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Reimbursement & Compliance Issues
Affecting Suppliers of g ppDMEPOS
AHLA Medicare/Medicaid Conference 2012
Jana Kolarik Anderson, PartnerNelson Mullins Riley & Scarborough, LLP
101 C tit ti A NW S it 900101 Constitution Avenue, NW, Suite 900Washington, D.C. 20001
Tel: 202-545-2960E il j k l ik@ l lli
13/30/2012
Email: [email protected]
Agenda1 i b d1. Reimbursement Landscape2. Enrollment 3. Supplier Standards4 Accreditation & Surety Bond4. Accreditation & Surety Bond
Requirements5 Stark Law and Anti kickback5. Stark Law and Anti-kickback
Considerations
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Reimbursement Landscapep
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What is DMEPOS?DMEPOS includes the following -
• Durable medical equipment (DME) – equipment furnished by a supplier or HHA that (1) canfurnished by a supplier or HHA that (1) can withstand repeated use, (2) is primarily and customarily used to serve a medical purpose, (3) generally is not useful to an individual in thegenerally is not useful to an individual in the absence of illness or injury and (4) is for use in the home. Examples – blood glucose monitors, h it l b d b li d lihospital beds, nebulizers, oxygen delivery systems & wheelchairs.
• Prosthetics – devices that replace all or part of an i l b d di kinternal body organ, e.g., cardiac pacemakers, cochlear implants, electrical nerve stimulators, and parenteral and enteral (PEN) nutrition.
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p
What is DMEPOS?
DMEPOS includes the following –• Orthotics and prosthetics – leg, arm, back & neck
braces (orthotics) and artificial legs, arms and eyes (prosthetics).
• Surgical dressings – include dressings and splits• Surgical dressings – include dressings and splits, casts and other devices used for the reduction of fractures and dislocations.
• Other items include therapeutic shoes for diabetics, home dialysis supplies and equipment, self-care home dialysis support services andself care home dialysis support services and institutional dialysis services and supplies and self-administered erythropoietin.
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Coverage
Medicare Benefit Policy Manual, ch. 15; Medicare Secondary Payer Manual; Medicare Program Integrity Manual
National Coverage Decisions (NCDs)• Medicare National Coverage Decisions Manual or
Medicare Coverage Database at www.cms.govl f ( )• Example – Coverage of TENS post-op (10.2) or as
DME (280.13) Local Coverage Decisions (LCDs)
• Medicare Coverage Database at www cms gov• Medicare Coverage Database at www.cms.gov• Look at specific DME MAC jurisdiction• Medicaid Example - NC DMA Botulinum Toxin
Treatment, Policy 1B-1Treatment, Policy 1B 1 Policy Articles
• Medicare Urological Supplies Policy Article regarding A4353 kit
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Medicare Coverage Database
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ARCHIVED Medicare Coverage Database
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Coverage - Medicare Program Integrity Manual
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Coverage – Medicare Secondary Payer Manual
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Medicare Coverage Database – LCD Example - Urological SuppliesExample - Urological Supplies
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Medicare Coverage Database – Policy Articles Example Urological SuppliesArticles Example – Urological Supplies
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Billing - DME MACs
There are 4 DME Medicare Administrative Contractors (or DME MACs) – they administer claims from DMEPOS suppliers.
MMA (2003) requires that CMS must re-compete MACs every 5 yearsMACs every 5 years.
Region A – NHIC Corp.Region B – National Government Services/NGSg /Region C – Cigna Government Services (CGS) AdministratorsRegion D – Noridian Administrative Services
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Billing - DME MACs
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Billing/Coding
Medicare Claims Processing Manual, ch. 20 (DMEPOS)
General Rules - DME MAC Supplier Manual by Jurisdiction, which provides information on -J , p• Physician Orders• Certificates of Medical Necessity (CMNs) and
DME MAC Information Forms (DIFs)DME MAC Information Forms (DIFs)• Medical Necessity Documentation• Proof of Delivery Requirements• Advanced Beneficiary Notice (ABNs)• Advanced Beneficiary Notice (ABNs)
Specific Item Rules – LCDs/Policy Articles
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Billing/Payment – Medicare Claims Processing ManualManual
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Billing - DME MAC Supplier Manual
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Billing/Coding - LCD Example –Urological SuppliesUrological Supplies
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Payment
During a Part A stay, DMEPOS is not separately billable.
Under Part B, DMEPOS is typically paid under a fee schedule.• The Pricing Data Analysis & Coding (PDAC)• The Pricing, Data Analysis & Coding (PDAC)
contactor (formerly known as the SADMERC) conducts coding verification and pricing of DMEPOS items.
• With the exception of customized items, a fee schedule amount is calculated for eachschedule amount is calculated for each item/category of DMEPOS that is identified by a code in the Healthcare Common Procedure
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Coding System (HCPCS).
Competitive Bidding Program
DMEPOS Competitive Bidding Program was statutorily mandated and was intended to begin in 2007.
Round One delayed in 2008 for 18 months, then MIPAA required CMS to terminate Round OneMIPAA required CMS to terminate Round One contracts.
MIPAA added a financial document review process and a requirement for contract suppliers to report contractor relationships.
Round One Rebid involved 9 of 10 metropolitanRound One Rebid involved 9 of 10 metropolitan statistical areas (MSAs) and 9 of 10 product categories of Round One.
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Competitive Bidding Program
Round One Rebid Results –• CMS received 6,215 bids from 1,011 suppliers during
60-day bidding period.60 day bidding period.• CMS awarded 1,217 contracts with 356 suppliers.• Small suppliers (with annual receipts less than $3.5
million) make up 51% of contract suppliers.CBIC i ll i h d i• CBIC estimates overall weighted average savings as 32%
Round Two –• Began late 2011 and was expanded from 70 to 91• Began late 2011 and was expanded from 70 to 91
MSAs and a total of 100 CBAs• National mail order component – covers all 50 states,
DC, Puerto Rico, U.S. Virgin Island, Guam and , , g ,American Samoa – diabetic testing strips - must offer at least 50% of all types (and must attest to the 50% compliance)
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Competitive Bidding Program – Round 2 ProductsProductsOxygen supplies & equipmentStandard power wheelchairs, scooters and relatedStandard power wheelchairs, scooters and related
accessoriesMail-order diabetic suppliesE t l t i t i t d liEnteral nutrients, equipment and suppliesContinuous positive airway pressure devices
(CPAPs), respiratory assist devices (RADs) and ( ) p y ( )related supplies and accessories
Hospital beds and related accessoriesWalkers and related accessoriesWalkers and related accessoriesSupport surfacesNegative pressure wound therapy pumps and
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grelated accessories
Competitive Bidding Round 2 Timeline HighlightsHighlights
November 30, 2011 – Bidding timeline announced February 9 2012 Registration closed February 9, 2012 – Registration closed February 29, 2012 – Financial Documents dueMarch 30, 2012 – TODAY – 60-day bid windowMarch 30, 2012 TODAY 60 day bid window
closing Fall 2012 – Target date for CMS to announce single
d b i h ipayment amounts and begin the contracting processSpring 2013 – Target date for CMS to announce
contract suppliers and begin contract suppliercontract suppliers and begin contract supplier education campaign
July 1, 2013 – Target date to implement Round 2 and i l il d d i
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national mail order contracts and prices
How to Participate in Competitive BiddingBidding Suppliers must meet the requirements in 42 CFR §
414.414.• Supplier Standards at 42 CFR § 424.57• Accreditation• Financial Standards• Licensure – for all locations identified in the bid(s) – a
competitive bidding area (CBA) can cross multiple states
Small suppliers (i.e., suppliers that generate $3.5 M or less in annual receipts, including MCR and non-MCR revenue) have the option to form networks of between 2-p20 members.
SNFs & nursing facilities – can bid as "specialty suppliers" and would be paid the single payment
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gamount for those items.
How to Participate in Competitive Bidding
Bidders may amend their bids as many times as necessary prior to the close of the 60-day bid window.
Bids must be bona fide (that was one of the problems in Bids must be bona fide (that was one of the problems in Round 1) – "rational and feasible for the bidder to furnish at the bid price"
Bidders may not bid against themselves for the same y gproduct category in the same CBA – this includes "commonly owned" or "commonly controlled" supplies.• "Commonly owned" supplies are described as those
where one or more of them has an ownership interestwhere one or more of them has an ownership interest totaling at least 5% in the other. (Ownership means possession of equity in the capital stock or profits of another.))
• "Commonly controlled" suppliers are those where one or more of the supplier's owners is also an officer, director or partner in another supplier.
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How to Participate in Competitive BiddingBiddingNoncontract suppliers that furnish competitively
bid items in a CBA are not eligible for MCR f h i l f hpayment for such items unless one or more of the
following exceptions apply –• Suppliers of grandfathered DME (e.g., Oxygen)• Repairs/replacement• Physicians and other practitioners who are
enrolled Medicare DMEPOS suppliers (canes, pp ( ,crutches, walkers, folding manual wheelchairs, blood glucose monitors and DME infusion pumps)pumps)
• PTs and OTs in private practice who are enrolled DMEPOS suppliers (off-the-shelf orthotics)
• Medicare secondary payer
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• Medicare secondary payer
Competitive Bidding Contracts
Suppliers that are awarded a contract must agree to furnish the competitively bid items for the full duration
f h i d h h h i CBAof the contract period throughout the entire CBA. Length of the contract may not exceed three (3) years. The contract supplier must furnish competitively bid The contract supplier must furnish competitively bid
items to any beneficiary who maintains a permanent residence in or who visits a CBA and who requests those items from the contract supplier. (Members of a networkitems from the contract supplier. (Members of a network may share that responsibility.)
Items supplied by the contract supplier must be the same items furnished to its other customers i e the supplieritems furnished to its other customers, i.e., the supplier should furnish Medicare and non-Medicare customers with the same selection of DMEPOS brands and
d t
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products.
Competitive Bidding Contract Suppliers -SubcontractorsSubcontractors
Contract suppliers may use subcontractors to assist them –them 1) To purchase inventory;2) To maintain and repair rented equipment;3) T d li M di d it d3) To deliver a Medicare-covered item; and 4) To setup and/or instruct on the use of the
Medicare-covered item. If using a subcontractor, the contract supplier must
ensure that the subcontractor is accredited, if li bl d t l ith th S liapplicable, and must comply with the Supplier
Standards Contract suppliers must disclose subcontractors
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Contract suppliers must disclose subcontractors and their accreditation status to CMS.
Enrollment
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Enrollment Basics
Enroll with the National Supplier Clearinghouse –website http://www.palmettogba.com/palmetto/providers.nsf/DocsCatHome/National%20Supplier%20Clearinghouse
Medicare Application – CMS form 855SppAll of the following enrollment requirements must
be in place prior to/on date of enrollment: (1) applicable licensure; (2) accreditation by one of 10applicable licensure; (2) accreditation by one of 10 approved accreditation organizations; (3) surety bond(s); (4) application fee paid through pay.gov; (5) meet all Supplier Standardsmeet all Supplier Standards
NSC site visit will occur pre- or post-enrollmentSeparate NPI/PTAN for each location (except
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locations used solely as warehouse/repair facilities)
2011 Enrollment Changes
Effective March 25, 2011, • Newly enrolling DMEPOS suppliers are
classified in the "high" risk category of fraud, waste or abuse under CMS' new enrollment standards;standards;
• Currently enrolled DMEPOS suppliers are classified in the "moderate" risk level.
Application fee (new enrollment, revalidation, new practice location) 2012 set at $523per applicationpractice location) – 2012 set at $523per application (for 2011 will be increased by CPI-U)
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2011 Enrollment Changes
Risk categories determine what screening procedures –• "Limited" risk – verification of provider/supplier-
specific requirements in the FHCPs, verification of licensure, and database checks.
• "Moderate" risk – all "limited" risk procedures PLUS punannounced pre- and post-enrollment site visits
• "High" risk – all "moderate" risk procedures PLUS fingerprint-based criminal history record check offingerprint based criminal history record check of Federal and State law enforcement databases
M di id d CHIP ill d t t d dMedicaid and CHIP programs will adopt same standards OR can add screening procedures or increase the risk level for categories of providers/suppliers.
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2011 Enrollment Rule's Additional ChangesChangesCMS can impose temporary moratorium on
enrollment for Medicare, Medicaid & CHIPenrollment for Medicare, Medicaid & CHIP programs
CMS can impose payment suspensions pending "credible allegations of fraud" unless "good cause" for the Medicare and Medicaid programsfor the Medicare and Medicaid programs
There will be cross-termination of provider/supplier p / ppparticipation if terminated under the Medicare, Medicaid or CHIP programs
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Change of Ownership
A stock deal that does not change the tax identification of a supplier is not a "change of
hi " ("CHOW") f f th M diownership" ("CHOW") for purposes of the Medicare enrollment rules. • In a stock deal, a change of information filing
(i l di l i f h 855S b(including relevant sections of the 855S must be submitted to update the file.
An asset purchase, consolidation or merger, p , g ,changing the tax identification number of the supplier, would be considered a CHOW, triggering a new application/new number.pp /
Simply put, whether there is a change in the tax identification determines whether there is a CHOW/new number required
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CHOW/new number required.
Change of Ownership & Competitive Bidding
Before the bid window closes – update the information related to the CHOW on the Request for Bids (RFB) forms in DBids. Also, resubmit all hardcopy documents reflecting the CHOW by close of the bid window. Also, notify NSC per usual.of the bid window. Also, notify NSC per usual.
During bid evaluation – bids will be evaluated based on the information provided as of the bid
i d l f i h illwindow close. Information on the new owner will not be used during this time period.
Post-contract – A contractor must notify CMS if it isPost contract A contractor must notify CMS if it is negotiating a CHOW 60 days prior to the anticipated close. (Other requirements are detailed in 414 422(d) )
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414.422(d).)
Supplier Standardspp
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30 Medicare Supplier Standards
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Supplier Standards/Proposed Rule
Supplier Standard #1 – supplier must operate a business in compliance with Federal and State laws.
If St t i li t f i h t i it• If a State requires licensure to furnish certain items or services, a DMEPOS supplier –
1. must be licensed; 2 t l th li d f i l f ll ti2. must employ the licensed professional on a full-time
or part-time basis; and 3. must not contract with an individual/entity to
provide the licensed services unless allowed by theprovide the licensed services, unless allowed by the State where the licensed services are being performed.
• The strike outs note the 2012 Final Rule changes to the 2010 Final Rule.
• 2012 Final Rule also replaces 3. with "may contract with an individual or other entity to provide the licensed services unless expressly prohibited by State law "
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services unless expressly prohibited by State law.
Supplier Standards
Supplier Standard #7 – Physical facility• Supplier must maintain a physical facility on an
"appropriate site "appropriate site.• An "appropriate site" must meet the following –
– Maintain a practice location that is at least 200 square feet (beginning 9/27/2010 and no later than 9/27/2013, d di h l t i t )*depending on when your lease terminates)*
– Is in a location accessible to the public, Medicare beneficiaries, CMS, NSC and its agents
– Is accessible and staffed during posted hours ofIs accessible and staffed during posted hours of operation
– Maintains a permanent visible sign in plain view and posts hours of operationI i l ti th t t i f t i b i– Is in a location that contains space for storing business records
– Is in a location that contains space for retaining the necessary ordering and referring documentation
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y g g
Supplier Standards/Proposed Rule
Supplier Standard #11 – Solicitation of Beneficiaries• 2010 Rule - DMEPOS suppliers cannot make
direct solicitation of Medicare beneficiaries by telephone, computer, email, instant messaging or in-person contacts without the beneficiary'sin-person contacts without the beneficiary s consent for the purpose of marketing.
• 2012 Final Rule goes back to the pre-2010 final rule, prohibiting telephone solicitation.
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Supplier Standard #11 - DMEPOS Telephone Solicitation Q&ASolicitation Q&A
Question 1: Under what circumstances can a DME supplier make telephone contract with a beneficiary pp p yregarding a Medicare-covered item?• Answer 1: If the beneficiary gave written permission
for the supplier to contact him/her, if the supplier has pp / ppalready provided a covered item to the beneficiary and the supplier is calling the beneficiary about such covered item or if the beneficiary has already received a covered item from the supplier in the last 15 months.
Question 2: Is a supplier returning a beneficiary's phone Q pp g y pcall considered an "unsolicited" contact?• Answer 2: No, in that scenario, the beneficiary
initiated the contract and is inviting a response from
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the supplier.
Supplier Standard #11 - DMEPOS Telephone Solicitation Q&ASolicitation Q&A
Question 3: If a supplier makes solicited contact with a beneficiary for a particular covered item, canwith a beneficiary for a particular covered item, can the supplier speak with the beneficiary about additional covered items during that same contact?• Answer 3: No if this is the first contact ever madeAnswer 3: No, if this is the first contact ever made
by the supplier to the beneficiary, then the supplier is prohibited from attempting to solicit the purchase of additional covered items sincethe purchase of additional covered items since the supplier only had permission to contact the beneficiary regarding the particular covered item
ib d b th h i i O th liprescribed by the physician. Once the supplier has provided the covered item to the beneficiary, then the other non-solicitation exceptions may
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apply.
Supplier Standards – Solicitation of BeneficiariesBeneficiaries
Supplier Standard #11 – Solicitation of Beneficiaries• A physician order does not constitute written• A physician order does not constitute written
permission from the beneficiary to contact the beneficiary.
• HOWEVER, if the physician contacts the supplier on behalf of the beneficiary with the beneficiary's knowledge then a supplier maybeneficiary s knowledge, then a supplier may contact the beneficiary to confirm or gather information needed to provide that particular covered item.
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Supplier Standards
Supplier Standard # 28 – A supplier must maintain ordering and referring documentation for 7 years ft th l i h b idafter the claim has been paid.
Supplier Standard # 30 – A supplier must be open to pp pp pthe public a minimum of 30 hours per week, except for those suppliers where –• A physician or a physical or occupationalA physician or a physical or occupational
therapist furnishes items to his/her own patients as part of his/her professional services or
• A supplier is working with custom-made• A supplier is working with custom-made orthotics and prosthetics.
Note: Suppliers that meet this 30-hour exception are permitted to be open "By Appointment Only "
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are permitted to be open "By Appointment Only."
Supplier Standards
Supplier Standard #29 – A supplier is prohibited from sharing a practice location (as that physical location is described on the CMS-855S) with any other Medicare supplier/provider except in the following circumstances:following circumstances:• Physician/NPP furnishing items to his/her
patients as part of his/her professional service;PT/OT f i hi it t hi /h ti t• PT/OT furnishing items to his/her own patients as part of his/her own professional service;
• DMEPOS supplier is co-located with and owned ppby an enrolled Medicare provider where DMEPOS supplier operates as a separate unit and meets the Supplier Standards
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and meets the Supplier Standards.
Accreditation/Surety Bond/ y
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Accreditation
As of 10/1/2009, DMEPOS suppliers must be accredited by a Medicare "deemed" accreditation organization ("AO") i d b i / i i billi i il if("AO") in order to obtain/maintain billing privileges if they furnish covered items and services.
Covered items and services include –• DME• Medical supplies• Home dialysis supplies and equipmentHome dialysis supplies and equipment• Therapeutic shoes• PEN nutrients, equipment and supplies• Blood products• Blood products• Transfusion medicine• Prosthetic devices
P th ti & O th ti
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• Prosthetics & Orthotics
Accreditation
NOTE: There is a difference between the Supplier Standards and the Quality Standards.• Suppliers must be in compliance with the
Supplier Standards to obtain/maintain Medicare billing privilegesbilling privileges.
• Suppliers must be in compliance with the Quality Standards to attain accreditation by a CMS-approved AO.
Certain supplier types are exempt from accreditation – physicians dentists orthotists prosthetists– physicians, dentists, orthotists, prosthetists, opticians, optometrists, audiologists, OTs, PTs and podiatrists.
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AccreditationCMS has deemed 10 AOs including the JointCMS has deemed 10 AOs – including the Joint
Commission, ACHC, ABC, BOC, CARF, CHAP, HCAA, NABP, TCT and NBAOs.
Quality Standards are divided into the followingQuality Standards are divided into the following areas –• Business Services – including Administration, Financial
Management, Human Resource Management, Consumer S i P f M P d S f dServices, Performance Management, Product Safety and Information Management
• General Product-Specific Service Standards – includes Preparation, Delivery and Setup, Training/Instruction to B fi i d C i d F llBeneficiary and Caregiver and Follow-up
• Appendix A – deals with respiratory equipment, supplies and services
• Appendix B – deals with manual wheelchairs and power bili d i i l di l h b d i imobility devices including complex rehab and assistive
technology.• Appendix C – deals with custom fabricated, custom fitted,
custom-made orthotics, prosthetic devices, soatic, ocular, and f l d d
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facial prosthetics and therapeutic shoes and inserts.
Surety Bond
As of October 2, 2009, each Medicare-enrolled DMEPOS supplier must have a surety bond.
Obtain through sureties identified on U.S. Department of Treasury's "Listing of Certified (Surety Bond) Companies" at www.fms.treas.gov
Bond – must be a continuous bond in an amount not less than $50,000 for each that has a separate NPI or a single bond that covers multiple locationsg p• For each location covered, the bond must identify
the location's TIN, legal business name, address, NPI NSC/PTAN numberNPI, NSC/PTAN number.
Higher bond amount will be required if "final adverse action"
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Surety Bond
Certain DMEPOS suppliers are exempt from surety bond requirements –
G t t d DMEPOS li (if th• Government-operated DMEPOS suppliers (if the DME supplier has provided CMS with a comparable surety bond under State law);p y );
• State-licensed orthotic and prosthetic personnel in private practice making custom-made orthotics and prosthetics if (1) the business is solelyand prosthetics if (1) the business is solely-owned and operated by the orthotic and prosthetic personnel, and (2) the business is only p p ybilling for orthotic, prosthetics and supplies;
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Surety Bond
Certain DMEPOS suppliers are exempt from surety bond requirements –• Physicians and nonphysician practitioners (as defined• Physicians and nonphysician practitioners (as defined
in section 1842(b)(18) of the Act) when items are furnished only to the physician or nonphysician
titi ' ti t t f hi hpractitioner's own patients as part of his or her physician service;
• Physical and occupational therapists in private practice if (1) the business is solely-owned and operated by the physical or occupational therapist; (2) the items are furnished only to the physical or y p yoccupational therapist's own patients as part of his or her professional service, and (3) the business is only billing for orthotics prosthetics and supplies
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billing for orthotics, prosthetics and supplies.
St k L & AKBSStark Law & AKBS Considerations
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Stark Law
"Designated health services" or "DHS" under the Stark Law includes -• Durable medical equipment (DME); • parenteral and enteral nutrients, equipment and
supplies;supplies; • prosthetics, orthotics and prosthetic devices and
supplies; and • outpatient prescription drugs.
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Stark Law
The Stark Law provides that "a physician who has a direct or indirect financial relationship with [a DHS] entity, or who has an immediate family member who has a direct or indirect financial relationship with the entity, may not make a referralrelationship with the entity, may not make a referral for the furnishing of DHS for which payment otherwise may be made under Medicare."
h i h f i h Further, an entity that furnishes DHS pursuant to a prohibited referral may not present or cause to be presented a claim or bill to the Medicare program or p p gto any individual, third party payer, or other entity for the DHS performed pursuant to the prohibited referral
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referral.
Stark Law
In order to avoid the Stark Law’s referral prohibitions, if the physician has a "direct or indirect financial relationship with [a DHS] entity" the financial relationship must meet an applicable exception.exception.
"Financial relationship" means (i) a direct or indirect ownership or investment
interest (as defined by 42 C.F.R. § 411.354(b)) in any entity that furnishes DHS or
(ii) a direct or indirect compensation(ii) a direct or indirect compensation arrangement (as defined by 42 C.F.R. § 411.354(c)) with an entity that furnishes DHS.
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Stark Law
The Stark Law applies not only to relationships between third-party DMEPOS suppliers and physicians, but also to a physician's referrals within his/her physician practice entity.
Under the Federal physician self-referral law (commonly known as the "Stark Law"), physicians and physician group practice entities may furnish DHS pursuant to the "in-office ancillary services" exception.exception.
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Stark Law
The types of DME that may be furnished under the IOAS exception are limited: (1) DME infusion pumps or (2) canes, crutches, walkers and folding manual wheelchairs, and blood glucose monitors that meet certain conditions.that meet certain conditions.
Note: For purposes of the in-office ancillary services exception, an item is "furnished" in the location
h h i i ll f dwhere the service is actually performed upon a patient or where an item is dispensed to a patient in a manner that is sufficient to meet the applicable ppMedicare payment and coverage rules.
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Stark Law – IOAS Exception
The services must meet the following conditions:1. Who –GENERALLY, they must be furnished personally by one of the following individuals: (i) the referring physician; (ii) a physician who is a member of the same group
ti th f i h i i (iii) i di id lpractice as the referring physician; (iii) an individual who is supervised by the referring physician or, if the referring physician is in a group practice, by another physician in the group practice provided that thephysician in the group practice, provided that the supervision complies with all other applicable Medicare payment and coverage rules for the services.Special DME Rule: DME is restricted in that it may onlySpecial DME Rule: DME is restricted in that it may only be furnished personally by the physician who ordered the DME, by another physician in the group practice or by an employee of the physician or the group practice.
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y p y p y g p p
Stark Law – IOAS Exception
2. Where –2. items must be furnished in one of the following locations:
(i) the same building (as defined at § 411 351) but not(i) the same building (as defined at § 411.351), but not necessarily in the same space or part of the building, in which all of the conditions of 42 C.F.R. § 411.355(b)(2)(i)(A), (B) or (C) are satisfied;
(ii) a centralized building (as defined at § 411.351) that is used by the group practice for the provision of some or all of the group practice's clinical laboratory services; or
(iii) li d b ildi ( d fi d i § 411 351) h i(iii) a centralized building (as defined in § 411.351) that is used by the group practice for the provision of some or all of the group practice's DHS (other than clinical laboratory services).services).
Special DME Rule: DME must exclusively be furnished in the "same building".
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g
Stark Law – IOAS Exception
3. How Billed - They are billed by one of the following: (i) the physician performing or supervising the service; (ii) the group practice of which the performing or supervising physician is a member under a billing number assigned to themember under a billing number assigned to the group practice; (iii) the group practice if the supervising physician is a "physician in the group practice" (as defined at § 411 351) under a billingpractice" (as defined at § 411.351) under a billing number assigned to the group practice; (iv) an entity that is wholly owned by or by that physician's group practice under the entity's own billing number or under a billing number assigned to the physician or group practice; or…
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physician or group practice; or…
Stark Law – IOAS Exception
3. How Billed (continued) - They are billed by one of the following: …(v) an independent third party billing company acting as an agent of the physician, group p y g g p y , g ppractice, or entity specified in subsections (i) through (iv) under a billing number assigned to the physician, group practice, or entity, provided that the billing arrangement meets the requirements of 42 C F R § 424 80(b)(5)meets the requirements of 42 C.F.R. § 424.80(b)(5).
Note: With regard to the billing requirements, a group practice may have and bill under more than onepractice may have, and bill under, more than one Medicare billing number, subject to any applicable Medicare program restrictions.
Special DME Rule - A physician or group practice that furnishes DME must meet all DME supplier standards set forth at 42 C.F.R. § 424.57(c).
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AKBS Considerations – Supply Closets
The OIG has had longstanding concern regarding space rental arrangements in physician office space.
"Consignment closets" (also called "supply closets") have been specifically mentioned in OIG guidance.
C i th t h t di i dConcern is that such arrangements are a disguised kickback from a supplier to a physician/group practice for referrals of DMEPOS items.
Arrangements should be structured to meet the AKBS rental safe harbor and the Stark Law's rental of office space exception as well as the Supplierof office space exception, as well as the Supplier Standards.
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QUESTIONS?Q
Jana Kolarik Andersonl 202 2960 90 1 39 8Tel: 202-545-2960 or 904-714-3948
Email: [email protected]
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