation and use with image analysis software. Poor staining can result in tissue not being scanned, inaccurate image analysis data—and in the worst case—a wrong diagnosis.

Traditionally, when glass slides are prepared, they are manually matched with the patient paperwork (including patient history, requisition and gross review), then delivered to the pathologist. With digital pathology, the process looks different. You now have whole slide images that need to be reconciled to the digital patient paperwork, then delivered to the pathologist. The only way to do this is with a laboratory information system (LIS), electronic medical record (EMR) integration, and bar codes. Bar codes will reduce human error, save time on the constant need for verification and re-checks, and improve quality assurance by tracking all specimens throughout the histology process.

Integration

The LIS and often the EMR need to share information with the digital pathology software to create a pathology picture archiving and communication system (PACS) that consolidates all patient paperwork, gross images and whole slide images for interpretation. This is the most important but also the most difficult piece for labs to handle. The process can be costly and require collaboration of two or more vendors, which can be a frustrating and hard process to manage. However, it can be accomplished with a plan, a budget and someone to manage the project.

Data Management

Many hospitals do not have adequate IT resources or the expertise to handle their already stressed storage demands. Yet these whole slide images have to be stored somewhere. Unfortunately, most IT departments do not understand the fundamentals of digital pathology. Pathology leaders and their lab personnel must improve communication with their IT departments and take an active role in educating IT on the realistic needs of the department now and over the next five years. Hospitals have to prepare for the increase in lab data and pathology images that will soon be their future.

To estimate your whole slide image storage needs, divide the number of surgical slides your lab generates per year by 3,500 to get an estimate of terabytes needed annually; 3,500 is the average number of whole slide images per one terabyte.

Healthcare providers are required to save medical records for a specified time; for most, this is a minimum of seven years. Security is not optional, and HIPAA mandates backup and disaster recovery plans for patient records, including all medical images. The specialty of pathology will not be an exception to the rule.

Interpretation

One goal of digital pathology is to enhance the sign-out process for pathologists. Pathologists should be able to sit down at a computer monitor to sign out digital cases retrieved from a pathology PACS system. Easy access to archived cases for disease progression or comparison, rapid case sharing and consultations, data mining for decision support and image analysis will all help improve the diagnostic process.

Powered by the rapid and endless growing portfolio of image analysis algorithms, pathology will transition from a qualitative to a quantitative discipline. Digital pathology partnered with image analysis will create the infrastructure necessary so pathologists can confidently determine the severity of a disease and predict responses to a target therapy.

Digital pathology streamlines laboratory workflow, enhances the sign-out process, and can improve diagnostic outcomes and treatment responses for patients while at the same time forge a new foundation for the use of pathology data to drive translational research and higher standards of care.

All Aboard! The Digital Pathology Bandwagon
Apr 1st, 2010 by alowe

Five years ago at the United States and Canadian Association of Pathology (USCAP) annual meeting, I was working for one of two slide scanner manufacturers exhibiting in a small booth trying to gain exposure and sell systems. A few years later, there were four or five companies, and this year there were SIXTEEN companies exhibiting digital pathology hardware and/or software solutions.  For the small group of people who have been in this industry for a long time, it’s amazing to see how far the field has evolved.  Here are a few of my digital pathology highlights from USCAP ’10.

A Step Forward

WG-26 met on March 20th to finalize Supplement 145, Whole Slide Imaging for Pathology, for submission to WG-6 who coordinates all changes to DICOM.  On March 25th, WG-6 approved the supplement, and it will go out to letter ballot within the next two weeks for a 49 day voting period.  Assuming a successful outcome, DICOM for whole slide images will be finalize this summer.  Many thanks to WG-26 for all of their hard work over the past five years as this standard will improve data management, interoperability, and workflow within pathology.

The Bandwagon

Several new companies were at USCAP this year offering digital pathology solutions including Leica, Philips, Motic, CRi and MikroScan Technologies.  Laboratory Information Systems (LIS) and middleware companies were highlighting integration with digital pathology companies increasing interoperability for pathology departments. In addition, numerous reference and contract laboratories were demonstrating their use of digital pathology to stay competitive and allow earlier and flexible access to images and their data.  Lastly, current market leaders Aperio, Bioimagene, Olympus, and 3DHistech were demonstrating impressive portfolios of hardware, software, and workflow solutions in their large, expanded booths.

Diagnostic Displays

If you visited the exhibit hall and met with any digital pathology companies, likely you were looking at whole slide images on a Barco diagnostic display.  I recently posted about diagnostic displays, and how they could play a key role in the future of digital pathology, and it was nice to see the industry support and response to diagnostic displays.

Whether it was during sessions, reviewing posters, walking the exhibit hall, or in conversations with colleagues; digital pathology was definitely a hot topic.  With all this excitement and advancement I cannot wait to see where we are next year, and to see who else will jump on the bandwagon!

The “Big Wave”
Jan 27th, 2010 by alowe

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I recently participated in an audio conference, provided by The Dark Report titled “New Opportunities for Your Lab’s LIS-EMR Interface: How to Profit From the Big Wave About to Hit Healthcare.”  The “Big Wave” is simply, the massive increase of physicians who will adopt a certified EMR system within the next 5 years.  In 2009, approximately 25,000 practices adopted an EMR, bringing the total physician adoption to  approximately 30% nationwide.  If the stimulus plan reaches it’s goal of 90% adoption by 2015, then adoption is going to more than double, with around 60,000 practices adopting per year starting this year.   But what does this mean for laboratories?

For a physician to get up to $44,000 in reimbursement dollars, available through Medicare, they must prove “meaningful use”.  There are three items on the “meaningful use” checklist that pertain to laboratories for phase 1, and they are:

  1. Computer physician order entry of tests, imaging studies, referrals, etc
  2. Lab test results- which many are doing or can do right now
  3. Reportable lab submission, meaning your lab reports coming into the EMR get reported to a public health agency

Basically lab orders have to be loaded up, set up in that EMR and adopted by the practice and its employees; lab results have to be deployed, and the lab reports will have to be shared with a public health agency.  It’s the first step in this process though that is going to have the largest impact on laboratories as their customers, physician practices,  are going to be demanding integration.   Thus, laboratories can either hope that their LIS will integrate with the physicians new EMR easily (but is IT integration ever easy?), or they can proactively use this opportunity to grow business and strengthen relationships with their practices.   Given that there are currently 11 certified EMR companies and an additional 30 pending certification, it is likely that your LIS will not support them all. You must become proactive!  So what do you do to manage the “Big Wave” about to hit laboratories?

  • Labs should reach out to their practices and find out where they are in their EMR selection process.  Ask to be involved in the process, that you are educated in “meaningful use”, and that lab integration needs to be part of their EMR solution
  • If you have a third-party partner, such as a middleware company or consultant, reach out to them for advice and guidance
  • Do an evaluation of  the physician groups and the type of EMR’s deployed in your area.  When a physician is already using an EMR find out about how their practice uses it and what the strengths and weaknesses are of the system.
  • If you have the means, dedicated an internal person to do this marketing research
  • Perform internal and external application assessment and readiness
  • Know your LIS applications strengths and weaknesses
  • Identify IT resources to help with integration to the practices
  • Create/maintain common order sets in native systems
  • Establish a cross-functional team who will help in strategizing and prioritizing which practices you should and will integrate with and on what time schedule
  • If you are a multi-service provider, consider bundling lab and DI as your market differentiators

Overall, be an informed leader in the process and don’t just wait for the “Big Wave” to hit you.

This information was presented by Pat Wolfram, Vice President of Marketing & Customer Services at Ignis Systems Corporation and Ruth Johanson, Information Technology Program Director at Providence Health & Services.   If you are interested in hearing this audio conference you can purchase a CD at The Dark Report, click here to learn more.

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