Medicare Program; Prior Authorization for Power Mobility Device (PMD) Demonstration, 46439-46441 [2012-19014]
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Federal Register / Vol. 77, No. 150 / Friday, August 3, 2012 / Notices
individual patients in Table 1 of the IJC
paper and their inappropriate impact on
the antibody values reported in Table II
of the IJC paper were reported in detail
by Respondent to the Managing Editor
in IJC in email communications dated
September 24 and 29, 2008.
Dr. Ravindranath has entered into a
Voluntary Settlement Agreement and
has voluntarily agreed for a period of
three (3) years, beginning on July 2,
2012:
(1) To have any PHS-supported
research supervised; Respondent agreed
that prior to the submission of an
application for PHS support for a
research project on which the
Respondent’s participation is proposed
and prior to Respondent’s participation
in any capacity on PHS-supported
research, Respondent shall ensure that a
plan for supervision of Respondent’s
duties is submitted to ORI for approval;
the supervision plan must be designed
to ensure the scientific integrity of
Respondent’s research contribution;
Respondent agreed that he shall not
participate in any PHS-supported
research until such a supervision plan is
submitted to and approved by ORI;
Respondent agreed to maintain
responsibility for compliance with the
agreed upon supervision plan;
(2) That any institution employing
him shall submit, in conjunction with
each application for PHS funds, or
report, manuscript, or abstract involving
PHS- supported research in which
Respondent is involved, a certification
to ORI that the data provided by
Respondent are based on actual
experiments or are otherwise
legitimately derived, that the data,
procedures, and methodology are
accurately reported in the application,
report, manuscript, or abstract, and that
the text in such submissions is his own
or properly cites the source of copied
language and ideas; and
(3) To exclude himself voluntarily
from serving in any advisory capacity to
PHS including, but not limited to,
service on any PHS advisory committee,
board, and/or peer review committee, or
as a consultant.
TKELLEY on DSK3SPTVN1PROD with NOTICES
FOR FURTHER INFORMATION CONTACT:
Director, Division of Investigative
Oversight, Office of Research Integrity,
1101 Wootton Parkway, Suite 750,
Rockville, MD 20852, (240) 453–8800.
John Dahlberg,
Director, Division of Investigative Oversight,
Office of Research Integrity.
[FR Doc. 2012–18990 Filed 8–2–12; 8:45 am]
BILLING CODE 4150–31–P
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Jkt 226001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Decision To Evaluate a Petition To
Designate a Class of Employees From
the Baker Brothers Site in Toledo,
Ohio, To Be Included in the Special
Exposure Cohort
National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention, Department of Health
and Human Services.
ACTION: Notice.
AGENCY:
NIOSH gives notice as
required by 42 CFR 83.12(e) of a
decision to evaluate a petition to
designate a class of employees from the
Bakers Brothers site in Toledo, Ohio, to
be included in the Special Exposure
Cohort under the Energy Employees
Occupational Illness Compensation
Program Act of 2000. The initial
proposed definition for the class being
evaluated, subject to revision as
warranted by the evaluation, is as
follows:
Facility: Baker Brothers.
Location: Toledo, Ohio.
Job Titles and/or Job Duties: All
employees who worked in any area.
Period of Employment: June 1, 1943 to
December 31, 1996.
FOR FURTHER INFORMATION CONTACT:
Stuart L. Hinnefeld, Director, Division
of Compensation Analysis and Support,
National Institute for Occupational
Safety and Health, 4676 Columbia
Parkway, MS C–46, Cincinnati, OH
45226, Telephone 877–222–7570.
Information requests can also be
submitted by email to DCAS@CDC.GOV.
SUMMARY:
John Howard,
Director, National Institute for Occupational
Safety and Health.
[FR Doc. 2012–19047 Filed 8–2–12; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–6042–N]
Medicare Program; Prior Authorization
for Power Mobility Device (PMD)
Demonstration
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
This notice announces a 3year Medicare Prior Authorization for
Power Mobility Device (PMD)
SUMMARY:
PO 00000
Frm 00067
Fmt 4703
Sfmt 4703
46439
Demonstration for certain PMD codes in
seven states where there have been high
incidences of fraudulent claims and
improper payments
DATES: This demonstration begins on
September 1, 2012.
FOR FURTHER INFORMATION CONTACT:
Daniel Schwartz, 410–786–4197.
Questions regarding the Medicare
Prior Authorization for PMD
Demonstration should be sent to
pademo@cms.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Power Mobility Devices have had
historically high incidents of fraud and
improper payments. PMD suppliers also
continue to be subject to significant law
enforcement investigation.
The Health Care Fraud Prevention
and Enforcement Action Team (HEAT)
Task Force was launched in May 2009
and is co-chaired by the Deputy
Secretary of HHS and the Deputy
Attorney General of DOJ. Medicare
Fraud Strike Force teams are a key
component of HEAT, since their
inception and based on data driven
investigations, prosecutors have filed
more than 600 cases charging more than
1,150 defendants who collectively billed
the Medicare program more than $2.9
billion in fraudulent claims. DME is a
primary focus of investigation for these
strike forces.
The Comprehensive Error Rate
Testing (CERT) Program noted in a 2010
Report 1 that 92.6 percent of claims for
motorized wheelchairs did not meet
Medicare coverage requirements.
Although we recognize that many
improper payments are not the result of
willful fraud, this error rate represents
over $822 million dollars in estimated
improper payments.
II. Legislative Authority
Section 402(a)(1)(J) of the Social
Security Amendments of 1967, 42
U.S.C. 1395b–1(a)(1)(J), authorizes the
Secretary to conduct demonstrations
designed to develop or demonstrate
improved methods for the investigation
and prosecution of fraud in the
provision of care or services provided
under the Medicare program. We plan to
conduct a demonstration that
implements a prior authorization
process for power mobility devices
(PMDs), an area with historically high
levels of fraud and improper payments,
to develop improved methods for the
investigation and prosecution of fraud
1 https://www.cms.gov/Research-Statistics-Dataand-Systems/Monitoring-Programs/CERT/
Downloads/CERT_Nov_2010_Appendix_-final.pdf
Supplemental Appendix, Table B2.
E:\FR\FM\03AUN1.SGM
03AUN1
TKELLEY on DSK3SPTVN1PROD with NOTICES
46440
Federal Register / Vol. 77, No. 150 / Friday, August 3, 2012 / Notices
in order to protect the Medicare Trust
Fund from fraudulent actions and the
resulting improper payments. We are
conducting this 3-year demonstration in
California, Florida, Illinois, Michigan,
New York, North Carolina, and Texas.
The beneficiary’s address as reported to
the Social Security Administration
(SSA) will determine participation in
the demonstration.
We believe this demonstration will
provide the agency with valuable data
through which the agency, working with
its partners, can develop new avenues
for combating the submission of
fraudulent claims to the Medicare
program for PMDs. We will share data
developed from this demonstration
within the agency, with our contractors,
and with our law enforcement partners
for further analysis and investigation.
We believe that data evidencing changes
in physician ordering and supplier
billing practices that coincide with this
demonstration could provide
investigators and law enforcement with
important information for determining
how and where to focus their
investigations concerning fraud in the
provision of PMDs. For instance, results
from this demonstration could
potentially indicate collaboration
between ordering physicians and
suppliers in submitting fraudulent
claims for PMDs. This data could assist
investigators and law enforcement in
targeting their investigations in this
area. Additionally, changes in billing
practices that result from this
demonstration could provide specific
leads for investigators and law
enforcement personnel. For instance,
where a supplier that frequently
submitted claims prior to the
demonstration stops submitting claims
during the demonstration, law
enforcement may determine it prudent
to investigate that supplier.
Data we will analyze will include the
following:
• Suppliers who no longer bill or
have a significant decrease in billing.
• Physicians/treating practitioners
with a high volume of submissions.
• Codes that show a dramatic
increase in use.
• Codes that show a dramatic
decrease in use.
The demonstration will likely have a
secondary benefit to help identify and
reduce improper payments. We
recognize that many improper payments
are not the result of willful fraud.
Information shared with law
enforcement will be limited to data on
those providers and suppliers who are
potentially submitting fraudulent claims
and other information that we believe
VerDate Mar<15>2010
17:33 Aug 02, 2012
Jkt 226001
covered item. The physician, treating
practitioner or supplier who submits the
request on behalf of the physician or
treating practitioner, is referred to as the
‘‘submitter.’’ In order to be affirmed, the
request for prior authorization must
meet all applicable rules, policies, and
National Coverage Determination
(NCD)/Local Coverage Determination
(LCD) requirements for PMD claims.
LCD requirements mandating
physician/treating practitioner
origination, such as the seven-element
order, face-to-face encounter
documentation and whatever other
clinical documentation is necessary,
must be completed by the physician/
treating practitioner regardless of which
entity is functioning as the submitter.
III. Provisions of the Notice
The supplier will still complete the
detailed product description regardless
This demonstration will implement a
prior authorization process for PMDs in of which entity is functioning as the
seven states where historically there has submitter.
After receipt of all relevant
been extensive evidence of fraud and
improper payments (CA, FL, IL, MI, NY, documentation, CMS or its agents will
make every effort to conduct a review
NC, and TX).
The prior authorization process under and postmark the notification of their
decision with the prior authorization
this demonstration is available for the
number within 10 business days.
following codes for Medicare payment:
Notification is provided to the
• Group 1 Power Operated Vehicles
physician/treating practitioner,
(K0800 through K0802 and K0812).
supplier, and the Medicare beneficiary
• All standard power wheelchairs
for the initial submission. If a
(K0813 through K0829).
• All Group 2 complex rehabilitative
subsequent prior authorization request
power wheelchairs (K0835 through
is submitted after a nonaffirmative
K0843).
decision on a prior authorization
• All Group 3 complex rehabilitative
request, then CMS or its agents will
power wheelchairs without power
make every effort to conduct a review
options (K0848 through K0855).
and postmark the notification of
• Pediatric power wheelchairs (K0890 decision with the prior authorization
and K0891).
number within 20 business days. These
• Miscellaneous power wheelchairs
timeframes will become part of the
(K0898).
contractors’ performance metrics.
Prior to the start of the demonstration,
There will also be a mechanism in
we have conducted and will continue to place to request an expedited review in
conduct outreach and education
emergency situations where a
including webinars, in-state meetings
practitioner indicates clearly, with
and other education sessions.
supporting rationale that the standard
Additional information about the
(routine) timeframe for a Prior
implementation of the prior
Authorization Decision (10 days) could
authorization demonstration is available seriously jeopardize the beneficiary’s
on the CMS Web site (go.cms.gov/
life or health. In these cases, the
PAdemo). In addition, suppliers who
contractor will conduct an expedited
have recently furnished and
review. The expedited request must be
practitioners who have recently ordered accompanied by the required supporting
a PMD for a beneficiary residing in a
documentation for this request to be
demonstration state will be notified via
considered complete thus commencing
certified letters about the demonstration the 48 hours for review. Inappropriate
prior to the start date of the
expedited requests may be downgraded
demonstration.
to standard requests. After conducting
Under this demonstration, a
an expedited review, CMS or its agents
physician, treating practitioner, or
will communicate a decision for the
supplier will be encouraged to submit to prior authorization request to the
their Durable Medical Equipment (DME) submitter within 48 hours of the
Medicare Administrative Contractor
complete submission.
(MAC) a request for prior authorization
The following explains the various
and all relevant documentation to
prior authorization scenarios:
• Scenario 1: When a submitter sends
support Medicare coverage of the PMD
item along with the written order for the a prior authorization request to the DME
will assist with the investigation and
prosecution of fraud.
Section 402(b) of the Social Security
Amendments of 1967 authorizes the
Secretary to waive requirements in Title
XVIII that relate to reimbursement and
payment in order to carry out the
demonstrations authorized under
section 402(a). In accordance with
section 402(b), the Secretary waives
certain requirements of sections 1834(a),
1834(j)(4) and 1879 of the Social
Security Act to the extent necessary to
implement this demonstration,
including, but not limited to, certain
payment and reimbursement regulations
set forth at 42 CFR part 414, Subpart D
and 42 CFR Part 411, Subpart K.
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TKELLEY on DSK3SPTVN1PROD with NOTICES
Federal Register / Vol. 77, No. 150 / Friday, August 3, 2012 / Notices
MAC with appropriate documentation
and all relevant Medicare coverage and
documentation requirements are met for
the PMD, then the DME MAC sends an
affirmative prior authorization decision
to the physician or treating practitioner,
supplier, and Medicare beneficiary.
When the claim is submitted to the DME
MAC by the supplier, it is linked to the
Prior Authorization via the claims
processing system and so long as all
applicable requirements in the
applicable NCD/LCD are met, the claim
is paid.
• Scenario 2: When a submitter sends
a prior authorization request but all
relevant Medicare coverage
requirements are not met for the PMD,
then the DME MAC sends a
nonaffirmative prior authorization
decision to the physician or treating
practitioner, supplier, and Medicare
beneficiary advising them that Medicare
will not pay for the item. A supplier can
deliver the PMD, and submit a claim
with a non-affirmative prior
authorization decision, at which point
the DME MAC would deny the claim.
The supplier and/or the beneficiary
would then have the Medicare denial
for secondary insurance purposes and
would have full appeal rights.
If an applicable PMD claim is
submitted without a prior authorization
decision it will be stopped and
documentation will be requested to
conduct medical review. After the first
3 months of the demonstration, we will
assess a payment reduction for claims
that, after review, are deemed payable,
but did not first receive a prior
authorization decision. As evidence of
compliance, the supplier must submit
the prior authorization number on the
claim in order to avoid a 25 percent
payment reduction. The 25 percent
payment reduction is non-transferrable
to the beneficiary and not subject to
appeal. In the case of capped rental
items, the payment reduction will be
applied to all claims in the series.
The 25-percent reduction in the
Medicare payment is for each payable
base claim not preceded by a prior
authorization request except in
competitive bidding areas. If a
competitive bid contract supplier
submits a payable claim for a
beneficiary with a permanent residence
in a competitive bidding area, that is
included in the supplier’s contract,
without first receiving a prior
authorization decision, that competitive
bid supplier would receive the
applicable single payment amount
under the competitive bid program, and
would not be subject to the 25-percent
reduction. These suppliers must still
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17:33 Aug 02, 2012
Jkt 226001
adhere to all other requirements of the
demonstration.
• Scenario 3: When a submitter sends
a prior authorization request where
documentation is incomplete, the prior
authorization request is sent back to the
submitter with an explanation about
what information is missing. The
submitter can rectify the situation and
resubmit the prior authorization request.
The physician or treating practitioner,
supplier, and Medicare beneficiary are
also notified.
• Scenario 4: When the DME supplier
fails to receive a prior authorization
decision, but nonetheless delivers the
item to the beneficiary and submits the
claim to the DME MAC for payment, the
PMD claim will be reviewed under
normal medical review processing
timeframes.
++ If the claim is determined to be not
medically necessary or insufficiently
documented, the claim will be denied.
The supplier and/or beneficiary can
appeal the claim denial. If the claim,
after review, is deemed not payable then
all current beneficiary/supplier liability
policies and procedures as well as
appeal rights remain in effect.
++ If the claim is determined to be
payable, it will be paid. However, 3
months after the start of the
demonstration, a 25-percent reduction
in the Medicare Payment will be
applied for failure to receive a prior
authorization decision before the
submission of a claim. This payment
reduction will not be applied for
competitive bidding program contract
suppliers submitting claims for
beneficiaries who maintain a permanent
residence in a Competitive Bidding Area
in their contracts according to the
Common Working File (CWF)); these
contract suppliers will continue to
receive the applicable single payment
amount under their contracts. The 25percent payment reduction is nontransferrable to the beneficiary for the
claims that are deemed payable. This
payment reduction will begin 3 months
after the start of the demonstration and
is not subject to appeal. In the case of
capped rental items the payment
reduction will be applied to all claims
in the series. After a claim is submitted
and processed, appeal rights are
available as they normally are.
Under the demonstration, we will
work to limit the impact on
beneficiaries. We will educate
beneficiaries as part of this protection.
If the prior authorization request is not
affirmed, and the claim is still
submitted by the supplier, the claim
will be denied in full, but beneficiaries
will continue to have all normal appeal
rights as well as the option of signing an
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Fmt 4703
Sfmt 4703
46441
Advance Beneficiary Notice in order to
receive and be liable for payment for a
denied PMD.
Additional information is available on
the CMS Web site at go.cms.gov/
PAdemo.
IV. Collection of Information
Requirements
We announced and solicited
comments for the information collection
requirements associated with the
Medicare Prior Authorization for Power
Mobility Device (PMD) Demonstration
for certain PMD codes in 60-day and 30day Federal Register notices that
published on February 7, 2012 (77 FR
6124) and May 29, 2012 (77 FR 31616),
respectively. The information collection
requirements are approved under OMB
control number 0938–1169.
Authority: Section 402(a)(1)(J) of the
Social Security Amendments of 1967.
Dated: July 30, 2012
Marilyn Tavenner,
Acting Administrator, Centers for Medicare
& Medicaid Services.
[FR Doc. 2012–19014 Filed 8–1–12; 4:15 pm]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0386]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Registration and
Product Listing for Owners and
Operators of Domestic Tobacco
Product Establishments and Listing of
Ingredients in Tobacco Products
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by September
4, 2012.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or emailed to
oira_submission@omb.eop.gov. All
SUMMARY:
E:\FR\FM\03AUN1.SGM
03AUN1
Agencies
[Federal Register Volume 77, Number 150 (Friday, August 3, 2012)]
[Notices]
[Pages 46439-46441]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-19014]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-6042-N]
Medicare Program; Prior Authorization for Power Mobility Device
(PMD) Demonstration
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces a 3-year Medicare Prior Authorization
for Power Mobility Device (PMD) Demonstration for certain PMD codes in
seven states where there have been high incidences of fraudulent claims
and improper payments
DATES: This demonstration begins on September 1, 2012.
FOR FURTHER INFORMATION CONTACT: Daniel Schwartz, 410-786-4197.
Questions regarding the Medicare Prior Authorization for PMD
Demonstration should be sent to pademo@cms.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Power Mobility Devices have had historically high incidents of
fraud and improper payments. PMD suppliers also continue to be subject
to significant law enforcement investigation.
The Health Care Fraud Prevention and Enforcement Action Team (HEAT)
Task Force was launched in May 2009 and is co-chaired by the Deputy
Secretary of HHS and the Deputy Attorney General of DOJ. Medicare Fraud
Strike Force teams are a key component of HEAT, since their inception
and based on data driven investigations, prosecutors have filed more
than 600 cases charging more than 1,150 defendants who collectively
billed the Medicare program more than $2.9 billion in fraudulent
claims. DME is a primary focus of investigation for these strike
forces.
The Comprehensive Error Rate Testing (CERT) Program noted in a 2010
Report \1\ that 92.6 percent of claims for motorized wheelchairs did
not meet Medicare coverage requirements. Although we recognize that
many improper payments are not the result of willful fraud, this error
rate represents over $822 million dollars in estimated improper
payments.
---------------------------------------------------------------------------
\1\ https://www.cms.gov/Research-Statistics-Data-and-Systems/Monitoring-Programs/CERT/Downloads/CERT_Nov_2010_Appendix_-final.pdf Supplemental Appendix, Table B2.
---------------------------------------------------------------------------
II. Legislative Authority
Section 402(a)(1)(J) of the Social Security Amendments of 1967, 42
U.S.C. 1395b-1(a)(1)(J), authorizes the Secretary to conduct
demonstrations designed to develop or demonstrate improved methods for
the investigation and prosecution of fraud in the provision of care or
services provided under the Medicare program. We plan to conduct a
demonstration that implements a prior authorization process for power
mobility devices (PMDs), an area with historically high levels of fraud
and improper payments, to develop improved methods for the
investigation and prosecution of fraud
[[Page 46440]]
in order to protect the Medicare Trust Fund from fraudulent actions and
the resulting improper payments. We are conducting this 3-year
demonstration in California, Florida, Illinois, Michigan, New York,
North Carolina, and Texas. The beneficiary's address as reported to the
Social Security Administration (SSA) will determine participation in
the demonstration.
We believe this demonstration will provide the agency with valuable
data through which the agency, working with its partners, can develop
new avenues for combating the submission of fraudulent claims to the
Medicare program for PMDs. We will share data developed from this
demonstration within the agency, with our contractors, and with our law
enforcement partners for further analysis and investigation. We believe
that data evidencing changes in physician ordering and supplier billing
practices that coincide with this demonstration could provide
investigators and law enforcement with important information for
determining how and where to focus their investigations concerning
fraud in the provision of PMDs. For instance, results from this
demonstration could potentially indicate collaboration between ordering
physicians and suppliers in submitting fraudulent claims for PMDs. This
data could assist investigators and law enforcement in targeting their
investigations in this area. Additionally, changes in billing practices
that result from this demonstration could provide specific leads for
investigators and law enforcement personnel. For instance, where a
supplier that frequently submitted claims prior to the demonstration
stops submitting claims during the demonstration, law enforcement may
determine it prudent to investigate that supplier.
Data we will analyze will include the following:
Suppliers who no longer bill or have a significant
decrease in billing.
Physicians/treating practitioners with a high volume of
submissions.
Codes that show a dramatic increase in use.
Codes that show a dramatic decrease in use.
The demonstration will likely have a secondary benefit to help
identify and reduce improper payments. We recognize that many improper
payments are not the result of willful fraud. Information shared with
law enforcement will be limited to data on those providers and
suppliers who are potentially submitting fraudulent claims and other
information that we believe will assist with the investigation and
prosecution of fraud.
Section 402(b) of the Social Security Amendments of 1967 authorizes
the Secretary to waive requirements in Title XVIII that relate to
reimbursement and payment in order to carry out the demonstrations
authorized under section 402(a). In accordance with section 402(b), the
Secretary waives certain requirements of sections 1834(a), 1834(j)(4)
and 1879 of the Social Security Act to the extent necessary to
implement this demonstration, including, but not limited to, certain
payment and reimbursement regulations set forth at 42 CFR part 414,
Subpart D and 42 CFR Part 411, Subpart K.
III. Provisions of the Notice
This demonstration will implement a prior authorization process for
PMDs in seven states where historically there has been extensive
evidence of fraud and improper payments (CA, FL, IL, MI, NY, NC, and
TX).
The prior authorization process under this demonstration is
available for the following codes for Medicare payment:
Group 1 Power Operated Vehicles (K0800 through K0802 and
K0812).
All standard power wheelchairs (K0813 through K0829).
All Group 2 complex rehabilitative power wheelchairs
(K0835 through K0843).
All Group 3 complex rehabilitative power wheelchairs
without power options (K0848 through K0855).
Pediatric power wheelchairs (K0890 and K0891).
Miscellaneous power wheelchairs (K0898).
Prior to the start of the demonstration, we have conducted and will
continue to conduct outreach and education including webinars, in-state
meetings and other education sessions. Additional information about the
implementation of the prior authorization demonstration is available on
the CMS Web site (go.cms.gov/PAdemo). In addition, suppliers who have
recently furnished and practitioners who have recently ordered a PMD
for a beneficiary residing in a demonstration state will be notified
via certified letters about the demonstration prior to the start date
of the demonstration.
Under this demonstration, a physician, treating practitioner, or
supplier will be encouraged to submit to their Durable Medical
Equipment (DME) Medicare Administrative Contractor (MAC) a request for
prior authorization and all relevant documentation to support Medicare
coverage of the PMD item along with the written order for the covered
item. The physician, treating practitioner or supplier who submits the
request on behalf of the physician or treating practitioner, is
referred to as the ``submitter.'' In order to be affirmed, the request
for prior authorization must meet all applicable rules, policies, and
National Coverage Determination (NCD)/Local Coverage Determination
(LCD) requirements for PMD claims.
LCD requirements mandating physician/treating practitioner
origination, such as the seven-element order, face-to-face encounter
documentation and whatever other clinical documentation is necessary,
must be completed by the physician/treating practitioner regardless of
which entity is functioning as the submitter. The supplier will still
complete the detailed product description regardless of which entity is
functioning as the submitter.
After receipt of all relevant documentation, CMS or its agents will
make every effort to conduct a review and postmark the notification of
their decision with the prior authorization number within 10 business
days. Notification is provided to the physician/treating practitioner,
supplier, and the Medicare beneficiary for the initial submission. If a
subsequent prior authorization request is submitted after a
nonaffirmative decision on a prior authorization request, then CMS or
its agents will make every effort to conduct a review and postmark the
notification of decision with the prior authorization number within 20
business days. These timeframes will become part of the contractors'
performance metrics.
There will also be a mechanism in place to request an expedited
review in emergency situations where a practitioner indicates clearly,
with supporting rationale that the standard (routine) timeframe for a
Prior Authorization Decision (10 days) could seriously jeopardize the
beneficiary's life or health. In these cases, the contractor will
conduct an expedited review. The expedited request must be accompanied
by the required supporting documentation for this request to be
considered complete thus commencing the 48 hours for review.
Inappropriate expedited requests may be downgraded to standard
requests. After conducting an expedited review, CMS or its agents will
communicate a decision for the prior authorization request to the
submitter within 48 hours of the complete submission.
The following explains the various prior authorization scenarios:
Scenario 1: When a submitter sends a prior authorization
request to the DME
[[Page 46441]]
MAC with appropriate documentation and all relevant Medicare coverage
and documentation requirements are met for the PMD, then the DME MAC
sends an affirmative prior authorization decision to the physician or
treating practitioner, supplier, and Medicare beneficiary. When the
claim is submitted to the DME MAC by the supplier, it is linked to the
Prior Authorization via the claims processing system and so long as all
applicable requirements in the applicable NCD/LCD are met, the claim is
paid.
Scenario 2: When a submitter sends a prior authorization
request but all relevant Medicare coverage requirements are not met for
the PMD, then the DME MAC sends a nonaffirmative prior authorization
decision to the physician or treating practitioner, supplier, and
Medicare beneficiary advising them that Medicare will not pay for the
item. A supplier can deliver the PMD, and submit a claim with a non-
affirmative prior authorization decision, at which point the DME MAC
would deny the claim. The supplier and/or the beneficiary would then
have the Medicare denial for secondary insurance purposes and would
have full appeal rights.
If an applicable PMD claim is submitted without a prior
authorization decision it will be stopped and documentation will be
requested to conduct medical review. After the first 3 months of the
demonstration, we will assess a payment reduction for claims that,
after review, are deemed payable, but did not first receive a prior
authorization decision. As evidence of compliance, the supplier must
submit the prior authorization number on the claim in order to avoid a
25 percent payment reduction. The 25 percent payment reduction is non-
transferrable to the beneficiary and not subject to appeal. In the case
of capped rental items, the payment reduction will be applied to all
claims in the series.
The 25-percent reduction in the Medicare payment is for each
payable base claim not preceded by a prior authorization request except
in competitive bidding areas. If a competitive bid contract supplier
submits a payable claim for a beneficiary with a permanent residence in
a competitive bidding area, that is included in the supplier's
contract, without first receiving a prior authorization decision, that
competitive bid supplier would receive the applicable single payment
amount under the competitive bid program, and would not be subject to
the 25-percent reduction. These suppliers must still adhere to all
other requirements of the demonstration.
Scenario 3: When a submitter sends a prior authorization
request where documentation is incomplete, the prior authorization
request is sent back to the submitter with an explanation about what
information is missing. The submitter can rectify the situation and
resubmit the prior authorization request. The physician or treating
practitioner, supplier, and Medicare beneficiary are also notified.
Scenario 4: When the DME supplier fails to receive a prior
authorization decision, but nonetheless delivers the item to the
beneficiary and submits the claim to the DME MAC for payment, the PMD
claim will be reviewed under normal medical review processing
timeframes.
++ If the claim is determined to be not medically necessary or
insufficiently documented, the claim will be denied. The supplier and/
or beneficiary can appeal the claim denial. If the claim, after review,
is deemed not payable then all current beneficiary/supplier liability
policies and procedures as well as appeal rights remain in effect.
++ If the claim is determined to be payable, it will be paid.
However, 3 months after the start of the demonstration, a 25-percent
reduction in the Medicare Payment will be applied for failure to
receive a prior authorization decision before the submission of a
claim. This payment reduction will not be applied for competitive
bidding program contract suppliers submitting claims for beneficiaries
who maintain a permanent residence in a Competitive Bidding Area in
their contracts according to the Common Working File (CWF)); these
contract suppliers will continue to receive the applicable single
payment amount under their contracts. The 25-percent payment reduction
is non-transferrable to the beneficiary for the claims that are deemed
payable. This payment reduction will begin 3 months after the start of
the demonstration and is not subject to appeal. In the case of capped
rental items the payment reduction will be applied to all claims in the
series. After a claim is submitted and processed, appeal rights are
available as they normally are.
Under the demonstration, we will work to limit the impact on
beneficiaries. We will educate beneficiaries as part of this
protection. If the prior authorization request is not affirmed, and the
claim is still submitted by the supplier, the claim will be denied in
full, but beneficiaries will continue to have all normal appeal rights
as well as the option of signing an Advance Beneficiary Notice in order
to receive and be liable for payment for a denied PMD.
Additional information is available on the CMS Web site at
go.cms.gov/PAdemo.
IV. Collection of Information Requirements
We announced and solicited comments for the information collection
requirements associated with the Medicare Prior Authorization for Power
Mobility Device (PMD) Demonstration for certain PMD codes in 60-day and
30-day Federal Register notices that published on February 7, 2012 (77
FR 6124) and May 29, 2012 (77 FR 31616), respectively. The information
collection requirements are approved under OMB control number 0938-
1169.
Authority: Section 402(a)(1)(J) of the Social Security
Amendments of 1967.
Dated: July 30, 2012
Marilyn Tavenner,
Acting Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. 2012-19014 Filed 8-1-12; 4:15 pm]
BILLING CODE 4120-01-P