PMSI - Settlement Solutions PMSI - Settlement Solutions

WCMSAP Soon to be Open to All Submitters

By , November 28, 2011 5:40 pm

waitOn July 5, 2011, CMS began pilot testing a program for the new Workers’ Compensation Medicare Set-Aside Portal (WCMSAP). Pilot testing of the WCMSAP has now been completed and CMS will be conducting a Town Hall conference call on November 29, 2011 from 1:00 to 3:00 pm (EST) to introduce the initiative to all submitters of proposed Workers’ Compensation Medicare Set-Asides (WCMSAs). During the conference call, CMS will answer questions regarding the WCMSAP. Submitters who wish to utilize the WCMSAP must first register and complete account setup.

After the Town Hall conference call, CMS will post links to the WCMSAP application and Computer Based Training (CBT) Modules on the WCMSAP section page under “Related Links Outside CMS.” The call in information for the WCMSAP Town Hall teleconference is:

  • Call in time: 1pm to 3pm
  • Call In Line: 1-800-603-1774
  • Conference ID: 29840615

PMSI was invited to participate in the pilot, along with select other submitters, and we have successfully submitted multiple claims via the WCMSAP. Implementation of the WCMSAP should improve the overall process by reducing turnaround times and the general delays experienced with the manual submission method. Users will be able to electronically submit the case as well as check the status and location of files. Receipt of the Case Control Number (CCN) will be immediate and all correspondence for cases submitted through the WCMSAP will be accessed through the portal rather than U.S. mail.

A couple of notable changes to the overall process are:

  • The WCMSAP will not accept cases that do not meet the review thresholds (the proposed total settlement amount is required to submit the case)
  • When CMS issues a developmental letter requesting additional information, submitters will only have 10 business days to respond prior to the case being closed by CMS

PMSI feels that the WCMSAP is an enhancement to the WCMSA submission process. The intent behind the WCMSAP is to provide better access to information pertaining to submitted cases and to allow for an improved experience when submitting MSAs to CMS. PMSI recommends that any organization or individual who frequently submits WCMSAs consider utilizing the portal.

Share

Denial of Medicare Coverage Continues

By , November 22, 2011 4:46 pm

On August 5, 2011, we discussed that with the transparency of claims being reported to Medicare via MMSEA Section 111, we have seen an increase in the instances of improper denial of coverage to Medicare beneficiaries.

This appears to be a widespread problem which is affecting not only the Medicare beneficiary, but the entire insurance industry. For our August 5th blog posting, please click here.

 

On November 16, 2011, CMS held a teleconference for liability insurance (including self-insurance), no-fault, and workers’ compensation, collectively recognized as Non-Group Health Plans (NGHP), to address MMSEA Section 111 technical issues. Several callers, including industry associations as well as insurance carriers, took the opportunity during the question and answer session to express their frustration to CMS regarding the issue of beneficiaries being inappropriately denied coverage due to the improper handling of information supplied during Section 111 reporting. The amount of discussion surrounding this issue confirms that it is a widespread issue and it was made very clear to CMS through these discussions that this is a very important issue requiring CMS’ immediate attention.

During the call, it was also noted that there is a perception by beneficiaries that the insurance industry is responsible for this issue because they do not fully understand the Medicare coordination of benefits process. One insurance industry association informed CMS they were recommending that Medicare beneficiaries contact their congressional leadership about specific instances where Medicare has improperly denied coverage.

The following instances of improper Medicare coverage denial were noted during the call:

  • Denial of coverage occurring when there is an open payment obligation and ongoing responsibility for medical (ORM) reported via Section 111
  • Denial of coverage when the proper ICD-9 codes are reported for the accepted injuries

CMS confirmed that they are aware of these issues, have received specific examples of inappropriate denial of benefits, and are looking into them. Over the last several months, CMS stated that they have been focused on outreach and education of contractors and providers to put a stop to this issue. Additionally, CMS indicated that they have not advised their contractors to deny claims solely because there is an open NGHP record of ORM without examining whether the payment sought was due to a specific illness/injury related to the ORM report.

CMS offered the following helpful hints to assist in reducing these issues:

  • For ORM reports, only submit ICD-9 codes related to the accepted injuries. For example, if ORM has been accepted for a broken arm, only ICD-9 codes related to the arm injury should be reported. ICD-9 codes pertaining to unrelated diagnoses such as hypertension and diabetes should not be included even if they appear on billing forms.
  • Assure proper ICD-9 codes are reported. Reporting vague or inaccurate ICD-9 codes can lead to improper denial of coverage.
  • Supply as many ICD-9 codes as needed to adequately document the injuries and diagnoses accepted (ORM) for that claim.
  • Responsible Reporting Entities (RREs) have the option to make an immediate report of ORM termination prior to their next assigned quarterly report submission by contacting the COBC Call Center at 1-800-999-1118 (specific instructions are in User Guide 3.2- need to provide link).
  • The Medicare Secondary Payer Recovery Contractor (MSPRC) is not the proper entity to contact regarding denial of Medicare coverage.

If all else fails, the beneficiary is not without recourse. CMS confirmed that there is an appeals process that the beneficiary can follow if they disagree with the denial. For further information on the Medicare appeals process please see our blog dated August 5, 2011.

While Section 111 reporting was created to assist in the recovery process, it has not been smooth sailing for all parties involved. The industry appears hopeful that CMS will take heed to the seriousness of this issue and take steps to correct problems on their end. However, in order to fully overcome these issues it will take the effort of not only CMS, but also everyone involved in this cumbersome and complex process.

Share

New FDA Approved Medications

By , November 18, 2011 12:50 pm

Prescription drug costs in workers’ compensation claims are rising, making it necessary for claims professionals to carefully evaluate this exposure and mitigate costs when possible.  Staying up to date on current pharmacy trends, including new medications introduced to the market and generic equivalents, is one piece of the equation to mitigating costs.

Every brand medication has a patent life and once the patent expires, generic equivalents will be introduced into the market at a lower cost.  Although there is no set brand versus generic price differential upon generic entry, there is a large cost savings that accompanies the generic release. The gap between brand and generic pricing widens as brand name medications continue to have annual (or quicker) increases to the AWP (average wholesale price), whereas the generic formulations do not generally experience annual inflation.  Some generic equivalents can launch at reductions of 70% from the brand medication price, which is a significant decrease.  

Recently, there have been several new medications and generic equivalents approved by the FDA that will have an impact on workers’ compensation claims.  Gralise (Gabapentin) is a new once-a-day dosing of Gabapentin which is FDA approved for post herpetic neuralgia pain.  It is to be taken once per day with the evening meal, which should lead to better patient compliance along with a better therapeutic outcome.  Gralise has been shown to produce fewer side effects than Lyrica and Neurontin (Gabapentin) and will more than likely gain in popularity among prescribers for its use in treating neuropathy and radiculopathy in chronic pain patients.  At this time, there is no pricing available for Gralise. 

For chronic pain management, a long acting (extended release) pain medication formulation is preferred over its short acting counterpart.   Both Nucynta ER (Tapentadol) and Tramadol ER 300mg- (generic Ultram ER 300mg), which are newly approved medications, fall into this category.  Nucynta ER and Tramadol ER are both pain medications approved by the FDA for treatment of moderate to severe pain requiring continuous, around the clock analgesia unlike their immediate release formulations, which are taken on an as needed basis.  The average cost of Nucynta ER 50mg twice a day for a month supply is $177.60 while Nucynta 50mg (immediate release) taken once every 4-6 hrs is $277.20; therefore, not only should the extended release formulation provide overall better pain control, but it would also be more cost effective. 

According to PMSI’s Drug Trends Report, Ultram ER is one of the top 20 brand medications prescribed in workers’ compensation.  Ultram ER and its generic Tramadol ER are dosed at once a day.  The average cost of brand Ultram ER 300mg is $279.90 for a one month supply while the generic Tramadol ER 300mg averages $162.30 per month.   Additionally, Tramadol ER is also less expensive than its immediate release formulation, which can be prescribed up to 8 tablets per day, at an average monthly cost of $189.60.

The above noted pricing differences creates an incentive to address the potential use of generic and/or long acting medications with the treating physician when an injured individual is being prescribed the brand or short acting medications, if a cost savings can be realized.  Sleep aids are commonly prescribed medications for workers’ compensation injuries when there are significant pain complaints and insomnia is present.  According to PMSI’s Drug Trends Report, Lunesta was noted to be the second most prescribed medication for insomnia in workers’ compensation.  Generic Lunesta (Eszopiclone) has now been FDA approved for the treatment of insomnia.  No release date or pricing for the generic has been released by its manufacturer as of today, but the approval of the generic formulation will likely impact medication transaction costs within the workers’ compensation community.

Keeping up to date on new drugs as well as generic formulations as they are approved by the FDA will help mitigate the rising cost of claims as well as provide for the potential of an overall better therapeutic response for the injured worker.

Share

Government Plans to Appeal U.S. v. Stricker

By , November 15, 2011 2:23 pm

According to an article titled “Government Appealing Medicare Set-Aside Suit” on WorkCompCentral (subscription required), the government plans to appeal the dismissal of U.S. v. Stricker, one of the largest Medicare reimbursement suits ever filed. The government recently filed a motion for reconsideration based upon a theory of “continuing accrual,” that the statute of limitations re-starts each time a class Plaintiff received a settlement payment. The motion for reconsideration was denied on August 12, 2011. For a copy of PMSI’s previous legal bulletins on U.S. v. Stricker please click here.

The WorkCompCentral article states that the Department of Justice has filed a notice of appeal with the U.S. 11th Circuit Court of Appeal, notifying the court that an appeal is forthcoming. Additionally, the article states that since learning of the impending appeal, the attorney defendants have filed a cross-appeal arguing that the three-year statute of limitations applies to them and that the government has until November 22nd to file their appellate brief, which will outline its specific arguments on appeal.  However, an extension of that deadline may be sought.

It will be interesting to see if the government puts forth its theory of “continuing accrual” yet again, and whether the U.S. 11th Circuit Court of Appeal will ultimately agree with the lower court’s decision that the Federal Claims Collection Act (FCCA) does apply to Medicare conditional payment matters, and that a six year statute of limitations applies if the underlying claim is a contract, and a three year statute of limitations applies if the underlying claim is a tort.

PMSI will continue to follow this matter and the arguments that are set forth in the government’s appeal. PMSI will also continue to follow and support the SMART Act, which seeks to clarify and set the government’s statute of limitations with regard to conditional payment demands at three years.

Share

Panorama Theme by Themocracy