Different Christmas, Same Story

Around this time of year wonder if my work will be reimbursed at 30% of what it was the year before or not.  Historically, not.  Actually small raises.  Now tangled up with an oil pipeline...Predict a cut on order of less than 10% if any...

December 20, 2011 — Medscape — The House today voted to reject a Senate bill postponing a 27.4% cut in Medicare reimbursement to physicians from January 1 to March 1, and to try to meld conflicting legislation through a House–Senate conference committee.

The tortured Congressional proceedings increase the odds that the cut will take effect New Year's Day.

The fight is not over physician compensation, but larger issues that have taken it hostage. The drama dates back to last Tuesday, when the Republican-controlled House voted 234 to 193 to approve a 2-year "doc fix" to the Medicare reimbursement crisis that would have given physicians a 1% raise in 2012 and 2013. This provision was a sideshow in a larger bill that would extend a temporary reduction in the Social Security payroll tax for 1 year, continue unemployment benefits for the long-term jobless, and force President Barack Obama to make a decision within 60 days on a permit for the controversial Keystone XL oil pipeline, which the GOP views as a giant jobs creator. The Obama administration had delayed the decision until 2013 to give it more time to study environmental concerns.

The Democrat-controlled Senate answered the House on Saturday by approving a 2-month extension of the payroll tax cut and unemployment benefits, along with a 2-month doc fix. The bill also includes a hurry-up timetable for the pipeline. In contrast to its counterpart in the House, the Senate measure passed with overwhelmingly bipartisan colors in an 89 to 10 vote.

CMS to Suspend Claims Processing in Early January

In tonight's vote, House Republicans followed the lead of House Speaker John Boehner (R-OH), who said earlier today that the Senate's short-term payroll tax cut extension "causes uncertainty for job creators." Tax policy conducted "2 months at a time" is the kind of Congressional decision-making, he added, that "has put our economy off its tracks." Just 2 days before, Boehner had called the Senate bill a "good deal." Democrats attribute his reversal to Tea Party pressure.

The differences over the legislation go beyond the timeframe. Senate Democrats would like to pay for a 1-year payroll tax cut extension and other provisions in part by raising taxes for millionaires. House Republicans prefer offsets such as freezing the pay of federal workers, raising Medicare premiums for high-income beneficiaries, and defunding portions of healthcare reform.

For the time being, Democrats and Republicans are in a holiday season stand-off. Just because the House Republicans voted today to take their payroll tax dispute to a bicameral conference committee does not oblige Senate Democrats to sit down at the table with them. Senate Majority Leader Harry Reid (D-NV) said yesterday that he will not reopen negotiations about a long-term version of the payroll tax cut extension until the House passes the Senate's 2-month deal, forged with Senate Republican leadership at Boehner's request, Reid noted.

This impasse leaves physicians with the prospect of members of Congress going home for the holidays without averting the 27.4% reduction in Medicare reimbursement set for January 1. Congress could postpone it retroactively when it goes back to work on January 17. Anticipating such an outcome, the Centers for Medicare and Medicaid Services (CMS) announced today that it would instruct its claims processing contractors to hold physician claims for the first 10 business days of January, or through January 17.

By putting claims in suspended animation, CMS can avoid paying them at the drastically reduced rate and wait for a more benign rate to kick in. CMS predicts that the interruption will have "minimal impact" on physician cash flow because a correct electronic claim cannot be paid until 14 calendar days after receipt anyway. Organized medicine counters that the CMS hold on claims processing still creates a financial hardship for practices that have payrolls to meet.

 

 

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

Real-time Colon Polyp Histopathology

Technologies Are Advancing But Face Some Hurdle
I was going along with story and understand the background, need and data to biopsy what amounts to normal or minimally abnormal tissue of no clinical significance until the author appropriately mentioned the key issue here for adopting this in the 3rd to last paragraph of the story.  We are not talking about missing a signifcant lesion that could be a precursor to a colon cancer down the road.  I undertand this even more if imaging technologies improve to appreciate at the in-vivo level what would be anticipated by histologic examination and predictive of morphology and hence clinical behavior and outcome. 
I also recognize that of the millions of colonoscopies that generate millions of biopsies, fewer biopsies means less cups of specimens, blocks, slides, images and of course, money.  My pathology brethren and I will look at more abnormal biopsies but fewer overall.  The percent of "normal colonic mucosa" diagnoses for colonoscopies goes down.  OK with all of that.  Also recognize that the savings of all the formalin, wax, glass, staining and printing equipment and supplies could save millions if not the billion in the article below.  That is good news too.  Medicare might yet be around for me when I need it.
Unless I missed it I don't see a pathologist referred to in here or interviewed or quoted about any of the downstream economic impact but that is OK too.  We all have a responsibility to control costs and the gastroenterologists here can do their part.  If it means saving lives and improving quality of life without unnecessary pathology, radiology, surgery or GI follow-ups, so be it.
Of course there is a small problem here.  Particularly for gastroenterologists that employ pathologists in their own in-office laboratories (IOL) and share in the revenue from collecting and producing a glass slide (technical services), if not part or all of the pathologist's professional services.
If an endoscopist with a IOL with the intent of processing biopsy specimens in a high-quality, under one roof, integrated clinicopathologic sign-out, etc... which are all possible and probable AND there more biopsies you do and the more tissue you process and the more money the endoscopist makes, you need one thing - the biopsies.
So, I am Dr. Rectum, a gastroenterologist who made the investment in space, equipment, supplies, probably some form of a AP laboratory information system and personnel, technical and professional, to provide full-service laboratory services, then I am probably not going to change my practice to doing fewer biopsies.  There are gains to be made in cost savings with increasing volume with histology processing.  If you have to run the machines and buy the pink and blue dyes, you can do so as effectively with more tissues and slides than you can with fewer. 
For the record, I am not suggesting for a minute (though some have with some data from CMS and others) that IOLs cause a spike in the number of biopsies being performed or parts being collected on a single case.  All I am saying is the community guys, particularly those with IOLs or other billing schemes that where fewer biopsies is a disincentive and hits their left hip rather than someone elses are not going to go for this. 
Chicago—After the American Society for Gastrointestinal Endoscopy (ASGE) released a key position statement in March, the concept of voluntarily not submitting certain diminutive colon polyps to histopathology took one step closer to becoming clinical practice, moving from academic centers to community endoscopy suites.

The ASGE’s position paper, “Preservation and Incorporation of Valuable Endoscopic Innovations (PIVI) on Real-time Endoscopic Assessment of the Histology of Diminutive Colorectal Polyps,” establishes a priori diagnostic and/or therapeutic thresholds for endoscopic technologies that will allow endoscopists to better determine which polyps pose a risk to patients (Rex DK et al. Gastrointest Endosc 2011;73:419-422).

The document states that provided a technology is 90% accurate in predicting surveillance intervals compared with standard histopathology, endoscopists can “resect and discard” polyps that are less than 5 mm based on their real-time assessment of histology. Alternatively, endoscopists can choose to leave suspected rectosigmoid hyperplastic polyps that are less than 5 mm in place.

“The general approach taken by the ASGE is that if a given technology meets the criteria with regard to performance, then the ASGE would endorse it,” explained Douglas Rex, MD, professor of medicine and director of endoscopy at Indiana University, in Indianapolis, who is first author of the ASGE position statement and chair of the PIVI committee.

Real-time Technologies in the Running

There are many ways to classify the available technologies for real-time polyp histologic evaluation, but two main groups emerge. One group, called virtual histology, comprises the imaging technologies that most closely mirror an actual histopathologic analysis, including endocytoscopy and confocal laser microscopy. These are capital-intensive, small-field, difficult-to-learn technologies, and may be less likely to gain a following in the market.

Endocytoscopy uses ultra-high magnification (450-1,125×) through a catheter-type endoscope that can be used in combination with chromoagents. Although endocytoscopy cannot reach a depth beyond superficial cell layers, it is considered virtual histology because it can provide an “optical biopsy,” similar to looking at a slide under a microscope.

Confocal laser microscopy can acquire high-resolution optical images at selected depths and creates a three-dimensional reconstruction of the interior of a specimen. The technology is currently available to physicians in the United States.

“Of these technologies, [confocal laser microscopy] is the best-studied; it provides real virtual histology; and I think it’s very effective at answering the simplest question, the one that the PIVI suggests is the greatest clinical need: ‘Is a polyp an adenoma or is it hyperplastic?’ ” Dr. Rex said.

Confocal laser microscopy comes with several downsides, however. The confocal laser microscope is a separate attachment to an endoscope and is relatively expensive compared with other real-time technologies. It also requires specialized training to accurately identify polyps, and perhaps most importantly, requires the endoscopist to take additional time during the colonoscopy to assess the image and make a judgment.

“I think it’s unlikely to be taken up on a widespread basis unless there is reimbursement for it, and I don’t think the reimbursement issues are clarified well enough,” said Dr. Rex.

The second group of real-time technologies uses less expensive, easy-to-use and readily available technologies, known as large-field or “push-button.” These technologies are now standard on the latest-generation colonoscopes. The large-field technologies include narrow-band imaging (Olympus), i-Scan (Pentax) and FICE (Fuji). Although each of the technologies is different, the principle behind them is the same: By passing a number of unique, filtered wavelengths of light through tissue, the images can be reconstructed to produce clearer, more distinct pictures of the mucosal surface, particularly the vasculature. By analyzing the “pit,” or vascular patterns, of polyps, endoscopists can determine whether they pose a risk to patients.

From Academic Centers to Community Endoscopy Suites

Presently, the biggest question is whether these technologies will translate to the gastroenterology community at large.

“In academic centers or those dedicated to this kind of research, the accuracy for predicting polyp types is very good, so the next real hurdle is how to get that into the broader community where the vast majority of colonoscopies are done,” said Michael Wallace, MD, professor of medicine and director of research for medicine in the Division of Gastroenterology and Hepatology at Mayo Clinic, Jacksonville, Fla., where he studies advanced endoscopic imaging technologies.

Many of the technologies are well studied in research environments. The PIVI statement, for example, cites more than four dozen studies, most within the last 10 years, looking at the accuracy of real-time technologies. Most of the studies have demonstrated an accuracy rate in the low 90th percentile, with rates dipping slightly for push-button, filtered-light technologies and often hitting 99% in studies of confocal laser microscopy.

Although actual data are lacking on how well the technologies perform in community settings, there is evidence that at least some of the techniques can be quickly learned. In a study published last year in Gastrointestinal Endoscopy (Raghavendra M et al. 2010;72:572-576), Dr. Rex and colleagues demonstrated that “narrow-band imaging can be learned in 20 minutes” among a group of endoscopists that included medical students and fellows as well as faculty. A short teaching session describing the differences in appearance between photos of hyperplastic and adenomatous polyps increased accuracy from 47.6% to 90.8% (P=0.0001) and raised interobserver agreement to a kappa score of 0.69.

Amit Rastogi, MD, has led similar studies with fellows at the Kansas City VA Medical Center, in Kansas, the findings of which were also published in Gastrointestinal Endoscopy (Rastogi A et al. 2009;69:716-722).

“I have a feeling that community gastroenterologists can easily learn these patterns,” he said. “Can it be learned and put into practice? Yes, absolutely.”

Another important advantage to voluntarily withholding certain diminutive polyps from histopathology is the substantial savings this will allow. One study reported that if endoscopists stopped sending diminutive polyps for histopathology, the health care system would save as much as $1 billion annually, said Dr. Rastogi, director of endoscopy at the Kansas City VA Medical Center and associate professor of medicine at the University of Kansas. A more conservative estimate was $33 million annually, still a significant savings (Hassan C. Clin Gastroenterol Hepatol 2010;8:865-869).

“Although the costs [per colonoscopy] are relatively low, when you multiply them by the number [of specimens] removed and by 14 million colonoscopies, the numbers become substantial,” said Dr. Wallace. Specifically, he said, roughly 14 million colonoscopies are done annually in the country each year, and about 50% of those generate a pathology specimen.

The Final Hurdles

The large-field, push-button technologies are now standard on new colonoscopes, but real-time histologic assessment has not become standard practice. Although real-time histologic technologies seem poised for widespread adoption, there are market forces, at least on an individual level, aligning against it.

“It’s very difficult to change practice,” said Dr. Rastogi. “As colonoscopists, we are used to removing all the polyps that we detect and sending them to pathology to get a diagnosis. We were trained to do that; that’s how we think we prevent colon cancer.”

One reflection of this mindset, at least for the time being, is that a “resect and discard” approach goes against the published policies of many hospitals as well as national colonoscopy guidelines.

“A lot of hospitals have a policy that if you remove tissue you are required to send it to pathology,” said Dr. Rex.

Currently, the national guidelines suggest that all significant polyps should be removed and subjected to histologic examination, so any other approach might be considered noncompliant, Dr. Wallace added. However, if studies confirm that real-time analysis is accurate in the community setting, these published policies will likely change as the prominent gastrointestinal societies endorse the new approach.

An issue in confirming the accuracy of real-time analysis in the community setting is that in vivo assessments take time. It may not be incredibly time-consuming on a per-polyp basis, but over the course of a day of colonoscopies, it can add up.

“You’re now asking the physician to spend an extra minute or two and sometimes a little more to diagnose a polyp and make a call,” Dr. Wallace said. “Physicians are already being pushed to do everything we do faster and more efficiently, see more patients, do more procedures. And this is yet another task that is not reimbursed at all.”

A bigger challenge, perhaps, comes from fear of medicolegal problems.

“In the minds of the endoscopists, there will be a medical-legal angle to this,” Dr. Rastogi said. “What if you leave behind a polyp that you thought was hyperplastic but actually the patient goes on to develop cancer? That lurking fear in the mind of the endoscopist can be a deterrent that prevents them from adopting this [practice].”

Dr. Wallace added, “If some untoward event occurs, the patient gets cancer in the next five or 10 years, the [patient] could look back and say you didn’t follow the guidelines.”

One more financial hurdle has to do with the perceived conflict of interest among gastroenterologists who employ pathologists in their surgery centers. There is a natural incentive to generate pathology in these settings. “Although I think physicians are ethical, there is an incentive in that setting, because you’re reimbursed for the pathology costs, not to change that practice,” Dr. Wallace said.

So, with these downsides, what would motivate a busy gastroenterologist to incorporate these technologies into his or her practice?

“That’s a valid philosophical question,” said Dr. Rastogi. “There might not be any immediate gain to the endoscopist, but I think if you look at it from a broader perspective you are saving a lot of health care dollars. The main advantage is cost savings to the health care system and all of us share some responsibility for that, especially in these troubled economic times.”


Dr. Rastogi disclosed having a commercial relationship with Olympus America. Dr. Rex reported relevant financial or other commercial relationships with American BioOptics, Avantis Medical Systems, Braintree Laboratories Inc., Check-Cap, Epigenomics AG, Given Imaging, Olympus America and Softscope Medical Technologies. Dr. Wallace reported relationships with Boston Scientific, Cook Medical, Fujinon, Mauna Kea Technologies and Olympus America.

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

PathXL BioBankā„¢ – a global solution for biobanking

Belfast, Northern Ireland: December 2011

Earlier this year, PathXL announced it had been commissioned to develop digital pathology software for the Northern Ireland Biobank.

Biobanks play a crucial role in diagnosis and the development of the new targeted treatments and stratefied therapies for cancer and other diseases, so PathXL has further developed it’s biobank solution and today is introducing PathXL Biobank™ to the global market.

PathXL Biobank™ is a fully web-enabled workflow management solution for biobanks. It provides a comprehensive platform for biosample management including the ability to create new sample records, manage patient consent, track sample preparation, store sample location, coordinate applications to the biobank and release of samples to researchers. Designed by pathologists, scientists, researchers, technicians and research nurses, PathXL Biobank™ provides an easily integrated web-based solution for new and well established biobanks.

Introducing Digital Pathology

Biobank DiagramPathXL Biobank™ allows the easy integration of digital slides and virtual microscopy for tissue section and tissue microarray storage. 

Web-based access and viewing of digital slides allows researchers to select the correct samples for their studies and provides tools for sample sharing and remote biomarker evaluation.   

PathXL has a longstanding reputation in digital pathology management and workflow – and they now bring this experience to biobanking.

The diagram illustrates the features of the PathXL Biobank™ workflow management solution. The secure, web-enabled platform provides an interface for key Biobank staff to manage the selection, collection, tracking, storage and distribution of samples.

The system integrates digital pathology and virtual microscopy allowing slides and TMAs to be shared online with researchers, and enabling data integration from other repositories. 

Dr Jackie James explains some of the benefits of working with PathXL;

“The PathXL Biobank system supports the developing biosample collection strategy for the NI Biobank.  In addition to managing sample collection, tracking and distribution, the system integrates digital pathology allowing web-based access to digital slides of the samples and tissue microarray management.  This is going to be important to our stratified medicine and biomarker discovery programmes at Queen's University, enabling researchers to view and assess samples before they make their applications.”

PathXL Biobank™ can be installed and configured to local needs in a matter of days, so no delays waiting for the IT project to complete. The software reduces errors in sample collection and retrieval and handles all the process and management aspects, allowing biobank staff to concentrate on sample preparation and high quality specimen collection. Researchers can remotely and securely identify correct samples for their studies allowing controlled sample sharing locally, nationally and internationally.

Professor Peter Hamilton, Chief Scientific Advisor with PathXL; 

“Biobanks may differ in their requirements according to their sample set and research needs, so PathXL Biobank™ has been designed flexibly to facilitate the creation of a tailored system for each specific customer.”

 

About PathXL
PathXL specialises in web-based software and workflows for Digital Pathology.  Its PathXL™ Manager product provides a robust, secure and open web-based platform to enable digital pathology users across all fields to manage, view and collaborate around virtual slides easily and efficiently.  In addition, PathXL provides a range of applications and workflows on top of PathXL™ Manager to deliver specific solutions to pathologists, scientists and students in Education, Research, Clinical and Biobanking settings. 

PathXL also provides a full range of supporting services, including scanning, hosting, image analysis and consultancy.  PathXL operates in the UK, Europe and North America.

PathXL is a privately owned company, headquartered in Belfast, Northern Ireland.

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

2nd International Scanner Contest (ISC) – Register Now

 

P. Hufnagl1, T. Schrader1, 2, M.G. Rojo3, A. Laurinavicius4, G. Kayser5, Y. Yagi6

1Institute for Pathology, Charité – Universitätsmedizin Berlin, Germany, 2University of Applied Sciences Brandenburg, Brandenburg, Germany, 3Servicio de Anatomia Patologica, Hospital General de Ciudad Real. 4National Centre of Pathology, Vilnius, Lithuania, 5Institute of Pathology, University of Freiburg, Freiburg, Germany, 6Massachusetts General Hospital, Boston, United States

All manufacturers of slide scanners are invited to participate in the Second International Scanner Contest (ISC) in Berlin, under the auspices of the European Society of Pathology, German Society of Pathology, and the Berufsverband Deutscher Pathologen e.V. (German Professional Organization of Pathologists).

The 1st ESC was a great success for manufacturers as well as for pathologists and other users. The results have influenced the ongoing development of scanners and the understanding of image quality and evaluation procedures. This contest helps to identify and clarify the specific requirements of image acquisition and digitalization in diagnostic pathology and initiates innovative discussions between developers, vendors and users.

Formerly established and recently re-evaluated criteria will increase the value of the contest, which may support customers to find the appropriate scanner for their specific tasks. Furthermore, the 2nd ISC will serve the manufacturers as a benchmark.

Schedule & Locations

 The contest consists of two phases as listed below.

 

Phase 1: Event of 2nd ISC in Berlin 

  • Venue: Berlin Congress Center
  • Schedule is linked to the 12th Annual Meeting of the Berufsverband Deutscher Pathologen e.V. (German Professional Organization of Pathologists) and the 96th Annual Meeting of the German Society of Pathology, May 31st – June 3rd, 2012

?      May 29th -30th, 2012: Scanning of slides in different disciplines (see below)

?      May 31st – June 3rd, 2012: Evaluation of the virtual slides by pathologists attending the 12th        meeting, preliminary evaluation and presentation of first results during a dedicated session.

  • Comment: Scanning takes place under supervision of referees. The contest room will be open to a restricted number of staff from each participating company between 8 a.m. and 6 p.m. only. Catering for the participants will be provided.

Phase 2: Presentation of results, award ceremony 

Report from 2nd ISC 

  • Venue: Scuola Grande di San Giovanni Evangelista, in Venice, Italy
  • Schedule is linked to the 11th European Congress on Telepathology and 5th International Congress on Virtual Microscopy, on June 6th to 9th 2012

 

Results & Award Ceremony 

  • Venue: Prague Congress Centre, Prague, Czech Republic
  • Schedule is linked to the 24th European Congress of Pathology, on Sept. 8th to13th, 2012

 

Contest Areas

 

The following table gives an overview of the planned domains of the 2nd International Scanner Contest:

No 

Domain 

Description 

# slides 

Criteria 

1 

High throughput

A: 20x

35 (H&E)

Speed, focus, particles

 

 

B: 40x

35 (H&E)

Speed, focus, particles

2 

Quality

A: 20x

10

Focus, manual quality assessment

 

 

B: 40x

10

Focus, manual quality assessment

3 

Image analysis and Quantification

Image analysis, quantification

3 TMA

Focus, quality, quantitative data

4 

Fluorescence

A: 20x

3

Focus, qualitative data

 

 

B: 40x

3

Focus, qualitative data

5 

Technical

Mesh grids,

color calibration slide

3

Geometry, scanning area, color fastness, acoustic camera

 

 

Sound check

 

 

 

 

Power consumption

 

 

 

General rules

Each company is invited to participate in any of the offered contests with one or more scanners. The organizing committee provides all glass slides. Independent referees who will be responsible for the handling of the slide series and the time measurements supervise the contest room.  The participating companies may participate at the contest with several different scanners. These scanners may be identical or of different types. The results will be analyzed and displayed separately if different scanners are used.  The participants are allowed to review and comment the evaluated results.

 

Evaluation of the results

The organizing scientists will supervise the evaluation process. Beside the evaluation criteria further parameters will be documented such as:

  • Scanning time for the test sets of High quality, Fluorescence
  • File size of resulting images
  • Number of scans failed/ broken slides/ software crashes
  • Additional technical parameters and capabilities

For the evaluation and presentation of results see http://scanner-contest.charite.de.

All involved parties are welcome to propose additional evaluation procedures.

 

Participants

Currently we have received completed registrations from seven vendors with nine devices overall. Two further vendors have announced their participation. Participants originate from Asia, Europe and North America. The ISC proves to be the global forum for Slide Scanner evaluation and benchmarking.

Registration for the 2012 contest is still open! 

Interested Slide Scanning vendors are invited to participate with their devices in the contest to evaluate and proof their individual strengths. Please register via online registration form: http://scanner-contest.charite.de/en/news/online_registration/

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

Posthum(or)ous recognition of Pick a Pathologist Pal Day

A reader recently let me know that I failed to recognize "Pick a Pathologist Pal Day" on Tuesday, December 13th:

Pick A Pathologist Pal Day

Wellcat strikes again with Pick A Pathologist Pal Day claiming Pathologists and coroners are an especially jovial lot, and befriending one of them offers an ongoing reminder than “tomorrow” is not necessarily a guarantee.

 They consider coroners and pathologists a happy group of people. They suggest being friends with one will help you realize tomorrow is no guarantee. Buddhists would call this "living in the now." Live in the Now suggests these methods for enjoying each moment:

* Say yes to the present moment by accepting it or taking action to make changes now (not later).

* Just breathe, focus on your breath.

* Stop and enjoy the details of your life.

Turns out beyond picking a pathologist day, sites such as these remind us that important interesting news happens everyday that is not nonsensical, like also being important to eating ice cream, music, end of war (sort of) and national cocoa day.

Read more at http://news.yahoo.com/dec-13-ice-cream-violins-day-20th-anniversary-234300678.html

Seems to be enough that marks December 13.  Perhaps they should move this pathologist pal day item to another less important day.  

And when is Digital Pathology Day, Immunohistochemistry Day or FISH Day?

 

 

 

 

 

 

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

UCT Digital Pathology Collection

An online catalogue with thousands of pathology specimens used as a teaching collection. Detailed cases and exhibitions are available.

This website gives electronic access to several thousand pathology specimens in our pathology teaching collection. It is intended for use by undergraduate and postgraduate students in the health sciences. There are currently three main catalogues for (1) the anatomical pathology collection (2) the forensic pathology collection and (3) the obstetrics and gynaecology collection. (A paediatric pathology section is in the pipeline).

This is an historical collection (begun in the 1920’s) so the cataloguing is rather old fashioned. The specimens are catalogued by organ or system e.g. “kidneys” and then by broad pathological category e.g. “neoplasms”. Each specimen has a brief description and commentary along with good quality photographs. The emphasis is on macroscopic pathology; we are aiming to include more radiographic imaging and also microscopy going forward.

The site also includes a more detailed section with “student cases” that are useful as teaching cases, "specialist cases" presenting unusual cases, and a few online exhibitions around special topics.

The website is a work in progress so much of our material is still in the process of being reviewed and uploaded. 

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

Ventana Medical Systems, Inc. and Advanced Cell Diagnostics Enter Worldwide Co-Promotion Agreement for Fully Automated RNA In Situ Hybridization Assay Systems

 

TUCSON, Ariz., Dec. 13, 2011 /PRNewswire/ -- Ventana Medical Systems Inc. (Ventana), a member of the Roche Group, and Advanced Cell Diagnostics Inc. (ACD), announced today they have entered a worldwide co-promotion agreement for the first commercially available, fully automated RNA in situ hybridization (ISH) assay system capable of robust detection and visualization of virtually any expressed gene in routine clinical specimens at single-molecule sensitivity.

VENTANA MEDICAL SYSTEMS, INC. MOUSE BRAIN TISSUE  mRNA of Nav1.7, a sodium channel, expressed in normal mouse brain tissue detected by automated RNAscope XT assay. Single mRNA molecules (i.e. the individual dots of the hybridization signal) can be observed in the paraventricular hypothalamic nucleus on both neuronal cell bodies and dendrites. This image is taken with 100x objective lens.  (PRNewsFoto/Ventana Medical Systems, Inc.) TUCSON, AZ UNITED STATES

(Photo: http://photos.prnewswire.com/prnh/20111213/DE21304 )

The two companies have partnered to automate this assay system on the VENTANA DISCOVERY series slide staining platforms. The product offerings are expected to become commercially available in the first quarter of 2012 and will initially be offered for research-use only (RUO) applications.

"Given the fact that the majority of biomarkers are discovered from genomic research and are RNA by nature, the automation of RNAscope represents an important milestone that will accelerate biomarker research into a new level of sophistication," said Dr. Yuling Luo, founder, president and CEO of ACD. "RNAscope will become an equally indispensable tool alongside immunohistochemistry, fluorescence in situ hybridization and polymerase chain reaction for researchers in life sciences and drug development."

Luo said the ability to generate robust and reproducible results from routine clinical specimens "makes the technology a compelling platform for clinical diagnostic applications in the foreseeable future."

The RNAscope® FFPE Reagent Systems automated on the VENTANA DISCOVERY ULTRA and DISCOVERY XT offers researchers a powerful tool with unprecedented levels of performance.

"The combination of RNAscope reagent system and our sophisticated and flexible DISCOVERY platform and detection systems delivers a powerful solution for biomarker discovery and validation," said Bill Crawford, director of marketing, Discovery, with Ventana. "It has significant potential to advance cell- and tissue-based biomarker analyses for future clinical and companion diagnostics development."

RNA in situ hybridization is an indispensable method to analyze gene expression in the context of tissue architecture in areas of oncology, virology, and neuroscience research. RNAscope is an award-winning breakthrough technology that provides researchers the unique capability to interrogate the function and disease relevance of any expressed genes in situ, especially for the approximately 5,000 genes and 15,000 non-coding RNAs in the human genome where no other technologies can adequately address. In addition, RNAscope allows researchers to tap into the estimated 400 million clinically-annotated, archived formalin-fixed paraffin-embedded (FFPE) tissue specimens for retrospective clinical studies in translational research.

The DISCOVERY XT and DISCOVERY ULTRA systems provide scientists and research professionals who require more than conventional IHC and ISH research methods with an array of fully automated applications, which improve flexibility and freedom and provide the necessary, reproducible results that optimize patient care.

About Advanced Cell Diagnostics, Inc.

Advanced Cell Diagnostics, Inc. (ACD) is a leader in the emerging field of molecular pathology, developing cell- and tissue-based diagnostic tests for personalized medicine. The company's products and services are based on its proprietary RNAscope® technology, the first multiplex fluorescent and chromogenic in situ hybridization platform capable of detecting and quantifying RNA biomarkers in situ at single-molecule sensitivity. ACD partners with pharmaceutical and biotechnology companies to validate biomarkers for targeted therapeutic development in cancer and other diseases. These partnerships provide the foundation for ACD to develop companion diagnostic tests in conjunction with partners' targeted therapeutics. ACD also pursues internal programs to develop proprietary diagnostic tests in cancer management. Learn more about ACD and RNAscope technology at http://www.acdbio.com.

About Ventana Medical Systems, Inc.

Ventana Medical Systems, Inc. ("VMSI") (SIX: RO, ROG; OTCQX: RHHBY), a member of the Roche Group, innovates and manufactures instruments and reagents that automate tissue processing and slide staining for cancer diagnostics. VENTANA solutions are used in clinical histology and drug development research laboratories worldwide. The company's intuitive, integrated staining, workflow management platforms, and digital pathology solutions optimize laboratory efficiencies to reduce errors, support diagnosis and inform treatment decisions for anatomic pathology professionals. Together with Roche, VMSI is driving personalized medicine through accelerated drug discovery and the development of "companion diagnostics" to identify the patients most likely to respond favorably to specific therapies. Visit http://www.ventana.com to learn more.

RNAscope products are for research use only and not intended for diagnostic applications.

RNAscope, HybEZ, CTCscope, and DNAscope are registered trademarks or trademarks of Advanced Cell Diagnostics, Inc. in the United States or other countries. All other trademarks are the property of their respective owners.

Ventana products are for in vitro diagnostic use for specific applications and are research use only for other applications. The VENTANA DISCOVERY products are for research use only. Not for use in diagnostic procedures.

SOURCE Ventana Medical Systems, Inc.

0
0
0

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

Transferring Laboratory Data Into The Electronic Medical Record: Technological Options For Data Migration In The Laboratory Information System

FREE Special Edition White Paper

download your report now!

Download Your FREE Special Report Today!
Simply Complete the Form Below

 

cover-white-paper-transfering-data-to-EHR

In an increasingly competitive economic environment for healthcare services, clinical diagnostic laboratories are looking at tools that can improve their efficiency and increase their profits. Of primary interest are sophisticated laboratory information systems (LIS) that can interact with the facility or institution’s electronic medical record (EMR) system and/or electronic health record (EHR).

Although the LIS concept is not new, advances in technology have made them more sophisticated than ever, offering clinical and non-clinical applications, Web-based connectivity, customizable configurations and rule-writing, scalability, and modular units that can offer data handling for the most cutting-edge laboratory techniques and testing.

The Dark Report is happy to offer our readers a chance to download our recently published FREE White Paper “Transferring Laboratory Data Into The Electronic Medical Record: Technological Options For Data Migration In The Laboratory Information System” at absolutely no charge. This free download will provide readers with a detailed explanation of technology options for data migration in the LIS System.

download your report now!

Among other topics, this FREE White Paper specifically addresses:

  1. Overview of the U.S. Clinical Laboratory System
  2. What is HL7’s mission statement?
  3. Software as a Service (SaaS)/ASP
  4. Selecting your lab’s LIS approach

For more about transferring lab data to EHR, please CLICK HERE

download your report now!

Table of Contents

Introduction — Page 3

Chapter 1.
 The Laboratory LIS and IT Environment — Page 4

Chapter 2. Challenges in the Current Marketplace for Moving Lab Data from LIS to EMR — Page 12

Chapter 3. Middleware — Page 19

Chapter 4. Software As A Service (SaaS)/ASP — Page 23

Chapter 5. Case Studies — Page 28

 Chapter 6. Selecting Your LIS Approach — Page 32

 Chapter 7. Implementing Your LIS Choice — Page 34

Conclusion — Page 36

 References — Page 37

Appendices

A-1 About Mark Terry — Page 39

A-2 About About NetLims — Page 40

A-3 About DARK Daily — Page 41

A-4 About The Dark Intelligence Group, Inc., and THE DARK REPORT — Page 42

A-5 About the Executive War College on Laboratory and Pathology Management — Page 43

A-6 About Julie Pekarek — Page 45

 Terms of Use — Page 48


download your report now!

 

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

Cutty Come Back

A colleague from Northwestern medical school and fellow despondent Bears fan sent this one along.  After getting Tebow'd in the fourth quarter earlier today I could not agree with this song more.  Thanks to "Chad in Portland - "Do you think you can throw left handed?" 4 minutes well spent.  Million views by weeks end as folks digest this latest Bears disaster.

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

Quorum Technologies Names XStor Systems Exclusive Pathology Image Storage Partner for Canadian Market

Partnership with Leading Biomedical Equipment Distributor Includes XStorPath™, a Digital Image Storage and Management Solution Developed Specifically for Pathologists

MOUNTAIN VIEW, Calif.--(BUSINESS WIRE)--XStor Systems, Inc., a provider of next-generation, specialty-specific digital imaging storage and connectivity solutions for radiology, pathology, and oncology, announced today an exclusive partnership with Quorum Technologies, Canada’s leading provider of microscope-based equipment and image processing solutions for scientists, clinicians and laboratories. Through this new partnership, Quorum will be the exclusive distributor of the XStorPath digital image storage and management system for the Canadian pathology market.

“Our patented technology is designed with the realities of today’s image intensive clinical workflow in mind”

“We are pleased Quorum recognizes the value XStor brings to today’s pathology lab, and we’re excited to be a key component of their digital pathology solutions family,” said Thomas Leahy, Executive Vice President of Sales and Marketing for XStor Systems.

XStorPath is a complete solution of onsite enterprise-class storage, pathology-centric management software and 24-hour remote support. Available for licensed purchase or as a pay-as-you-go subscription, XStorPath is designed to make it easy and inexpensive for pathology labs of every size to implement a digital imaging workflow. XStorPath’s vendor-independent platform ensures seamless integration with whole-slide imaging (WSI) scanners from all major equipment vendors.

“For the past 25 years, we’ve made it our mission to thoroughly understand the needs of clinical labs and help them achieve their goals with integrated, robust and flexible imaging systems,” said John Arbuckle, CEO of Quorum Technologies. “Our partnership with XStor Systems will help us to provide pathology labs with a complete digital workflow solution with tools developed specifically for their needs.”

XStor’s distribution partnership with Quorum also includes current and upcoming image storage and connectivity solutions. Using image caching technology patented by XStor, storage management software optimizes image data access and retrieval speed across a distributed care environment without compromising security or scalability.

“Our patented technology is designed with the realities of today’s image intensive clinical workflow in mind,” said Syed Hamdani, President and CEO of XStor Systems. “By developing storage management solutions optimized for multi-location and multi-vendor environments, clinicians and labs can improve the lifecycle of patient care.”

About XStor Systems

XStor Systems, Inc., provides next-generation digital image storage and connectivity solutions to meet radiology, oncology and emerging digital pathology market needs. XStor’s vendor-neutral archiving and connectivity platform enables hospitals, clinics and clinical research labs to intelligently organize and instantly retrieve digital images and relevant patient information. With highly scalable solutions that leverage existing infrastructure, XStor accommodates rapid growth without compromising data security, quality and availability. To learn more, please visit http://www.xstorsystems.com.

About Quorum Technologies

Quorum Technologies Inc. is a private Canadian owned enterprise located in Guelph, Ontario. The company develops and integrates scientific instruments and is the largest independent provider of Microscope based imaging systems in Canada. Quorum is a leader in advanced Live Cell Imaging platforms and holds over half a dozen patents with several others in process. Through its technology transfer relationships with Canadian Universities, Quorum is helping to bring new innovative technologies to market for use in preclinical research, drug development and personalized medicine. http://www.quorumtechnologies.com

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

Applications Pre-Sales Consultant / Specialist, Healthcare (Lab Workflow, IHC, Pathology)

Aperio is hiring. See below fron LinkedIn

Aperio - Vista, CA (Greater San Diego Area)

Job Description

This person will be directly involved with the sales team and responsible for pre-sales activities with prospective and existing customers. You will also have interaction with other departments including Operations, Marketing, Development and Quality.

(Internal Job Title - Digital Pathology Consultant - This is a regular employee position with Aperio, consulting with our customers and potential customers)

In this position you will:

  • Perform in-house and field based activities including but not limited to:
    • Pre-sales on-site and / or WebEx presentations regarding Aperio hardware, software and applications, including workflow, Spectrum Plus, Image Analysis and basic IT infrastructure
    • Communication with prospective customers to determine optimal configuration and applications for pre-sales demonstrations for assigned accounts
    • Continuous product improvement feedback from the field
  • Attend assigned tradeshows
  • Assist in writing support material for customers
  • Participate in project management for key accounts
  • Attend user meetings

Source:
http://feeds.feedburner.com/DigitalPathologyBlog

The achilles tendon. Part 2: biomechanics

This Podcast about "The achilles tendon" has been created by Marc Schmitz, director of http://www.kinecare.nl and founder of http://www.facebook.com/anatomyphysiotherapy 38 references have been used for this videopresentation about anatomy of the achilles tendon. A list of the references can be downloaded on http://www.kinecare.nl Like it, Share it

See the original post:
The achilles tendon. Part 2: biomechanics

Rouge Valley Health System – Synoptic Pathology Reporting – Video

**Rouge Valley Health System's submission for ImagineNation Outcomes Challenge - Clinical Synoptic Reporting** Sharon Howe, Debra McLeod and Dr. Helena Haile Meskel present Rouge Valley Health System's solution for clinical synoptic reporting. Using mTuitive's xPert for Pathology, Rouge Valley is able to capture structured data for all their pathology cases.

View post:
Rouge Valley Health System - Synoptic Pathology Reporting - Video

Pathology – Intro+Code Injection (With Lyrics) – Video

From the album Legacy of the Ancients (2010) Lyrics: Infected by will saliva will secrete DNA strands complete Living cells evolve and mutate Brain neurons regenerate A war of consciousness A war of our minds Accounts of the elders Guards of forbidden knowledge An ancient race will rise Reality is only what we perceive Operation majority directs all technology Collected to advance through the stars Code Injection The Jason Society 32 strong Designate lies and deception of truth and control Code inject - Code inject - Code inject - Code inject Sigma is responsible with communications With the beyond... Infected by will control is complete DNA strands - Maji Dead cells evolve and mutate Brain experiment delete A war of consciousness A war on our minds Note: All credit goes to Pathology and the respective owners of this material.

Continue reading here:
Pathology - Intro+Code Injection (With Lyrics) - Video