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Member Update Article |
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ASCP Urges CMS to Implement Tough Anti-“Pod” Regulations, Fix SGR
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On October 10, ASCP submitted its comment letter on the 2007 Physician Fee Schedule
(PFS) and urged the Centers for Medicare & Medicaid Services (CMS) to adopt strict
regulatory provisions to prevent abusive billing practices by “pod” or “condo” laboratories.
These laboratories participate in “contractual joint ventures,” enabling clinicians
and other entities to capture the revenues resulting from the referral of pathology
services.
ASCP urged CMS to clarify Medicare regulations that reassignment of benefits rules
pertaining to contractual arrangements are subject to program integrity safeguards
relating to the right of payment for diagnostic tests. ASCP also advocated that
the regulations for payment of the technical component be amended so that when a
reassignment involves a contractual arrangement with a physician or other supplier
who performs the test, payment may not exceed the lowest of the physician or other
supplier's net charge to the billing physician or medical group, the billing physician's
or medical group's actual charge, or the fee schedule amount for the service that
would be allowed if the physician or other supplier billed directly. ASCP hopes
these changes to the Medicare rules would minimize the ability of pod laboratories
to unfairly compete for anatomic pathology services.
ASCP also urged the Administration to work with Congress to fix the flawed sustainable
growth rate (SGR) formula, which has resulted in negative annual updates in the
Physician Fee Schedule (PFS). ASCP noted that “the negative update, combined with
the 5 percent reduction in pathologist practice expenses means pathologists could
see more than a 10 percent reduction in Medicare reimbursement rates in 2007, assuming
Congress does not act to stop the negative 5.1% SGR update.”
ASCP supported CMS’s proposal to adjust the direct practice expense inputs for flow
cytometry CPT codes 88184 and 88185, per supplemental data submitted by the American
Clinical Laboratory Association. CMS had planned to make these changes previously
but held off after other medical specialty societies opposed the Agency’s supplemental
survey methodology. ASCP’s letter was in response to CMS’ proposed physician fee
schedule rule, which was published in the Federal Register on August 22nd. ASCP’s
comments also addressed the date of service, independent laboratory billing, and
clinical laboratory diagnostic tests.
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