Reimbursement News
Hold April Claims for Services Paid Under the 2010 PFS
On March 23rd, President Obama signed into law H.R. 3950, the Patient Protection and Affordable Care Act. Subsequently, the House passed H.R. 4872, the Health Care and Education Reconciliation Act of 2010 by a 220-207 vote; it was signed by President Obama, thus ending the one-year healthcare reform debate. Among other changes, the Reconciliation Bill modifies the imaging services equipment utilization rate and reduces the technical component payment for sequential imaging services on contiguous body parts. The bill is estimated to cost $940 billion over 10 years and is intended to provide coverage for 32 million uninsured by 2019. The Centers for Medicare and Medicaid Services (CMS) will propose imaging-related implementation policies in their proposed 2011 Medicare Physician Fee Schedule rules to be released early this summer.
A brief summary of the major provisions of the Affordable Care Act and the Reconciliation Bill that impact providers follows.
Equipment Utilization Rate:
Under a provision in the Reconciliation Bill, the equipment utilization rate assumption for expensive diagnostic imaging equipment (priced over $1 million) will increase to 75 percent in 2011 and subsequent years. This new provision will override the utilization rate policy published in the 2010 Medicare Physician Fee Schedule (MPFS) final rule, which transitions the increase in the equipment utilization rate to 90 percent over 4 years for equipment costing over $1 million. The 75 percent utilization rate will be applied to all existing CT and MRI codes listed in the CMS rule regardless of when the system was acquired (before or after the effective date of the legislation) or the price actually paid. CMS will subject new CT and MRI codes to the 75 percent utilization rate if the cost of the equipment is $1 M or greater. Currently, CMS assigns an equipment code to a procedure code based on what is considered the "typical" cost incurred in acquiring the system. The fact that some centers might use a different type of equipment platform for a particular code is irrelevant and this fact is neither reported nor known. Similarly, if a used CT is purchased at a cost less than $1 million or the CT is leased it will not change the application of 75 percent use rate (payment) for the service under the MPFS. While the Reconciliation Bill limits the 75 percent utilization rate increase to MR and CT services, CMS is free to propose use rate increases to other imaging modalities. For now, the use rate for all other physician fee schedule imaging modality codes remains at 50 percent.
Contiguous Body Parts Reduction:
The reduction in the technical component payment for sequential imaging services on contiguous body parts during the same visit is increased from 25 percent to 50 percent.
[FULL STORY]
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Accreditation
ACR adds NM, PET to Online Accreditation
The American College of Radiology (ACR) of Reston, VA, has launched a new program that allows facilities to receive accreditation online for nuclear medicine and positron emission tomography (PET) programs. The society has added the modalities to its ACRedit system, which uses online technology to enable facilities to move through the accreditation process in half the time, according to the society.
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ACRedit online application
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ICANL Releases New 2010 Standards
The revised 2010 ICANL Standards become effective July 1, 2010. Laboratories may apply using either the new Standards or the 2008 version for a period of three months. Applications submitted after October 1, 2010 must be in compliance with the 2010 ICANL Standards.
The majority of changes are a clarification or explanation of the previous Standards. There are several areas where the guidelines are now more "relaxed." However, there are four areas of significant change:
- Technical Director Qualifications
- Stress Test Supervision
- Imaging and Non-imaging Equipment Quality Control
- Appropriate Use Criteria (AUC)
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Industry News
New FDA Regulations for the Production of PET Radiopharmaceuticals
In a December 2009 response to the Food and Drug Modernization Act of 1997, the FDA established new regulations for production of PET radiopharmaceuticals, slated to go into effect on Dec. 12, 2011. Prior to the new guidelines, PET radiopharmaceuticals were aggregated under the practice of pharmacy regulations. Debate continues to rage over who actually stands to gain--and who will lose-- with the new regulations.
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Clinical Practice
18F NaF PET Imaging Detects Skeletal Trauma in Child Abuse Cases
18F NaF Sodium Fluoride PET had greater sensitivity in the overall detection of fractures related to child abuse than did baseline skeletal survey and was superior in the detection of rib fractures in particular, according to a study published in the April issue of Radiology.
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MI LifeNet Spotlight
18F Sodium Fluoride Bone Imaging
18F Sodium Fluoride was one of the first bone imaging agents used in the 1960s until the introduction of 99mTc bone imaging agents, which were more readily available and better suited to the technology at that time. Today, however, PET radiopharmaceuticals and PET scanners are more widely available and 18F Sodium Fluoride as a PET bone imaging agent is experiencing a resurgence.
The 18F Sodium Fluoride Bone Imaging clinical module covers basic imaging techniques, provides studies related to oncology and general orthopedics, and demonstrates how 18F sodium fluoride is poised to reenter mainstream clinical imaging.
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Molecular Imaging News
Latest News from Molecular Imaging Insight Magazine
To view for the latest edition of Molecular Imaging Insight magazine and learn of more news in molecular imaging, click here.
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