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Many AOPA Concerns Included in Ways and Means Committee Draft Bill Addressing Medicare Fraud, RACs, and ALJ Delays

AOPA has been anticipating that the House Ways & Means Committee will be putting forward a bill to address Medicare fraud, hospitals, RACs and the long delays for ALJ hearings. Our strategy has involved working closely with two representatives who have been working on their own bills to address RAC problems, Reps. Renee Ellmers (R-NC), author of H.R. 5083: The Medicare DMEPOS Audit Improvement and Reform (AIR) Act of 2014, and Mark Meadows (R-NC), whose bill is still being drafted. Several provisions of great importance to O&P, and language grafted from the O&P Alliance RAC Audit draft legislative language have been recommended by AOPA, with support of our Alliance partners, for inclusion in these two bills. H.R. 5083 includes language to legitimatize the prosthetist/orthotist’s notes as a legitimate part of the medical record and language to require CMS to track specific data on O&P RAC appeals, distinct from the current data spanning indiscriminately ONLY ALL of DMEPOS claims.

The strategy has been that having these provisions appear in bills already crafted by GOP legislators would make it far more likely that these provisions would find their way into the bigger Ways and Means Committee bill, which will be on a faster track for enactment. On Thursday, November 19, Rep. Kevin Brady (R-TX), the Chair of the House Ways and Means Health Subcommittee released a 146-page working draft of his bill. This is the second draft of this bill (AOPA had provided our input on the initial draft just before our Las Vegas meeting).

This draft includes the following provisions of interest/concern to O&P professionals:

• Language to recognize the prosthetist/orthotists’ records and notes as being a legitimate part of the medical record;
• A broad provision instructing CMS to publish the specific requirements they have for payment of lower limb prosthetic claims;
• Instituting a 30-day required ‘discussion period’ between auditor and provider before an audited claim is transmitted to the DME MAC for adjustment or recoupment;
• Language is included to require collection of audit data for O&P distinct from the rest of DME data;
• Two provisions instructing CMS to develop data-driven claims resolution/ settlement offers for Part B claims like O&P, generally paralleling the settlement offers of RACs that CMS has already extended to Part A hospital claims;
• A lengthy provision to initiate a bundled payment system for several specific Medicare episodes of care (surgery and all services 90 days thereafter). While currently limited to: hip/knee joint replacement, lumbar spine fusion, coronary artery bypass graft; heart valve replacement; percutaneous coronary stenting; and colon resection, we are concerned that it would give the Secretary discretion to add additional procedures or services.

Like all legislation, there are things here that we would like, and others that give us great pause. Clearly, the strategy AOPA has invoked to advance some of the provisions we have favored has been borne out, and clearly there is much more work to be done. AOPA will continue working with the Ways & Means staff and legislators sympathetic on O&P issues to try to refine and remedy some of the rough edges with this draft bill. We will keep members apprised of any developments. The 146-page bill may accessed here. Of greatest interest are pages 38-41, 54, 62-63, and 105-133.

AOPA to Testify Today during SBA Hearing on Regulatory Fairness

AOPA will be testifying during today’s Regional SBA Hearing being held in Seattle, WA titled “Regulatory Fairness Hearing for Small Business.”  AOPA will testify on behalf of our members on the RAC and Pre-payment audit practices jeopardizing the economic viability of our members.

You may read AOPA’s submitted testimony online.

Background

This hearing is being held by the U.S. Small Business Administration, Office of the National Ombudsman. The National Ombudsman assists small businesses with unfair and excessive regulatory enforcement by federal agencies including repetitive audits or investigations, excessive fines, penalties, retaliation or other unfair regulatory enforcement actions. The National Ombudsman acts as a “troubleshooter” between small businesses and federal agencies by receiving comments and complaints from small businesses and then directing those comments and complaints to the appropriate federal agency for a high-level review.

The hearing is designed to provide small business owners, community and business leaders with an opportunity to discuss issues regarding Federal Regulatory Compliance and enforcement.  While this hearing is one of the regularly held hearings mandated by the law that set up the Regulatory Fairness Office and is designed as a general session for all kinds of small business government abuse issues, we plan to use this opportunity to voice concerns about the CMS regulatory issues plaguing O&P small businesses.

The SBA will also be holding another Regulatory Fairness Hearing on June 21, 20913 in Davenport, Iowa from 8:30 am- 11:30 am.

 

Next Medicare Open Door Forum to Discuss the CMS Proposed Physician Documentation Template Scheduled for June 13, 2013

The Centers for Medicare and Medicaid Services has announced that the second of several Open Door Forums to discuss the proposed physician documentation template for O&P services will be held on Thursday, June 13, 2013 from 4pm-5pm EDT.

AOPA encourages all of its members to participate on this call and provide feedback to CMS regarding its proposed physician template.  AOPA will be represented on the call and is developing an alternate template for submission to CMS.

Questions regarding this issue may be directed to Joe McTernan or Devon Bernard via email.

 

AOPA Files Lawsuit Against CMS

American Orthotic & Prosthetic Association Files Lawsuit Against Medicare Arising from Unfair Medicare RAC/Pre-payment Audits, Where No Fraud Exists, and Challenges Unlawful Changes to Medicare Standard for Care of Medicare Amputees

Today, the American Orthotic and Prosthetic Association (AOPA) filed suit against HHS/Medicare in the Federal District Court for the District of Columbia, seeking relief from the unfair and unauthorized actions of the Center for Medicare and Medicaid Services, primarily via actions of its RAC auditors and DME MACs relating to physician documentation requirements.

AOPA President, Thomas F. Kirk stated, “Today, AOPA has stated empathically that we will not stand by when government acts inappropriately to threaten either the quality of care we provide to our patients or the economic viability of the small businesses and providers that comprise the orthotics and prosthetics profession.”

AOPA’s suit arises with respect to Medicare actions that began in August 2011 the HHS Office of Inspector General released a flawed, and in some respects amateurish, report alleging fraud in the O&P field where there essentially was none. The report: (1) misunderstood that patients don’t go to their physician when their prosthesis is not working properly; (2) misunderstood that it is not unusual that most Medicare amputees may not see the ‘referring physician’ who first prescribed their prosthetic care because that physician is commonly the surgeon who amputated their limb; (3) created extensive confusion about whether bi-lateral amputees should have both prostheses on a single claim or two separate claims; (4) leapt to conclusions of fraud because claims costs had increased with a fixed number of Medicare amputee beneficiaries while failing to recognize that Iraq-Afghanistan had prompted a quantum leap in technology (and a related incremental increase in unit cost) which together with CMS-approved O&P fee schedule increases (after years of ‘freeze’) had indeed driven per capita increases; and (5) failed to track as required by BIPA 427 whether or not care providers were, or were not, qualified providers under federal law. But the worst thing this flawed OIG report did was trigger an adverse change in the quality of patient care for Medicare beneficiaries.

Someone at Medicare should have known better. CMS leadership or its DME MAC contractors should have pointed out the flaws in this OIG report and pushed back. But no one did. In fact, without any process for the stakeholder input that is guaranteed by federal law, CMS also in August 2011, through the actions of its DME MAC contractors, dramatically revised the standards by which a prosthetic claim would be judged for reimbursement approval. This was done by simply circulating unilaterally a “Dear Physician” letter. We believe that in doing so Medicare violated the law, specifically the federal Administrative Procedure Act and the Medicare Act. Then CMS contractors/auditors proceeded to apply this ill-conceived new standard retroactively to claw back money on claims which no one asserts involved any fraud, but which originated years before CMS contractors devised the new “standard.”

AOPA has recounted efforts O&P has over the past 20 months to try to explain and persuade CMS that its actions on this matter are unfair, contrary to the statutes and detrimental to the care provided to Medicare beneficiaries. The introduction of the new ‘standard’ and audits were done in the name of saving Medicare dollars against the backdrop of the Affordable Care Act’s promise to extract $750 billion over ten years from Medicare providers. RAC auditors’ independence is fundamentally compromised by the fact that they are paid a commission based on a percentage of the claims dollars they claw back. Last month, thirty-five members of the U.S. House recently signed a letter to the Secretary of HHS seeking relief for O&P and our Medicare patients. AOPA’s lawsuit maintains that the OIG/CMS action has changed the standard of care, often forcing practitioners to choose between meeting the patient’s immediate need for a prosthesis by providing a less sophisticated device, rather than endure long delays in care triggered by the paper chase with physicians. The truth is that CMS wants physicians to provide more documentation, but isn’t willing to pay them any more. According to AOPA Executive Director, Thomas F. Fise, “(M)any patient care facilities have closed or been sold as a result of these Medicare-induced financial pressures, and you have said if we can’t find a way to get this problem fixed, the entire field is at grave risk. Under these dire circumstances, AOPA, having exhausted all other prospects for relief, has little choice but to place this matter, and the future of our profession as well as the quality of care delivered to Medicare amputee beneficiaries, in the hands of the courts.”

Review the complaint AOPA has filed.

Reminder Regarding RAC ADR Limits for O&P Services

AOPA would like to remind its members that revised limits for Additional Documentation Requests (ADRs) for RAC audits involving O&P claims were implemented as of April 3, 2013.

While the ADR calculation remains unchanged at 10% of claims submitted during the previous year, divided by 8, for each 45 day period, CMS has limited the number of ADR requests for O&P providers to a maximum of 10 ADR requests every 45 days.

AOPA has received several reports where members have received ADR requests after April 3, 2013 that exceed the maximum of 10.

If you receive more than 10 ADR requests from a RAC auditor within a 45 day period, please contact the RAC contractor immediately to challenge the request.  In addition, please contact Joe McTernan so that AOPA may address this issue with CMS directly.

Policy Forum Makes Big Impact on Raising Congressional Concerns over RAC Audits

AOPA Executive Director, Tom Fise, brought the Board of Directors up to date in a recent email on how AOPA members attending the Policy Forum took the lead in urging their legislators in the House of Representatives to sign-on to the letter Rep. Tammy Duckworth and Rep Brett Guthrie will send to HHS Secretary Sebelius.  Subsequently, all AOPA members were urged to contact their legislators and to request they sign-on to the Sebelius letter.

Click here to read the letter to Secretary Sebelius.

EXCERPTS FROM FISE EMAIL UPDATING AOPA BOARD ON RAC AUDITS

“With March drawing to a close, it makes sense to provide an update on AOPA’s and related efforts on the RAC/pre-payment audit issues.  In terms of this issue, it was very fortuitous that we decided to hold the Policy Forum earlier than usual this year, as a great deal has happened since we saw most of you at the AOPA Policy Forum, March 12-13.

“Let me start with background on RAC issues in hospitals.  Many of you are probably familiar with the fact that a few months back the American Hospital Association sued CMS challenging its RAC audit policies.  The specific dispute is a bit different from ours but related.  RAC auditors have roundly challenged claims involving patients who were admitted as inpatients and received certain procedures, claiming the admission was improper, clawing back the entire Medicare payment to the hospital with the assertion that the procedure could have been done on an outpatient basis.  Hospitals have massively appealed these audit results up the chain to the ALJ claiming that even if the auditor is correct regarding the admission decision, Medicare ought to at least allow the payment the hospital would have received if the patient had received the procedure on an outpatient basis at the hospital.

“I have been told that these appeals to ALJ have succeeded in securing partial payment in 90-95 percent of cases that have gone that far.  On March 13, CMS released its proposed regulations to implement such partial payment AND also issued a new administrative policy that they would start making the partial payment immediately, even before the conclusion of the rulemaking process for the new regulation, in any such case where an audit contested the full inpatient hospital tab (see email attached).  This is a very important precedent that was achieved after the AHA filed suit, and the AHA gave nothing in return for the CMS commitment to the new regulation and interim administrative policy that approved partial payment, i.e., AHA did not withdraw its suit against Medicare.

“You may also recall that on March 8, just before the Policy Forum, we had written four letters to CMS audit/DME MAC contractor chief George Mills, questioning several policies those contractors had implemented (click here to see letters).   I was not surprised to receive an email from George Mills, responding to two of the four letters (Letters one & two) we had delivered to him.  The AOPA letters/requests on the issues of K-level and the legitimacy of the prosthetist’s notes remain pending in front of George Mills, still awaiting action.

“There remain a good many items in motion, energized largely by the AOPA Policy Forum.   Reps. Duckworth and Guthrie circulated a “Dear Colleague” letter to all Members of the House, encouraging them to sign-on to the letter to Secretary Sebelius.  AOPA has mounted a strong outreach both to Policy Forum attendees and to all AOPA members, offering an easy pathway for them to contact their House Representative urging them to exercise the opportunity to Sign-on  to the letter.  Within the past 5 day AOPA members have sent letters to approximately 250 Congressional offices seeking endorsement of the Duckworth/Guthrie letter.  While many members of Congress are reluctant to ‘sign-on’ to such joint letters,  we are still hopeful of securing commitments from a good number of House members to sign-on in advance of the April 10 close-out date when the letter will be finalized and delivered by Duckworth and Guthrie, with as many signatures as can be garnered–so the heat is building at CMS

“The high level of activity on the RAC and pre-payment audit issue, especially since the Policy Forum seems to have prompted some confusion among CMS staffers.  For example, we’ve been informed by Hill staffers that CMS has been representing to Congressional staffers that AOPA is already working with CMS on their planned physician template rule making (we will work with them if and when they ask us to–and odds are they will ask–but as yet they haven’t).”

End of Fise Email

 

AOPA’s Concerns Prompts CMS to Modify Limits for RAC Audits

AOPA’s continuing conversation and efforts to convince CMS of the cash flow killing harm to patient care and member patient care facilities imposed by the pervasive and aggressive RAC audits together with aggressive AOPA member advocacy with their legislators flowing from the Policy Forum appears to have borne some fruit.

The Centers for Medicare and Medicaid Services has announced that, effective April 3, 2013, it has modified the number of Additional Documentation Requests (ADRs) that a RAC auditor may make for DMEPOS suppliers.

For most DMEPOS suppliers, the limits remain unchanged from last year. The number of ADRs a RAC may make per 45 days is limited to 10% of all claims submitted under a single Tax ID for the previous calendar year, divided by 8.

For suppliers who are classified in categories 52, 53, 56, or 57 however, there is a limit of no more than 10 ADR requests per 45 days. The provider taxonomy codes mentioned above are defined as follows:

  • 52—Medical Supply Company with Prosthetist
  • 53—Medical Supply Company with Orthotist-Prosthetist
  • 56—Individual Certified Prosthetist
  • 57—Individual Certified Prosthetist-Orthotist

The fact that CMS has modified the RAC ADR guidelines to include a limit of no more than 10 ADR requests for claims from companies providing prosthetics is a significant development in AOPA’s efforts to challenge the egregious and aggressive audit practices that RAC auditors have been using. While it does not represent, in any respect, a comprehensive solution to the challenges that RAC audits represent, it does represent an acknowledgement of the negative impact RAC audits have had on the provision of medically necessary services by qualified O&P professionals.

AOPA has contacted CMS and requested that they also consider a similar limit of no more than 10 ADRs per 45 days for suppliers classified as follows:

  • 51—Medical Supply Company with Orthotist
  • 55—Individual Certified Orthotist

CMS has indicated that it will consider including these categories in a future update to the RAC ADR limits. If and when this change is made, AOPA will notify its membership.

AOPA can assist members to ensure that their organization is enrolled in Medicare under the proper provider taxonomy code. Questions on how to do this or any other questions regarding this issue may be directed to Joe McTernan or Devon Bernard.
This action is distinct from CMS’ response to AOPA’s letter of March 8, referenced in a prior AOPA Smartbrief, notifying CMS that Performant Recovery, Inc., the Jurisdiction A RAC contractor, was incorrectly applying the provider based ADR limit calculation to O&P suppliers resulting in more ADR requests than regulations allow. CMS has corrected this situation and Performant Recovery has rescinded RAC audits that exceeded the limits of the supplier based calculation. If you are interested in reviewing those communications, they are accessible at: March 8th letter & CMS Response.