Agency Information Collection Activities: Submission for OMB Review; Comment Request, 67603-67605 [E7-23163]
Download as PDF
rmajette on PROD1PC64 with NOTICES
Federal Register / Vol. 72, No. 229 / Thursday, November 29, 2007 / Notices
review the external review draft
document titled, ‘‘An Exploratory
Study: Assessment of Modeled Dioxin
Exposure in Ceramic Art Studios’’ (EPA/
600/R–06/044A). The draft document
was prepared by the National Center for
Environmental Assessment (NCEA)
within EPA’s Office of Research and
Development. The purpose of this report
is to describe an exploratory
investigation of potential dioxin
exposures to artists/hobbyists who use
ball clay to make pottery and related
products. Dermal, inhalation and
ingestion exposures to clay were
measured at the ceramics art department
of Ohio State University in Columbus,
OH. Estimates of exposure were made
based on measured levels of clay in the
studio air, deposited on surrogate food
samples and on the skin of artists. EPA
is releasing this draft document solely
for the purpose of pre-dissemination
peer review under applicable
information quality guidelines. This
document has not been formally
disseminated by EPA. It does not
represent and should not be construed
to represent any Agency policy or
determination.
On October 4, 2007, EPA announced
a 45-day public comment period on the
draft document (72 FR 56756). The
public comment period has closed as of
November 19, 2007. The public
comment period and the external peerreview panel workshop are separate
processes that provide opportunities for
all interested parties to comment on the
document. All public comments
submitted have been forwarded to EPA’s
contractor, Eastern Research Group, Inc.
(ERG), and provided to the external
peer-review panel members prior to the
workshop for consideration during
discussions at the workshop.
In preparing a final report, EPA will
consider the public comments
submitted to EPA’s docket during the
public comment period, and the
comments and, recommendations from
the external peer-review workshop,
including any oral public comments
made at the workshop.
DATES: The peer-review panel workshop
will begin on Wednesday, January 16,
2008, at approximately 9 a.m. and end
at 5 p.m. Members of the public may
attend the peer-review panel workshop.
Time will be set aside on the morning
of January 16, 2008 for registered
attendees who wish to make brief oral
comments (for more information refer to
the instructions for registration below).
ADDRESSES: Eastern Research Group
(ERG), an EPA contractor for external
scientific review, will convene an
independent panel of experts and
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14:52 Nov 28, 2007
Jkt 211001
organize and conduct the peer-review
workshop to review this draft
document. The peer-review workshop
will be held at the Navy League
Building, 2300 Wilson Boulevard,
Arlington, Virginia 22201.
Observers may attend the peer-review
workshop through a registration process
by calling ERG’s conference line
between the hours of 9 a.m. and 5:30
p.m. EST at (781) 674–7374 or toll free
at (800) 803–2833, or by faxing a
registration request to (781) 674–2906
(please reference the ‘‘Dioxin/Cermics
Peer-Review Panel Workshop’’ and
include full address and contact
information) or by sending an e-mail to
Meetings@erg.com (Subject line: Dioxin/
Ceramics Peer-Review Panel Workshop;
Body: include full address and contact
information). Pre-registration is strongly
recommended as space is limited, and
registration will be accepted on a firstcome, first-served basis. The deadline
for pre-registration is Monday, January
7, 2008. If space allows, registrations
will continue to be accepted after this
date, including on-site registration.
Time will be set aside to hear comments
from observers, and individuals will be
limited to a maximum of five minutes
during the morning of the day of the
workshop. When you register, please
inform ERG that you wish to make
comments during the comment period.
The draft document, ‘‘An Exploratory
Study: Assessment of Modeled Dioxin
Exposure in Ceramic Art Studios,’’ is
available primarily via the Internet on
the National Center for Environmental
Assessment(s home page under the
Recent Additions and the Data and
Publications menus at https://
www.epa.gov/ncea. A limited number of
paper copies are available from the
NCEA Information Management Team;
telephone: 202–564–3261; facsimile:
202–565–0050.
If you are requesting a paper copy,
please provide your name, mailing
address, and the document title, ‘‘An
Exploratory Study: Assessment of
Modeled Dioxin Exposure in Ceramic
Art Studios’’. Copies are not available
from ERG and copies will not be
available at the workshop.
FOR FURTHER INFORMATION CONTACT:
Questions regarding information,
registration, and logistics for the
external peer-review workshop should
be directed to Eastern Research Group,
110 Hartwell Avenue, Lexington, MA
02421–3136; telephone: (781) 674–7374
or toll free at (800) 803–2833; facsimile:
(781) 674–2906; e-mail:
Meetings@erg.com.
If you need technical information
about the document, please contact John
PO 00000
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Fmt 4703
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67603
Schaum, National Center for
Environmental Assessment (NCEA);
telephone: 202–564–3237; facsimile:
202–565–0078; e-mail
schaum.john@epa.gov.
Dated: November 21, 2007.
Peter W. Preuss,
Director, National Center for Environmental
Assessment.
[FR Doc. E7–23158 Filed 11–28–07; 8:45 am]
BILLING CODE 6560–50–P
FEDERAL ELECTION COMMISSION
Sunshine Act Meeting Notice
Federal Election Commission.
Thursday, November
29, 2007, at 10 a.m.
PLACE: 999 E Street, NW., Washington,
DC (Ninth Floor).
STATUS: This meeting will be open to the
public.
AGENCY:
DATES AND TIMES:
THE FOLLOWING ITEM HAS BEEN ADDED TO
THE AGENDA: Advisory Opinion 2007–30:
Chris Dodd for President, Inc., by Marc
E. Elias, Esq.
PERSON TO CONTACT FOR INFORMATION:
Mr. Robert Biersack, Press Officer,
Telephone: (202) 694–1220.
Mary W. Dove,
Secretary of the Commission.
[FR Doc. 07–5892 Filed 11–27–07; 3:06 pm]
BILLING CODE 6715–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10054, CMS–R–
118 and CMS–10246]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS), Department of Health
and Human Services, is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this burden
estimate or any other aspect of this
collection of information, including any
of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
AGENCY:
E:\FR\FM\29NON1.SGM
29NON1
rmajette on PROD1PC64 with NOTICES
67604
Federal Register / Vol. 72, No. 229 / Thursday, November 29, 2007 / Notices
performance of the Agency’s function;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
1. Type of Information Collection
Request: Extension without change of a
currently approved collection; Title of
Information Collection: Recognition of
payment for new technology services for
New Technology ambulatory payment
classification (APC) groups under the
Outpatient Prospective Payment System
and Supporting Regulations in 42 CFR
part 419; Use: CMS needs to keep pace
with emerging new technologies and
make them accessible to Medicare
beneficiaries in a timely manner. It is
necessary that CMS continue to collect
appropriate information from interested
parties such as hospitals, medical
device manufacturers, pharmaceutical
companies and others that bring to
CMS’ attention specific services that
they wish us to evaluate for New
Technology APC payment. The
information that CMS seeks to continue
to collect is necessary to determine
whether certain new services are
eligible for payment in New Technology
APCs, to determine appropriate coding
and to set an appropriate payment rate
for the new technology service. The
intent of these provisions is to ensure
timely beneficiary access to new and
appropriate technologies. Interested
parties such as hospitals, device
manufacturers, pharmaceutical
companies, and physicians use this
information to apply for New
Technology APC payments for certain
services covered in the Outpatient
Prospective Payment System. Form
Numbers: CMS–10054 (OMB #: 0938–
0860); Frequency: Reporting—Once;
Affected Public: Business or other forprofits; Number of Respondents: 15;
Total Annual Responses: 15; Total
Annual Hours: 180.
2. Type of Information Collection
Request: Reinstatement without change
of a previously approved collection;
Title of Information Collection: Quality
Improvement (formerly Peer Review)
Organization Contracts: Solicitation of
Statements of Interest from In-State
Organizations, General Notice and
Supporting Regulations in 42 CFR,
475.102, 475.103, 475.104, 475.105,
475.106; Use: The criteria that an
organization must satisfy in order to be
eligible for a Medicare Quality
Improvement Organization (QIO)
contract are specified by law and set
forth in sections 1152 and 1153 of the
VerDate Aug<31>2005
14:52 Nov 28, 2007
Jkt 211001
Social Security Act (the Act). In very
basic terms, the applicant organization
must demonstrate that it is either a
physician-sponsored or physicianaccess organization. The qualifications
for in-State status for an otherwise
qualified QIO organization are also set
forth in section 1153(i)(3) of the Act.
To comply with section 1153 of the
Act, we must publish the solicitation of
statements of interest from qualified inState organizations no later than January
31, 2008. We wish to publish notice of
contract expiration dates and the time
periods during which interested,
qualified organizations may submit
statements of interest and proposals for
these contracts substantially sooner than
the January 2008 deadline, in order to
give maximal notice and opportunity to
all qualified and potentially interested
organizations. We are soliciting
information in the form of responses to
our request for statements of interest
from qualified in-State organizations
who may wish to compete for the QIO
contracts for their respective States. The
responses should contain an indication
of interest and information
demonstrating the interested
organizations’ eligibility to qualify as a
QIO under the requirements of sections
1152 and 1153 of the Act. Form
Number: CMS–R–118 (OMB #: 0938–
0526); Frequency: Reporting—On
occasion; Affected Public: Business or
other for-profit; Number of
Respondents: 53; Total Annual
Responses: 53; Total Annual Hours: 1.
3. Type of Information Collection
Request: New collection; Title of
Information Collection: Cost and
Resource Utilization (CRU) Data
Collection for the Medicare Post Acute
Care Payment Reform Demonstration;
Use: The CRU data collection is part of
the Post-Acute Care Payment Reform
Demonstration mandated by Section
5008 of the Deficit Reduction Act of
2005. This demonstration is intended to
address problems with the current
Medicare payment systems for postacute care services, including those for
Long Term Care Hospitals, Inpatient
Rehabilitation Facilities, Skilled
Nursing Facilities, and Home Health
Agencies. Each of these four types of
providers currently has a separate
prospective payment system (PPS) with
its own case-mix groups, payment units,
and rates. Each case-mix grouper uses a
unique set of items to measure patients,
making it difficult to compare severity,
costs, and outcomes across settings.
These four provider types form a
continuum of care where patients may
overlap in terms of the conditions being
treated, but they primarily differ in
terms of the severity of the patients’
PO 00000
Frm 00012
Fmt 4703
Sfmt 4703
medical or functional impairments. The
current payment methods are designed
as silos that do not recognize the
potential overlap in case mix or the
complimentary nature of the services
across an episode, nor does it allow for
standardized measures of costs across
settings since each PPS was developed
independently using different
measurement systems and underlying
assumptions.
The Post-Acute Care Payment Reform
Demonstration will examine the relative
costliness and outcomes of post acute
cases admitted to different settings for
similar conditions. The work will differ
from past attempts in this area because
it will use a standardized case mix tool
for measuring patient severity and a
standardized resource data collection
tool in all four post acute settings.
Specifically, the legislation requires that
CMS provide information on both the
fixed and variables costs for each
individual treated in post acute care
settings.
The CRU data collection instruments
are designed to collect a provider’s
routine costs to specific patients
because in general, nurses’ and many
other direct care providers’ time spent
on behalf of specific patients and on
activities not patient-specific, is not
reported. In addition, charges for
therapist services reported on claims
may not sufficiently measure true
relative differences in therapy resource
costs among patients. The data will be
used, along with Medicare claims and
cost report data, to examine substitution
issues: how do costs and outcomes
differ for post acute care patients with
similar case mix acuity when treated in
one of the various settings. The results
will be used to provide CMS and the
Congress information on setting-neutral
payment models, revisions to single
setting payment systems, current
discharge placement patterns, and
patient outcomes across settings.
Since the August 24, 2007, Federal
Register notice (72 FR 48645), we have
made minor changes to the CRU
instrument in response to public
comments and internal review. The
changes are primarily wording changes
and direction clarifications. These
changes are not expected to impact the
data collection burden. Form Number:
CMS–10246 (OMB #: 0938–New);
Frequency: Reporting and
Recordkeeping; Affected Public: Private
Sector—Business or other for-profits
and not-for-profit institutions; Number
of Respondents: 138; Total Annual
Responses: 61,589; Total Annual Hours:
28,783.
To obtain copies of the supporting
statement and any related forms for the
E:\FR\FM\29NON1.SGM
29NON1
Federal Register / Vol. 72, No. 229 / Thursday, November 29, 2007 / Notices
proposed paperwork collections
referenced above, access CMS Web site
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786–
1326.
To be assured consideration,
comments and recommendations for the
proposed information collections must
be received by the OMB desk officer at
the address below, no later than 5 p.m.
on December 31, 2007.
OMB Human Resources and Housing
Branch, Attention: Carolyn Lovett, New
Executive Office Building, Room 10235,
Washington, DC 20503, Fax Number:
(202) 395–6974.
Dated: November 21, 2007.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E7–23163 Filed 11–28–07; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services, HHS
[Document Identifier: CMS–10165, CMS–
2552–96 and CMS–10008]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS) is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this burden
estimate or any other aspect of this
collection of information, including any
of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
1. Type of Information Collection
Request: Revision of a currently
rmajette on PROD1PC64 with NOTICES
AGENCY:
VerDate Aug<31>2005
14:52 Nov 28, 2007
Jkt 211001
approved collection; Title of
Information Collection: Electronic
Health Record; Use: The purpose of this
demonstration project is to reward the
delivery of high-quality care supported
by the adoption and use of electronic
health records in small to medium-sized
primary care physician practices. While
this is separate and distinct from the
Medicare Care Management
Performance (MCMP) Demonstration, it
expands upon the foundation created by
the MCMP Demonstration, which was
mandated by Section 649 of the
Medicare Prescription Drug,
Improvement and Modernization Act of
2003. The electronic health record
demonstration will be operational for a
5-year period and will be operated
under section 402 demonstration waiver
authority. The information to be
obtained as part of the application form
is necessary to document basic
information for physician practices that
intend to participate in this
demonstration initiative. Form Number:
CMS–10165 (OMB#: 0938–0965);
Frequency: Once; Affected Public:
Private sector—Business or other forprofit; Number of Respondents: 2,400;
Total Annual Responses: 2,400; Total
Annual Hours: 520.
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Hospital and
Health Care Complexes Cost Report and
supporting Regulations in 42 CFR
413.20 and 413.24; Use: This Cost
Report Form is filed annually by
freestanding providers participating in
the Medicare program to effect year end
cost settlement for providing services to
Medicare beneficiaries. The CMS–2552–
96 cost report is needed to determine
the amount of reimbursable cost, based
upon the cost limits, that is due these
providers furnishing medical services to
Medicare beneficiaries. Form Number:
CMS–2552–96 (OMB #: 0938–0050);
Frequency: Yearly; Affected Public:
Private sector—Business or other forprofit and Not-for-profit institutions;
Number of Respondents: 6,175; Total
Annual Responses: 6,175; Total Annual
Hours: 4,090,474.
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Process and
Information Required to Determine
Eligibility of Drugs, Biologicals, and
Radiopharmaceutical Agents for
Transitional Pass-Through Status Under
the Hospital Outpatient Prospective
Payment System (OPPS); Use: Section
1833(t)(6) of the Social Security Act
provides for temporary additional
payments or ‘‘transitional pass-through
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Fmt 4703
Sfmt 4703
67605
payments’’ for certain drugs and
biological agents. Interested parties such
as hospitals, pharmaceutical companies,
and physicians can apply for
transitional pass-through payment for
drugs and biologicals used with services
covered under the OPPS. CMS uses this
information to determine if the criteria
for making a transitional pass-through
payment are met and if an interim
Healthcare Common Procedure Coding
System (HCPCS) code for a new drug or
biological is necessary. Form Number:
CMS–10008 (OMB #: 0938–0802);
Frequency: Once; Affected Public:
Private sector—Business or other forprofit; Number of Respondents: 10;
Total Annual Responses: 10; Total
Annual Hours: 160.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web site
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786–
1326.
To be assured consideration,
comments and recommendations for the
proposed information collections must
be received at the address below, no
later than 5 p.m. on January 28, 2008.
CMS, Office of Strategic Operations
and Regulatory Affairs, Division of
Regulations Development—C, Attention:
Bonnie L Harkless, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
Dated: November 21, 2007.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E7–23164 Filed 11–28–07; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Gastrointestinal Drugs Advisory
Committee; Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
E:\FR\FM\29NON1.SGM
29NON1
Agencies
[Federal Register Volume 72, Number 229 (Thursday, November 29, 2007)]
[Notices]
[Pages 67603-67605]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-23163]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10054, CMS-R-118 and CMS-10246]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid
Services (CMS), Department of Health and Human Services, is publishing
the following summary of proposed collections for public comment.
Interested persons are invited to send comments regarding this burden
estimate or any other aspect of this collection of information,
including any of the following subjects: (1) The necessity and utility
of the proposed information collection for the proper
[[Page 67604]]
performance of the Agency's function; (2) the accuracy of the estimated
burden; (3) ways to enhance the quality, utility, and clarity of the
information to be collected; and (4) the use of automated collection
techniques or other forms of information technology to minimize the
information collection burden.
1. Type of Information Collection Request: Extension without change
of a currently approved collection; Title of Information Collection:
Recognition of payment for new technology services for New Technology
ambulatory payment classification (APC) groups under the Outpatient
Prospective Payment System and Supporting Regulations in 42 CFR part
419; Use: CMS needs to keep pace with emerging new technologies and
make them accessible to Medicare beneficiaries in a timely manner. It
is necessary that CMS continue to collect appropriate information from
interested parties such as hospitals, medical device manufacturers,
pharmaceutical companies and others that bring to CMS' attention
specific services that they wish us to evaluate for New Technology APC
payment. The information that CMS seeks to continue to collect is
necessary to determine whether certain new services are eligible for
payment in New Technology APCs, to determine appropriate coding and to
set an appropriate payment rate for the new technology service. The
intent of these provisions is to ensure timely beneficiary access to
new and appropriate technologies. Interested parties such as hospitals,
device manufacturers, pharmaceutical companies, and physicians use this
information to apply for New Technology APC payments for certain
services covered in the Outpatient Prospective Payment System. Form
Numbers: CMS-10054 (OMB : 0938-0860); Frequency: Reporting--
Once; Affected Public: Business or other for-profits; Number of
Respondents: 15; Total Annual Responses: 15; Total Annual Hours: 180.
2. Type of Information Collection Request: Reinstatement without
change of a previously approved collection; Title of Information
Collection: Quality Improvement (formerly Peer Review) Organization
Contracts: Solicitation of Statements of Interest from In-State
Organizations, General Notice and Supporting Regulations in 42 CFR,
475.102, 475.103, 475.104, 475.105, 475.106; Use: The criteria that an
organization must satisfy in order to be eligible for a Medicare
Quality Improvement Organization (QIO) contract are specified by law
and set forth in sections 1152 and 1153 of the Social Security Act (the
Act). In very basic terms, the applicant organization must demonstrate
that it is either a physician-sponsored or physician-access
organization. The qualifications for in-State status for an otherwise
qualified QIO organization are also set forth in section 1153(i)(3) of
the Act.
To comply with section 1153 of the Act, we must publish the
solicitation of statements of interest from qualified in-State
organizations no later than January 31, 2008. We wish to publish notice
of contract expiration dates and the time periods during which
interested, qualified organizations may submit statements of interest
and proposals for these contracts substantially sooner than the January
2008 deadline, in order to give maximal notice and opportunity to all
qualified and potentially interested organizations. We are soliciting
information in the form of responses to our request for statements of
interest from qualified in-State organizations who may wish to compete
for the QIO contracts for their respective States. The responses should
contain an indication of interest and information demonstrating the
interested organizations' eligibility to qualify as a QIO under the
requirements of sections 1152 and 1153 of the Act. Form Number: CMS-R-
118 (OMB : 0938-0526); Frequency: Reporting--On occasion;
Affected Public: Business or other for-profit; Number of Respondents:
53; Total Annual Responses: 53; Total Annual Hours: 1.
3. Type of Information Collection Request: New collection; Title of
Information Collection: Cost and Resource Utilization (CRU) Data
Collection for the Medicare Post Acute Care Payment Reform
Demonstration; Use: The CRU data collection is part of the Post-Acute
Care Payment Reform Demonstration mandated by Section 5008 of the
Deficit Reduction Act of 2005. This demonstration is intended to
address problems with the current Medicare payment systems for post-
acute care services, including those for Long Term Care Hospitals,
Inpatient Rehabilitation Facilities, Skilled Nursing Facilities, and
Home Health Agencies. Each of these four types of providers currently
has a separate prospective payment system (PPS) with its own case-mix
groups, payment units, and rates. Each case-mix grouper uses a unique
set of items to measure patients, making it difficult to compare
severity, costs, and outcomes across settings. These four provider
types form a continuum of care where patients may overlap in terms of
the conditions being treated, but they primarily differ in terms of the
severity of the patients' medical or functional impairments. The
current payment methods are designed as silos that do not recognize the
potential overlap in case mix or the complimentary nature of the
services across an episode, nor does it allow for standardized measures
of costs across settings since each PPS was developed independently
using different measurement systems and underlying assumptions.
The Post-Acute Care Payment Reform Demonstration will examine the
relative costliness and outcomes of post acute cases admitted to
different settings for similar conditions. The work will differ from
past attempts in this area because it will use a standardized case mix
tool for measuring patient severity and a standardized resource data
collection tool in all four post acute settings. Specifically, the
legislation requires that CMS provide information on both the fixed and
variables costs for each individual treated in post acute care
settings.
The CRU data collection instruments are designed to collect a
provider's routine costs to specific patients because in general,
nurses' and many other direct care providers' time spent on behalf of
specific patients and on activities not patient-specific, is not
reported. In addition, charges for therapist services reported on
claims may not sufficiently measure true relative differences in
therapy resource costs among patients. The data will be used, along
with Medicare claims and cost report data, to examine substitution
issues: how do costs and outcomes differ for post acute care patients
with similar case mix acuity when treated in one of the various
settings. The results will be used to provide CMS and the Congress
information on setting-neutral payment models, revisions to single
setting payment systems, current discharge placement patterns, and
patient outcomes across settings.
Since the August 24, 2007, Federal Register notice (72 FR 48645),
we have made minor changes to the CRU instrument in response to public
comments and internal review. The changes are primarily wording changes
and direction clarifications. These changes are not expected to impact
the data collection burden. Form Number: CMS-10246 (OMB :
0938-New); Frequency: Reporting and Recordkeeping; Affected Public:
Private Sector--Business or other for-profits and not-for-profit
institutions; Number of Respondents: 138; Total Annual Responses:
61,589; Total Annual Hours: 28,783.
To obtain copies of the supporting statement and any related forms
for the
[[Page 67605]]
proposed paperwork collections referenced above, access CMS Web site
address at https://www.cms.hhs.gov/PaperworkReductionActof1995, or e-
mail your request, including your address, phone number, OMB number,
and CMS document identifier, to Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786-1326.
To be assured consideration, comments and recommendations for the
proposed information collections must be received by the OMB desk
officer at the address below, no later than 5 p.m. on December 31,
2007.
OMB Human Resources and Housing Branch, Attention: Carolyn Lovett,
New Executive Office Building, Room 10235, Washington, DC 20503, Fax
Number: (202) 395-6974.
Dated: November 21, 2007.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. E7-23163 Filed 11-28-07; 8:45 am]
BILLING CODE 4120-01-P