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The Dark Report
 

      Headlines - January 16, 2006
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R. Lewis Dark: Coding Edits Are a Potential Hammerblow to Pathology

DURING THE NEXT SIX MONTHS, WE WILL WITNESS an intense debate between the pathology profession and the Medicare/Medicaid bureaucracy. This battle will center around the proposed MUEs (Medically Unbelievable Edits) which place restrictions on the units of service per patient per day on key CPT codes widely used in laboratory medicine.

As you will read in our lead story on pages 2-3, news of this proposal only surfaced in mid-December, just as the holiday season kept folks from paying close attention to business issues and government proposals. It is still a matter"under wraps," because confidentiality agreements cover the information about proposed restrictions on service that was distributed by a Medicare contractor to the American Medical Association and medical specialty associations. It is why neither the Medicare program nor recipients of this information have made it public.

What caught the attention of pathologists was the proposal to restrict use of CPT code 88305 to two units of service per patient per day. But that is not the limit of the bad news. The Medicare contractor proposes to place restrictions on approximately 1,200 CPT codes involving anatomic pathology and clinical laboratory services. By itself, the 88305 restriction is a potential hammerblow to pathology because it covers a procedure that makes up as much as 50% of the services performed by some individual pathologists.

As the laboratory industry responds to this ill-conceived Medicare coding initiative, there are no guarantees that the final decisions affecting 88305 and other laboratory CPTs will be satisfactory to the pathology and laboratory community. This will be a major story of 2006 and you can expect to read more about it in the pages of THE DARK REPORT.

For my part, I believe the very fact that Medicare launched a contractor on a project to propose restrictions on service, based on MUE standards, across all medical specialties, represents a more serious threat. Regardless of whether this round of CPT code edits originated because of incompetence, ignorance, or intent to restrain utilization (thereby reducing costs), the fact that some Medicare officials wanted to go down this road is a sign of the growing pressure they face to control spending—and their lack of creativity in how to solve that problem.



Proposed Coding Edits May Restrict 88305 Use

Full range of proposed edits promises bad news for both pathology groups and clinical labs

CEO SUMMARY: When the Medicare contractor tasked with developing MUEs (Medically Unbelievable Edits) for this year's Correct Coding Initiative work released the proposed list of edits to the AMA, it didn't take long for the bad news to reach the pathology profession. Restriction on units of service per patient are proposed for approximately 80 pathology CPTs and almost 1,100 clinical laboratory CPTs.



AD PathLabs Is Closed, Assets & Clients Are Sold

Local pathology laboratory picks up pieces, but considers the transaction as fraught with risk

CEO SUMMARY: AD PathLabs, Inc. was a regional anatomicpathology company built around a unique business model: it would provide technical AP services to local hospitals and other clients and allow referring physicians to perform the professional services on the cases they referred to AD PathLabs. After four years of operations, AD PathLabs closed its doors and investors liquidated the company.



Failure of AD Pathlabs: Structural Weakness?

Can any AP lab business model separate AP technical and professional and succeed?

CEO SUMMARY: AD PathLabs is the latest in a string of business disappointments. Over the past decade, a number of anatomic pathology companies have proven that they can grow rapidly—attracting substantial volumes of specimens. But these companies seem to hit a financial wall that leads their owners to sell the firms to more traditional laboratory companies. Is there a fatal flaw in these business models?



Luminex and PerkinElmer Ink Licensing Agreement

Company known for high-volume systems will explore applications in clinical diagnostics

CEO SUMMARY: PerkinElmer's interest in the multiplex capabilities of Luminex's xMap technology led to this new licensing agreement. PerkinElmer's instrument systems played a major role in accelerating the work of the Human Genome Project. Now, besides bioresearch applications, PerkinElmer wants to look for opportunities to develop high-volume, multi-analyte assays for in vitro diagnostics.



Lab Industry Briefs:

PREDICTIVE TESTING FOR RECURRENT BREAST CANCER

CUTS IN FLOW CYTOMETRY REIMBURSEMENT AFFECT BRLI EARNINGS

NEWFOUNDLAND AND LABRADOR NOW OPERATE PATIENT REGISTRY



New Instrument Targets Cervical Cancer Detection

Georgia company is developing diagnostic device for real-time detection of cancer in docs' offices

CEO SUMMARY: Guided Therapeutics, Inc. of Norcross, Georgia is working to develop proprietary technology into an improved method for detecting cervical cancer. It wants to give ob-gyns and other physicians an instrument system that can be used in the office to provide real-time results to patients. The procedure will be non-invasive and it will determine results by using both morphological and biochemical analysis.


INTELLIGENCE:

MEDICAL BOOKS AND JOURNALS ARE MUCH NEEDED IN IRAQ

NEW COO AT LABCORP

 

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