Medicare Program; Prior Authorization of Non-Emergent Hyperbaric Oxygen (HBO) Therapy, 69488-69490 [2014-27578]
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determinations of ITL situations; and
surveyor documentation that includes a
detailed deficiency statement that
clearly supports the determination of
manner and degree of non-compliance
and the appropriate level of citation.
• Section 488.8(a)(2)(iv), to
strengthen surveyor documentation to
include sufficient detail to support the
determination of the manner and degree
of non-compliance and the appropriate
level of deficiency citation.
• Section 489.13, related to the
effective date of accreditation for
facilities undergoing a survey for
purposes of its initial participation in
Medicare; to ensure the effective date of
accreditation when deficiencies have
been identified, and to ensure it is
consistent with CMS regulatory
requirements.
• To ensure comparability with the
survey process requirements at
§ 488.26(d), TJC must have—
++ Updated its accreditation process
policies to clarify that all surveys for
TJC’s Medicare ASC accreditation
program are conducted unannounced.
++ Updated its accreditation process
policies to ensure all required follow-up
surveys for its Medicare ASC
accreditation program meet the
Medicare requirements.
++ Revised its accreditation process
policies to clarify that the appropriate
level of citation be made when an
Immediate Threat to Health or Safety is
identified.
++ Clarified its survey policies in the
surveyor activity guide (SAG) to address
how ‘‘Special Issue Resolution’’ is
handled during surveys lasting only 1
day.
++ Updated its ASC accreditation
process policies to clearly demonstrate
that the policies are related to ASCs and
not hospitals.
• Section 488.28(a), to include all
documented observations of noncompliance and all internal,
uncompleted Plans for Improvement
(PFI) listed in the accredited ASC’s
‘‘Statement of Condition (SOC) to
correct Life Safety Code Deficiencies’’
into the survey report. In addition, TJC
will provide CMS with rationale for
each standard for which TJC has
determined will not require a citation of
non-compliance when a single
observation has been made.
• Complied with section 1861(e)(9)(C)
of the Act, to require that waiver and
equivalency requests submitted by
accredited organizations for Life Safety
Code deficiencies that would result in
unreasonable hardship for such a
facility to resolve and would not
jeopardize patient health or safety, be
VerDate Sep<11>2014
18:00 Nov 20, 2014
Jkt 235001
reviewed by TJC, and forwarded to CMS
for approval, as appropriate.
• To demonstrate comparability with
minimum eligibility requirements for
Initial surveys, increased the minimum
number of patients/volume of services
from three patients served with one
active at the time of survey, to ten
patients served, with one active at the
time of survey.
• To comply with TJS’s own policies,
TJS must—
++ Ensure its surveyors complete the
ASC Infection Control Worksheet on
every survey.
++ Ensure its surveyors observe at
least one surgery during every survey.
++ Ensure that the minimum number
of medical records have been reviewed
on every survey.
++ Ensure that findings noted on the
Infection Control Worksheet are
integrated into the survey report
findings.
B. Term of Approval
Based on our review and observations
described in section III of this final
notice, we approve TJC as a national
accreditation organization for ASCs that
request participation in the Medicare
program, effective December 20, 2014
through December 20, 2020.
To verify TJC’s continued compliance
with the provisions of this final notice,
we will conduct a follow-up corporate
on-site visit and survey observation
within 18 months of the date of
publication of this final notice.
V. Collection of Information
Requirements
This document does not impose
information collection requirements,
that is, reporting, recordkeeping or
third-party disclosure requirements.
Consequently, there is no need for
review by the Office of Management and
Budget under the authority of the
Paperwork Reduction Act of 1995 (44
U.S.C. Chapter 35).
Dated: November 5, 2014.
Marilyn Tavenner,
Administrator, Centers for Medicare &
Medicaid Services.
[FR Doc. 2014–27577 Filed 11–20–14; 8:45 am]
BILLING CODE 4120–01–P
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–6064–N]
Medicare Program; Prior Authorization
of Non-Emergent Hyperbaric Oxygen
(HBO) Therapy
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
This notice announces a 3year Medicare Prior Authorization
model for non-emergent hyperbaric
oxygen therapy services in the states of
Illinois, Michigan, and New Jersey
where there have been high incidences
of improper payments for these services.
DATES: The model will begin on March
1, 2015 in Michigan, New Jersey, and
Illinois.
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
Jennifer McMullen, (410) 786–7635.
Questions regarding the Medicare
Prior Authorization Model for NonEmergent Hyperbaric Oxygen (HBO)
Therapy should be sent to HBOPA@
cms.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Hyperbaric Oxygen (HBO) therapy is
a modality used for treatment of wounds
in which the entire body is exposed to
oxygen under increased atmospheric
pressure. HBO therapy is covered as
adjunctive therapy only after there have
been no measurable signs of healing
during at least 30 consecutive days of
treatment with standard wound therapy,
and must be used in addition to
standard wound care. Wounds must be
evaluated at least every 30 days during
administration of HBO therapy.
Continued treatment with HBO therapy
is not covered if measurable signs of
healing have not been demonstrated
within any 30-day period of treatment.
Medicare issued a National Coverage
Determination (NCD) for HBO therapy
in 2002, which lists clinical conditions
for which HBO therapy is medically
necessary and clinical conditions for
which HBO therapy is not medically
necessary, and therefore; not covered by
Medicare. The NCD can be found in the
Medicare National Coverage
Determinations Manual (CMS Pub. No.
100–03), Chapter 1, Part 1, Section
20.29, and in the NCD database at
https://www.cms.gov/medicare-coveragedatabase/details/nca-decision-memo.
aspx?NCAId=37&bc=AiAAAAAAA
gAAAA%3d%3d&. In addition, some of
E:\FR\FM\21NON1.SGM
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the Medicare Administrative
Contractors (MACs) have Local
Coverage Determinations (LCDs) that
expand on the NCD.
In 2000, a report by the HHS Office
of Inspector General 1 on hyperbaric
oxygen therapy found the following:
• $14.2 million (of $49.9 million in
allowed charges for outpatient hospital
departments and physicians) was paid
in error, either for beneficiaries who
received treatments for non-covered
conditions or when documentation did
not adequately support HBO.
• An additional $4.9 million was paid
for treatments deemed to be excessive.
• Lack of testing and treatment
monitoring raised quality of care
concerns.
Data from CMS’ Chronic Condition
Warehouse were used to determine state
rankings based on average number of
sessions per beneficiary. States were
then ranked by expenditures. Illinois,
Michigan, and New Jersey were selected
as the initial states for the model
because they ranked in the top three for
average number of sessions per
beneficiary.
Section 1115A of the Social Security
Act (the Act) authorizes the Secretary to
test innovative payment and service
delivery models to reduce program
expenditures, while preserving or
enhancing the quality of care furnished
to Medicare, Medicaid, and Children’s
Health Insurance Program beneficiaries.
Section 1115A(d)(1) of the Act
authorizes the Secretary to waive such
requirements of Titles XI and XVIII and
of sections 1902(a)(1), 1902(a)(13), and
1903(m)(2)(A)(iii) of the Act as may be
necessary solely for purposes of carrying
out section 1115A of the Act with
respect to testing models described in
section 1115A(b) of the Act. For this
model, consistent with this standard, we
will waive such provisions of sections
1834(a)(15) and 1869(h) of the Act that
limit our ability to conduct prior
authorization. We have determined that
the implementation of this model does
not require the waiver of any fraud and
abuse law, including sections 1128A,
1128B, and 1877 of the Act. Thus,
providers and suppliers affected by this
model must comply with all applicable
fraud and abuse laws. While these
provisions are specific to durable
medical equipment (DME) and
physician services, we will waive any
portion of these sections as well as any
portion of 42 CFR 410.20(d) of the
regulations, which implements section
1869(h) of the Act, that could be
1 Office of Inspector General, Hyperbaric Oxygen
Therapy, Its Use and Appropriateness, October
2000.
VerDate Sep<11>2014
18:00 Nov 20, 2014
Jkt 235001
construed to limit our ability to conduct
prior authorization.
II. Provisions of the Notice
We plan to implement a 3-year
Medicare Prior Authorization process
for non-emergent HBO therapy rendered
in 3 states (Illinois, Michigan, and New
Jersey). These states were selected as the
initial states for the model because of
their high utilization and improper
payment rates for this service. The
model will begin in Michigan, New
Jersey, and Illinois on March 1, 2015.
We plan to test whether prior
authorization helps reduce
expenditures, while maintaining or
improving quality of care, using a model
that would establish a prior
authorization process for non-emergent
HBO therapy to reduce utilization of
services that do not comply with
Medicare policy.
We plan to use this prior
authorization process to ensure that all
relevant clinical or medical
documentation requirements are met
before services are rendered to
beneficiaries and before claims are
submitted for payment. This prior
authorization process will further
ensure that payment complies with
Medicare documentation, coverage,
payment, and coding rules.
The use of prior authorization will not
create new clinical documentation
requirements. Instead, it will require the
same information that is already
required to support Medicare payment,
just earlier in the process. Prior
authorization allows facilities to address
issues with claims prior to rendering
services.
The prior authorization process under
this model will be available for the
following code for Medicare payment:
C1300—Hyperbaric oxygen under
pressure, full body chamber, per 30
minute interval.
Prior authorization is only needed for
the facility payment part of the HBO
therapy service. However, if a facility
does not have prior authorization, or has
a non-affirmed prior authorization, the
associated physician claims with the
following code will be subject to
medical review: 99183—Physician
attendance and supervision of
hyperbaric oxygen, per session.
Of the 15 covered clinical conditions
listed in the NCD, the following 6 will
be available for prior authorization:
• Preparation and preservation of
compromised skin grafts (not for
primary management of wounds).
• Chronic refractory osteomyelitis,
unresponsive to conventional medical
and surgical management.
PO 00000
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69489
• Osteoradionecrosis as an adjunct to
conventional treatment.
• Soft tissue radionecrosis as an
adjunct to conventional treatment.
• Actinomycrosis, only as an adjunct
to conventional therapy when the
disease process is refractory to
antibiotics and surgical treatment.
• Diabetic wounds of the lower
extremities in patients who meet the
following three criteria:
++ Patient has Type I or Type II
diabetes and a lower extremity wound
that is due to diabetes.
++ Patient has a wound classified as
Wagner grade III or higher.
++ Patient has failed an adequate
course of wound therapy as defined in
the NCD.
A provisional affirmative prior
authorization decision, justified by the
beneficiary’s condition, may affirm up
to 36 treatments in a 12-month period.
A provisional affirmation is a
preliminary finding that a future claim
submitted to Medicare for the service
likely meets Medicare’s coverage,
coding, and payment requirements. A
provisional affirmative decision can be
for all or part of the requested number
of treatments. If additional treatments
are needed, a subsequent prior
authorization request must be
submitted.
Prior to the start of the model, we will
conduct (and thereafter will continue to
conduct) outreach and education to
facilities that provide HBO therapy, as
well as to beneficiaries, through such
methods as Open Door Forums,
frequently asked questions (FAQs) on
our Web site, other Web site postings,
and educational materials issued by the
Medicare Administrative Contractors
(MACs). Additional information about
the implementation of the prior
authorization model is available on the
CMS Web site at https://go.cms.gov/
PAHBO.
Under this model prior authorization
process, the facility or beneficiary will
be encouraged to submit to the MAC a
request for prior authorization along
with all relevant documentation to
support Medicare coverage of the HBO
therapy. In order to be affirmed, the
request for prior authorization must
meet all applicable rules and policies,
and any NCD and Local Coverage
Determination (LCD) requirements for
HBO therapy.
After receipt of all relevant
documentation, the MACs will make
every effort to conduct a review and
postmark the notification of their
decision on a prior authorization
request within 10 business days for an
initial submission. Notification will be
provided to the submitter of the prior
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69490
Federal Register / Vol. 79, No. 225 / Friday, November 21, 2014 / Notices
authorization request (and, upon
request, to the beneficiary if he or she
was not the original submitter). If a
subsequent prior authorization request
is submitted after a non-affirmative
decision on an initial prior
authorization request, the MACs will
make every effort to conduct a review
and postmark the notification of their
decision on the request within 20
business days.
A facility or beneficiary may request
an expedited review when the standard
timeframe for making a prior
authorization decision could jeopardize
the life or health of the beneficiary. If
the MAC agrees that the standard review
timeframe would put the beneficiary at
risk, the MAC will make reasonable
efforts to communicate a decision
within 2 business days of receipt of all
applicable, Medicare-required
documentation. As this model is for a
non-emergent service only, we expect
requests for expedited reviews to be
extremely rare.
The following describes examples of
various prior authorization scenarios:
• Scenario 1: When a facility or
beneficiary submits a prior
authorization request to the MAC with
appropriate documentation and all
relevant Medicare coverage and
documentation requirements are met for
the HBO therapy, the MAC will send a
provisional affirmative prior
authorization decision to the submitter
(and, upon request, to the beneficiary if
he or she was not the original
submitter). When the claim is submitted
to the MAC, it is linked to the prior
authorization via the claims processing
system and the claim is paid so long as
all Medicare coding, billing, and
coverage requirements are met.
However, after submission, the claim
could be denied for technical reasons,
such as the claim being a duplicate
claim or being for a date of service after
a beneficiary’s death.
• Scenario 2: When a facility or
beneficiary submits a prior
authorization request but all relevant
Medicare coverage requirements are not
met, the MAC will send a nonaffirmative prior authorization decision
to the submitter (and, upon request, to
the beneficiary if he or she was not the
original submitter), advising them that
Medicare will not pay for the service.
The facility or beneficiary may then
resubmit the request with
documentation showing that Medicare
requirements have been met.
Alternatively, a facility could render the
service, and submit a claim with a nonaffirmative prior authorization tracking
number, at which point the MAC would
deny the claim. The facility or the
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18:00 Nov 20, 2014
Jkt 235001
beneficiary would then have the
Medicare denial for secondary
insurance purposes and would have the
opportunity to submit an appeal of the
claim denial if they believe Medicare
coverage was denied inappropriately.
• Scenario 3: When a facility or
beneficiary submits a prior
authorization request with incomplete
documentation, a detailed decision
letter will be sent to the submitter (and,
upon request, to the beneficiary if he or
she was not the original submitter) with
an explanation of what information is
missing. The facility or beneficiary can
rectify the situation and resubmit the
prior authorization request with
appropriate documentation.
• Scenario 4: When a facility renders
a service that is subject to the prior
authorization process to a beneficiary,
and submits the claim to the MAC for
payment without requesting a prior
authorization, the claim will be stopped
for prepayment review and
documentation will be requested.
++ If the claim is determined to be
not medically necessary or to be
insufficiently documented, the claim
will be denied, and all current policies
and procedures regarding liability for
payment will apply. The facility and/or
beneficiary can appeal the claim denial
if they believe the denial was
inappropriate.
++ If the claim is determined to be
payable, it will be paid.
Under the model, we will work to
limit any adverse impact on
beneficiaries and to educate
beneficiaries about the process. If a prior
authorization request is not affirmed,
and the claim is still submitted by the
facility, the claim will be denied in full,
but beneficiaries will continue to have
all applicable administrative appeal
rights.
Only one prior authorization request
per beneficiary per designated time
period can be provisionally affirmed. If
the initial facility cannot complete the
total number of HBO treatments (for
example, the initial facility closes or the
beneficiary moves out of the area), the
initial request is cancelled. In this
situation, a subsequent prior
authorization request may be submitted
for the same beneficiary and must
include the required documentation in
the submission. If multiple facilities are
providing HBO treatments to the
beneficiary during the same or
overlapping time period, the prior
authorization decision will only cover
the facility indicated in the
provisionally affirmed prior
authorization request. Any facility
submitting claims for which no prior
authorization request is recorded will be
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Frm 00070
Fmt 4703
Sfmt 4703
subject to 100 percent pre-payment
medical review of those claims.
Additional information is available on
the CMS Web site at https://go.cms.gov/
PAHBO.
III. Collection of Information
Requirements
Section 1115A(d)(3) of the Act, as
added by section 3021 of the Affordable
Care Act, states that chapter 35 of title
44, United States Code (the Paperwork
Reduction Act of 1995), shall not apply
to the testing and evaluation of models
or expansion of such models under this
section. Consequently, this document
need not be reviewed by the Office of
Management and Budget under the
authority of the Paperwork Reduction
Act of 1995 (44 U.S.C. 35).
Authority: Section 1115A of the Social
Security Act.
Dated: October 8, 2014.
Marilyn Tavenner,
Administrator, Centers for Medicare &
Medicaid Services.
[FR Doc. 2014–27578 Filed 11–20–14; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–1464–N]
Medicare Program; Town Hall Meeting
on FY 2016 Applications for New
Medical Services and Technology AddOn Payments
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice of meeting.
AGENCY:
This notice announces a
Town Hall meeting in accordance with
section 1886(d)(5)(K)(viii) of the Social
Security Act (the Act) to discuss fiscal
year (FY) 2016 applications for add-on
payments for new medical services and
technologies under the hospital
inpatient prospective payment systems
(IPPS). Interested parties are invited to
this meeting to present their comments,
recommendations, and data regarding
whether the FY 2016 new medical
services and technologies applications
meet the substantial clinical
improvement criterion.
DATES: Meeting Date: The Town Hall
Meeting announced in this notice will
be held on Tuesday, February 3, 2015.
The Town Hall Meeting will begin at
9:00 a.m. Eastern Standard Time (e.s.t.)
and check-in will begin at 8:30 a.m.
e.s.t.
SUMMARY:
E:\FR\FM\21NON1.SGM
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Agencies
[Federal Register Volume 79, Number 225 (Friday, November 21, 2014)]
[Notices]
[Pages 69488-69490]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-27578]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-6064-N]
Medicare Program; Prior Authorization of Non-Emergent Hyperbaric
Oxygen (HBO) Therapy
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces a 3-year Medicare Prior Authorization
model for non-emergent hyperbaric oxygen therapy services in the states
of Illinois, Michigan, and New Jersey where there have been high
incidences of improper payments for these services.
DATES: The model will begin on March 1, 2015 in Michigan, New Jersey,
and Illinois.
FOR FURTHER INFORMATION CONTACT: Jennifer McMullen, (410) 786-7635.
Questions regarding the Medicare Prior Authorization Model for Non-
Emergent Hyperbaric Oxygen (HBO) Therapy should be sent to
HBOPA@cms.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Hyperbaric Oxygen (HBO) therapy is a modality used for treatment of
wounds in which the entire body is exposed to oxygen under increased
atmospheric pressure. HBO therapy is covered as adjunctive therapy only
after there have been no measurable signs of healing during at least 30
consecutive days of treatment with standard wound therapy, and must be
used in addition to standard wound care. Wounds must be evaluated at
least every 30 days during administration of HBO therapy. Continued
treatment with HBO therapy is not covered if measurable signs of
healing have not been demonstrated within any 30-day period of
treatment.
Medicare issued a National Coverage Determination (NCD) for HBO
therapy in 2002, which lists clinical conditions for which HBO therapy
is medically necessary and clinical conditions for which HBO therapy is
not medically necessary, and therefore; not covered by Medicare. The
NCD can be found in the Medicare National Coverage Determinations
Manual (CMS Pub. No. 100-03), Chapter 1, Part 1, Section 20.29, and in
the NCD database at https://www.cms.gov/medicare-coverage-database/details/nca-decision-memo.aspx?NCAId=37&bc=AiAAAAAAAgAAAA%3d%3d&. In
addition, some of
[[Page 69489]]
the Medicare Administrative Contractors (MACs) have Local Coverage
Determinations (LCDs) that expand on the NCD.
In 2000, a report by the HHS Office of Inspector General \1\ on
hyperbaric oxygen therapy found the following:
---------------------------------------------------------------------------
\1\ Office of Inspector General, Hyperbaric Oxygen Therapy, Its
Use and Appropriateness, October 2000.
---------------------------------------------------------------------------
$14.2 million (of $49.9 million in allowed charges for
outpatient hospital departments and physicians) was paid in error,
either for beneficiaries who received treatments for non-covered
conditions or when documentation did not adequately support HBO.
An additional $4.9 million was paid for treatments deemed
to be excessive.
Lack of testing and treatment monitoring raised quality of
care concerns.
Data from CMS' Chronic Condition Warehouse were used to determine
state rankings based on average number of sessions per beneficiary.
States were then ranked by expenditures. Illinois, Michigan, and New
Jersey were selected as the initial states for the model because they
ranked in the top three for average number of sessions per beneficiary.
Section 1115A of the Social Security Act (the Act) authorizes the
Secretary to test innovative payment and service delivery models to
reduce program expenditures, while preserving or enhancing the quality
of care furnished to Medicare, Medicaid, and Children's Health
Insurance Program beneficiaries.
Section 1115A(d)(1) of the Act authorizes the Secretary to waive
such requirements of Titles XI and XVIII and of sections 1902(a)(1),
1902(a)(13), and 1903(m)(2)(A)(iii) of the Act as may be necessary
solely for purposes of carrying out section 1115A of the Act with
respect to testing models described in section 1115A(b) of the Act. For
this model, consistent with this standard, we will waive such
provisions of sections 1834(a)(15) and 1869(h) of the Act that limit
our ability to conduct prior authorization. We have determined that the
implementation of this model does not require the waiver of any fraud
and abuse law, including sections 1128A, 1128B, and 1877 of the Act.
Thus, providers and suppliers affected by this model must comply with
all applicable fraud and abuse laws. While these provisions are
specific to durable medical equipment (DME) and physician services, we
will waive any portion of these sections as well as any portion of 42
CFR 410.20(d) of the regulations, which implements section 1869(h) of
the Act, that could be construed to limit our ability to conduct prior
authorization.
II. Provisions of the Notice
We plan to implement a 3-year Medicare Prior Authorization process
for non-emergent HBO therapy rendered in 3 states (Illinois, Michigan,
and New Jersey). These states were selected as the initial states for
the model because of their high utilization and improper payment rates
for this service. The model will begin in Michigan, New Jersey, and
Illinois on March 1, 2015.
We plan to test whether prior authorization helps reduce
expenditures, while maintaining or improving quality of care, using a
model that would establish a prior authorization process for non-
emergent HBO therapy to reduce utilization of services that do not
comply with Medicare policy.
We plan to use this prior authorization process to ensure that all
relevant clinical or medical documentation requirements are met before
services are rendered to beneficiaries and before claims are submitted
for payment. This prior authorization process will further ensure that
payment complies with Medicare documentation, coverage, payment, and
coding rules.
The use of prior authorization will not create new clinical
documentation requirements. Instead, it will require the same
information that is already required to support Medicare payment, just
earlier in the process. Prior authorization allows facilities to
address issues with claims prior to rendering services.
The prior authorization process under this model will be available
for the following code for Medicare payment: C1300--Hyperbaric oxygen
under pressure, full body chamber, per 30 minute interval.
Prior authorization is only needed for the facility payment part of
the HBO therapy service. However, if a facility does not have prior
authorization, or has a non-affirmed prior authorization, the
associated physician claims with the following code will be subject to
medical review: 99183--Physician attendance and supervision of
hyperbaric oxygen, per session.
Of the 15 covered clinical conditions listed in the NCD, the
following 6 will be available for prior authorization:
Preparation and preservation of compromised skin grafts
(not for primary management of wounds).
Chronic refractory osteomyelitis, unresponsive to
conventional medical and surgical management.
Osteoradionecrosis as an adjunct to conventional
treatment.
Soft tissue radionecrosis as an adjunct to conventional
treatment.
Actinomycrosis, only as an adjunct to conventional therapy
when the disease process is refractory to antibiotics and surgical
treatment.
Diabetic wounds of the lower extremities in patients who
meet the following three criteria:
++ Patient has Type I or Type II diabetes and a lower extremity
wound that is due to diabetes.
++ Patient has a wound classified as Wagner grade III or higher.
++ Patient has failed an adequate course of wound therapy as
defined in the NCD.
A provisional affirmative prior authorization decision, justified
by the beneficiary's condition, may affirm up to 36 treatments in a 12-
month period. A provisional affirmation is a preliminary finding that a
future claim submitted to Medicare for the service likely meets
Medicare's coverage, coding, and payment requirements. A provisional
affirmative decision can be for all or part of the requested number of
treatments. If additional treatments are needed, a subsequent prior
authorization request must be submitted.
Prior to the start of the model, we will conduct (and thereafter
will continue to conduct) outreach and education to facilities that
provide HBO therapy, as well as to beneficiaries, through such methods
as Open Door Forums, frequently asked questions (FAQs) on our Web site,
other Web site postings, and educational materials issued by the
Medicare Administrative Contractors (MACs). Additional information
about the implementation of the prior authorization model is available
on the CMS Web site at https://go.cms.gov/PAHBO.
Under this model prior authorization process, the facility or
beneficiary will be encouraged to submit to the MAC a request for prior
authorization along with all relevant documentation to support Medicare
coverage of the HBO therapy. In order to be affirmed, the request for
prior authorization must meet all applicable rules and policies, and
any NCD and Local Coverage Determination (LCD) requirements for HBO
therapy.
After receipt of all relevant documentation, the MACs will make
every effort to conduct a review and postmark the notification of their
decision on a prior authorization request within 10 business days for
an initial submission. Notification will be provided to the submitter
of the prior
[[Page 69490]]
authorization request (and, upon request, to the beneficiary if he or
she was not the original submitter). If a subsequent prior
authorization request is submitted after a non-affirmative decision on
an initial prior authorization request, the MACs will make every effort
to conduct a review and postmark the notification of their decision on
the request within 20 business days.
A facility or beneficiary may request an expedited review when the
standard timeframe for making a prior authorization decision could
jeopardize the life or health of the beneficiary. If the MAC agrees
that the standard review timeframe would put the beneficiary at risk,
the MAC will make reasonable efforts to communicate a decision within 2
business days of receipt of all applicable, Medicare-required
documentation. As this model is for a non-emergent service only, we
expect requests for expedited reviews to be extremely rare.
The following describes examples of various prior authorization
scenarios:
Scenario 1: When a facility or beneficiary submits a prior
authorization request to the MAC with appropriate documentation and all
relevant Medicare coverage and documentation requirements are met for
the HBO therapy, the MAC will send a provisional affirmative prior
authorization decision to the submitter (and, upon request, to the
beneficiary if he or she was not the original submitter). When the
claim is submitted to the MAC, it is linked to the prior authorization
via the claims processing system and the claim is paid so long as all
Medicare coding, billing, and coverage requirements are met. However,
after submission, the claim could be denied for technical reasons, such
as the claim being a duplicate claim or being for a date of service
after a beneficiary's death.
Scenario 2: When a facility or beneficiary submits a prior
authorization request but all relevant Medicare coverage requirements
are not met, the MAC will send a non-affirmative prior authorization
decision to the submitter (and, upon request, to the beneficiary if he
or she was not the original submitter), advising them that Medicare
will not pay for the service. The facility or beneficiary may then
resubmit the request with documentation showing that Medicare
requirements have been met. Alternatively, a facility could render the
service, and submit a claim with a non-affirmative prior authorization
tracking number, at which point the MAC would deny the claim. The
facility or the beneficiary would then have the Medicare denial for
secondary insurance purposes and would have the opportunity to submit
an appeal of the claim denial if they believe Medicare coverage was
denied inappropriately.
Scenario 3: When a facility or beneficiary submits a prior
authorization request with incomplete documentation, a detailed
decision letter will be sent to the submitter (and, upon request, to
the beneficiary if he or she was not the original submitter) with an
explanation of what information is missing. The facility or beneficiary
can rectify the situation and resubmit the prior authorization request
with appropriate documentation.
Scenario 4: When a facility renders a service that is
subject to the prior authorization process to a beneficiary, and
submits the claim to the MAC for payment without requesting a prior
authorization, the claim will be stopped for prepayment review and
documentation will be requested.
++ If the claim is determined to be not medically necessary or to
be insufficiently documented, the claim will be denied, and all current
policies and procedures regarding liability for payment will apply. The
facility and/or beneficiary can appeal the claim denial if they believe
the denial was inappropriate.
++ If the claim is determined to be payable, it will be paid.
Under the model, we will work to limit any adverse impact on
beneficiaries and to educate beneficiaries about the process. If a
prior authorization request is not affirmed, and the claim is still
submitted by the facility, the claim will be denied in full, but
beneficiaries will continue to have all applicable administrative
appeal rights.
Only one prior authorization request per beneficiary per designated
time period can be provisionally affirmed. If the initial facility
cannot complete the total number of HBO treatments (for example, the
initial facility closes or the beneficiary moves out of the area), the
initial request is cancelled. In this situation, a subsequent prior
authorization request may be submitted for the same beneficiary and
must include the required documentation in the submission. If multiple
facilities are providing HBO treatments to the beneficiary during the
same or overlapping time period, the prior authorization decision will
only cover the facility indicated in the provisionally affirmed prior
authorization request. Any facility submitting claims for which no
prior authorization request is recorded will be subject to 100 percent
pre-payment medical review of those claims.
Additional information is available on the CMS Web site at https://go.cms.gov/PAHBO.
III. Collection of Information Requirements
Section 1115A(d)(3) of the Act, as added by section 3021 of the
Affordable Care Act, states that chapter 35 of title 44, United States
Code (the Paperwork Reduction Act of 1995), shall not apply to the
testing and evaluation of models or expansion of such models under this
section. Consequently, this document need not be reviewed by the Office
of Management and Budget under the authority of the Paperwork Reduction
Act of 1995 (44 U.S.C. 35).
Authority: Section 1115A of the Social Security Act.
Dated: October 8, 2014.
Marilyn Tavenner,
Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. 2014-27578 Filed 11-20-14; 8:45 am]
BILLING CODE 4120-01-P