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Termination of the BlueCard Program Runs Afoul of State and Federal Regulations

Blue plans attempting to reconcile the non-standard claims filing rules imposed by BCBS associated with the termination of the BlueCard program are running afoul of state and federal regulations; from non-adherence to HIPAA electronic standards to ignoring state assignment laws.
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Who if anyone benefits from the dismantling of the BlueCard® program?

The new system turns a straightforward process into an unnecessarily complicated and expensive one. Is the BCBS Association, forcing the Blues to enforce their exclusivity arrangements that disadvantage regional labs and prohibit them from competing in the market place?
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Recorded Webinar - What We Learned in Our First Million 5010 Production Claims

The 5010 conversion is that it's so broad and complex that there are bound to be issues. The key to success is your ability to identify, investigate and resolve those issues and ensure you have the resources available to do those things.
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4 Reasons Molecular Dx Labs May Not Benefit From New CED Program

Diagnostic services already face challenges in recouping R&D costs. Lower fee schedules, coverage for "investigational" services likely to stifle investment and development.
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3 Red Flags Behind the 5010 Enforcement Delay. More than a Format Change; Guidance Required on Comments and Edits

It is not surprising that CMS had to delay enforcement of 5010 compliance in light of the fact that even the small payor community, including a number of MACs and Medicaids, were unable to test and implement 5010 files in production timely; let alone the thousands of providers primarily relying on unprepared clearinghouses and software vendors. A number of payors had announced delays in advance of CMS that they would not meet the deadline, such as Medi-Cal of California which had announced it would not be ready until 2013.
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3 Ways Palmetto's MolDx Program May Jeopardize Labs

By forcing labs to obtain a Z code prior to submission of any claim and by defining tests with non-coverage as investigational, Palmetto is effectively attempting to close the loop for providers utilizing the appeal process to obtain coverage. With the MolDx program guidelines, Palmetto's second LCD (Non-standardized organ panels) targeting Molecular Diagnostics tests by eliminating any coding that requires more than one CPT code to report, is even more deliberate in its attempt to eliminate adherence to established coding guidelines and consequently, the use of the Medicare laboratory and physician fee schedules.
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Labs "Very Nervous" About Palmetto GBA /CMS Contract, New Z-Codes and LCDs

Palmetto GBA announced that they obtained a new contract with CMS to develop a registry for Molecular diagnostic tests that would establish a new Z-code for each test using McKesson's proprietary software.
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HIPAA 5010 contingency plan needed, says MGMA

MGMA’s research suggests that critical coordination among many practices and their trading partners has not yet occurred. Practices that do not successfully implement Version 5010 by the Jan. 1, 2012, compliance date face possible disruption in cash flow, say experts. The Medical Group Management Association (MGMA) is calling on the Department of Health and Human Services (HHS) to issue a HIPAA 5010 contingency plan permitting health plans to adjudicate claims that may not have all the required data.
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White Paper Explains 5 Key Trends Driving CEOs to Next Generation Revenue Cycle Management

The rapid and wide-ranging changes to healthcare are magnified in the diagnostic services segment because diagnostic services influence 70% of healthcare decisions. Diagnostic service providers who fail to rapidly and aggressively adapt to this ever-changing environment do so at their peril. Because the RCM system is the system of record and therefore the lifeblood of any diagnostic service organization, a dramatic rethinking of the role of RCM systems is necessary to ensure service providers continue to successfully compete in the health services market.
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Increased Focus on Compliance Puts Pressure On Labs

With the government’s increased enforcement efforts and arsenal, the need for a comprehensive and highly effective compliance plan has never been greater. With the passage of PPACA in March 2010, a compliance program is now a legal requirement for providers participating in Medicare or Medicaid programs. A defined compliance program is also essential for clinical laboratories to survive and succeed, as well as for lab owners looking to exit the industry through a merger or acquisition.

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