Medicare Program; Town Hall Meeting on the FY 2021 Applications for New Medical Services and Technologies Add-On Payments, 53732-53734 [2019-21750]
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53732
Federal Register / Vol. 84, No. 195 / Tuesday, October 8, 2019 / Notices
Dated: October 2, 2019.
Sandra Cashman,
Executive Secretary, Centers for Disease
Control and Prevention.
[FR Doc. 2019–21864 Filed 10–7–19; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–1722–N]
Medicare Program; Town Hall Meeting
on the FY 2021 Applications for New
Medical Services and Technologies
Add-On 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) 2021 applications for add-on
payments for new medical services and
technologies under the hospital
inpatient prospective payment system
(IPPS). Interested parties are invited to
this meeting to present their comments,
recommendations, and data regarding
whether the FY 2021 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 Monday, December 16, 2019
and Tuesday December 17, 2019 (the
number of new technology applications
submitted will determine if a second
day for the meeting is necessary; see the
SUPPLEMENTARY INFORMATION section for
details regarding the second day of the
meeting and the posting of the
preliminary meeting agenda). The Town
Hall Meeting will begin each day at 9:00
a.m. Eastern Standard Time (e.s.t.) and
check-in will begin at 8:30 a.m. e.s.t.
Deadline for Registration for
Participants (not Presenting) at the
Town Hall Meeting: The deadline to
register to attend the Town Hall Meeting
is 5:00 p.m. e.s.t. on Monday, December
9, 2019.
Deadline for Requesting Special
Accommodations: The deadline to
submit requests for special
accommodations is 5 p.m. e.s.t. on
Monday, November 25, 2019.
Deadline for Registration of Presenters
at the Town Hall Meeting: The deadline
to register to present at the Town Hall
Meeting is 5 p.m. e.s.t. on Monday,
November 18, 2019.
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SUMMARY:
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Deadline for Submission of Agenda
Item(s) or Written Comments for the
Town Hall Meeting: Written comments
and agenda items for discussion at the
Town Hall Meeting, including agenda
items by presenters, must be received by
5 p.m. e.s.t. on Monday, November 25,
2019.
Deadline for Submission of Written
Comments after the Town Hall Meeting
for consideration in the FY 2021 IPPS
proposed rule: Individuals may submit
written comments after the Town Hall
Meeting, as specified in the ADDRESSES
section of this notice, on whether the
service or technology represents a
substantial clinical improvement. These
comments must be received by 5:00
p.m. e.s.t. on Friday, January 3, 2020, for
consideration in the FY 2021 IPPS
proposed rule.
ADDRESSES: Meeting Location: The
Town Hall Meeting will be held in the
main Auditorium in the central building
of the Centers for Medicare & Medicaid
Services located at 7500 Security
Boulevard, Baltimore, MD 21244–1850.
In addition, we are providing two
alternatives to attending the meeting in
person—(1) there will be an open tollfree phone line to call into the Town
Hall Meeting; or (2) participants may
view and participate in the Town Hall
Meeting via live stream technology or
webinar. These options are discussed in
section II.B. of this notice.
Registration and Special
Accommodations: Individuals wishing
to participate in the meeting must
register by following the on-line
registration instructions located in
section III of this notice or by contacting
staff listed in the FOR FURTHER
INFORMATION CONTACT section of this
notice. Individuals who need special
accommodations should contact staff
listed in the FOR FURTHER INFORMATION
CONTACT section of this notice.
Submission of Agenda Item(s) or
Written Comments for the Town Hall
Meeting: Each presenter must submit an
agenda item(s) regarding whether a FY
2021 application meets the substantial
clinical improvement criterion. Agenda
items, written comments, questions or
other statements must not exceed three
single-spaced typed pages and may be
sent via email to newtech@cms.hhs.gov.
FOR FURTHER INFORMATION CONTACT:
Michelle Joshua, (410) 786–6050,
michelle.joshua@cms.hhs.gov; or
Michael Treitel, (410) 786–4552,
michael.treitel@cms.hhs.gov.
Alternatively, you may forward your
requests via email to newtech@
cms.hhs.gov.
SUPPLEMENTARY INFORMATION:
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Sfmt 4703
I. Background on the Add-On Payments
for New Medical Services and
Technologies Under the IPPS
Sections 1886(d)(5)(K) and (L) of the
Social Security Act (the Act) require the
Secretary to establish a process of
identifying and ensuring adequate
payments to acute care hospitals for
new medical services and technologies
under Medicare. Effective for discharges
beginning on or after October 1, 2001,
section 1886(d)(5)(K)(i) of the Act
requires the Secretary to establish (after
notice and opportunity for public
comment) a mechanism to recognize the
costs of new services and technologies
under the hospital inpatient prospective
payment system (IPPS). In addition,
section 1886(d)(5)(K)(vi) of the Act
specifies that a medical service or
technology will be considered ‘‘new’’ if
it meets criteria established by the
Secretary (after notice and opportunity
for public comment). (See the fiscal year
(FY) 2002 IPPS proposed rule (66 FR
22693, May 4, 2001) and final rule (66
FR 46912, September 7, 2001) for a more
detailed discussion.) As finalized in the
FY 2020 IPPS/LTCH PPS final rule,
technologies which are eligible for the
alternative new technology pathway for
transformative new devices or the
alternative new technology pathway for
Qualified Infectious Disease Products do
not need to meet the requirement under
42 CFR 412.87(b)(1) that the technology
represent an advance that substantially
improves, relative to technologies
previously available, the diagnosis or
treatment of Medicare beneficiaries.
These medical devices or products will
also be considered new and not
substantially similar to an existing
technology for purposes of new
technology add-on payment under the
IPPS. (See the FY 2020 IPPS/LTCH PPS
final rule (84 FR 42292 through 42297)
for additional information.)
In the FY 2020 IPPS/LTCH PPS final
rule (84 FR 42289 through 42292), we
codified in our regulations at § 412.87
the following aspects of how we
evaluate substantial clinical
improvement for purposes of new
technology add-on payments under the
IPPS in order to determine if a new
technology meets the substantial
clinical improvement requirement:
• The totality of the circumstances is
considered when making a
determination that a new medical
service or technology represents an
advance that substantially improves,
relative to services or technologies
previously available, the diagnosis or
treatment of Medicare beneficiaries.
• A determination that a new medical
service or technology represents an
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advance that substantially improves,
relative to services or technologies
previously available, the diagnosis or
treatment of Medicare beneficiaries
means—
++ The new medical service or
technology offers a treatment option for
a patient population unresponsive to, or
ineligible for, currently available
treatments;
++ The new medical service or
technology offers the ability to diagnose
a medical condition in a patient
population where that medical
condition is currently undetectable or
offers the ability to diagnose a medical
condition earlier in a patient population
than allowed by currently available
methods, and there must also be
evidence that use of the new medical
service or technology to make a
diagnosis affects the management of the
patient; or
++ The use of the new medical
service or technology significantly
improves clinical outcomes relative to
services or technologies previously
available as demonstrated by one or
more of the following:
—A reduction in at least one clinically
significant adverse event, including a
reduction in mortality or a clinically
significant complication.
—A decreased rate of at least one
subsequent diagnostic or therapeutic
intervention (for example, due to
reduced rate of recurrence of the
disease process).
—A decreased number of future
hospitalizations or physician visits.
—A more rapid beneficial resolution of
the disease process treatment
including, but not limited to, a
reduced length of stay or recovery
time; an improvement in one or more
activities of daily living; an improved
quality of life; or, a demonstrated
greater medication adherence or
compliance.
++ The totality of the circumstances
otherwise demonstrates that the new
medical service or technology
substantially improves, relative to
technologies previously available, the
diagnosis or treatment of Medicare
beneficiaries.
• Evidence from the following
published or unpublished information
sources from within the United States or
elsewhere may be sufficient to establish
that a new medical service or
technology represents an advance that
substantially improves, relative to
services or technologies previously
available, the diagnosis or treatment of
Medicare beneficiaries: Clinical trials,
peer reviewed journal articles; study
results; meta-analyses; consensus
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statements; white papers; patient
surveys; case studies; reports;
systematic literature reviews; letters
from major healthcare associations;
editorials and letters to the editor; and
public comments. Other appropriate
information sources may be considered.
• The medical condition diagnosed or
treated by the new medical service or
technology may have a low prevalence
among Medicare beneficiaries.
• The new medical service or
technology may represent an advance
that substantially improves, relative to
services or technologies previously
available, the diagnosis or treatment of
a subpopulation of patients with the
medical condition diagnosed or treated
by the new medical service or
technology.
Section 1886(d)(5)(K)(viii) of the Act
requires that as part of the process for
evaluating new medical services and
technology applications, the Secretary
shall do the following:
• Provide for public input regarding
whether a new service or technology
represents an advance in medical
technology that substantially improves
the diagnosis or treatment of Medicare
beneficiaries before publication of a
proposed rule.
• Make public and periodically
update a list of all the services and
technologies for which an application is
pending.
• Accept comments,
recommendations, and data from the
public regarding whether the service or
technology represents a substantial
improvement.
• Provide for a meeting at which
organizations representing hospitals,
physicians, manufacturers and any
other interested party may present
comments, recommendations, and data
to the clinical staff of CMS as to whether
the service or technology represents a
substantial improvement before
publication of a proposed rule.
The opinions and presentations
provided during this meeting will assist
us as we evaluate the new medical
services and technology applications for
FY 2021. In addition, they will help us
to evaluate our policy on the IPPS new
technology add-on payment process
before the publication of the FY 2021
IPPS proposed rule.
II. Town Hall Meeting Format and
Conference Call/Live Streaming
Information
A. Format of the Town Hall Meeting
As noted in section I. of this notice,
we are required to provide for a meeting
at which organizations representing
hospitals, physicians, manufacturers
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53733
and any other interested party may
present comments, recommendations,
and data to the clinical staff of CMS
concerning whether the service or
technology represents a substantial
clinical improvement. This meeting will
allow for a discussion of the substantial
clinical improvement criterion for the
FY 2021 new medical services and
technology add-on payment
applications. Information regarding the
applications can be found on our
website at https://www.cms.gov/
Medicare/Medicare-Fee-for-ServicePayment/AcuteInpatientPPS/
newtech.html.
The majority of the meeting will be
reserved for presentations of comments,
recommendations, and data from
registered presenters. The time for each
presenter’s comments will be
approximately 10 to 15 minutes and
will be based on the number of
registered presenters. Individuals who
would like to present must register and
submit their agenda item(s) via email to
newtech@cms.hhs.gov by the date
specified in the DATES section of this
notice.
Depending on the number of
applications received, we will
determine if a second meeting day is
necessary. A preliminary agenda will be
posted on the CMS website at https://
www.cms.gov/Medicare/Medicare-Feefor-Service-Payment/AcuteInpatient
PPS/newtech.html. by November 8,
2019 to inform the public of the number
of days of the meeting.
In addition, written comments will
also be accepted and presented at the
meeting if they are received via email to
newtech@cms.hhs.gov by the date
specified in the DATES section of this
notice. Written comments may also be
submitted after the meeting for our
consideration. If the comments are to be
considered before the publication of the
FY 2021 IPPS proposed rule, the
comments must be received via email to
newtech@cms.hhs.gov by the date
specified in the DATES section of this
notice.
B. Conference Call, Live Streaming, and
Webinar Information
For participants who cannot attend
the Town Hall Meeting in person, an
open toll-free phone line will be made
available. Continue to check our website
at: https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
AcuteInpatientPPS/newtech.html for
updated dial-in number and
instructions.
Also, there will be an option to view
and participate in the Town Hall
Meeting via live streaming technology
or webinar. Information on the option to
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Federal Register / Vol. 84, No. 195 / Tuesday, October 8, 2019 / Notices
participate via live streaming
technology or webinar will be provided
through an upcoming listserv notice and
posted on the New Technology website
at https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
AcuteInpatientPPS/newtech.html.
Continue to check the website for
updates.
C. Disclaimer
We cannot guarantee reliability for
live streaming technology or a webinar.
III. Registration Instructions
The Division of Acute Care in CMS is
coordinating the meeting registration for
the Town Hall Meeting on substantial
clinical improvement. While there is no
registration fee, individuals planning to
attend the Town Hall Meeting in person
must register to attend.
Registration may be completed online at the following web address:
https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
AcuteInpatientPPS/newtech.html.
Select the link at the bottom of the page
‘‘Register to Attend the New Technology
Town Hall Meeting’’. After completing
the registration, online registrants
should print the confirmation page(s)
and bring it with them to the meeting.
If you are unable to register on-line,
you may register by sending an email to
newtech@cms.hhs.gov. Please include
your name, address, telephone number,
email address and fax number. If seating
capacity has been reached, you will be
notified that the meeting has reached
capacity.
IV. Security, Building, and Parking
Guidelines
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Because this meeting will be located
on Federal property, for security
reasons, any persons wishing to attend
the meeting must register by the date
specified in the DATES section of this
notice. Please allow sufficient time to go
through the security checkpoints. If you
are attending the Town Hall Meeting in
person, we suggest that you arrive at
7500 Security Boulevard no later than
8:30 a.m. e.s.t. so that you will be able
to arrive promptly for the meeting.
Security measures include the
following:
• Presentation of government-issued
photographic identification to the
Federal Protective Service or Guard
Service personnel.
Note: The REAL ID Act established
minimum security standards for license
issuance and production and prohibits
Federal agencies from accepting for certain
purposes driver’s licenses and identification
cards from states not meeting the Act’s
minimum standards. We encourage the
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21:50 Oct 07, 2019
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public to visit the DHS website at https://
www.dhs.gov/real-id prior to the new
technology town hall meeting for updated
information.
• All Foreign National visitor
requests must be submitted 12 business
days prior to the scheduled visitor to
allow for processing.
• Inspection of vehicle’s interior and
exterior (this includes engine and trunk
inspection) at the entrance to the
grounds. Parking permits and
instructions will be issued after the
vehicle inspection.
• Inspection, via metal detector or
other applicable means of all persons
entering the building. We note that all
items brought to CMS, whether personal
or for the purpose of presentation or to
support a presentation, are subject to
inspection. We cannot assume
responsibility for coordinating the
receipt, transfer, transport, storage, setup, safety, or timely arrival of any
personal belongings or items used for
presentation or to support a
presentation.
Note: Individuals who are not registered in
advance will not be permitted to enter the
building and will be unable to attend the
meeting in person. The public may not enter
the building earlier than 45 minutes prior to
the convening of the meeting.
All visitors must be escorted in all
areas other than the lower level lobby
and cafeteria area and first floor
auditorium and conference areas in the
Central Building. Seating capacity is
limited to the first 250 registrants.
Effective June 1, 2018, Federal
Protective Services (FPS) has
implemented new security screening
procedures at all CMS Baltimore
locations to align with national
screening standards. Please allow extra
time to clear security prior to the
beginning of the meeting. Employees,
contractors and visitors must place all
items in bins for screening, including
the following:
• Any items in your pockets.
• Belts, hats, jackets & coats (not suit
jackets or sport coats).
• Purses, laptop computers, and cell
phones.
• Larger items (for example computer
bags) can be placed directly onto the
conveyer.
In the event the metal detector beeps
when you walk through a security guard
will run a hand-held metal detector over
you—
• If the metal detector does not alarm,
you are cleared to enter;
• If the hand-held metal detector
alarms, the guard will pat down the area
of the body where the metal detector
alarmed; or
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• If footwear alarms, it will need to be
removed and placed in a bin for x-ray
screening.
If you believe that you have a
disability that will cause you to require
reasonable accommodation to comply
with the new process, please contact
reasonableaccommodationprogram@
cms.hhs.gov as soon as possible.
Dated: September 26, 2019.
Seema Verma,
Administrator, Centers for Medicare &
Medicaid Services.
[FR Doc. 2019–21750 Filed 10–4–19; 11:15 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare and Medicaid
Services
Privacy Act of 1974; System of
Records
Centers for Medicare &
Medicaid Services (CMS), Department
of Health and Human Services (HHS).
ACTION: Notice of a modified system of
records.
AGENCY:
In accordance with
requirements of the Privacy Act of 1974,
as amended, the Department of Health
and Human Services (HHS) is updating
an existing system of records
maintained by the Centers for Medicare
& Medicaid Services (CMS), system No.
09–70–0550, titled ‘‘Medicare Retiree
Drug Subsidy Program’’ (RDSP), and
renaming it ‘‘Retiree Drug Subsidy
(RDS), HHS/CMS/CM.’’ This system
collects and maintains information
about individuals who are qualifying
covered retirees so that accurate and
timely subsidy payments may be made
to plan sponsors who continue to offer
actuarially equivalent prescription drug
coverage to the qualifying covered
retirees.
SUMMARY:
In accordance with 5 United
States Code (U.S.C.) 552a(e)(4) and (11),
this notice is applicable October 8,
2019, subject to a 30-day period in
which to comment on the new and
revised routine uses, described below.
Please submit any comments by
November 7, 2019.
ADDRESSES: Written comments should
be submitted by mail or email to: CMS
Privacy Act Officer, Division of
Security, Privacy Policy & Governance,
Information Security & Privacy Group,
Office of Information Technology, CMS,
Location N1–14–56, 7500 Security
Blvd., Baltimore, MD 21244–1870, or
walter.stone@cms.hhs.gov.
DATES:
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Agencies
[Federal Register Volume 84, Number 195 (Tuesday, October 8, 2019)]
[Notices]
[Pages 53732-53734]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-21750]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-1722-N]
Medicare Program; Town Hall Meeting on the FY 2021 Applications
for New Medical Services and Technologies Add-On Payments
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice of meeting.
-----------------------------------------------------------------------
SUMMARY: 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) 2021 applications for add-on payments for new
medical services and technologies under the hospital inpatient
prospective payment system (IPPS). Interested parties are invited to
this meeting to present their comments, recommendations, and data
regarding whether the FY 2021 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 Monday, December 16, 2019 and Tuesday December 17, 2019
(the number of new technology applications submitted will determine if
a second day for the meeting is necessary; see the SUPPLEMENTARY
INFORMATION section for details regarding the second day of the meeting
and the posting of the preliminary meeting agenda). The Town Hall
Meeting will begin each day at 9:00 a.m. Eastern Standard Time (e.s.t.)
and check-in will begin at 8:30 a.m. e.s.t.
Deadline for Registration for Participants (not Presenting) at the
Town Hall Meeting: The deadline to register to attend the Town Hall
Meeting is 5:00 p.m. e.s.t. on Monday, December 9, 2019.
Deadline for Requesting Special Accommodations: The deadline to
submit requests for special accommodations is 5 p.m. e.s.t. on Monday,
November 25, 2019.
Deadline for Registration of Presenters at the Town Hall Meeting:
The deadline to register to present at the Town Hall Meeting is 5 p.m.
e.s.t. on Monday, November 18, 2019.
Deadline for Submission of Agenda Item(s) or Written Comments for
the Town Hall Meeting: Written comments and agenda items for discussion
at the Town Hall Meeting, including agenda items by presenters, must be
received by 5 p.m. e.s.t. on Monday, November 25, 2019.
Deadline for Submission of Written Comments after the Town Hall
Meeting for consideration in the FY 2021 IPPS proposed rule:
Individuals may submit written comments after the Town Hall Meeting, as
specified in the ADDRESSES section of this notice, on whether the
service or technology represents a substantial clinical improvement.
These comments must be received by 5:00 p.m. e.s.t. on Friday, January
3, 2020, for consideration in the FY 2021 IPPS proposed rule.
ADDRESSES: Meeting Location: The Town Hall Meeting will be held in the
main Auditorium in the central building of the Centers for Medicare &
Medicaid Services located at 7500 Security Boulevard, Baltimore, MD
21244-1850.
In addition, we are providing two alternatives to attending the
meeting in person--(1) there will be an open toll-free phone line to
call into the Town Hall Meeting; or (2) participants may view and
participate in the Town Hall Meeting via live stream technology or
webinar. These options are discussed in section II.B. of this notice.
Registration and Special Accommodations: Individuals wishing to
participate in the meeting must register by following the on-line
registration instructions located in section III of this notice or by
contacting staff listed in the FOR FURTHER INFORMATION CONTACT section
of this notice. Individuals who need special accommodations should
contact staff listed in the FOR FURTHER INFORMATION CONTACT section of
this notice.
Submission of Agenda Item(s) or Written Comments for the Town Hall
Meeting: Each presenter must submit an agenda item(s) regarding whether
a FY 2021 application meets the substantial clinical improvement
criterion. Agenda items, written comments, questions or other
statements must not exceed three single-spaced typed pages and may be
sent via email to [email protected].
FOR FURTHER INFORMATION CONTACT: Michelle Joshua, (410) 786-6050,
[email protected]; or Michael Treitel, (410) 786-4552,
[email protected]. Alternatively, you may forward your
requests via email to [email protected].
SUPPLEMENTARY INFORMATION:
I. Background on the Add-On Payments for New Medical Services and
Technologies Under the IPPS
Sections 1886(d)(5)(K) and (L) of the Social Security Act (the Act)
require the Secretary to establish a process of identifying and
ensuring adequate payments to acute care hospitals for new medical
services and technologies under Medicare. Effective for discharges
beginning on or after October 1, 2001, section 1886(d)(5)(K)(i) of the
Act requires the Secretary to establish (after notice and opportunity
for public comment) a mechanism to recognize the costs of new services
and technologies under the hospital inpatient prospective payment
system (IPPS). In addition, section 1886(d)(5)(K)(vi) of the Act
specifies that a medical service or technology will be considered
``new'' if it meets criteria established by the Secretary (after notice
and opportunity for public comment). (See the fiscal year (FY) 2002
IPPS proposed rule (66 FR 22693, May 4, 2001) and final rule (66 FR
46912, September 7, 2001) for a more detailed discussion.) As finalized
in the FY 2020 IPPS/LTCH PPS final rule, technologies which are
eligible for the alternative new technology pathway for transformative
new devices or the alternative new technology pathway for Qualified
Infectious Disease Products do not need to meet the requirement under
42 CFR 412.87(b)(1) that the technology represent an advance that
substantially improves, relative to technologies previously available,
the diagnosis or treatment of Medicare beneficiaries. These medical
devices or products will also be considered new and not substantially
similar to an existing technology for purposes of new technology add-on
payment under the IPPS. (See the FY 2020 IPPS/LTCH PPS final rule (84
FR 42292 through 42297) for additional information.)
In the FY 2020 IPPS/LTCH PPS final rule (84 FR 42289 through
42292), we codified in our regulations at Sec. 412.87 the following
aspects of how we evaluate substantial clinical improvement for
purposes of new technology add-on payments under the IPPS in order to
determine if a new technology meets the substantial clinical
improvement requirement:
The totality of the circumstances is considered when
making a determination that a new medical service or technology
represents an advance that substantially improves, relative to services
or technologies previously available, the diagnosis or treatment of
Medicare beneficiaries.
A determination that a new medical service or technology
represents an
[[Page 53733]]
advance that substantially improves, relative to services or
technologies previously available, the diagnosis or treatment of
Medicare beneficiaries means--
++ The new medical service or technology offers a treatment option
for a patient population unresponsive to, or ineligible for, currently
available treatments;
++ The new medical service or technology offers the ability to
diagnose a medical condition in a patient population where that medical
condition is currently undetectable or offers the ability to diagnose a
medical condition earlier in a patient population than allowed by
currently available methods, and there must also be evidence that use
of the new medical service or technology to make a diagnosis affects
the management of the patient; or
++ The use of the new medical service or technology significantly
improves clinical outcomes relative to services or technologies
previously available as demonstrated by one or more of the following:
--A reduction in at least one clinically significant adverse event,
including a reduction in mortality or a clinically significant
complication.
--A decreased rate of at least one subsequent diagnostic or therapeutic
intervention (for example, due to reduced rate of recurrence of the
disease process).
--A decreased number of future hospitalizations or physician visits.
--A more rapid beneficial resolution of the disease process treatment
including, but not limited to, a reduced length of stay or recovery
time; an improvement in one or more activities of daily living; an
improved quality of life; or, a demonstrated greater medication
adherence or compliance.
++ The totality of the circumstances otherwise demonstrates that
the new medical service or technology substantially improves, relative
to technologies previously available, the diagnosis or treatment of
Medicare beneficiaries.
Evidence from the following published or unpublished
information sources from within the United States or elsewhere may be
sufficient to establish that a new medical service or technology
represents an advance that substantially improves, relative to services
or technologies previously available, the diagnosis or treatment of
Medicare beneficiaries: Clinical trials, peer reviewed journal
articles; study results; meta-analyses; consensus statements; white
papers; patient surveys; case studies; reports; systematic literature
reviews; letters from major healthcare associations; editorials and
letters to the editor; and public comments. Other appropriate
information sources may be considered.
The medical condition diagnosed or treated by the new
medical service or technology may have a low prevalence among Medicare
beneficiaries.
The new medical service or technology may represent an
advance that substantially improves, relative to services or
technologies previously available, the diagnosis or treatment of a
subpopulation of patients with the medical condition diagnosed or
treated by the new medical service or technology.
Section 1886(d)(5)(K)(viii) of the Act requires that as part of the
process for evaluating new medical services and technology
applications, the Secretary shall do the following:
Provide for public input regarding whether a new service
or technology represents an advance in medical technology that
substantially improves the diagnosis or treatment of Medicare
beneficiaries before publication of a proposed rule.
Make public and periodically update a list of all the
services and technologies for which an application is pending.
Accept comments, recommendations, and data from the public
regarding whether the service or technology represents a substantial
improvement.
Provide for a meeting at which organizations representing
hospitals, physicians, manufacturers and any other interested party may
present comments, recommendations, and data to the clinical staff of
CMS as to whether the service or technology represents a substantial
improvement before publication of a proposed rule.
The opinions and presentations provided during this meeting will
assist us as we evaluate the new medical services and technology
applications for FY 2021. In addition, they will help us to evaluate
our policy on the IPPS new technology add-on payment process before the
publication of the FY 2021 IPPS proposed rule.
II. Town Hall Meeting Format and Conference Call/Live Streaming
Information
A. Format of the Town Hall Meeting
As noted in section I. of this notice, we are required to provide
for a meeting at which organizations representing hospitals,
physicians, manufacturers and any other interested party may present
comments, recommendations, and data to the clinical staff of CMS
concerning whether the service or technology represents a substantial
clinical improvement. This meeting will allow for a discussion of the
substantial clinical improvement criterion for the FY 2021 new medical
services and technology add-on payment applications. Information
regarding the applications can be found on our website at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/AcuteInpatientPPS/newtech.html.
The majority of the meeting will be reserved for presentations of
comments, recommendations, and data from registered presenters. The
time for each presenter's comments will be approximately 10 to 15
minutes and will be based on the number of registered presenters.
Individuals who would like to present must register and submit their
agenda item(s) via email to [email protected] by the date specified
in the DATES section of this notice.
Depending on the number of applications received, we will determine
if a second meeting day is necessary. A preliminary agenda will be
posted on the CMS website at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/AcuteInpatientPPS/newtech.html. by November 8, 2019
to inform the public of the number of days of the meeting.
In addition, written comments will also be accepted and presented
at the meeting if they are received via email to [email protected] by
the date specified in the DATES section of this notice. Written
comments may also be submitted after the meeting for our consideration.
If the comments are to be considered before the publication of the FY
2021 IPPS proposed rule, the comments must be received via email to
[email protected] by the date specified in the DATES section of this
notice.
B. Conference Call, Live Streaming, and Webinar Information
For participants who cannot attend the Town Hall Meeting in person,
an open toll-free phone line will be made available. Continue to check
our website at: https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/AcuteInpatientPPS/newtech.html for updated dial-in number and
instructions.
Also, there will be an option to view and participate in the Town
Hall Meeting via live streaming technology or webinar. Information on
the option to
[[Page 53734]]
participate via live streaming technology or webinar will be provided
through an upcoming listserv notice and posted on the New Technology
website at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/AcuteInpatientPPS/newtech.html. Continue to check the website
for updates.
C. Disclaimer
We cannot guarantee reliability for live streaming technology or a
webinar.
III. Registration Instructions
The Division of Acute Care in CMS is coordinating the meeting
registration for the Town Hall Meeting on substantial clinical
improvement. While there is no registration fee, individuals planning
to attend the Town Hall Meeting in person must register to attend.
Registration may be completed on-line at the following web address:
https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/AcuteInpatientPPS/newtech.html. Select the link at the bottom of the
page ``Register to Attend the New Technology Town Hall Meeting''. After
completing the registration, online registrants should print the
confirmation page(s) and bring it with them to the meeting.
If you are unable to register on-line, you may register by sending
an email to [email protected]. Please include your name, address,
telephone number, email address and fax number. If seating capacity has
been reached, you will be notified that the meeting has reached
capacity.
IV. Security, Building, and Parking Guidelines
Because this meeting will be located on Federal property, for
security reasons, any persons wishing to attend the meeting must
register by the date specified in the DATES section of this notice.
Please allow sufficient time to go through the security checkpoints. If
you are attending the Town Hall Meeting in person, we suggest that you
arrive at 7500 Security Boulevard no later than 8:30 a.m. e.s.t. so
that you will be able to arrive promptly for the meeting.
Security measures include the following:
Presentation of government-issued photographic
identification to the Federal Protective Service or Guard Service
personnel.
Note: The REAL ID Act established minimum security standards
for license issuance and production and prohibits Federal agencies
from accepting for certain purposes driver's licenses and
identification cards from states not meeting the Act's minimum
standards. We encourage the public to visit the DHS website at
https://www.dhs.gov/real-id prior to the new technology town hall
meeting for updated information.
All Foreign National visitor requests must be submitted 12
business days prior to the scheduled visitor to allow for processing.
Inspection of vehicle's interior and exterior (this
includes engine and trunk inspection) at the entrance to the grounds.
Parking permits and instructions will be issued after the vehicle
inspection.
Inspection, via metal detector or other applicable means
of all persons entering the building. We note that all items brought to
CMS, whether personal or for the purpose of presentation or to support
a presentation, are subject to inspection. We cannot assume
responsibility for coordinating the receipt, transfer, transport,
storage, set-up, safety, or timely arrival of any personal belongings
or items used for presentation or to support a presentation.
Note: Individuals who are not registered in advance will not be
permitted to enter the building and will be unable to attend the
meeting in person. The public may not enter the building earlier
than 45 minutes prior to the convening of the meeting.
All visitors must be escorted in all areas other than the lower
level lobby and cafeteria area and first floor auditorium and
conference areas in the Central Building. Seating capacity is limited
to the first 250 registrants.
Effective June 1, 2018, Federal Protective Services (FPS) has
implemented new security screening procedures at all CMS Baltimore
locations to align with national screening standards. Please allow
extra time to clear security prior to the beginning of the meeting.
Employees, contractors and visitors must place all items in bins for
screening, including the following:
Any items in your pockets.
Belts, hats, jackets & coats (not suit jackets or sport
coats).
Purses, laptop computers, and cell phones.
Larger items (for example computer bags) can be placed
directly onto the conveyer.
In the event the metal detector beeps when you walk through a
security guard will run a hand-held metal detector over you--
If the metal detector does not alarm, you are cleared to
enter;
If the hand-held metal detector alarms, the guard will pat
down the area of the body where the metal detector alarmed; or
If footwear alarms, it will need to be removed and placed
in a bin for x-ray screening.
If you believe that you have a disability that will cause you to
require reasonable accommodation to comply with the new process, please
contact [email protected] as soon as possible.
Dated: September 26, 2019.
Seema Verma,
Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. 2019-21750 Filed 10-4-19; 11:15 am]
BILLING CODE 4120-01-P