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Billing Alert for Long-Term Care, June 2015

Star razing: Providers face quality rating dips after system recalibration

Note: For more recent coverage of the Nursing Home Compare star rating system, see the November 2014 and January 2015 issues of PPS Alert for Long-Term Care.

 

On February 12, CMS announced the dawn of Nursing Home Compare 3.0, a version update marked by a major recalibration of the popular consumer search site’s five-star quality rating system. When the agency debuted the retooled feature just one week later, almost a third of nursing homes had shed at least one star from their overall rating?a change that some provider advocates say baffled industry business partners and consumers alike.

"What we’ve heard is confusion," says David Gifford, MD, senior vice president of quality and regulatory affairs at the American Health Care Association (AHCA), a national trade association for long-term care providers. "The public’s asking, ‘Why did you lose a star?’ "

 

Recalibration rundown

The five-star rating system scores a given nursing home in three domains, the general characteristics of which were preserved during the recalibration:

1.Quality measures (QM) pulled from MDS documentation completed by the facility.

2.Staffing levels identified in a form completed by the facility during its annual state inspection. The rating in this domain is calculated based on scores in two subcategories: 1) the number of hours RNs have worked per resident day in the two-week period leading up to the survey, and 2) the total number of hours worked by RNs, licensed practical nurses, CNAs, and physical therapists within the same time frame.

3.Health inspection reports that detail the facility’s performance on the latest three annual surveys, as well as the outcomes of any complaint investigations conducted within that time frame.

 

The methodology CMS uses to translate these individual component scores into a facility’s overall rating was also spared in the February calculation updates: The health ­inspection component?the only rating domain that doesn’t hinge on data submitted directly by a facility?still serves as the bedrock of the score. From there, one star can be added or subtracted based on the staffing component. The same goes for the quality measure score.

The recalibration instead targeted the two so-called self-reported categories, weeding the field of top performers in these arenas by:

1.Increasing the difficulty of achieving a staffing rating of four stars, which now requires nursing homes to earn four stars in either the RN or total staffing subcategory.

2.Ratcheting up the number of points necessary to earn a QM rating of two or more stars?a move that significantly redistributed providers along the rating scale. CMS reports that since the recalibration, the number of nursing homes with four- or five-star QM ratings has plunged from about 80% to 49%, while the number of facilities with one star in this arena has climbed from 8.5% to 13%. In total, ­Gifford says a staggering two-thirds of providers experienced a change in their QM score.

3.Incorporating two antipsychotic measures that have long been reported on Nursing Home Compare (one targeting rates of use among short-stay residents, the other aimed at their long-stay counterparts) into QM scoring methodology.

 

In addition to kindling major rating changes in the quality and staffing domains, the February shake-up also tided a shift of up to two stars in facilities’ overall ratings.

According to AHCA, overall score changes that can be wholly attributed to the quality and staffing calculation updates are as follows:

  • About 29% of providers lost one star
  • 2% lost two stars
  • Less than 1% gained a star

 

Note: These statistics don’t account for the additional star shifts experienced in February by some providers whose health inspection data was updated at the time of the recalibration.

 

Curbing the ratings creep

The recent recalibration builds on the controversy that has embroiled the star system since the New York Times published its August 2014 exposé claiming the ratings’ reliance on self-reported measures enabled facilities to game the system. This position, the author and some consumer advocacy groups say, is backed by the steep climb of top-ranked facilities over the years (a climb that the new calibration has since stemmed).

But providers and their advocates bristled at these charges, instead attributing the influx of four- and five-star ratings seen prior to the recalibration to the industry’s fierce commitment to improving care delivery.

Although stakeholder factions are still contesting the primary drivers of the historic ratings creep, it’s undeniable that, with calculation methodology left largely unchecked in the six-year expanse between the advent of the star system and its February recalibration, ratings had trended upward.

When the five-star system was first inaugurated in December 2008, the number of top and bottom ratings awarded in a given category hovered within a few percentage points of their counterparts in the other two domains. However, between 2009 and 2013, the volume of nursing homes with an overall rating of five stars jumped more than 10%, while the number of facilities with one star fell more than 11%.

Because the health inspection rating is calculated using a state-specific fixed distribution (with five stars awarded to the top 10% of facilities, one star granted to the bottom 20% of performers, and the remaining star counts doled out in equal shares among the middle 70%), the skyward trajectory of the overall ratings can be traced exclusively to hikes in staffing and quality scores over the years.

Between 2009 and 2013, the proportion of four- and five-star ratings in the staffing domain increased about 13%, while these ratings soared almost 33% in the quality arena, according to data released by CMS contractor Abt Associates.

"We’ve seen the number of high five-star rated buildings increase, increase, increase," says Thomas Martin, senior research analyst at PointRight Inc., a healthcare analytics consulting firm in Cambridge, Massachusetts. "We were moving toward almost half of the industry being a five star in the quality domain."

These disproportionate leaps in QM scores shook many stakeholders’ trust in the system, according to Richard J. Mollot, executive director at the Long Term Care Community Coalition (LTCCC), a New York City?based advocacy group for elders and people with disabilities.

"It got to the point where it was hard to pay any attention at all to the quality measures," Mollot explains, recalling the site profiles of facilities with one-star ratings in the inspection and staffing categories and a five-star QM score. "It was just kind of bizarre."

Although most stakeholders seem to acknowledge that the spiraling ratings needed to be reined in, provider advocates worry that the steep drop-offs triggered by CMS’ drastic response will sully the reputations of well-performing facilities and ignite unintended operational consequences.

Nursing Home Compare was launched in 1998?and augmented by the five-star system a decade later?to facilitate consumers’ searches for facilities that best fit their specific care needs. But today, the reach of the site extends well beyond these original bounds. Far-flung entities (e.g., accountable care organizations, managed care plans, liability insurance carriers, and the U.S. Department of Housing and Urban Development) have appropriated the star ratings to determine facilities’ business worth, and consequently, Gifford says some providers have fielded calls from these stakeholders inquiring about sudden rating drops.

"It looks like . . . industrywide, nursing home practices have suddenly dipped and quality has decreased, but that’s not really the case," adds Martin.

 

Stakeholders support antipsychotics crackdown

Although Gifford decries the aggressiveness and abruptness of CMS’ score rebasing, he says AHCA backs the agency’s inclusion of antipsychotic measures in QM calculations?a decision that speaks to the growing precedence of this focus in the healthcare realm.

As Americans are living longer with more complex conditions, and nursing homes have consequently experienced an influx of residents with dementia, regulatory efforts to quell the use of antipsychotics are gaining momentum.

"Antipsychotic drugging . . . is, I think, one of the most important issues that we’re looking at today," ­Mollot says. "It’s emblematic of care in general for a lot of facilities in terms of . . . how staff are trained to meet the needs of their residents."

Although providers have already made significant strides in this domain, CMS and patient-centered groups like LTCCC say there’s a lot of work left to do.

For example, though the industry managed to whittle usage of antipsychotics by 15% between calendar years (CY) 2011 and 2013, CMS hopes to double this statistic by the end of CY 2016. And despite current progress, LTCCC reports that roughly 20% of residents nationwide were still on antipsychotic drugs in December 2014.

Because many providers focus on boosting ratings to attract prospective clients and business partners, Mollot thinks CMS’ decision to integrate antipsychotic use into rating calculations will fuel more necessary improvements in this arena.

Despite garnering support from provider and consumer advocates, the new QM measures left some participants in a February open door forum wary about the then-impending rating system updates. A couple callers voiced concerns that the incorporation of the short stay antipsychotic usage measure would penalize nursing homes for drugs prescribed to residents during prior stays at the hospital. One participant worried the new spotlight on antipsychotics would misrepresent her facility’s usage of the drugs among its unique population of residents with severe mental health issues.

 

Star striking justified, but too abrupt

Despite generally favorable receptions of the antipsychotic measure additions to QM ratings, some provider advocates had championed a much more graduated approach to getting the star system up to speed. For example, Gifford recounts AHCA’s suggestion to bump up the cutoff score needed to qualify for a given star count (called a cut point by CMS) on a quarterly basis, adding that he hopes CMS will still adopt such a method for the subsequent rounds of rating updates the agency already has in the pipeline.

"Each time they add new measures, if they’re going to rebase [ratings], that’s just going to add more confusion," Gifford explains. "I think there’s a better way that hopefully they’ll consider next time going forward."

He adds that employing an incremental method to adjust star cut points and calculations would also benefit the intended users of Nursing Home Compare, who would be able to make more meaningful judgments about a facility’s succession of star ratings?an ability Gifford says would be hampered by future iterations of this year’s recalibration, which rendered providers’ ratings between January and February incongruous.

"Rebasing this every couple years [would mean] that all prior ratings have no meaning compared to the new ratings," Gifford explains.

But while providers and their backers believe February’s jarring rating updates could malign nursing homes’ performance, consumer advocates say the rampant score inflation prior to the recalibration also misled consumers. "[The rating system] really wasn’t fair before for consumers," says Mollot. "You’re seeing a much more accurate rating now."

For this reason, Mollot finds many of the attempts he’s seen throughout the industry to characterize lowered ratings as mere byproducts of CMS’ more stringent calculation methodology too reductive. Instead, he urges providers to consider the full context of the agency’s decision to carry out the rating overhauls and reflect on whether star losses reveal any gaps in current care practices.

"If providers are thinking about [the recalibration] in a constructive way, that will be really useful to them in terms of the quality of care overall in the facility and . . . in terms of customer satisfaction, too," Mollot says. "The more accurate the information is, the more useful it will be for the nursing home[s] . . . to improve their care, and that’s really what we all want."

Despite the growth opportunities he thinks the recalibration presents, Mollot acknowledges the importance of explaining to alarmed clients that it is also the direct impetus of some sudden rating reductions.

But Martin thinks this feat may be easier said than done, given the minutiae of the rating calculation methodology. He recommends underscoring that the changes reflect higher expectations from CMS, rather than newfound performance lapses on the facility’s end.

"The five-star methodology has raised the bar," he says. "[CMS’] grading criteria has gotten more difficult, even though the facility didn’t necessarily take a dip in quality."

In addition, Gifford suggests trying out the language CMS posted on Nursing Home Compare post-recalibration to highlight the lack of comparability between QM scores introduced in January and their immediate predecessors.

"Many nursing homes will see a lower quality measure rating as a result of these changes, even though the underlying QM data may not have changed," CMS recently wrote on the "How we calculate ratings" page of the site. "Because of these changes, it is not appropriate to compare a facility’s QM ratings that appear in February with those that appeared in earlier months."

Mollot says anticipating tough questions from clients is a best practice that should extend beyond the scope of recalibration fallouts. For example, if a surveyor identifies a deficiency during an annual inspection, a provider should brace for queries about what its staff are doing to address the issue?and have a corrective plan in place to ensure the prepared answer is more than lip service.

 

Catch falling stars

In addition to strategically educating concerned clients on rating changes carried by the recalibration, Mollot and Gifford urge providers to use the revised scoring methodology as a tool to identify their facility’s specific hot spots and guide targeted quality improvement efforts.

Gifford recommends consulting the latest version of the rating system user’s guide, which CMS updated in February to reflect the new quality and staffing star cut points ushered in by the recalibration.

"One of the nice things in the changes is CMS actually provided the rates on each of the quality measures that you need to achieve a better score," says Gifford. "We’ve been encouraging members to look at those rates related to the points and figure out how much better they have to get on which measures to improve their score."

Martin echoes this recommendation, stressing the importance of determining a given facility’s proximity to the next star count in each domain.

"If you just understood where those cut points were and how close you were, you could get a feel for what you need to do to improve," he explains. "You might be one hour of nursing time away from the next star."

Because of the heightened emphasis on reducing antipsychotic drug usage, Mollot also recommends strengthening dementia care practices?a move he says doesn’t necessarily demand major resource expenditures or new hires. Sometimes, he says, a simple change in approach?such as delaying a distressed resident’s scheduled bath?is all it takes to overcome the use of chemical restraints and recoup time traditionally spent subduing difficult behaviors. This refocusing can allow staff to dedicate additional efforts to other facility needs and, in turn, boost star ratings.

"Providers who are moving to provide better dementia care will see benefits, and hopefully that will incentivize others as well," Mollot says.

Once nursing homes pinpoint their performance gaps and growth opportunities, Gifford suggests turning to national initiatives (e.g., the one developed by AHCA) or established quality improvement programs (e.g., the Baldrige Performance Excellence Program) for frameworks to transform performance goals into operational realities.

 

More changes on the horizon

Although providers may still be seeing stars after the February recalibration, CMS is far from done with its overhauls to the rating system.

In particular, experts are keenly anticipating the agency’s deployment of an electronic reporting system that will both cull staffing numbers from a nursing home’s payroll records and report this data on a quarterly basis, ultimately transforming it into star ratings, Mollot says. CMS recently announced that it intends to collect data through the system on a voluntary basis beginning October 1, 2015, and to mandate the industry’s nationwide reporting in this manner beginning July 1, 2016.

Gifford says CMS is also readying a handful of new staffing and quality measures for integration into star calculations in the not-so-distant future, including rates of turnover, retention, rehospitalization, and discharge to the community?prospects about which he is cautiously optimistic.

For his part, Mollot would like to see CMS regularly update criteria and refine calculation methodologies across all rating categories to undercut what he calls the tendency of some industry players to "teach to the test" by applying quick-fix strategies to bump up ratings rather than launching genuine quality improvement initiatives.

As CMS continues to flesh out the criteria within each rating domain, Gifford hopes the agency will find a way to continue representing the entire spectrum of insurers weighed in today’s ratings. Although current scores reflect all residents, regardless of their payer type, the proposed rehospitalization and discharge to community measures could be based on claims data that isn’t collected for all coverage plans.

"If this information is going to be used for [consumer] choice, it should reflect the full panel of individuals who are cared for by a provider," Gifford explains.

But despite stakeholders’ misgivings, Mollot stresses that the revamped rating system is an important tool for the nursing home community. "Nursing Home Compare, even with its imperfections, is by far the most valuable resource for people in terms of choosing a nursing home," he explains. "Capturing quality in an accurate way . . . is an important thing, and I think that benefits the good providers, as well as consumers."

 

Stakeholders take NOTICE of mounting ­observation status reform legislation

In mid-March, the U.S. House of Representatives unanimously approved the Notice of Observation Treatment and Implication for Care Eligibility ­(NOTICE) Act (H.R. 876). As a result, the bill is now poised to become the first to gain legal standing among a collection of proposed legislation aimed at remedying today’s fallout from observation status.

Reforming this outpatient designation?which leaves affected Medicare beneficiaries eligible only for Part B coverage?has drawn support from an unlikely assemblage of healthcare stakeholders in the acute, postacute, and beneficiary advocacy spheres.

"We’ve been working very closely with a very broad coalition of groups around [observation status], and it’s a coalition of groups where sometimes we’re on different sides of issues, but as it pertains to this issue, we’ve been completely and totally united," says Clifton J. Porter II, senior vice president of government relations at the American Health Care Association, a national trade association for long-term care providers.

The reason behind this widespread traction: Today’s heavy-handed application of observation status is having devastating effects on those in acute and postacute settings. The designation often disrupts a beneficiary’s eligibility for Medicare coverage in SNFs following a hospital stay, sparking patient confusion and potentially narrowing the client pool for long-term care providers.

In addition, the outpatient designation severely limits Medicare coverage in the hospital itself, ­slapping beneficiaries with a copayment for each individual service rendered during an observation stay instead of the one-time deductible granted during the Part A inpatient alternative. In addition, patients are expected to pay for prescription charges that accumulate during an observation stay.

Because of these potential liabilities, observation status has traditionally been reserved for patients who undergo brief hospital stints, during which time clinicians are charged with assessing whether they are ill enough to warrant inpatient admission or well enough to return home. However, as Recovery Auditors (RA) have ramped up scrutiny on the appropriateness of inpatient stay determinations, hospitalists have become much more liberal in their use of observation status, applying it to stays as long as a week, says Diane Brown, BA, CPRA, director of postacute education at HCPro, a division of BLR, in Danvers, Massachusetts. She underscores the huge impact on beneficiaries, many of whom are left in the dark about their outpatient status and its ramifications until long after their stay has ended.

"The beneficiaries who weren’t aware that they hadn’t been officially admitted come out of the hospital, and then they get whacked with a bill," says Brown.

And underlying the recent outcrop of beneficiaries under observation is a flawed foundational concept that fails to account for the clinical services provided in the hospital, says Ann M. Sheehy, MD, MS, associate professor and division head of hospital medicine at the University of Wisconsin School of Medicine and Public Health.

"We can deliver the same exact care to two patients that are in the beds next to each other?one is observation, one is inpatient?for three nights, and the inpatient gets to go to a nursing home and have the Medicare coverage; the outpatient does not," she explains. "That’s just really hard to swallow."

 

Flying under RA radars

Observation status has been a provision of the Medicare benefit since the program’s inception in 1965, but healthcare providers attribute the backlash facing beneficiaries today to the instatement of the nationwide Recovery Audit Contractor Program (now known simply as the Recovery Audit Program) nearly half a century later.

RAs are charged with combating reported instances of fraud and abuse throughout the healthcare system by detecting and recouping improper payments, such as those for noncovered, incorrectly coded, and duplicative services. However, because RAs are paid on a contingency basis, healthcare providers argue there’s a financial incentive for them to target practices that will yield the biggest monetary reward while providing the least grounds for contest, a strategy that Brown says has inspired them to take a hard line on regulations with obvious gray areas, like observation status.

"If you’re going to be paid that way . . . you want to find the low-hanging fruit," says Brown. "[Observation status is] a broad-based rule . . . and unless you have a lot of concrete examples to support a broad-based rule, nobody knows how it really works, and so the RAs took advantage of that."

Since CMS began phasing in the national RA program as directed by the Tax Relief and Health Care Law of 2006, the prevalence of observation status designation has soared. According to a March 2014 report by the Medicare Payment Advisory Commission, the number of outpatient observation claims increased 88% between 2006 and 2012?a trend that runs counter to financial motivation for hospitals, which are paid less for care delivered to a patient under observation than for that provided during an inpatient stay, even if the services are equivalent in both cases.

For their part, RAs deny responsibility for the climb. ­After a July 2014 Senate hearing that addressed observation status, the American Coalition for Healthcare Claims Integrity, an RA trade association, issued a statement stressing that the contractors audit less than 2% of Medicare records from any given provider and only focus on CMS-approved billing hot spots.

"While our coalition agrees that the use of observation status has evolved from its initial intent and administrators should work to clarify these payment policies, the suggestion that the Recovery Audit Contractor (RAC) program has caused this issue is false," Becky Reeves, spokesperson for the group, said in the statement.

But this alleged audit rate of less than 2% doesn’t hold for providers across the board, according to Sheehy, who points to a recent study she led that found RAs performed complex Part A audits on 8% of the total inpatient encounters had by three academic hospitals from 2010 to 2013. Complex reviews, as opposed to their automated or semi-automated counterparts, produce the vast majority of RA recoupments.

Regardless of disputes over the reasons behind observation status spikes, CMS introduced the two-midnight rule in 2013 in an effort to curtail them. Through the provision, the agency sought to clarify that hospitals can consider beneficiaries whose stays are expected to last at least two nights inpatients without the fear of RA review. But enforcement of the rule has been repeatedly delayed since its introduction, lambasted by hospitals as arbitrary, reductive, and potentially punitive toward innovations used to reduce lengths of stay.

Because many healthcare providers maintain that hikes in observation status are tied to RA scrutiny, Sheehy thinks major reform in both domains is necessary to make progress throughout the industry.

To that end, CMS and a couple of its RA contractors are currently locked in disputes over the terms of new contracts, which propose revisions to the way RAs are paid?a possible effort by CMS to discourage faulty recoupment of payments and to unclog RA decision appeal logjams.

SNF implications

Although hospitals are at the heart of the observation status crisis, those in the postacute sector are also feeling the fallout. SNFs are often the next stop for recently hospitalized patients whose stays have been deemed observation, such as those who will require short-term intensive therapy services after a medical illness. But days spent under observation don’t count toward the three consecutive days a beneficiary must remain in the hospital before Medicare coverage for subsequent nursing home care kicks in?a rule that is itself contentious. Some say the requirement flies in the face of continuum-wide pushes to return beneficiaries to the community as often and as quickly as possible.

"The reality is that the sooner a patient is out of the hospital, the better," says Porter. "Requiring a patient to be in a hospital for three days before they can access a benefit that gets them out of the hospital and ultimately on their way home seems a bit archaic to me."

And now that the requirement is increasingly tangled with observation stays, more and more patients are disqualified from SNF coverage, forcing them to choose between paying for rehabilitation services entirely out of pocket and jeopardizing their recovery by forgoing the follow-up care deemed necessary by their doctors.

Sheehy recalls the first time she witnessed the detrimental effects of such a decision. It was 2010, and she had just treated a woman who had stayed three nights in the hospital following a recent cancer diagnosis. At the time of discharge, Sheehy decided to order nursing home services for the patient, who was weak and dehydrated. But when Sheehy informed her case manager of this plan, she was told that the patient?a longtime Medicare contributor?would have to pay the cost in full because she had been under observation during her entire stay.

"All she should have had to do was worry about getting better," says Sheehy. "Now she was worried about her bill and how she was going to take care of herself at home because she didn’t have the resources to pay for a nursing home on her own."

But not all patients are granted even this modicum of warning that subsequent services won’t be covered?a shortfall that saddles SNF providers with the task of verifying the hospital admission status of prospective clients and communicating bad news to those whose nursing home stay wouldn’t be covered by Medicare.

Brown says hospitals sometimes compound this burden by retrospectively deciding to tag a stay as observation, potentially leaving nursing home providers as blindsided as residents come billing time.

 

The NOTICE Act only sets stage for reform

These knowledge gaps are precisely what theNOTICE Act targets. The bill would amend the Social Security Act with a provision requiring hospitals to provide oral and written notice to patients placed under observation for more than 24 hours, the reason for this designation, and its implications for service coverage within 36 hours of the classification, or, if the stay is shorter, upon discharge.

Advocates say the bill is an important move toward empowering beneficiaries to make informed decisions about their healthcare.

"They deserve to know [their status] in the hospital, so I think this transparency measure is a very good one," says Sheehy, though she adds that the bill would also increase pressure on hospital employees, who would be expected to create, supply, and test comprehension of additional paperwork, thereby upholding a regulation that doesn’t sit we

HCPro.com – Billing Alert for Long-Term Care

Billing Alert for Long-Term Care, July 2015

CMS sets sights on future quality, payment initiatives in 2016 SNF PPS proposed rule

In mid-April, CMS released its proposed SNF PPS rule for fiscal year (FY) 2016. Though the rulemaking document is an annual ritual, this year’s iteration, which experts who spoke with HCPro predict will pass largely unaltered, departed from its recent predecessors in one distinct aspect: its preoccupation with long-term projects.

"It was not a … rule like we’ve had in recent years," says Judy Wilhide Brandt, RN, BA, RAC-MT, C-NE, principal at Judy Wilhide MDS Consulting, Inc., in Virginia Beach, Virginia.

In lieu of remedying small-scale, immediate concerns (like FY 2015’s COT OMRA fix), the FY 2016 proposed rule lays the framework for SNF-specific value-based purchasing (VBP) and quality reporting programs (QRP)?two more distant initiatives that, through their ongoing integrations in different settings, promise to reshape long-standing paradigms, business models, and care practices across the care continuum in the coming years.

But despite the unusual foresight of the latest SNF rule, experts say its provisions hold few surprises, as the two far-off programs they detail are products of high-profile legislation passed last year:

  • The Improving Medicare Post-Acute Care Transformation (IMPACT) Act of 2014 calls for the phasing in of various quality improvement and reporting initiatives throughout postacute care (PAC), including a SNF QRP. The legislation also requires the creation of standardized reporting metrics that allow for more equitable comparisons of care delivery strategies, patient outcomes, and overall performance across the various PAC settings (i.e., SNFs, home health agencies, inpatient rehabilitation facilities, and long-term care hospitals).
  • The Protecting Access to Medicare Act (PAMA) of 2014 added new subsections to the Social Security Act that authorize the establishment of a SNF VBP program beginning in FY 2019, under which value-based incentive payments will be distributed to SNFs based on their performance on designated quality metrics.

Payment update

In addition to these long-term projects, experts say the one major constant of annual CMS rulemaking?the payment update?was also familiar territory this year.

CMS projects that aggregate reimbursement to SNFs will increase by 1.4% ($ 500 million) in FY 2016. The proposed bump would be the result of a 2.6% market basket increase combined with two 0.6% reductions, one stemming from the forecast error adjustment, and the other from the multi-factor productivity adjustment.

But although the anticipated increase is within normal bounds?Brandt says the industry is accustomed to an annual boost between 1% and 2%?Maureen McCarthy, RN, BS, RAC-CT, president and CEO of Celtic Consulting, LLC, in Torrington, Connecticut, had hoped that SNFs would see a higher market basket raise next fiscal year. Although McCarthy says the multi-factor productivity adjustment and the forecast error affect reimbursement rates each year, she says this year’s adjustments may also be intended to fund some of the proposal’s other initiatives that center on improving quality of care and patient satisfaction. Still, McCarthy prefers this strategy over ones that would divest providers after payment was awarded or that would only target certain SNFs.

"It’s the least punitive," she explains. "It’s money we haven’t gotten yet, so it’s easier to lose."

 

Payroll-based staffing reporting

The other major change addressed in the proposed rule that will actually hit providers next fiscal year is an electronic system for submitting staffing data pulled directly from payrolls, which CMS plans to debut this October for volunteer SNF testing. The so-called payroll-based journal (PBJ) is a response to the Affordable Care Act (ACA)’s call for the introduction of more accountability into the SNF staff reporting sphere by creating a method to electronically submit data on direct care staff (including agency and contract workers). The ACA requires that such a system fulfill the following criteria:

  • Culls data that is verifiable and auditable, such as that from payrolls
  • Specifies the job classification of each employee (e.g., RN, LPN, licensed vocational nurse, CNA, therapist, or other medical personnel) and the number of care hours each employee category provides per resident day
  • Distinguishes data on agency and contract staff from that on SNF employees
  • Tracks employee turnover and tenure
  • Includes data on resident census and case mix
  • Facilitates public reporting on a regular schedule

 

Although CMS has long been developing a qualifying system and periodically updating the industry about its progress, the FY 2016 proposed rule offers a more comprehensive discussion of how the agency plans to implement these ACA stipulations. Most strikingly, the rule reiterates CMS’ recent announcement that all SNFs will be required to submit data through the PBJ beginning July 1, 2016.

Although this wholesale shift in staff reporting is coming up fast, McCarthy says the details of its execution aren’t yet set in stone. She therefore urges SNFs to parse CMS’ proposals in this domain to bring to light any potential snares, including:

  • How the PBJ will consider corporate nurses who aren’t on a facility’s payroll but may perform direct care.
  • What documentation will be required to support the new collection system. For example, will the CMS-671 and CMS-672 forms feed the PBJ until CMS develops a more tailored alternative?
  • How the PBJ will account for time worked by salaried employees. Although full-time staff are typically thought to spend 40 hours per week on the job, McCarthy says many salaried direct care staff work 50- to 60-hour weeks, meaning a facility could have higher staffing levels at any given time than the size of its workforce would suggest.

 

Despite these lingering uncertainties, Brandt believes that CMS recognizes the gravity of the industry’s upcoming transition to a much more robust?and complex?reporting mechanism. In turn, she’s optimistic that the agency will implement the new system methodically, accounting for industry feedback and not jeopardizing honest performers.

"I trust that their goal is that it be fair and reliable, so I trust that people who are staffing to acuity are going to be just fine," she says.

Despite Brandt’s confidence in the ability of worthy providers to acclimate to the upcoming shift, Bonnie G. Foster, RN, BSN, MEd, long-term care consultant in Columbia, South Carolina, doesn’t think they should have to. Foster sees the PBJ as a symbol of the government’s misplaced distrust in an industry largely composed of scrupulous providers that are trying their best to field unforeseeable staffing challenges (e.g., last-minute callouts and heavy turnover) as they arise.

But others don’t have such a high view of the SNF provider community. In addition to fulfilling legislative mandates, the government hopes that the PBJ will quell worries expressed by industry stakeholders about the validity of today’s self-reported staffing data?worries that were stoked by an August 2014 New York Times exposé that charged some in the long-term care setting with artificially inflating reported staffing levels to fare better on Nursing Home Compare’s star ratings.

Of course, many providers have denounced these charges. Some, like Brandt, believe that they represent only a small proportion of providers?providers that may soon be exposed through the verifiable PBJ data.

"The people who have been spending their time trying to manipulate the data and … figure out ways to beef up staffing before a survey … all of those tricks are going away if these measures get implemented," Brandt says.

But Foster fears the PBJ could have the reverse effect, driving providers to enlist staff whose titles look the best on paper (or screens) rather than those who are the most qualified. For example, with increasing pressure from CMS and consumer advocates to bump up levels of RN staffing and supervision at SNFs (which will be more easily identifiable in an electronic reporting system), LPNs with years of nursing and management experience may fall by the wayside, Foster explains.

"I don’t want people to put staffing down there to satisfy the system," she says. "That part scares me a lot."

Regardless of her qualms about the forthcoming reporting system, Foster says providers have some work to do to brace for the additional staffing scrutiny ahead.

For example, while SNFs have adopted flexible intake practices to stay competitive in an evolving industry (e.g., admitting new residents late at night and on weekends), Foster says many haven’t synced their staffing schedules with these new patterns, potentially leaving a workforce that is undermanned or underqualified to cope with peak admission periods.

"If you’re going to continue to admit at those strange hours, then you better be sure that all of your staff understand everything," she says.

In addition to improving general staffing strategies, Brandt says providers should focus on understanding the specifics of the forthcoming PBJ.

"People need to read the draft manual on submitting staffing data, and it’s not too early to start preliminary talks about how they’re going to comply," she explains, encouraging providers to begin priming staffing data for the new collection process by identifying the employees who will be responsible for reporting through the system, kick-starting training initiatives, and setting away necessary budget today.

 

QRP

To satisfy provisions of the IMPACT Act that task CMS with collecting quality data, the agency is proposing to build a SNF QRP that considers the three quality measures outlined in the table below.

Under the QRP, SNFs would be required to submit certain data on these measures beginning in FY 2018, as well as on any other focuses CMS finalizes in future rulemaking. In addition, the IMPACT Act dictates that providers failing to comply with these reporting requirements will be penalized with a 2% reduction in their annual payment update.

These prospective QRP requirements will carry significant changes in SNFs’ approaches to quality improvement. The proposed fall and functional status measures have not yet been approved by the National Quality Forum for SNFs, and the latter measure could see in an additional MDS component: Section GG. This new section, which would prompt SNFs to evaluate the functional abilities and goals of residents at the start and end of care, would also foretell a new required assessment for facilities to complete when a beneficiary is discharged from a Medicare Part A stay but does not leave the facility?a status shift that CMS says affects 30% of SNF residents.

Brandt has encountered some providers that are wary about the prospect of an additional assessment on top of their already heavy documentation load?not to mention the associated data capture, training, and resource distribution changes it could carry. However, she thinks these fears are overstated because much of Section GG is pulled straight from the Continuity Assessment Record and Evaluation (CARE) item set, a tool that’s been in development since the 2005 enactment of the Deficit Reduction Act compelled CMS to examine the consistency of payment incentives across the various Medicare providers. CMS states that the CARE tool, which is an output of this directive, is "designed to standardize assessment of patients’ medical, functional, cognitive, and social support status across acute and post-acute settings." And Brandt says it has long been on the radars of central SNF departments.

"The CARE tool has been around for a long time now, and if you read through [Section GG], it’s what therapy has been doing, maybe in different formats, every time they do an evaluation in the discharge summary," she says, explaining that, consequently, many rehab providers already have the tool in their software and have been collecting data through it for some time.

"The MDS community needs to realize that adding a section to the MDS doesn’t mean that it’s going to add more to the job of the MDS coordinator," she says.

Beyond the new quality considerations CMS has posed, the agency also seeks to redefine the current bounds of the industry’s skin integrity measure. Although SNFs are presently required to submit data on changes in their residents’ skin integrity, this measurement is restricted to the development of stage 1?4 pressure ulcers that occur or worsen during facility stays. CMS is proposing to broaden this reporting criteria for SNFs (and other PAC providers) to include:

  • Unstageable pressure ulcers
  • Suspected deep tissue injuries
  • Stage 1 or 2 pressure ulcers that become unstageable due to slough or eschar (indicating progression to a stage 3 or 4 pressure ulcer) after admission

 

CMS points out that since SNFs are already required to complete items related to unstageable pressure ulcers in the MDS, the revision would require a change in the way the agency calculates the measure but would not increase the data collection burden for SNFs.

In addition, by capturing more incidences of decline, CMS says these proposed updates?which are backed by a number of experts and the agency’s own data analyses?could potentially reveal a wider range of SNF performance, improving "the ability of the quality measure to discriminate between poor- and high-performing facilities."

Brandt thinks this attempt to better discern the success of pressure ulcer prevention throughout the provider community demonstrates CMS’ overarching proposal strategy: to elevate hard workers and undercut bad actors.

"Facilities that have been sincerely and tirelessly working on achieving the highest quality of care are going to rise to the surface," she says. "There are nursing facilities all over this country that have been … doing what they can to prevent injuries from falls, preventing pressure ulcers, and I think they’re going to shine."

In addition to putting the necessary frameworks in place to highlight today’s top-performing facilities, ­McCarthy says the QRP proposals can serve as a road map for providers on shakier ground to launch targeted quality improvement initiatives.

"I think providers should take a look at what’s going to be reported for 2018 … and then look at those quality metrics within their own organizations," she says, adding that facilities should pay particular attention to the proposed methods of collecting and scoring quality data.

"They have the opportunity to correct some issues before [there’s] mandatory reporting if CMS will allow it," she continues, explaining that the agency is soliciting public comments through the proposed rule on whether to give providers this head start.

However, Brandt cautions facilities to avoid putting too much stock in the formulas for calculating these quality measures until they are finalized.

 

VBP

In addition to putting the finishing touches on the QRP’s initial aims, CMS is considering another quality-related focus intended to shape future payments dispensed through the setting’s forthcoming VBP program: the SNF 30-day all-cause readmission measure (SNFRM), which CMS specifies would assess the rate of unplanned readmissions among SNF residents that occur within 30 days of discharge from an inpatient hospital. However, McCarthy says CMS has failed to disclose whether the measure would also penalize providers for hospital readmissions that occur within 30 days after discharge from the SNF itself.

To gather preliminary data for the potential introduction of this metric?whose development was first kindled by PAMA?in October 2016, CMS plans to require facilities to report certain rehospitalization rates starting this October.

Beyond the prospect of an imminent reporting start date tied to its contents, Brandt thinks the SNFRM is significant for another reason: It would be calculated using data from claims rather than MDS documentation, an unprecedented move in the SNF quality domain and one that wouldn’t require any additional data collection or submission by providers.

"It’s kind of historic that we’ve finally got our first measure that is not MDS-based," says Brandt, who believes that the financial tie-ins carried by both the VBP and QRP will further undermine bad actors by stripping them of their primary motivation: monetary reward.

"I think the people who are in long-term care for the goal of providing the service of quality care and who are interested in quality outcomes are going to rise to the surface," she says. "I think people who are in long-term care for any other reason are going to be leaving."

Foster is more ambivalent about the financial incentives (and disincentives) that will soon underlie key performance metrics in the sector. She says that although the forthcoming measures?and their monetary drivers?target long-standing industry shortcomings, she thinks they paint with too broad a brush.

"It’s your entire building is doing a good job, or your entire building is not doing a good job," she says.

Foster worries that this stance could penalize facilities that take on the most compromised residents or reward those whose emphasis on producing favorable bodily outcomes jeopardizes the psychosocial health of the individuals they serve.

 

Today’s strategies for future success

Despite the far-off focuses of CMS’ latest SNF rulemaking, experts warn providers against lapsing into complacency in the absence of more urgent proposals. They stress that the changes, although distant, are likely to become finalized without major revision. Further, the sweeping scope of QRP and VBP demands preparation from providers today to facilitate compliance and operational stability down the road.

To address the spirit of these changes?the facilitation of effective and efficient care?Foster urges SNFs to implement new restorative nursing programs (or modernize existing ones) with an eye to addressing CMS’ focuses, such as functional status and rehospitalization. Foster says this latter quality indicator, in particular, has been an historic pain point in the industry.

"We’re just worried about the people that keep going back and forth to the hospital as [if through] a revolving door," she explains. To combat this issue, Foster says restorative programs should target services that have traditionally landed residents back in the hospital even though SNFs are equipped to render them, such as providing extra hydration through IVs.

Currently, Foster?who has extensive experience helping facilities implement restorative strategies?says many providers are failing to capitalize on the benefits of a formal restorative program, instead opting for one-off interventions (e.g., designating nursing staff to take residents for a walk once or twice a week) and dedicating the bulk of their resources to enriching therapy offerings. Although some experts say that therapy has been gaining priority throughout the industry as an adaptation to today’s influx of patients seeking short-term intensive SNF rehab services, Foster argues that restorative nursing is a more sustainable practice in some respects. For example, she says that Medicare-covered SNF therapy services have federal cost caps, while restorative programs oftentimes have no mandated expiration date.

Thus, Foster urges providers to shift some of their focus to modeling restorative programs after their often more robust therapy counterparts (e.g., by framing the program with concrete, measurable goals). Not only does Foster believe a restorative mindset will align a facility’s practices with large-scale regulatory shifts, but she says it can breed better connectivity between therapy and nursing departments, thereby fostering a unified vision of care.

In order to build a restorative program that can achieve these manifold benefits in time for the implementation of QRP and VBP measures, Foster says providers need to get started soon.

"It’s going to take you a year to get it right," she explains, citing chronic industry shortfalls as barriers to speedy implementation.

In particular, Foster says providers need to strengthen communication with physicians and the families of residents. She believes many rehospitalizations can be attributed to insistence by families that a SNF readmit a resident to the hospital for any change in condition?even one a facility is capable of remedying.

"When nurses call the families to let them know … "Something’s changed in your loved one," families are notorious for saying, ‘We’ll just send them to the hospital,’ and that’s what [SNFs] do," she says.

To combat families’ reflexive panic and facilities’ equally knee-jerk acquiescence, Foster urges SNFs to sit down with partnering physicians to write a concrete strategy for addressing condition changes. The document should list the specific events a facility can handle on its own and detail the procedures it will use to do so. This will arm SNFs and physicians with an official document to assure families that the SNF is well-equipped to stabilize their loved one’s condition after certain adverse events.

But SNFs’ current communication shortfalls aren’t restricted to external stakeholders, according to Foster, who also charges the industry with insufficient education, particularly among frontline staff. In turn, these lapses can trigger subpar care, inaccurate documentation, and high turnover among mismanaged and frustrated employees. For example, Foster says that documentation among a facility’s CNAs can be erratic and inconsistent, especially regarding a given resident’s functional status, which must be captured multiple times each day and can be evaluated very differently by varying frontline staff members.

To begin clearing up disparate clinical understandings, Foster recommends focusing training efforts around the component of the MDS that corresponds to functional status. "If nothing else, just teach Section G," she says?a directive that seems particularly fitting, given the potential implementation of Section GG, which would build on the functional data already captured today.

Beyond ramping up education, Foster proposes an unconventional solution for warding off critical quality lapses: establishing a mentor program that assigns a qualified staff member to remain by each newly admitted resident’s side for the first two days of his or her stay, a period during which Foster believes the lion’s share of adverse incidents occurs.

"Everything bad happens within the first 48 hours of admission," she says, explaining that she’s seen mentor programs targeted to this time frame reduce fall rates.

But before getting too caught up in planning any full-fledged program refurbishments, McCarthy urges providers to take advantage of the public reporting period on the proposed rule?in effect through June 15?to point out to CMS any perceived issues, discrepancies, or oversights (e.g., surrounding the PBJ and SNFRM) that could jeopardize the future success of their facility.

"Providers really should use that opportunity to voice their concerns to CMS on what issues they think may negatively impact them," she explains. "Because once they become public, they become public, and there’s no opportunity to correct the information that’s out there."

In many respects, the proposed rule provides a first glimpse into CMS’ big-picture plans for the industry in the years ahead. Although it glazes over some key nuances of the agency’s potential execution strategy, Brandt is optimistic the proposal will ultimately introduce new, more reliable methods of upholding virtuous SNFs that have been overshadowed in recent years by the industry’s small, yet potent faction of abusers.

"I think that all the good, decent, honest nursing home operators have ever asked for was a fair chance and to be measured realistically on a level playing field, and I think this is a great step in that direction," she says. "I’m excited to see what’s going to happen in our industry in the coming years."

 

Navigating the LTC technology landscape:How SNFs are using HIT, POC tools

When it comes to technology, SNFs and their fellow postacute care (PAC) providers are rapidly approaching a crossroads: Find a way to overcome resource gaps to speed adoption efforts, or risk facing new compliance issues down the line as the use of innovative technologies to facilitate data sharing, performance comparison, and patient-centered care across settings and sectors become staples in the modern provision of healthcare.

The increasing precedence of technology is not only reshaping traditional attitudes toward healthcare delivery along the continuum, but could derail providers that don’t keep pace with innovations that fuel new approaches.

“Technology has become a business imperative, frankly,” says Majd Alwan, PhD, senior vice president of technology at LeadingAge, a Washington, D.C.?based trade association for nonprofit aging services providers, and executive director of the organization’s Center for Aging Services Technologies (CAST). “Without the right technologies, you will not be getting in your referrals … either because you do not have the competencies and are ­costing your trading partners money … or because you don’t have the proper documentation and analytics to demonstrate that you have better results than competitors.”

 

Historic PAC gaps

Although legislators are working to catalyze technology adoption through policy and regulation, PAC providers have historically been passed over for the associated financial incentives (e.g., CMS’ twilighting electronic health record [EHR] incentive programs) in favor of their acute care counterparts.

Until recently, SNFs have also been overlooked in national research on technology adoption. Alwan says the most recent data on usage among nursing home providers across the country is a 2009 research paper whose findings are based on survey results from 2004.

But policymakers aren’t blind to these lapses, says Jennie Harvell, senior policy analyst in the Office of the Assistant Secretary for Planning and Evaluation in the U.S. Department of Health and Human Services (HHS). She explains that while widespread technology adoption initiatives have so far homed in on the acute and primary care spheres, PAC providers are increasingly the targets of federal grants awarded to state- and community-based implementation projects.

“I think [HHS] is aware of … who the EHR incentive programs targeted, and who the EHR incentive programs did not, and so they have made some grant programs available that support technology development and use by long-term and postacute care providers,” she says.

In addition, she explains that CMS reinvigorated national technology research efforts in the sector this year by launching a voluntary survey to analyze if and how PAC providers are using health information technology (HIT) to coordinate care transitions and support their clinical services?an effort that the agency hopes will help it better understand the current benefits and barriers to adoption. The survey will close on April 3.

 

Mounting incentives

CMS’ recent initiatives aren’t the only moves that suggest an increased push to understand and further flesh out the role technology plays in long-term care.

More legislative evidence includes the PAC-centered Improving Medicare Post-Acute Care Transformation (IMPACT) Act of 2014, which sailed through a notoriously fragmented Congress last year and is slated to propel the development of standardized, interoperable assessment data for the sector.

Also in 2014, the Obama administration issued a handful of executive actions that CMS has begun using to recalibrate the star rating system featured on Nursing Home Compare.

The actions also allocated funding from the IMPACT Act to kick-start CMS’ development of an electronic reporting system that will collect nursing homes’ staffing numbers based on payroll data and post this information on Nursing Home Compare. Development is currently underway, and CMS expects to mandate nationwide nursing home reporting through the system by the end of fiscal year 2016.

In addition to setting-specific incentives on the horizon, Alwan says the overarching shift in care priorities illustrated by new payment and care delivery models offers significant indirect motivation for SNFs as well. He points to increasing opportunities for high-performing facilities to reap financial rewards and referrals through bundled payments, participation in accountable care organizations (ACO), and contributions to hospital success in readmission reduction programs.

 

Major technology landmarks in healthcare

Because of this increasing precedence, the healthcare technology market is awash with tools intended to spur operational efficiency and clinical success.

For example, according to the Office of the National Coordinator for Health Information Technology (ONC), HIT is an umbrella term that encompasses a host of technologies that can facilitate the storage, sharing, and analysis of health data by patients and their providers.

Notable HIT subsets and offshoots include:

  • Health information exchange

HCPro.com – Billing Alert for Long-Term Care

Billing Alert for Long-Term Care, August 2015

OIG releases its FY 2015 mid-year update

The Office of Inspector General (OIG) released its fiscal year (FY) 2015 Mid-Year Update last week. The update summarizes new and ongoing reviews and activities that OIG plans to pursue with respect to HHS programs during the current fiscal year and beyond.

The OIG’s job is to detect fraud, waste, and abuse; identify opportunities to improve healthcare program economy; and to hold "accountable those who do not meet program requirements or who violate Federal health care laws." The OIG conducts audits and investigation, and can impose civil monetary penalties where appropriate, so its Work Plan is often of great interest to those working with federal healthcare programs. As a summary of some of the OIG’s enforcement initiatives, the Work Plan can serve as a useful resource for companies when training and when planning internal audits. 

The FY mid-year update includes several initiatives central to long-term care providers.

 

Medicare Part A billing by SNFs

The OIG will describe changes in SNF billing practices from FYs 2011 to 2013. Prior OIG work found that SNFs increasingly billed for the highest level of therapy even though beneficiary characteristics remained largely unchanged. The OIG also found that SNFs billed one-quarter of all 2009 claims in error; this erroneous billing resulted in $ 1.5 billion in inappropriate Medicare payments. CMS has made substantial changes to how SNFs bill for services for Medicare Part A stays.

CMS’ future plans include:

  • phasing in bundling options
  • continued growth and development of ACO models of reimbursement tied to outcomes and quality of care
  • the elimination of using the amount of therapy delivered as an incentive for payment
  • conducting outcome studies on therapy delivered under Medicare Part B

 

Diane Brown, director of postacute education at HCPro explains that, "These plans will likely contribute to better care and improved transitions in care as well as be linked to appropriate payment. When implemented, much of the time spent by facilities on navigating COTs and other labor intensive tasks could be eliminated."

As Kathy W. O’Neal, RN, RAC-CT, LNHA, from Crossroads Medical Management can attest to, "There were numerous changes with Part A billing practices associated with the implementation of MDS 3.0. Probably the most significant was that on the five-day assessment, projecting therapy minutes were removed. Another significant change is that a change of therapy (COT) assessment is required every seven days if a resident in a rehab RUG category that receives more or less therapy minutes and/or the number of modalities changes enough to cause the resident to fall into another RUG category. This practice was created as a response to the thought process that SNFs were being paid for a therapy that was not needed and/or provided. These changes have created a tremendous increase in the number of assessments needed, with the resulting billing rules associated that are confusing for providers. A large percentage of my time is consumed with audits and appeals associated with Part A stays, mainly Medicare replacement policies, and often it seems that the insurance companies providing the replacement policies do not understand PPS billing. It is very frustrating but has become a routine part of our industry."

 

State agency verification of deficiency corrections

The OIG will determine whether state survey agencies verified correction plans for deficiencies identified during nursing home recertification surveys. A prior OIG review found that one state survey agency did not always verify that nursing homes corrected deficiencies identified during surveys in accordance with federal requirements. Federal regulations require nursing homes to submit correction plans to the state survey agency or CMS for deficiencies identified during surveys. CMS requires state survey agencies to verify the correction of identified deficiencies through on-site reviews or by obtaining other evidence of correction.

 

Program for national background checks for long-term-care employees

The OIG will review the procedures implemented by participating states for long-term care facilities or providers to conduct background checks on prospective employees and providers who would have direct access to patients and determine the costs of conducting background checks. Further, the OIG will determine the outcomes of the states’ programs and determine whether the programs led to any unintended consequences. Section 6201 of the Patient Protection and Affordable Care Act (ACA) requires the Secretary of Health and Human Services to carry out a nationwide program for states to conduct national and state background checks for prospective direct patient access employees of nursing facilities and other long-term care providers.

The program is administered by CMS. To carry out the nationwide program, CMS has issued solicitations for grant awards. All states, the District of Columbia, and U.S. territories are eligible to be considered for a grant award. OIG is required under the ACA to submit a report to Congress evaluating this program upon its conclusion. This mandated work is ongoing, and an interim report will be issued prior to the program’s conclusion.

O’Neal approves of this initiative, saying that, "I agree with any additional background screening to ensure our residents are cared for in a safe and caring environment."

Although the OIG’s oversight extends to other programs under the U.S. Department of Health & Human Services, the majority of its resources go toward combating fraud, waste, and abuse in Medicare and Medicaid.

You can review the entire mid-year update to the 2015 Work Plan on the OIG’s website.

 

Medicare myths

Editor’s note: This article is excerpted from the book Long-Term Care Skilled Services: How to Document for Proper Medicare Reimbursement, by Elizabeth Malzahn-McLaren.

 

Throughout my years of educating providers on the inner workings of the Medicare program, whether it was a boot camp class for newcomers or a refresher course for those in the business for years, there are always instances where I am able to "myth-bust" Medicare. With any program, especially one that has been in existence for 60 years, there are bound to be some myths out there about how the program works.

 

Myth #1: A psychiatric resident will not qualify for Medicare Part A skilled services.

Although most psychiatric services will not qualify as Medicare Part A skilled services, there are some instances when a resident will qualify coming straight from the hospital, at least for a short period of time.

First you need to determine if the stay in the psychiatric hospital meets the three-day qualifying hospital requirement. If it does, the next area to review is whether the care meets the requirements for skilled services under Medicare Part A.

The resident may need to have his or her medications adjusted; there also can be potential for an adverse drug reaction if medications were changed. In addition, depending on the time spent in the hospital, there may have been some deterioration and the resident may have therapy orders upon discharge from the hospital. Other areas to review include hearing, speech, and vision (Section B of the Minimum Data Set [MDS]); ­cognitive patterns (Section C); mood (Section D); behavior (Section E); functional status (Section G); and medications (Section N) … just to name a few!

 

Myth #2: You can cover a resident for the first five days to observe and assess his or her condition.

The Centers for Medicare & Medicaid Services (CMS) provides no time frame of minimum or maximum time covered; however, there is the ability to use administrative presumption of coverage. Remember, though, that the use of the administrative presumption is reserved only for residents being directly admitted from a three-day qualifying hospital stay. In addition, this administrative presumption only covers up to and including the assessment reference date (ARD), if no skilled need is identified on the initial admission/readmission MDS. The regulation indicates that a resident can be skilled "until the condition of the patient is stabilized." Typically, skilled care for observation and assessment lasts for a few weeks or less.

 

Myth #3: A new diagnosis triggers a new benefit period.

This is one of the most dangerous Medicare myths out there. It can impact not only resident care, but also customer service, and it can have a significant financial impact as well. The only way a resident can earn a new 100-day benefit period under SNF Medicare Part A is to complete a 60-day period of wellness. The calculation for earning a new benefit period is based on two criteria:

  • Determining when skilled services ended
  • Counting days

There is no magic formula to earning a new benefit period. Let us review an example to illustrate how the calculation should work.

A resident completed a 100-day Medicare benefit period on December 31. The resident remained skilled under Medicare Part B, receiving therapy services until January 31. Beginning February 1, the resident was no longer at a skilled level of care. Based on the counting of 60 days, the resident would be eligible for a new benefit period on April 2 (assuming 28 days in February). However, we need to review each day between February 1 and April 2 to make sure none of the following occurred:

  • Did the resident receive any services that would qualify the resident under a Medicare skilled level of care while in the SNF during that time period? For example, was the resident picked back up under a Medicare Part B plan of care that met the skilled level of care requirements?
  • Did the resident have any inpatient admissions to the hospital during that time period?

 

If the answer to either of these questions is yes, then the resident did not earn a new 100-day benefit period based on either the provision of skilled services or failure to meet the 60-day period of wellness requirement.

There is one small wrinkle in this calculation of benefit periods. If a resident leaves the SNF and continues to receive a skilled service while residing at home, for example, this would not impact the benefit period. When reviewing skilled services received, Medicare is only looking at skilled services received while in a SNF or as an inpatient of a hospital. Skilled services rendered to a beneficiary in the home setting do not impact the Medicare Part A SNF benefit period calculation.

 

Myth #4: All residents who are receiving tube feeding are always skilled and always will be skilled.

This statement is both true and false. The caveat lies with the level of calories and fluid the resident is taking in through the tube. Residents who meet the 26%?50% of calories and 501 cc of fluid per day via the feeding tube, or residents who receive 51% or more of calories via the feeding tube will automatically qualify for ­Medicare Part A benefits in a SNF. Additionally, they are required to continue on Medicare to use a full 100-day benefit period until they drop below such levels on an MDS. These levels will also continue that spell of illness and prevent the resident from attaining the 60-day period of wellness to qualify for a new 100-day benefit period.

Residents who meet the caloric and fluid requirements of 26%?50% of caloric intake and 501 cc of fluid daily via the tube or residents who receive 51% of more of caloric intake from the tube will remain at a skilled level of care for a full 100 days, as long as they remain at those levels. In addition, the resident will not qualify for a new 100-day benefit period unless he or she:

  • Drops below the calorie and fluid levels previously identified for 60 consecutive days without any other skilled service in the SNF or inpatient hospital stay
  • Remains at those calorie and fluid levels identified previously but discharges to home with skilled services being provided in the home for 60 consecutive days

 

Myth #5: As long as there is an inpatient hospital stay or Medicare Part A SNF stay within the last 30 days, we can pick the resident back up on Medicare Part A.

Although this is partly true, the most important criteria to using the 30-day window is relating the reason for coverage back to the original hospitalization or a condition that arose during treatment. If the reason to pick the resident back up under Medicare Part A is completely unrelated to the original hospitalization or subsequent SNF stay, the criteria outlined in the regulation regarding the 30-day transfer rules are not met, and the resident should not be put back on Medicare Part A.

 

Myth #6: A resident on Medicare Part A in a SNF can never leave the SNF for an overnight leave of absence.

Often, a resident is unable to leave the SNF due to the complexity of the services being rendered in the SNF. That said, a couple of items need to be reviewed before determining if an overnight leave of absence (LOA) is feasible:

  • Can the resident safely be away from the SNF, and can the family or responsible party be taught to safely meet the resident’s needs while out of the SNF?
  • Are the absences infrequent in nature and not for prolonged periods of time?

 

Obviously, the first question is important to make sure the resident can be properly cared for during the LOA. It is always necessary to consult with the resident’s physician to notify him or her of the LOA request and get some feedback from the physician’s point of view on whether the LOA is feasible. The second question relates more to being sure that the practical matter criteria also discussed in Chapter 3 is being met. If a resident is able to leave the SNF on a weekly basis for an overnight visit, or if the resident leaves for prolonged periods of time three times per week to attend an off-site bingo game, for example, it is doubtful that the practical matter criterion is being met. Remember, one of the four criteria related to meeting the skilled services requirement in a SNF is the practical matter criterion in Section 30.7 of the Medicare Benefit Policy Manual (Pub. 100-02):

As a practical matter, considering economy and efficiency, the daily skilled services can be provided only on an inpatient basis in a SNF (see §30.7).

 

That said, although a resident may safely be able to go on LOAs frequently or for prolonged periods of time, the question becomes: Is the SNF the most appropriate place for that resident to receive those skilled services?

 

Myth #7: You never have to issue more than one notice regarding a Medicare stay at the same time.

If only that were a true statement. There are so many notices that it can be confusing trying to understand which notice is issued under what circumstances. To further complicate things, there are times when more than one notice will be issued at relatively the same time. Chapter 30, Section 261 of the Medicare Claims Processing Manual:

Delivery of the NOMNC does not replace the required delivery of other mandatory notices, including ABNs. Notice delivery must be determined by the individual NOMNC requirements per this section and ABN delivery requirements per §1879 of the Act and per guidance in this chapter. Both the NOMNC and an ABN may be required in certain instances.

 

This same manual section notes the following example of when both notices would be issued:

A beneficiary’s Part A stay is ending because skilled level care is no longer medically necessary and the beneficiary wishes to remain in the SNF receiving custodial care. The beneficiary must receive the NOMNC two days prior to the end of coverage. A SNFABN must also be delivered before custodial care begins.

 

Myth #8: There is never an instance where no notice is required at the end of Medicare coverage.

This is untrue! When a beneficiary exhausts his or her 100-day benefit period in the SNF, there is no notice required. The Beneficiary Notification Initiative (BNI) process allows beneficiaries to be notified and have the ability to appeal decisions being made by providers in relation to their Medicare coverage; the end of the 100-day SNF benefit period is not a provider decision, but rather a statutory end of coverage based on the Medicare guidelines, and there is nothing that the beneficiary can challenge or appeal. That said, it is recommended to communicate the end of the 100-day benefit period to the beneficiary, but no formal notice or form is required.

 

Bolster billing compliance: Implement a Medicare Part A triple-check process

Medicare billing is a domain rife with payer offshoots and evolving regulations that can be difficult to navigate without a strategy to weather claim scrutiny and withstand the gaze of CMS’ various auditing contractors.

Enter the triple-check process, a time-tested internal auditing strategy used by proactive long-term care providers to facilitate billing accuracy and compliance the first time a UB-04 claim form is submitted. As its name suggests, triple check is a layered verification process that involves staff members from billing, nursing, and therapy departments?the three core disciplines required to submit a clean claim. But this sturdy foundation is also pliable, allowing a facility to easily adapt the procedure to the various types of claims it files.

Read on for an expert iteration of the triple-check process, which is modified from the HCPro book The Medicare Billing Manual for Long-Term Care, written by Frosini Rubertino, RN, BSN, C-NE, CDONA/LTC. This specific triple-check procedure is designed to mobilize key staff to ensure accuracy and timely submission of Part A claims.

 

Procedure

Each month, the SNF will collect all Medicare Part A billing information ready for submission and enlist the following individuals to carry out their designated roles in verifying the accuracy of these items: administrator, director of nursing, MDS coordinator, facility rehab director or designee, business office manager, medical records personnel, and central supply staff.

The following is a breakdown of each of these staff members’ responsibilities in the triple-check process:

Business office manager and medical records personnel

  • Verify that the qualifying stay information recorded on the UB-04 aligns with that on the medical records face sheet.

 

Business office manager

  • Verify that each resident has benefit days available in the HIPAA Eligibility Transaction System.
  • Verify the admit date on the UB-04 aligns with the date in the manual census log.
  • Verify covered service dates listed on the UB-04 align with those in the Medicare and manual census logs.
  • Verify that a resident’s financial file contains a signed and completed Medicare Secondary Payer form whenever applicable.

 

Business office manager and MDS coordinator

  • Verify that ADLs are correct and are supported by documentation. Confirm that staff have coded all other contributory items (e.g., mood, IVs).
  • Verify that ARDs on each MDS align with the occurrence dates found at form locators (FL) 31?34 on the UB-04.
  • Verify that the RUG level listed on each MDS aligns with that found at FL 44 on the UB-04.
  • Verify that the assessment type for each MDS aligns with the modifier found at FL 44 on the UB-04.
  • Verify that the number of accommodation units listed on the UB-04 aligns with the assessment type for each MDS. Verify that the total number of accommodation units aligns with corresponding covered service dates.

 

Facility rehab director, MDS coordinator, and business office manager

  • Verify that physical therapy minutes listed on the daily treatment grid align with those noted in the service log. Align the days and minutes documented in the MDS with those on the treatment grid. Align the number of units billed on the UB-04 with those in the service log.
  • Verify that each principal diagnosis is accurate, that all secondary diagnoses support skilled care, and that every ICD-9 code corresponds to an appropriate diagnosis.
  • Verify that occupational therapy minutes recorded on the daily treatment grid align with those in the service log. Align the days and minutes in the MDS with those on the treatment grid. Align the number of units billed on the UB-04 with those in the service log.
  • Verify that speech therapy minutes listed on the daily treatment grid align with those noted in the service log. Align the days and minutes in the MDS with those on the treatment grid. Align the number of units billed on the UB-04 with those in the service log.

 

DON and medical records personnel

  • Verify each resident’s need for Medicare skilled intervention by reviewing supporting clinical documentation that corresponds with the dates of service listed in the manual census log.
  • Verify that each (re)certification form has been completed and signed by the appropriate physician.
  • Verify that each physician order has been obtained and implemented.
  • Verify that each chart reflects appropriate charting guidelines. Confirm that charting has been completed at least once in every 24-hour period, relates to skilled service provided, and supports therapy.

 

Facility rehab director

  • Verify that physician orders include rehabilitation.
  • Verify that each evaluation notes the prior level of function.
  • Verify that clinical documentation contains a progress note establishing the need for continued skilled intervention.

 

Administrator

  • Chair the triple-check meeting (detailed below), and ensure that the entire process is completed by appropriate staff each month before Medicare claims are submitted. Participation in the triple check will allow the administrator to monitor the effectiveness of key operational processes carried out by the facility’s ­interdisciplinary team (IDT) on an ongoing basis.

Triple-check meeting and audit tool

Each of the SNF’s triple-check participants should complete their respective duties prior to the Medicare triple-check meeting, which will be held monthly before the SNF bills for a given batch of services. In other words, the meeting is not an occasion for staff to complete their initial claim component(s). Instead, it’s a chance for IDT members to cross-check the work of their colleagues by verifying the accuracy of claim items that others have completed, thereby ensuring each element has been studied by multiple sets of eyes.

The triple-check meeting will also serve as the platform for the SNF’s business office manager to document the completion of each integral item on a billing claim using the triple-check audit tool, an internal checklist-type document that will be included in every month-end closing report.

Using this audit tool, the manager will denote items verified as correct during the triple-check meeting with an "X." He or she will mark items identified as incorrect with an "O" and, in the remarks section of the document, record the steps the team will take to obtain the correct information. Items initially found to be incorrect but rectified during the meeting should still be marked with an "O" to better track any practice patterns that could lead to billing slipups and inform future training activities.

The business office manager will call for any claim found to have errors during the triple-check meeting to be put on hold until it is amended. Once staff have made necessary revisions, the manager will indicate these correction(s) and the corresponding date(s) in the remarks section of the audit tool. He or she will then contact a corporate entity to review the changes and ultimately grant approval to submit the claim.

 

SNF therapy contracts: Your risks and what you need to know Q&A

Editor’s note: The following Q&A was written by Reginald Hislop III.

 

Q: When we receive proposals from various therapy companies, they all represented that they would increase our Part A and Part B billings. Should this somehow be incorporated into the ­contract?

 

A: Yes. Absolutely. If they’re willing to say that to you and they tell you, "That’s the reason why you’re going to go with us is because we’re going to do this," I am going to hold them accountable for that, and I first want to know how you determine that and how are you going to do that because I’m going to tell them right there before we even get to a contract, I’m going to say that they need to fundamentally prove it. How do you know it, how’s it going to happen, and be prepared because yeah, you’re going to put in the contract, you’re going to represent it, it’s going to be legal and you’re going to do it over what period of time? I’m then going to hold them accountable for it.

Otherwise, it becomes a common game of therapy contractors: "We’re going to make your world so much better than the last group that was in here." I’ve never seen a contractor come in and say, "We looked at your last experience with your last therapy contractor and the amount of stuff that they were doing, and by the way, we got to tell you, it really makes us nervous, and fundamentally if you go with us, we’re going to shrink your revenue by 15% because we think there’s a whole bunch of erroneous and falsely billed claims." I’ve never seen that happen. Everybody comes in and says, "Yes, we can improve your performance over this group, and we’re going to do it by a pretty impressive margin, and your revenue is going to go up, your claims are going to go up." I want to know how they’re going to do that, I want it in the contract, and I want full transparency. I want to know over what time period, because without that, they haven’t actually validated they will be able to do that. That’s a standard pitch, and they have never yet been expected in many cases to be accountable for those kind of numbers. It’s just a sales pitch, but, if they’re going to say it, I want it in the contract.

 

Q: Would the indemnification clause you mentioned, indemnification not just for the therapy component but the whole amount?how can the therapy company indemnify money they did not receive?

 

A: How can they indemnify money they did not receive? We’re not talking about necessarily indemnification for money they received. We’re talking about indemnification for services that they provided as part of the representation that all of our services that we provide are going to be compliant and in concert with the law. Since the SNF is responsible for that, my responsibility then is to negotiate with that company and say, "By the way, if in fact we’re involved in this work and you’re going to be part of this process and you’re going to have input in terms of what we RUG, what we bill, part of our triple check and all the rest of that other kind of stuff, there is dollars on the table, and anything that you did that was illegal, unethical, or improper that caused us to lose revenue as a result of your actions and your documentation, all those other kinds of things because you’re going to represent to me that you’re going to do this, you’re going to properly manage and supervise your employees and all those other kinds of things, that if in fact you didn’t do that, you’re going to be responsible not just for what we paid you but also for what your bad acts caused this facility." Yes, I can indemnify them for that because they are part and parcel to that. They’re going to represent to me that they’re going to do this the right way, and if they don’t, then they’re going to have shared risk for anything that occurs that they were responsible for or could be tied to them that cost my facility money or my organization money.

 

Q: How do we hold the therapy provider accountable for an 80% productivity level?

 

A: You actually monitor their productivity levels. Their treatment records should be open. Their minutes should be open. I should be able to see when they were on-site, what their time was spent on this site, what I was billed for because I’m being billed for their time. And I should be able to go to treatment logs and treatment records and look at what their billing time was and th

HCPro.com – Billing Alert for Long-Term Care

Medical Polymers Market To 2015 – Polyvinyl Chloride (pvc) Dominating The Medical Devices

Summary

GBI Researchs report, Medical Polymers Market to 2015 provides in-depth analysis of the global medical polymers market with revenue forecasts up to 2015. It analyses medical polymers market based on product types. Revenue forecasts, which include historical statistics of the market, are provided for all the major regions of the world. The factors that drive and restrain the growth of the medical polymers market are also analyzed in the report. In addition, the research provides market share analysis of the leading medical polymers producers for all the major regions of the world.

Scope

– Medical polymers market globally and for key regions.
– Medical polymers market revenues data from 2005 to 2009 and forecast for six years to 2015.
– Coverage of the various product types.
– Detailed analysis of the key drivers, restraints and challenges for the medical polymers market in all the major regions.
– Information on the competitive landscape with the revenue shares of the leading companies in the major regions of the world.

Reasons to buy

– Develop business strategies by understanding the trends and developments that are driving the medical polymers market.
– Design and develop your product development, marketing and sales strategies.
– Develop market-entry and market expansion strategies.
– Identify key companies best positioned to take advantage of the emerging market opportunities.
– Benchmark different geographies by the historic and forecasted growth of the global medical polymers market.
– Capitalize by identifying the medical polymers market segments poised for strong growth.
– Identify macro and micro-economic trends shaping and driving the global medical polymers market.

Table of Contents :

1 Table of Contents 6
1.1 List of Tables 9
1.2 List of Figures 10
2 Introduction 12
2.1 GBI Report Coverage 12
3 Global Medical Polymers Market 13
3.1 Global Medical Polymers Market Drivers 13
3.1.1 Varied Properties of Plastics 13
3.1.2 Technological Advances 13
3.1.3 Preference for Plastics as a Packaging Material 13
3.1.4 The Rising Incidence of Diseases and Increasing Public Health Awareness 13
3.1.5 Production of Low Weight Medical Devices 13
3.2 Global Medical Polymers Market Restraints 13
3.2.1 Proper Management of Medical Waste 13
3.2.2 Indestructibility of Plastics 13
3.3 Global Medical Polymers Market to 2015 14
3.4 Global Medical Polymers Market Breakdown By Product in 2009 16
3.5 Global Medical Polymer Market Breakdown by Region in 2009 17
3.6 Global Medical Polymers Market Breakdown By Product and Region in 2009 18
3.6.1 Polyvinyl Chloride (PVC) based Medical Polymers 18
3.6.2 Polypropylene (PP) based Medical Polymers 19
3.6.3 Polyethylene (PE) based Medical Polymers 20
3.6.4 Other Polymers 21
3.7 Global Medical Polymers Market End Use Classification and Forecasts to 2015 22
3.7.1 Medical Devices Market and Forecasts 22
3.7.2 Medical Packaging Market and Forecasts 24
3.8 Global Medical Polymers: Major Players 26
3.8.1 Bayer AG 26
3.8.2 Celanese Corporation 27
3.8.3 Eastman Chemical Company 27
3.8.4 Dow Chemical Comapny 28
3.8.5 E. I. du Pont de Nemours and Company 28
3.8.6 Exxon Mobil Corporation 29
4 Global Polyvinyl Chloride (PVC) based Medical Polymers Market 30
4.1 Market Introduction and Overview 30
4.2 Applications of PVC 30
4.3 Advantages of PVC based Medical Polymers 30
4.4 Disadvantages of PVC based Medical Polymers 31
4.5 Strategic Analysis by Geographic Region and Forecasts to 2015 31
4.5.1 North America Market Analysis and Forecasts 31
4.5.2 North America Price Analysis and Forecasts 33
4.5.3 Europe Market Analysis and Forecasts 35
4.5.4 Europe Price Analysis and Forecasts 37
4.5.5 Asia Market Analysis and Forecasts 39
4.5.6 Asia Price Analysis and Forecasts 41
4.6 Strategic Analysis by End Use Classification 43
5 Global Poly Propylene (PP) based Medical Polymers Market 44
5.1 Market Introduction and Overview 44
5.2 Applications of PP 44
5.3 Advantages of PP based Medical Polymers 44
5.4 Strategic Analysis by Geographic Regions and Forecasts to 2015 45
5.4.1 North America Market Analysis and Forecasts 45
5.4.2 North America Price Analysis and Forecasts 47
5.4.3 Europe Market Analysis and Forecasts 49
5.4.4 Europe Price Analysis and Forecasts 51
5.4.5 Asia Market Analysis and Forecasts 53
5.4.6 Asia Price Analysis and Forecasts 55
5.5 Strategic Analysis by End Use Classification 57

For more information, please visit :
http://www.aarkstore.com/reports/Medical-Polymers-Market-to-2015-Polyvinyl-Chloride-PVC-Dominating-the-Medical-Devices-and-Packaging-Markets-79679.html

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Billing Alert for Long-Term Care, May 2015

Common consolidated billing issues facing SNFs

Consolidated billing can be a challenge for any facility, and many SNFs continue to face confusion over which services are included or excluded. "Confusion over consolidated billing could result in missed reimbursement opportunities and rejected claims," says Maureen McCarthy, RN, BS, vice president of clinical reimbursement at National Healthcare Associates and president of Celtic Consulting in Goshen, Connecticut.

The following is a list of common consolidated billing questions facilities are facing and what your SNF can do to address these issues today.

 

1. I can’t find the Medicare fee schedule for a given charge from the hospital. What do I do? How much do I owe the hospital?

When a facility gets a bill for consolidated billing from a hospital, it usually does not have the fee-for-service reimbursement amount specifically listed. Instead, it will list the complete amount, including the hospital’s allowable markup for the services provided.

"Many facilities have a difficult time realizing how much they should be paying the hospital," says McCarthy.

Facilities often have trouble finding the codes to bill for the correct service. Here’s an example: A hospital bills a facility for hyperbaric chamber services. The bill amount was listed as $ 7,000. The question for the facility to consider is:

  • What exactly are we being billed for?
  • How much would Medicare pay for these services?

 

When faced with questions like these, the first step facilities should take is to determine where they need to look up the billing codes. Most facilities may access CMS’ physician fee schedule lookup. This tool, which can be found at www.cms.gov/apps/physician-fee-schedule/overview.aspx, will help you understand many of the charges billed by the hospital.

It is important to note that there are numerous sources of Medicare allowable payments outside the physician fee schedule, according to Bill Ulrich, president of Consolidated Billing Services, Inc., in Spokane, Washington. These include:

  • Ambulance services
  • Durable medical equipment, prosthetics, orthotics, and supplies (DMEPOS)
  • Parenteral and enteral nutrition (PEN)
  • Drug services
  • Clinical laboratory services
  • Ambulatory Payment Classification (APC)
  • Splints, casts, etc.

 

For these services, there is no single or correct payment option, and there are a number of places facilities may need to look outside of the physician fee schedule.

In answering the question, "How much do I pay?" many facilities are missing a critical first step: Put "under arrangement" transactions in place with outside providers of services, including hospitals, says Ulrich. "CMS says that the entity shall look to the SNF for payment and they have told the SNF it must pay, but never has CMS said, at what level," he explains. "It’s the ‘arrangement’ that sets price, and absent that, state law controls cases where there is a payment dispute. Although we all encourage it, one cannot assume you pay the fee schedule or the fee schedule less co-pay."

 

2. Do I pay the technical component or the professional component of a provided service? What is the difference between these two components?

This question relates to any of the consolidated billing portion or Medicare Part B services. Under consolidated billing, the SNF is only responsible for paying the technical component of a bill?not the professional component, which is billed by the vendor straight to Medicare Part B.

When billing Medicare, vendors will receive payments under their own provider numbers because they are providing the professional service separately. The SNF has an arrangement with the vendor to supply the service to the resident, so you are only responsible for the technical component.

"The most important thing you can do to avoid confusion in this area of consolidated billing is to provide education on what these two components are and how they involve the SNF," McCarthy says.

Along with education of these components, a related issue facilities face is being asked to pay "facility fees," according to Ulrich. "While CMS says professional fees are not bundled, the hospital and ambulatory surgical center (ASC) bill for the facility portion of the professional services using the professional service code," Ulrich says. "It is important to understand that when the SNF is billed for one of these codes by the hospital or ASC they are not seeking reimbursement for the professional component but rather for the facility overhead associated with the services."

 

3. Are all forms of chemotherapy excluded under consolidated billing? What happens if the resident changes the chemotherapy they receive after admission to the SNF?

While the SNF Help file for consolidated billing provides information on chemotherapy drugs, the variety of drug treatments can cause confusion for billers when using consolidated billing.

"If a patient is on one type of chemotherapy when they are admitted to a SNF, it does not mean that they will stay on the same chemotherapy treatment throughout their stay," says McCarthy. "Their treatments may change and this is very important to understand."

Certain types of chemotherapy may be excluded under consolidated billing; however, other types are included and are reimbursable. This often leaves billers asking "Do I have to pay for it or not?"

"Many facilities may shy away from taking chemo patients because they were under the assumption that chemo was not paid for," McCarthy says. "This is incorrect?some of it is paid for, and facilities need to be aware of the differences."

When working with a chemotherapy patient, either the billers or the admissions staff?depending on who has the responsibility?should begin by contacting the provider from which they are getting their chemotherapy. This may be a hospital, chemotherapy center, cancer center, physician’s office, etc., to find out exactly which type of chemotherapy medication they are receiving.

"The provider was likely billing someone prior to that patient coming into the SNF, so if you can get the code that they are billing under, you can use that information to look up the type of chemotherapy provided," says McCarthy.

Speak to the physician prior to admission to determine:

  • The likelihood that the patient will switch the type of chemotherapy he or she is receiving
  • How long he or she will be on current chemotherapy medication and/or others

The goal of these questions is to help your facility understand what your cost will be for the length of the resident’s stay.

 

4. How far back can the hospital or physician provider go to send my facility a bill for any given service under consolidated billing? Is there an expiration date for submitting a bill?

There is not actually a window or a closing date for this, according to McCarthy. "We only have 120 days to adjust a Medicare claim, but we are receiving bills for people who have had stays back in 2010."

In the past, SNFs were not receiving a lot of bills because hospitals were being paid by a Medicare carrier and their business facilities were being paid by a fiscal intermediary. The records between the two were not overlapping, so both facilities were billing and all of the claims, regardless of duplication, were accepted.

Since the billing has become more transparent through reform efforts, SNFs are seeing more bills from hospitals. "When a hospital initially submits a bill, they may not be aware that the patient is or was a Medicare beneficiary," McCarthy says. "Then when their claim is denied, it’s not until they get back around to dealing with it that the SNF will see the bill. It generally shouldn’t take that long, but sometimes there are cases when it does."

Consider the following example: A person is in a no-fault auto accident. The no-fault insurance company says that it will pay for the necessary medical services. The capitated amount the insurance company is providing runs out prior to all of the services provided and the resident is switched over to Medicare Part A. The facility does not find out about the transition to Part A until after the initial bill has been sent.

It is particularly important to be aware of this when you are dealing with a situation where the payer source changes, says McCarthy. "Whether the resident is using auto insurance, Worker’s Compensation insurance, or another form of insurance, if they then ran out of money and switched to Medicare while in a stay at the facility, you don’t find that out until later," she explains.

 

5. Do I still have to pay a bill if the patient has already discharged or if they have expired?

Yes, in this situation, facilities must still pay for the billed services, if they received the services while covered under Medicare Part A. "Even if the resident owes your facility money, the facility still has to pay these bills," McCarthy says.

 

6. Is the ambulance ride covered?

Ambulance services are not categorically excluded from consolidated billing, according to CMS. However, certain types of ambulance transportation are separately billable in specific situations. According to CMS, these situations include:

  • An ambulance trip that transports a beneficiary from the SNF at the end of a stay, when it occurs in connection with one of the following events, is not subject to consolidated billing.
    • A trip for an inpatient admission to a Medicare-participating hospital or critical access hospital (CAH)
    • A trip to the beneficiary’s home to receive services from a Medicare-participating home health agency under a plan of care
    • A trip to a Medicare-participating hospital or CAH for the specific purpose of receiving emergency services or certain other intensive outpatient services that are not included in the SNF’s comprehensive care plan
    • A formal discharge (or other departure) from the SNF that is not followed by readmission to that or another SNF by midnight of that same day
  • An ambulance trip from the SNF to the hospital for the receipt of excluded types of outpatient hospital services. Since a beneficiary’s departure from the SNF to receive excluded outpatient hospital services is considered to end the beneficiary’s status as a SNF resident for consolidated billing purposes, any associated ambulance trips are excluded as well. Moreover, once the beneficiary’s SNF resident status has ended in this situation, it does not resume until the point at which the beneficiary actually arrives back at the SNF; accordingly, the return ambulance trip from the hospital to the SNF would also be excluded from consolidated billing.
  • When a beneficiary leaves the SNF to receive off-site services other than the excluded types of outpatient hospital services described previously and then returns to the SNF, he or she retains the status of a SNF resident with respect to the services furnished during the absence from the SNF. Accordingly, ambulance services provided in connection with these services would remain subject to consolidated billing, even if the purpose of the trip is to receive a particular type of service (such as a physician service) that is excluded from consolidated billing.
  • When an individual leaves a SNF via ambulance and does not return to that or another SNF by midnight, the day is not a covered Part A day, and CB would not apply. However, a beneficiary’s departure from a SNF is not considered to be a "final" departure for CB purposes if he or she is readmitted to that or another SNF by midnight of the same day. Therefore, when a beneficiary travels directly from SNF 1 and is admitted to SNF 2 by midnight of the same day, that day is a covered Part A day for the beneficiary, and CB applies.
    • A medically necessary ambulance trip would be bundled back to SNF 1 since the beneficiary would continue to be considered a resident of SNF 1 (for CB purposes) up until the actual point of admission to SNF 2. However, it should be noted that in addition to the "medical necessity" criterion pertaining specifically to ambulance transports under the SNF benefit (i.e., the patient’s medical condition is such that transportation by any means other than ambulance would be contraindicated), coverage in this context also involves the underlying requirement of being reasonable and necessary for diagnosing or treating the patient’s condition.
    • For example, a transfer between two SNFs would be considered reasonable and necessary in a situation where needed care is unavailable at the originating SNF, thus necessitating a transfer to the receiving SNF in order to obtain that care.
    • By contrast, a SNF-to-SNF transfer that is prompted by non-medical considerations (such as a patient’s personal preference to be placed in the receiving SNF) is not considered reasonable and necessary for diagnosing or treating thepatient’s condition and, thus, would not be bundled back to the originating SNF.
  • If a SNF’s Part A resident requires transportation to a physician’s office and meets the general medical necessity requirement for transport by ambulance (i.e., using any other means of transport would be medically contraindicated), then the ambulance roundtrip is the responsibility of the SNF and is included in the PPS rate.
  • Medicare does not provide any coverage at all under Part A or Part B for any non-ambulance forms of transportation, such as ambulette, wheelchair van, or litter van. In order for the Part A SNF benefit to cover transportation via ambulance, the ambulance transportation must be medically necessary. This means that in a situation where it is medically feasible to transport a SNF resident by means other than an ambulance, ambulance service will not be covered.

 

As with other situations of non-coverage, where the resident may be financially liable, the SNF must provide appropriate notification to the resident of services available in the facility and of charges for those services, including any charges for services not covered under Medicare or by the facility’s per diem rate.

 

7. Do I have to adjust my paid claims to show the charges for a late bill from a bundled service?

As mentioned previously, SNFs only have 120 days to adjust a claim, but it would be in the provider’s best interest to ensure that all of the services paid for by the SNF for a particular resident under consolidated billing are stated, according to McCarthy. This is important because that will accurately document the amount?in services and dollars?that your facility is spending on Medicare patients.

This information should be included in your cost report under the different revenue codes. "A common problem we see here is related to ambulance services," McCarthy says. "The problem is that the ambulance providers don’t send their billed claims until the SNFs bills have already gone out." As a result, many facilities aren’t adding this information to their claim because it is significantly later and it is already a paid claim.

Just remember that all of the charges that resident incurs for Medicare Part A and B should be reflected on the claim.

 

8. Should I post all ancillary services my resident receives on my monthly claims?

Yes, all of the ancillary services should be included on monthly claims.

While ancillary service providers are a lot later to send the information to facilities, billers still need to show CMS all of the services that the facility is spending on Medicare covered patients. This is necessary to ensure that each patient is actually receiving the services they require.

 

9. Are FDA-approved drugs covered by Medicare if a resident is prescribed the drug for an off-label treatment?

There is a growing number of SNF’s residents that are being prescribed FDA-approved drugs for off-label conditions, according to Ulrich. "These off-label uses can really add up when the SNF is not aware of the coverage limitations set by CMS," Ulrich says.

For example, consider the drug Basiliximab (Simulect®), which was FDA-approved on May 12, 1998 for the following indicated use: kidney transplant?prophylaxis of acute organ rejection in patients receiving renal transplantation when used as part of an immunosuppressive regimen that includes cyclosporine and corticosteroids. The Medicare allowable single dose cost for Basiliximab is $ 2,442.92 per 20mg (vial), which can bundled to the SNF.

However, Simulect® is also commonly used to treat the following (off-label) conditions:

  • Atopic dermatitis
  • Psoriasis
  • Ulcerative colitis
  • Uveitis
  • Scleromyxedema
  • Graft versus host disease (a complication that may occur after a stem cell or bone marrow transplant)
  • Prevention of liver (and other organs) transplant rejection

 

The off-label treatments are not Medicare-approved costs.

 

Ready for ICD-10?

Ensure your facility’s training is on track

 

Editor’s note: Karen Fabrizio, RHIA CHTS-CP CPRA, recently presented "ICD-10 Coding and Documentation for Long-Term Care," a 90-minute webinar hosted by HCPro.

Fabrizio is an AHIMA Approved ICD-10-CM/PCS trainer and a medical record administrator and HIPAA privacy and security officer at Van Duyn Home and Hospital, a 513-bed SNF in Syracuse, New York. During the webcast, she identified common documentation pitfalls and reviewed ways that SNFs can prepare their documentation and policies for the transition to ICD-10 on October 1, 2015.

Fabrizio recently shared her suggestions for how to get ready for ICD-10 with Billing Alert for Long-Term Care. Recordings of the webcast can be purchased on CD at http://hcmarketplace.com/coding-and-documentation-for-longterm-care.

 

Q: What did you want SNFs to take away from your webcast?

A: My underlying objective was to really identify how important documentation is for accurate and thorough coding and to identify areas that facilities can take a look at across all disciplines.

The identification of a diagnosis is a physician’s responsibility; however, when you get some of the specificity sometimes from different disciplines, a physician may not pick up on the dominate side or the non-dominate side for a stroke, but a physical therapist or an occupational therapist definitely will be focused on that. So it’s looking at documentation on an interdisciplinary standpoint.

So far I’ve highlighted 10 diagnoses that are pretty common. I talk about the pitfalls of bad documentation and things to consider for providing good documentation.

The second takeaway is: I feel very strongly that facilities need to have a coding policy so that if you have multiple people coding or multiple people interpreting codes, they all come up with the same interpretation.

For instance, there is a code for history of falls. It’s important for the facility to determine when they are going to use it. You certainly don’t want to use history of falls for someone who has only fallen once and broken his or her leg. But if someone has fallen frequently, whether or not there is injury, that’s a code that is going to be important for facilities to consider how they are going to use it.

Unfortunately, the whole coding system is new, so there are not a lot of guidelines in terms of you need to have fallen three times in six months to be able to use that code. I think we’ll start to see that develop, but that doesn’t mean a facility can’t make that interpretation now.

For example, in my facility that I worked at previously, we had an interpretation that if someone had fallen three times within six months, we would code that as a history of falls, and if someone had fallen once previously with a significant injury, we would use that code as well.

So, my plan is to identify areas that we should seriously think about how we’re coding it and when we should consider using a specific code.

 

Q: What should SNFs be doing now to plan for this transition and improve their documentation? Should they begin training staff now?

A: There is mixed thoughts about the training. I think the training should be done soon and I think someone in the facility should be in the process of starting that in-depth training. But if you don’t use it you lose it; it’s a corny phrase, but you don’t want to learn how to do ICD-10 and then not do anything with it.

So I think the facilities should identify a group of people to be part of their stakeholder task force. They need to have their implementation and transition team and have at least one individual become comfortable with the classification system, and that person can go back and lead discussions?not necessarily be the chief decision maker?but lead discussions to say chapter-by-chapter, how are we going to address the endocrine? How are we going to address the neurological system? Do we want to use external cause codes? I think you need someone with that knowledge. It’s unfortunate though, because I don’t know if a lot of facilities really have the resources to do that.

 

Q: Can you walk our readers through a couple of examples of coding issues that facilities might run into?

A: Sure. So a doctor commonly says that a patient has diabetes. If he doesn’t identify type one or type two diabetes, the coding guidelines say we have to assume that it’s type two. The problem you run into is that type one diabetes is generally maintained on insulin and affects other systems. So if we don’t have good documentation by applying the rules, I would have to code diabetes as type two diabetes, and that might not represent the patient at all.

The other spinoff of that is we really need to identify whether a person is maintained on insulin and whether it’s to control a type one or type two diabetes, or if it’s a short-term use just to bring things back around. When a person is coming in from home and we have our intake people writing down his or her list of meds, and they add insulin, and I see a person that is type two diabetes and on insulin, I have to ask whether or not that is just a short time use of insulin to supplement their diabetes or if this person really does have type one diabetes.

In long-term care it does not directly impact our reimbursement because we are reimbursed by the RUGs. However, with the nation moving toward quality improvement surveys and Medicare making sure skilled services are appropriate and medically necessary, our coding that we do in long-term care is greatly affected by the coding they do in acute care prior, and can affect our discharges to a home health service.

 

Q: What are facilities still unprepared for regarding the transition to ICD-10?

A: I don’t think a lot of facilities are aware of how long it’s going to take to do the coding. We’ve jumped to one more code that requires us to be more specific and I have heard that a patient record could take up to twice as long to code under ICD-10, just because it is more specific and you’re learning a new system. For example, I know in ICD-9 UTI is 599.0. In ICD-10 I know it starts with an "N" and maybe has a "39," but then it’s getting into all the specifics. Part of it is that transition of it, but you’re getting into more specificity.

I think historically, long-term care facilities have utilized generic codes and maybe have used cheat sheets to be able to quickly assign codes, and that’s going to be very difficult to do with ICD-10.

 

Q: Anything else that facilities should be thinking about?

A: The other big thing is that this really needs to be multidisciplinary. Very few facilities have the resources of an educated or credentialed health information manager, but they are fortunate to have individuals with other backgrounds who may be comfortable with coding. But you have to include everyone in this process.

 

Don’t forget the billers

Most ICD-10 training is focused on coding, but don’t forget to train your billing staff, says Maureen McCarthy, president of Celtic Consulting in Goshen, Connecticut, and vice president of clinical reimbursement for National HealthCare Associates based in Lynbrook, New York.

Billers need to understand how changes introduced by ICD-10 codes will affect their work, McCarthy says. They should be comfortable with what codes will look like under the ICD-10 system as well as any software changes related to ICD-10.

CMS has announced that MACs will host an ICD-10 testing week from March 3?7, allowing providers to submit test claims. MACs are expected to provide more information through their websites and listservs.

McCarthy recommends that billers take advantage of the testing week to prepare for the official ICD-10 implementation on October 1. She also recommends that billers check their state and national professional organizations for ICD-10 training.

"There’s a lot of information out there for clinicians, but there’s not a lot for billers," McCarthy says. "The earlier billers can get their claims tested with their new software systems, the better off they’ll be."

 

Common SNF billing struggles

Written by Lisa McIntire and Julie Bilyeu of BKD, LLP.

With ever changing billing requirements and increased payer scrutiny, skilled nursing facility (SNF) billing personnel encounter more challenges than ever. Providers that don’t stay on top of changes that impact billing are at risk for noncompliance and decreased cash flow. Oftentimes billing issues can be avoided with ongoing education, consistent review of outstanding accounts receivable, and a thorough process for pre-submission claims review.

 

Lack of understanding about payment methodology

It sounds simple enough, but understanding how each payer reimburses for services is critical to determining if claims are paid correctly.

Important components of Medicare payment methodology include knowing when rates change annually. This can be confusing since Part A rates are updated in October, while coinsurance and Part B rates change each January. If the new rates aren’t loaded into billing software in a timely manner, accounts receivable will not be accurate, which can make follow-up daunting.

Other considerations include accounting for the 2% sequestration cut that has been in effect since April 1, 2013, and the Multiple Procedure Payment Reduction (MPPR) that applies to certain therapy service codes, both of which your software may or may not apply automatically.

Knowing what to expect in reimbursement from insurance primary and Medicare Advantage (MA) plans can also be confusing. Providers often mistakenly assume these plans pay according to Medicare guidelines; however, contracted providers are generally paid a daily rate based on level of care or charges billed. Insurance payment rates may not change, depending on how often the contract is renegotiated, so it is advisable to review your contract on an annual basis.

Determining patient out-of-pocket costs is another burden, as it can vary greatly by payer. But the earlier patients are notified of their financial responsibility, the higher the likelihood the SNF will be able to collect.

 

Overlooked adjustments and bad debt write-offs

A common theme surrounding aged accounts receivable (AR) is that the claims have paid, but a balance or credit balance remains after the payment was applied. Just because the claim paid does not mean the situation is finalized. If a balance remains after payment posting, further investigation is in order?and the sooner, the better.

Otherwise, these incorrect balances build up over time, making it difficult and time-consuming to determine later if claims were correctly paid or if there are balances that need to be collected or reported as overpayments. This also contributes to inaccurate AR, which can lead to increased scrutiny by stakeholders as well as unrealistic expectations about cash yet to be collected. However, these issues can be easily avoided by researching any discrepancies at the time payments are posted as well as determining?and resolving?the core issue.

As previously mentioned, incorrect rates in billing software is a common contributor to inaccurate AR balances. Depending on the state, Medicaid rates may change as often as quarterly, which requires even more diligence in ensuring they are correct. Not adjusting for sequestration and MPPR, as detailed on the Medicare remittance advices (RAs), is another reason why balances remain after claims have paid.

For providers with a high volume of MA claims, contractual adjustments can come in many forms, depending on how

HCPro.com – Billing Alert for Long-Term Care

Is 2015 cpt manual obsolete??

PLEASE ADVISE!
I passed the exam and ICD-10 updates in 2015, however remained at my (current) medical billing job.
I remain with an "Apprentice Status" to date… never found coding work and sadly, lost hope of working as a coder…however,
A job opportunity has come up!!!
I must test and was advised to, "be strong on using modifier 24, 25 & 57; Inpatient, OBS, admits, D.C. and Critical Care. ICD10, Concurrent Care".
I only have 2015 CPT Manual and ICD-10 Complete Draft Code Set in my possession. I’ve dusted them off and am eager to "refresh" my memory.
I don’t know who to askCan I still use these books?
I feel lost and don’t know where to begin!
All input is welcome! Thanking you in advance!

Medical Billing and Coding Forum

OIG releases its FY 2015 mid-year update

OIG releases its FY 2015 mid-year update

The Office of Inspector General (OIG) released its fiscal year (FY) 2015 Mid-Year Update last week. The update summarizes new and ongoing reviews and activities that OIG plans to pursue with respect to HHS programs during the current fiscal year and beyond.

The OIG’s job is to detect fraud, waste, and abuse; identify opportunities to improve healthcare program economy; and to hold "accountable those who do not meet program requirements or who violate Federal health care laws." The OIG conducts audits and investigation, and can impose civil monetary penalties where appropriate, so its Work Plan is often of great interest to those working with federal healthcare programs. As a summary of some of the OIG’s enforcement initiatives, the Work Plan can serve as a useful resource for companies when training and when planning internal audits. 

The FY mid-year update includes several initiatives central to long-term care providers.

 

Medicare Part A billing by SNFs

The OIG will describe changes in SNF billing practices from FYs 2011 to 2013. Prior OIG work found that SNFs increasingly billed for the highest level of therapy even though beneficiary characteristics remained largely unchanged. The OIG also found that SNFs billed one-quarter of all 2009 claims in error; this erroneous billing resulted in $ 1.5 billion in inappropriate Medicare payments. CMS has made substantial changes to how SNFs bill for services for Medicare Part A stays.

CMS’ future plans include:

  • phasing in bundling options
  • continued growth and development of ACO models of reimbursement tied to outcomes and quality of care
  • the elimination of using the amount of therapy delivered as an incentive for payment
  • conducting outcome studies on therapy delivered under Medicare Part B

 

Diane Brown, director of postacute education at HCPro explains that, "These plans will likely contribute to better care and improved transitions in care as well as be linked to appropriate payment. When implemented, much of the time spent by facilities on navigating COTs and other labor intensive tasks could be eliminated."

As Kathy W. O’Neal, RN, RAC-CT, LNHA, from Crossroads Medical Management can attest to, "There were numerous changes with Part A billing practices associated with the implementation of MDS 3.0. Probably the most significant was that on the five-day assessment, projecting therapy minutes were removed. Another significant change is that a change of therapy (COT) assessment is required every seven days if a resident in a rehab RUG category that receives more or less therapy minutes and/or the number of modalities changes enough to cause the resident to fall into another RUG category. This practice was created as a response to the thought process that SNFs were being paid for a therapy that was not needed and/or provided. These changes have created a tremendous increase in the number of assessments needed, with the resulting billing rules associated that are confusing for providers. A large percentage of my time is consumed with audits and appeals associated with Part A stays, mainly Medicare replacement policies, and often it seems that the insurance companies providing the replacement policies do not understand PPS billing. It is very frustrating but has become a routine part of our industry."

 

State agency verification of deficiency corrections

The OIG will determine whether state survey agencies verified correction plans for deficiencies identified during nursing home recertification surveys. A prior OIG review found that one state survey agency did not always verify that nursing homes corrected deficiencies identified during surveys in accordance with federal requirements. Federal regulations require nursing homes to submit correction plans to the state survey agency or CMS for deficiencies identified during surveys. CMS requires state survey agencies to verify the correction of identified deficiencies through on-site reviews or by obtaining other evidence of correction.

 

Program for national background checks for long-term-care employees

The OIG will review the procedures implemented by participating states for long-term care facilities or providers to conduct background checks on prospective employees and providers who would have direct access to patients and determine the costs of conducting background checks. Further, the OIG will determine the outcomes of the states’ programs and determine whether the programs led to any unintended consequences. Section 6201 of the Patient Protection and Affordable Care Act (ACA) requires the Secretary of Health and Human Services to carry out a nationwide program for states to conduct national and state background checks for prospective direct patient access employees of nursing facilities and other long-term care providers.

The program is administered by CMS. To carry out the nationwide program, CMS has issued solicitations for grant awards. All states, the District of Columbia, and U.S. territories are eligible to be considered for a grant award. OIG is required under the ACA to submit a report to Congress evaluating this program upon its conclusion. This mandated work is ongoing, and an interim report will be issued prior to the program’s conclusion.

O’Neal approves of this initiative, saying that, "I agree with any additional background screening to ensure our residents are cared for in a safe and caring environment."

Although the OIG’s oversight extends to other programs under the U.S. Department of Health & Human Services, the majority of its resources go toward combating fraud, waste, and abuse in Medicare and Medicaid.

You can review the entire mid-year update to the 2015 Work Plan on the OIG’s website.

HCPro.com – Billing Alert for Long-Term Care

2015 new CPT Codes for RADIATION THERAPY


Radiation therapy codes underwent significant changes for 2015. Teletherapy isodose planning and brachytherapy codes now include the basic dosimetry calculation and IMRT codes now include guidance and tracking. Also radiation treatment delivery codes were deleted in 2015.

77306  Teletherapy isodose plan; simple (1 or 2 unmodified ports directed to a single area of interest), includes basic dosimetry calculation(s)

77307  Teletherapy isodose plan; complex (multiple treatment areas, tangential ports, the use of wedges, blocking, rotational beam, or special beam considerations), includes basic dosimetry calculation(s)

77316  Brachytherapy isodose plan; simple (calculation[s] made from 1 to 4 sources, or remote afterloading brachytherapy, 1 channel), includes basic dosimetry calculation(s)

77317  Brachytherapy isodose plan; intermediate (calculation[s] made from 5 to 10 sources, or remote afterloading brachytherapy, 2-12 channels), includes basic dosimetry calculation(s)

77318  Brachytherapy isodose plan; complex (calculation[s] made from over 10 sources, or remote afterloading brachytherapy, over 12 channels), includes basic dosimetry calculation(s)

77385  Intensity modulated radiation treatment delivery (IMRT), includes guidance and tracking, when performed; simple

77386  Intensity modulated radiation treatment delivery (IMRT), includes guidance and tracking, when performed; complex

77387  Guidance for localization of target volume for delivery of radiation treatment delivery, includes intrafraction tracking, when performed

See also complete list of 2015 CPT Changes


Coding Ahead

2015 CROSSWALK FOR LAB CODES

TEST CODE DESCRIPTION OLD CPT CODE NEW CPT CODE
6MAM 6 MAM SCREEN RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
TYL ACETAMINOPHEN 82003 80329 (HCPCS G6039)
ACETAM ACETAMINOPHEN, URINE 82003 80327 (HCPCS G6039)
ACET ACETONE 84600 80320
ALC20 ALCOHOL SCREEN RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
ALC ALCOHOL, ETHYL SERUM OR PLASMA 82055 80320 (HCPCS G6040)
ALPRAZ ALPRAZOLAM (XANAX) 80154 80346 (HCPCS G6031)
ALTAMP ALTERNATE AMPHETAMINES SCREEN 80101 (HCPCS G0431) 80301 (HCPCS G0431)
AMITR AMITRIPTYLINE AND METABOLITE 80152, 80182 80335 (HCPCS G6030, G6037)
AMPH AMPHETAMINE SCREEN RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
BARBS BARBITURATE SCREEN RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
MSBAR BARBITURATES (GCMS) 82205 80345 (HCPCS G6043)
BENZLC BENZODIAZEPINE CONF (LCMSMS) 80154 80347 (HCPCS G6031)
BENZ BENZODIAZEPINE SCREEN RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
BHPVGT BILL ONLY HPV GENTOTYPE 16/18 REFLEX 87621 87625
BHPVHR BILL ONLY HPV HIGH RISK REFLEX 87621 87624
CBUPS BUPRENORPHINE CMPLNC SCRN RFLX 80101 80301 (HCPCS G0431)
BUTALB BUTALBITAL (FIORINAL) 82205 80345 (HCPCS G6043)
THCQ CANNABINOID (THC) QUANTIFICATION 82542 80349
CAN20 CANNABINOID SCREEN (20) RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
CAN50 CANNABINOIDS SCREEN (50) RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
MSTHC CARBOXY-THC (GCMS) 82542 80324
CHLORP CHLORPROMAZINE (THORAZINE) 84022 80342 (HCPCS G6057)
CLON CLONAZEPAM (CLONOPIN) 80154 80346 (HCPCS G6031)
CLORAZ CLORAZEPATE 80154 80346 (HCPCS G6031)
MSCOC COCAINE METAB (GCMS) 82520 80353 (HCPCS G6044)
COC COCAINE SCREEN RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
CDA COMPLEX DRUG ANALYSIS 80299 80377
CPMETD COMPLIANCE CONFIRM METHADONE 83840 80358 (HCPCS G6053)
KETAMS CONFIRM KETAMINE (GCMS) 82542 80357
NIC COTININE 83887 80302 (HCPCS G6055)
DESIP DESIPRAMINE 80160 80335 (HCPCS G6032)
DIAZ DIAZEPAM AND NORDIAZEPAM 80154 80346 (HCPCS G6031)
DOXMP DOXEPIN AND METABOLITE 80166 80335 (HCPCS G6034)
OPCONQ DRUGS OF ABUSE CONF, QUANT, OPIATES 83925 80364 (HCPCS G6056)
ESTF ESTROGENS, TOTAL 82679, 82670 82671
ETGU ETHYL GLUCURONIDE, UR RFLX 80101 (HCPCS G0431) 80302 (HCPCS G0431)
ETGA ETHYL GLUCURONIDE/SULFATE 83789 80321
ETHY ETHYLENE GLYCOL 82693 80320
FENTU FENTANYL/NORFENTANYL (LCMSMS) 83925 80354 (HCPCS G6056)
FLUPH FLUPHENAZINE 84022 80342 (HCPCS G6057)
FLURAZ FLURAZEPAM 82742 80346 (HCPCS G6031)
GHBMS GAMMA-HYDROXUBUTYRIC ACID SCR 82542 80375
GIBPNL GI BACTERIAL PCR PANEL 87798 x 4 87505
HPVGTY HPV GENOTYPE 16/18 87621 x 2 87625
HPVHRD HPV HIGH RISK 87621 87624
HPVWGT HPV HIGH RISK REFLEX 87621 87624
IMDES IMIPRAMINE AND METABOLITE 80174, 80160 80335 (HCPCS G6036, G6032)
IALC ISOPROPYL ALCOHOL 84600 80320
LDISO LD ISOENZYMES 83516, 83625 83625, 83615
LIB LIBRIUM AND METABOLITE 80154 80346 (HCPCS G6031)
PAPHPV LIQUID BASED PAP, PAP AND HPV Dependent on diagnosis, 87621 Dependent on diagnosis, 87624
PAP30 LIQUID PAP + HPV (RFLX 16/18) Dependent on diagnosis, 87621 Dependent on diagnosis, 87624
LOR LORAZEPAM 80154 80346 (HCPCS G6031)
MSMEP MEPERIDINE (GCMS) 83925 80362 (HCPCS G6056)
MEPU MEPERIDINE SCREEN RFLX 80101 (HCPCS G0431) 80302 (HCPCS G0431)
MEPHOB MEPHOBARBITAL 82205 80345 (HCPCS G6043)
CARMEP MEPROBAMATE 83805, 80299 80369 (HCPCS G6052), 80299
MEPROB MEPROBAMATE, URINE 83805 80302 (HCPCS G6052)
METD METHADONE RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
METDL METHAMPHETAMINE D/L ISOMERS 82542 80324 (HCPCS G6042)
MSUX METHSUXIMIDE (CELONTIN) 83858, 80299 80339 (HCPCS G6054), 80299
MALC METHYL ALCOHOL 84600 80320
NICMUR NICOTINE & METABOLITES, URINE 83887 80323 (HCPCS G6055)
NORT NORTRIPTYLINE 80182 80335 (HCPCS G6037)
OPI OPIATE SCREEN RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
BOXCOD OXYCODONE CONFIRM REFLEX TEST 83925 80364 (HCPCS G6056)
OXYS OXYCODONE SCREEN RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PMCARI PAIN MANAGE CARI/MEPRO 80101 (HCPCS G0431) 80302 (HCPCS G0431)
PMACET PAIN MANAGEMENT ACETAMINOPHEN 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PMALC PAIN MANAGEMENT ALCOHOL RFLX 82055 (HCPCS G0431) 80301 (HCPCS G0431)
PMAAMP PAIN MANAGEMENT ALT AMP RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PBAR PAIN MANAGEMENT BARB CONFIRM 82205 80345 (HCPCS G6043)
PMBARB PAIN MANAGEMENT BARBITURATES RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PBEN PAIN MANAGEMENT BENZ CONFIRM 80154 80347 (HCPCS G6031)
PBUP PAIN MANAGEMENT BUPRE CONFIRM 83925 80348 (HCPCS G6058)
PMBUP PAIN MANAGEMENT BUPRENORPHINE RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PCOC PAIN MANAGEMENT COCAINE CONF 82520 80353 (HCPCS G6044)
PMCOC PAIN MANAGEMENT COCAINE RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PMETGS PAIN MANAGEMENT ETG/ETS RFLX 80101 (HCPCS G0431) 80302 (HCPCS G0431)
PFENT PAIN MANAGEMENT FENTANYL CONF 83925 80354 (HCPCS G6056)
PMFEN PAIN MANAGEMENT FENTANYL RFLX 80101 (HCPCS G0431) 80302 (HCPCS G0431)
PMMEP PAIN MANAGEMENT MEPERIDINE RFLX 80101 (HCPCS G0431) 80302 (HCPCS G0431)
PMETC PAIN MANAGEMENT METHADONE CONF 83840 80358 (HCPCS G6058)
PMMETH PAIN MANAGEMENT METHADONE RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PMOPI PAIN MANAGEMENT OPIATES 83925 80356, 80365, 80364 (HCPCS G6056)
PM1 PAIN MANAGEMENT PANEL 1 RFLX 80101 x 7 (HCPCS G0431), 83925 80301, 80364 (HCPCS G0431, G6056)
PM2 PAIN MANAGEMENT PANEL 2 RFLX 80101 x 10 (HCPCS G0431), 83925 80301, 80361 (HCPCS G0431, G6056)
PM3 PAIN MANAGEMENT PANEL 3 RFLX 80101 x 13 (HCPCS G0431), 83925 80301, 80364 , 80302 x 2 (HCPCS G0431, G6056)
PM4 PAIN MANAGEMENT PANEL 4 RFLX 80101 x 17 (HCPCS G0431), 83925 80301, 80364, 80302 x 6 (HCPCS G0431, G6056)
PPROC PAIN MANAGEMENT PROPOXY CONF 83925 80367 (HCPCS G6056)
PMPROP PAIN MANAGEMENT PROPOXY RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PTHCC PAIN MANAGEMENT THC CONFIRM 82542 80349
PMTHC PAIN MANAGEMENT THC RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PMTRAM PAIN MANAGEMENT TRAMADOL RFLX 80101 80302 (HCPCS G0431)
PALTAP PAIN MGMT ALT AMP CONFIRM 82145 80301 (HCPCS G6042)
PMAMP PAIN MGMT AMP/METHAMPHETAMINE RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PMBENZ PAIN MGMT BEZODIAZEPINES RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PMPCP PAIN MGMT PHENCYCLIDINE RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PENTO PENTOBARBITAL 82205 80345 (HCPCS G6043)
PERPH PERPHENAZINE (TINLAFAR) 84022 80342 (HCPCS G6057)
PCP PHENCYCLIDINE RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
PNA2 PRENATAL ANEUPLOIDY W/SEX 84999 81420
MSPRO PROPOX/NORPROPOXYPHENE (GCMS) 82542 80367 (HCPCS G6056)
PROP PROPOXYPHENE RFLX 80101 (HCPCS G0431) 80301 (HCPCS G0431)
SAL SALICYLATES 80196 80329 (HCPCS G6038)
SYNCAN SYNTHETIC CANNABINOIDS SCREEN RFLX 80101 (HCPCS G0431) 80302 (HCPCS G0431)
MSTRAM TRAMADOL (GCMS) 82542 80373 (G6056)
TRAMU TRAMADOL SCREEN RFLX 80101 (HCPCS G0431) 80302 (HCPCS G0431)
TCA TRICYCLIC DETECTION 80101 80301 (HCPCS G0431)
VOLAT VOLATILES 84600 80320
TCA TRICYCLIC DETECTION 80101 80301 (HCPCS G0431)
VOLAT VOLATILES 84600 80320
CONFO1 CONFIRMATION BILLING – 1 80102 80375
ACETAZ ACETAZOLAMIDE 82491 80375
AMOX AMOXAPINE/ACTIVE METABOLITE 82492 80335
ARI ARIPIPRAZOLE 83789 80342
BACLQT BACLOFEN, SERUM 83789 80369
BENUQ BENZODIAZEPINES PANEL, URINE 80154 80347 (G6031)
BMSBAR BILL ONLY BARBITURATES CONFIRM
80345 (G6043)
BMSBUP BILL ONLY BUPRENORPHINE CONFIRM 80348 (G6056)
BMSCAR BILL ONLY CARI MEPR CONFIRM 80369 (G6052)
BMSCOC BILL ONLY COCAINE CONFIRM 80353 (G6044)
BMSAPX BILL ONLY EXTENDED AMPHET CONFIRM 80324 (G6042), 80359
BLSDS BILL ONLY LSD SERUM 83789 80323
BLSDU BILL ONLY LSD URINE 83789 80323
BMSMEP BILL ONLY MEPERIDINE CONFIRM 80362 (G6056)
BMSMET BILL ONLY METHADONE CONFIRM 80358 (G6053)
BMETDA BILL ONLY METHADONE CONFIRM REFLEX TEST 83840 80358 (G6053)
BMSPRO BILL ONLY NORPROPOXY CONFIRM 80367 (G6056)
BMSPCP BILL ONLY PHENCYCLIDINE CONFIRM 83992
BMSTHC BILL ONLY THC CONFIRM 80349
BMSTRA BILL ONLY TRAMADOL CONFRIM 80373 (G6056)
BRET BRETYLIUM TOSYLATE 82491 80375
CANNQS CANNABINOIDS QUANTITATION 82542 80349
CHLORS CHLORALHYDRATE 82491 82441
CHLUR CHLORALHYDRATE, URINE RANDOM 82491 82441
TAG CIMETIDINE 82491 80375
CELEX CITALOPRAM 83789 80332
CLOBAZ CLOBAZAM, SERUM OR PLASMA 80154 80339 (G6031)
CLONID CLONIDINE 83789 80375
COCQTS COCAINE AND METABOLITES 82520 80353 (G6044)
CONFO1 CONFIRMATION BILLING – 1 80102 80375
CONFO2 CONFIRMATION BILLING – 2 80102 x 2 80375
CONFO3 CONFIRMATION BILLING – 3 80102 x 3 80375
DANT DANTRIUM 80299 80369
DEXMR DEXTROMETHORPHAN/METABOLITE 82492 80362 (G6056)
DOXY DOXYLAMINE 82491 80375
DRUSER DRUG SCREEN, SERUM RFLX 80101 X 11 80301 (G0431)
DRASER DRUG/ALCOHOL SCRN, SERUM RFLX 82055, 80101 X 11 80301 X 2 (G0431, G6040)
DUL DULOXETINE 83789 80332
DYP DYPHYLLINE 82491 80329
ESCI ESCITALOPRAM 83789 80332
EXDS EXTENDED DRUG SURVEY REFLEX 80301, 80302, 80337, 80339, 80342, 80332, 80369, 80364, 80376, 80324, 80338, 80360
EZOMET EZOGABINE AND METABOLITE 83789 80339
FENSTN FENTANYL AND METABOLITE 83925 80354 (G6056)
FENTBF FENTANYL AND METABOLITE, BLOOD 83925 80354 (G6056)
FLEX FLEXERIL 83789 80369
FLUNCO FLUNITRAZEPAM & METABOLITE UA REF 80100 80304 (G0431)
LUVOX FLUVOXAMINE 82491 80332
FURUQ FUROSEMIDE QUANTITATION 83789 80375
GABAPU GABAPENTIN, URINE 80171 80355
GLIPI GLIPIZIDE 82491 80375
GLY GLYBURIDE 82491 80375
HYDROCODONE HYDROCODONE, FREE 83925 80361 (G6056)
HYDRME HYDROMORPHONE, FREE 83925 80361 (G6056)
KETACO KATAMINE & METABOLITE (REFLEXIVE) 80100 80304 (G0431)
LACOS LACOSAMIDE 83789 80339
LDLPS LDL PARTICLE SIZE 83704, 82465, 83883 83701, 83721
LETM LEFLUNOMIDE MET (THERAPEUTIC) 83789 80375
LETP LEFLUNOMIDE MET PRE PREGNANCY 83789 80375
LOXA LOXAPINE 82491 80342
LSDSCO LSD RFLX 80101 80302 (G0431)
LSDUCO LSD, URINE RFLX 80101 80302 (G0431)
LUD MAPROTILINE 82491 80335
MEP MEPERIDINE 83925 80362
MEPHE MEPHENYTOIN AND METABOLITE 82492 80339
MERCA6 MERCAPTOPURINE/METAB, BLOOD 83789 80375
METMBN METHADONE AND METABOLITE 83840 80358 (G6053)
METHA METHAQUALONE 82542 80368
RITA METHYLPHENIDATE 83789 80360
RITAUR METHYLPHENIDATE, URINE RANDOM 83789 80360
MIRTQ MIRTAZAPINE, QUANTITATION 82491 80335
MOB MOBAN 83789 80342
MOR MORICIZINE 82491 80375
NAP NAPROXEN 82491 80329
NARDIL NARDIL 82491 80338
NEFAZQ NEFAZODONE QUANTITATION 82491 80338
OPISCO OPIATES RFLX 80101 X 2 80301 (G0431)
OPIFRT OPIATES, FREE AND TOTAL, SERUM 83925 X 2 80356, 80361, 80365 X 2 (G6056 X 2)
OPIFUS OPIATES, FREE SERUM / PLASMA 83925 80356, 80361, 80365 (G6056)
OPCONQ OPIATES, SERUM QUANT 83925 80364 (G6056)
OPITSP OPIATES, TOTAL SERUM OR PLASMA 83925 80361, 80365 (G6056)
PAROX PAROXETINE 83789 80332
PREGAS PREGABALIN, SERUM OR PLASMA 83789 80366
PREGAU PREGABALIN, URINE 83789 80366
QUETQT QUETIAPINE, SERUM 83789 80342
RIS RISPERIDONE AND METABOLITE 83789 80342
RUFIN RUFINAMIDE 83789 80339
SILVER SILVER 83788 83789
SILVER.U SILVER, URINE RANDOM 83788 83789
SPAU S-PHENYLMERCAPTURIC ACID, URINE 82570, 83789 82570, 83921
TAPNUS TAPENTADOL, URINE RFLX 80101 80302 (G0431)
THIODZ THIORIDAZINE/METABOLITE QUANT 84022 80342
TOC TOCAINIDE 82491 80375
TOPIM TOPIRAMATE 83789 80201
MSTRAM TRAMADOL (GCMS) 80373 (G6056)
TRIFLU TRIFLUOPERAZINE 83789 80342
TRIMEN TRIMETHOPRIM 83789 80375
TRIMIP TRIMIPRAMINE AND METABOLITE 82492 80335
VALPFR VALPROIC ACID, FREE 80164 80165
VENLAM VENLAFAXINE AND METABOLITE 83789 80338
VERAPA VERAPAMIL, SERUM OR PLASMA 82491 80375
ZIPRA ZIPRASIDONE, SERUM OR PLASMA 83789 80342
BUPRO BUPRIOPION, SERUM OR PLASMA 80299 80338
CLOMIP CLOMIPRAMINE AND METABOLITE, SERUM 80299 80335
CUMB12 CORDSTAT 12 DRUG SCR PNL 80101 x 12 80301, 80302 x 2 (G0431)
CUM12A CORDSTAT 12 SCR W/ALC 80101 x 12, 80100 80301, 80302 x 3 (G0431, G6040)
CUMB13 CORDSTAT 13 DRUG SCR PNL 80101 x 13 80301, 80302 x 2 (G0431)
CUM13A CORDSTAT 13 SCR W/ALC 80101 x13, 80100 80301, 80302 x 3 (G0431, G6040)
CUMB5 CORDSTAT 5 DRUG SCR PNL 80101 x 5 80301 (G0431)
CUMB7 CORDSTAT 7 DRUG SCR PNL 80101 x 7 80301 (G0431)
CUMB9 CORDSTAT 9 DRUG SCR PNL 80101 x 9 80301 (G0431)
DHTT DIHYDROTESTOSTERONE, LCMSMS 82651 80327
ETHOT ETHOTOIN 80299 80339
ETG ETHYL GLUCORONIDE REFLEX TEST 80100 80301 (G0431)
FELB FELBAMATE 80299 80339
FLUOX FLUOXETINE AND METABOLITE 80299 80332
IBU IBUPROFEN 80299 80329
MEC12A MECONIUM 12 DRUG + ALC 80101 x 12, 80100 80301, 80302 x 3 (G0431, G6040)
MEC12 MECONIUM 12 DRUG SCREEN 80101 x 12 80301, 80302 x 2 (G0431)
MEC13A MECONIUM 13 DRUG + ALC 80101 x 13, 80100 80301, 80302 x 3 (G0431, G6040)
MEC13 MECONIUM 13 DRUG SCREEN 80101 x 13 80301, 80302 x 2 (G0431)
MEC5A MECONIUM 5 DRUG + ALC 80101 x 5, 80100 80301, 80302 (G0431, G6040)
MEC5 MECONIUM 5 DRUG SCREEN 80101 x 5 80301 (G0431)
MEC7 MECONIUM 7 DRUG SCREEN 80101 x 7 80301 (G0431)
MEC7A MECONIUM 7 DRUG SCRN + ALC 80101 x 7, 80100 80301, 80302 (G0431, G6040)
MEC9SC MECONIUM 9 DRUG SCREEN 80101 x 9 80301 (G0431)
NICMSP NICOTINE AND METABOLITES – CONFIRMATION 83887 80323 G6055)
OLANZ OLANZAPINE 80299 80342
ORAL10 ORAL FLUID 10 80101 x 10 80301 (G0431)
ORAL12 ORAL FLUID 12 80101 x 12 80301, 80302 x 2 (G0431)
ORAL5 ORAL FLUID 5 80101 x 5 80301 (G0431)
ORAL7 ORAL FLUID 7 80101 x 7 80301 (G0431)
ORAL9 ORAL FLUID 9 80101 x 9 80301 (G0431)
PCATMA PCA3 – PROSTATE CANCER BIOMARKER BY TRANSCRIPTION-MEDIATED AMPLIFICATION 81478 81313
PROTRI PROTRIPTYLINE, SERUM OR PLASMA 80299 80335
SERT SERTRALINE 80299 80342
THIOTH THIOTHIXENE 80299 80342
TRAZ TRAZADONE 80299 80338

Reference: http://www.paml.com/Files/Miscellaneous/CPT%20List%20for%20Website%20120514.pdf


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