Medicare Program; Public Meeting in Calendar Year 2007 for New Clinical Laboratory Tests Payment Determinations, 29330-29331 [E7-9525]
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Federal Register / Vol. 72, No. 101 / Friday, May 25, 2007 / Notices
Federal Protective Service or Guard
Service personnel before entering the
building.
• Security measures include
inspection of vehicles, inside and out, at
the entrance to the grounds.
• In addition, all persons entering the
building must pass through a metal
detector.
• All items brought into CMS—
including personal items such as
desktops, cell phones, palm pilots,
etc.—are subject to physical inspection.
• The public may enter the building
30–45 minutes before the meeting
convenes each day.
• All visitors must be escorted in
areas other than the lower and first-floor
levels in the Central Building.
• The main-entrance guards will
issue parking permits and instructions
upon arrival at the building.
IX. Special Accommodations
Individuals requiring sign-language
interpretation or other special
accommodations must send a request
for these services to the DFO by 5 p.m.
(e.s.t.), Wednesday, August 29, 2007.
Authority: Section 1833(t)(9) of the Act (42
U.S.C. 13951(t)). The Panel is governed by
the provisions of Pub. L. 92–463, as amended
(5 U.S.C. Appendix 2).
(Catalog of Federal Domestic Assistance
Program No. 93.773, Medicare-Hospital
Insurance; and Program No. 93.774,
Medicare-Supplementary Medical Insurance
Program)
Dated: May 1, 2007.
Leslie V. Norwalk,
Acting Administrator, Centers for Medicare
& Medicaid Services.
[FR Doc. E7–9521 Filed 5–24–07; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–1546–N]
Medicare Program; Public Meeting in
Calendar Year 2007 for New Clinical
Laboratory Tests Payment
Determinations
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
jlentini on PROD1PC65 with NOTICES
AGENCY:
SUMMARY: This notice announces a
public meeting to discuss payment
determinations for specific new
Physicians’ Current Procedural
Terminology (CPT) codes for clinical
laboratory tests. The meeting provides a
forum for interested parties to make oral
VerDate Aug<31>2005
17:34 May 24, 2007
Jkt 211001
presentations and submit written
comments on the new codes that will be
included in Medicare’s Clinical
Laboratory Fee Schedule for calendar
year 2008, which will be effective on
January 1, 2008. The meeting will
address technical issues relating to
payment determinations for a specified
list of new clinical laboratory codes.
The development of the codes for
clinical laboratory tests is performed by
the CPT Editorial Panel and will not be
discussed at the CMS meeting.
DATES: The public meeting is scheduled
for Monday, July 16, 2007 from 10 a.m.
to 2 p.m.
ADDRESSES: The public meeting will be
held in the main auditorium of the
central building of the Centers for
Medicare & Medicaid Services (CMS)
located at 7500 Security Boulevard,
Baltimore, Maryland 21244.
FOR FURTHER INFORMATION CONTACT:
Anita Greenberg, (410) 786–4601.
SUPPLEMENTARY INFORMATION:
I. Background
Section 531(b) of the Medicare,
Medicaid, and SCHIP Benefits
Improvement and Protection Act of
2000 (BIPA), Pub. L. 106–554, mandated
procedures that permit public
consultation for payment
determinations for new clinical
laboratory tests under Part B of title
XVIII of the Social Security Act (the
Act) in a manner consistent with the
procedures established for
implementing coding modifications for
International Classification of Diseases
(ICD–9–CM). The procedures and public
meeting announced in this notice for
new clinical laboratory tests are in
accordance with the procedures
published on November 23, 2001 in the
Federal Register (66 FR 58743) to
implement section 531(b) of BIPA. Also,
section 942(b) of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA), Pub.
L. 108–173, added section
1833(h)(8)(B)(iii) of the Act, which
required that we establish by regulation
procedures for determining the basis for,
and amount of, payment for new
clinical laboratory tests. In the calendar
year (CY) 2007 physician fee schedule
final rule (71 FR 69701 through 69704),
we adopted new 42 CFR subpart G
regarding payment for new clinical
diagnostic laboratory tests. Under 42
CFR 414.506, we annually convene a
meeting that includes representatives of
CMS officials involved in determining
payment amounts to receive individual
comments and recommendations (and
data on which the recommendations are
based).
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
A newly created CPT code can either
represent a refinement or modification
of existing test methods, or a
substantially new test method. The
newly created CPT codes for the
calendar year 2007 will be listed at the
web site https://www.cms.hhs.gov/
ClinicalLabFeeSched on or after June 18,
2007.
The first method, called crosswalking, is used when a new test is
determined to be similar to an existing
test, multiple existing test codes, or a
portion of an existing test code. The
new test code is then assigned the
related existing local fee schedule
amounts and resulting national
limitation amount. The second method,
called gap-filling, is used when no
comparable, existing test is available.
When using this method, instructions
are provided to each Medicare carrier to
determine a payment amount for its
geographic area(s) for use in the first
year, and the carrier-specific amounts
are used to establish a national
limitation amount for following years.
For each new clinical laboratory test
code, a determination must be made to
either cross-walk or to gap-fill, and, if
cross-walking is appropriate, to know
which tests to cross-walk.
II. Meeting Format
This meeting is open to the public.
The on-site check-in for visitors will be
held from 9:30 to 10 a.m., followed by
opening remarks. Registered individuals
may discuss and recommend payment
determinations for specific new CPT
codes for the 2008 Clinical Laboratory
Fee Schedule.
Oral presentations must be brief, and
must be accompanied by three written
copies. Presenters may also make copies
available for approximately 50 meeting
participants. Presenters should address
the new test code(s) and descriptor, the
test purpose and method, costs, charges,
and make a recommendation with
rationale for using one of two methods
(cross-walking or gap-fill) for
determining payment for new clinical
laboratory codes. Presentations that do
not address the six items may be
considered incomplete and not
considered by CMS when making a
payment determination. We will request
missing information following the
meeting in order to prevent a
recommendation from being considered
incomplete.
A summary of the new codes and the
payment recommendations that are
presented during the public meeting
will be posted on our Web site by
September 7, 2007 and can be accessed
at https://www.cms.hhs.gov/
ClinicalLabFeeSched. In addition, the
E:\FR\FM\25MYN1.SGM
25MYN1
Federal Register / Vol. 72, No. 101 / Friday, May 25, 2007 / Notices
summary will list other comments
received on or before 15 days after the
meeting, or August 1, 2007. The
summary will also display CMS’
tentative payment determinations, and
interested individuals may submit
written comments on the tentative
payment determinations by September
21, 2007 to the address specified in the
summary.
III. Registration Instructions
We are coordinating the public
meeting registration. Beginning June 18,
2007 registration may be completed online at https://www.cms.hhs.gov/
ClinicalLabFeeSched. The following
information must be submitted when
registering: Name; company name;
address; telephone number(s); and Email address(es).
When registering, individuals who
want to make a presentation must also
specify which new clinical laboratory
test code(s) they will be presenting. A
confirmation will be sent upon receipt
of the registration.
Registration Deadline: Individuals
must register by July 11, 2007.
jlentini on PROD1PC65 with NOTICES
IV. Security, Building, and Parking
Guidelines
The meeting will be held in a Federal
government building; therefore, Federal
security measures are applicable. In
planning your arrival time, we
recommend allowing additional time to
clear security. In order to gain access to
the building and grounds, participants
must bring a government-issued photo
identification and a copy of your written
meeting registration confirmation.
Persons without proper identification
may be denied access to the building.
Individuals who are not registered in
advance will not be permitted to enter
the building and will be unable to
attend the meeting. The public may not
enter the building earlier than 30 to 45
minutes prior to the convening of the
meeting.
Security measures also include
inspection of vehicles, inside and out at
the entrance to the grounds. In addition,
all persons entering the building must
pass through a metal detector. All items
brought to CMS, whether personal or for
the purpose of demonstration or to
support a presentation, are subject to
inspection.
V. Special Accommodations
Individuals attending a meeting who
are hearing or visually impaired and
have special requirements, or a
condition that requires special
assistance, should provide the
information upon registering for the
meeting.
VerDate Aug<31>2005
17:34 May 24, 2007
Jkt 211001
Authority: Section 1102, 1833(h), and 1871
of the Social Security Act (42 U.S.C. 1302, 42
U.S.C. 13951, and 42 U.S.C. 1395hh)
(Catalog of Federal Domestic Assistance
Program No. 93.774, Medicare—
Supplementary Medical Insurance Program)
Dated: March 22, 2007.
Leslie V. Norwalk,
Acting Administrator, Centers for Medicare
& Medicaid Services.
[FR Doc. E7–9525 Filed 5–24–07; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3172–N]
Medicare Program; Meeting of the
Medicare Coverage Advisory
Committee—July 18, 2007
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
SUMMARY: This notice announces a
public meeting of the Medicare
Evidence Development Coverage
Advisory Committee (MedCAC or
Committee), formerly the Medicare
Coverage Advisory Committee (MCAC).
The Committee generally provides
advice and recommendations about
whether scientific evidence is adequate
to determine whether certain medical
items and services are reasonable and
necessary under the Medicare statute.
This meeting concerns percutaneous
transluminal angioplasty (PTA) and
stenting of the renal arteries.
Notice of this meeting is given under
the Federal Advisory Committee Act (5
U.S.C. App. 2, section 10(a)).
DATES: Meeting Date: The public
meeting will be held on Wednesday,
July 18, 2007 from 7:30 a.m. until 4:30
p.m., eastern daylight time (e.d.t.).
Deadlines for Registration and
Request for Special Accommodations:
Registration must be completed no later
than 5 p.m., e.d.t. on Monday, July 9,
2007. Request for special
accommodations must be received by 5
p.m., e.d.t. Tuesday, July 10, 2007.
Deadlines for Written Comments and
Presentations: Written comments and
presentations must be received by June
18, 2007, 5 p.m., e.d.t. Presentations,
once submitted, are final. No further
changes to the presentation can be
accepted after submission.
ADDRESSES: Meeting Location: The
meeting will be held in the main
auditorium of the Centers for Medicare
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
29331
& Medicaid Services, 7500 Security
Boulevard, Baltimore, MD 21244.
Presentation and Comment
Submission: Interested persons may
present data, information, or views
orally or in writing on issues pending
before the Committee. Presentation and
written comments must be submitted by
e-mail to
Michelle.Atkinson@cms.hhs.gov or by
regular mail to Michelle Atkinson,
Executive Secretary for MedCAC,
Centers for Medicare & Medicaid
Services, Office of Clinical Standards
and Quality, Coverage and Analysis
Group, C1–09–06, 7500 Security
Boulevard, Baltimore, MD 21244.
Registration and Special
Accommodations: Individuals wishing
to participate or who need special
accommodations, or both, may register
by phone or e-mail by contacting Maria
Ellis at 410–786–0309 or
Maria.Ellis@cms.hhs.gov no later than 5
p.m., e.d.t on Monday, July 9, 2007.
Persons attending the meeting who are
hearing or visually impaired, or have a
condition that requires special
assistance or accommodations, are
asked to contact Michelle Atkinson,
Executive Secretary for MedCAC, no
later than July 9, 2007.
Web site: You may access up-to-date
information on this meeting at https://
www.cms.hhs.gov/FACA/
02_MCAC.asp#TopOfPage.
FOR FURTHER INFORMATION CONTACT:
Michelle Atkinson, Executive Secretary
for MedCAC, 410–786–2881;
Michelle.Atkinson@cms.hhs.gov;
Centers for Medicare & Medicaid
Services, OCSQ—Coverage and Analysis
Group, C1–09–06, 7500 Security
Boulevard, Baltimore, MD 21244).
SUPPLEMENTARY INFORMATION:
I. Background
On December 14, 1998, we published
a notice in the Federal Register (63 FR
68780) to describe the Medicare
Coverage Advisory Committee (MCAC),
which provides advice and
recommendations to CMS about clinical
issues.
This notice announces the July 18,
2007 public meeting of the Committee.
During this meeting, the Committee will
discuss evidence and hear presentations
from the public concerning the use of
PTA and stenting of the renal arteries
for the treatment of atherosclerotic renal
artery stenosis (ARAS). The clinical
outcomes in the Medicare population
will be discussed. MedCAC will review
the following kinds of evidence:
• The most informative measures of
clinical outcomes.
• Indications.
E:\FR\FM\25MYN1.SGM
25MYN1
Agencies
[Federal Register Volume 72, Number 101 (Friday, May 25, 2007)]
[Notices]
[Pages 29330-29331]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-9525]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-1546-N]
Medicare Program; Public Meeting in Calendar Year 2007 for New
Clinical Laboratory Tests Payment Determinations
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces a public meeting to discuss payment
determinations for specific new Physicians' Current Procedural
Terminology (CPT) codes for clinical laboratory tests. The meeting
provides a forum for interested parties to make oral presentations and
submit written comments on the new codes that will be included in
Medicare's Clinical Laboratory Fee Schedule for calendar year 2008,
which will be effective on January 1, 2008. The meeting will address
technical issues relating to payment determinations for a specified
list of new clinical laboratory codes. The development of the codes for
clinical laboratory tests is performed by the CPT Editorial Panel and
will not be discussed at the CMS meeting.
DATES: The public meeting is scheduled for Monday, July 16, 2007 from
10 a.m. to 2 p.m.
ADDRESSES: The public meeting will be held in the main auditorium of
the central building of the Centers for Medicare & Medicaid Services
(CMS) located at 7500 Security Boulevard, Baltimore, Maryland 21244.
FOR FURTHER INFORMATION CONTACT: Anita Greenberg, (410) 786-4601.
SUPPLEMENTARY INFORMATION:
I. Background
Section 531(b) of the Medicare, Medicaid, and SCHIP Benefits
Improvement and Protection Act of 2000 (BIPA), Pub. L. 106-554,
mandated procedures that permit public consultation for payment
determinations for new clinical laboratory tests under Part B of title
XVIII of the Social Security Act (the Act) in a manner consistent with
the procedures established for implementing coding modifications for
International Classification of Diseases (ICD-9-CM). The procedures and
public meeting announced in this notice for new clinical laboratory
tests are in accordance with the procedures published on November 23,
2001 in the Federal Register (66 FR 58743) to implement section 531(b)
of BIPA. Also, section 942(b) of the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003 (MMA), Pub. L. 108-173,
added section 1833(h)(8)(B)(iii) of the Act, which required that we
establish by regulation procedures for determining the basis for, and
amount of, payment for new clinical laboratory tests. In the calendar
year (CY) 2007 physician fee schedule final rule (71 FR 69701 through
69704), we adopted new 42 CFR subpart G regarding payment for new
clinical diagnostic laboratory tests. Under 42 CFR 414.506, we annually
convene a meeting that includes representatives of CMS officials
involved in determining payment amounts to receive individual comments
and recommendations (and data on which the recommendations are based).
A newly created CPT code can either represent a refinement or
modification of existing test methods, or a substantially new test
method. The newly created CPT codes for the calendar year 2007 will be
listed at the web site https://www.cms.hhs.gov/ClinicalLabFeeSched on or
after June 18, 2007.
The first method, called cross-walking, is used when a new test is
determined to be similar to an existing test, multiple existing test
codes, or a portion of an existing test code. The new test code is then
assigned the related existing local fee schedule amounts and resulting
national limitation amount. The second method, called gap-filling, is
used when no comparable, existing test is available. When using this
method, instructions are provided to each Medicare carrier to determine
a payment amount for its geographic area(s) for use in the first year,
and the carrier-specific amounts are used to establish a national
limitation amount for following years. For each new clinical laboratory
test code, a determination must be made to either cross-walk or to gap-
fill, and, if cross-walking is appropriate, to know which tests to
cross-walk.
II. Meeting Format
This meeting is open to the public. The on-site check-in for
visitors will be held from 9:30 to 10 a.m., followed by opening
remarks. Registered individuals may discuss and recommend payment
determinations for specific new CPT codes for the 2008 Clinical
Laboratory Fee Schedule.
Oral presentations must be brief, and must be accompanied by three
written copies. Presenters may also make copies available for
approximately 50 meeting participants. Presenters should address the
new test code(s) and descriptor, the test purpose and method, costs,
charges, and make a recommendation with rationale for using one of two
methods (cross-walking or gap-fill) for determining payment for new
clinical laboratory codes. Presentations that do not address the six
items may be considered incomplete and not considered by CMS when
making a payment determination. We will request missing information
following the meeting in order to prevent a recommendation from being
considered incomplete.
A summary of the new codes and the payment recommendations that are
presented during the public meeting will be posted on our Web site by
September 7, 2007 and can be accessed at https://www.cms.hhs.gov/
ClinicalLabFeeSched. In addition, the
[[Page 29331]]
summary will list other comments received on or before 15 days after
the meeting, or August 1, 2007. The summary will also display CMS'
tentative payment determinations, and interested individuals may submit
written comments on the tentative payment determinations by September
21, 2007 to the address specified in the summary.
III. Registration Instructions
We are coordinating the public meeting registration. Beginning June
18, 2007 registration may be completed on-line at https://
www.cms.hhs.gov/ClinicalLabFeeSched. The following information must be
submitted when registering: Name; company name; address; telephone
number(s); and E-mail address(es).
When registering, individuals who want to make a presentation must
also specify which new clinical laboratory test code(s) they will be
presenting. A confirmation will be sent upon receipt of the
registration.
Registration Deadline: Individuals must register by July 11, 2007.
IV. Security, Building, and Parking Guidelines
The meeting will be held in a Federal government building;
therefore, Federal security measures are applicable. In planning your
arrival time, we recommend allowing additional time to clear security.
In order to gain access to the building and grounds, participants must
bring a government-issued photo identification and a copy of your
written meeting registration confirmation. Persons without proper
identification may be denied access to the building.
Individuals who are not registered in advance will not be permitted
to enter the building and will be unable to attend the meeting. The
public may not enter the building earlier than 30 to 45 minutes prior
to the convening of the meeting.
Security measures also include inspection of vehicles, inside and
out at the entrance to the grounds. In addition, all persons entering
the building must pass through a metal detector. All items brought to
CMS, whether personal or for the purpose of demonstration or to support
a presentation, are subject to inspection.
V. Special Accommodations
Individuals attending a meeting who are hearing or visually
impaired and have special requirements, or a condition that requires
special assistance, should provide the information upon registering for
the meeting.
Authority: Section 1102, 1833(h), and 1871 of the Social
Security Act (42 U.S.C. 1302, 42 U.S.C. 13951, and 42 U.S.C. 1395hh)
(Catalog of Federal Domestic Assistance Program No. 93.774,
Medicare--Supplementary Medical Insurance Program)
Dated: March 22, 2007.
Leslie V. Norwalk,
Acting Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. E7-9525 Filed 5-24-07; 8:45 am]
BILLING CODE 4120-01-P