Agency Information Collection Activities: Submission for OMB Review; Comment Request, 25182-25183 [2012-10225]
Download as PDF
25182
Federal Register / Vol. 77, No. 82 / Friday, April 27, 2012 / Notices
Respondents: 2,700,000; Total Annual
Responses: 2,700,000; Total Annual
Hours: 1,360,000. (For policy questions
regarding this collection contact Debbie
Skinner at 410–786–7480. For all other
issues call 410–786–1326.)
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.
In commenting on the proposed
information collections please reference
the document identifier or OMB control
number. To be assured consideration,
comments and recommendations must
be submitted in one of the following
ways by June 26, 2012:
1. Electronically. You may submit
your comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) accepting comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number llllllll,
Room C4–26–05, 7500 Security
Boulevard, Baltimore, Maryland 21244–
1850.
Dated: April 24, 2012.
Martique Jones,
Director, Regulations Development Group,
Division B Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–10231 Filed 4–26–12; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
mstockstill on DSK4VPTVN1PROD with NOTICES
[Document Identifier CMS–10102, CMS–R–
263 and CMS–855(O)]
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
AGENCY:
VerDate Mar<15>2010
17:44 Apr 26, 2012
Jkt 226001
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
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: Revision of a currently
approved collection;
Title of Information Collection:
National Implementation of Hospital
Consumer Assessment of Healthcare
Providers and Systems (HCAHPS); Use:
The HCAHPS (Hospital Consumer
Assessment of Healthcare Providers and
Systems) survey is the first national,
standardized, publicly reported survey
of patients’ perspectives of hospital
care. HCAHPS (pronounced ‘‘H-caps’’),
also known as the CAHPS® Hospital
Survey, is a survey instrument and data
collection methodology for measuring
patients’ perceptions of their hospital
experience. While many hospitals have
collected information on patient
satisfaction for their own internal use,
until HCAHPS there was no national
standard for collecting and publicly
reporting information about patient
experience of care that allowed valid
comparisons to be made across hospitals
locally, regionally and nationally.
Three broad goals have shaped
HCAHPS. First, the survey is designed
to produce data about patients’
perspectives of care that allow objective
and meaningful comparisons of
hospitals on topics that are important to
consumers. Second, public reporting of
the survey results creates new
incentives for hospitals to improve
quality of care. Third, public reporting
serves to enhance accountability in
health care by increasing transparency
of the quality of hospital care provided
in return for the public investment.
With these goals in mind, the Centers
for Medicare & Medicaid Services (CMS)
has taken substantial steps to assure that
the survey is credible, useful, and
practical. Hospitals implement HCAHPS
under the auspices of the Hospital
Quality Alliance (HQA), a private/
public partnership that includes major
hospital and medical associations,
PO 00000
Frm 00062
Fmt 4703
Sfmt 4703
consumer groups, measurement and
accrediting bodies, government, and
other groups that share an interest in
improving hospital quality. Both the
HQA and the National Quality Forum
have endorsed HCAHPS.
The enactment of the Deficit
Reduction Act of 2005 created an
additional incentive for acute care
hospitals to participate in HCAHPS.
Since July 2007, hospitals subject to the
Inpatient Prospective Payment System
(IPPS) annual payment update
provisions (‘‘subsection (d) hospitals’’)
must collect and submit HCAHPS data
in order to receive their full IPPS annual
payment update. IPPS hospitals that fail
to publicly report the required quality
measures, which include the HCAHPS
survey, may receive an annual payment
update that is reduced by 2.0 percentage
points. Non-IPPS hospitals, such as
Critical Access Hospitals, may
voluntarily participate in HCAHPS.
The Patient Protection and Affordable
Care Act of 2010 (Pub. L. 111–148)
includes HCAHPS among the measures
to be used to calculate value-based
incentive payments in the Hospital
Value-Based Purchasing program,
beginning with discharges in October
2012.
Currently the HCAHPS survey asks
discharged patients 27 questions about
their recent hospital stay. The survey
contains 18 core questions about critical
aspects of patients’ hospital experiences
(communication with nurses and
doctors, the responsiveness of hospital
staff, the cleanliness and quietness of
the hospital environment, pain
management, communication about
medicines, discharge information,
overall rating of hospital, and would
they recommend the hospital). The
survey also includes four items to direct
patients to relevant questions, three
items to adjust for the mix of patients
across hospitals, and two items that
support Congressionally-mandated
reports.
This revision is being submitted in
order to add five new items to the
survey: three items that comprise a Care
Transitions composite; one item that
asks whether the patient was admitted
through the emergency room; and one
item that asks about the patient’s overall
mental health. This marks the first
addition of items to the HCAHPS
Survey since its national
implementation in 2006. Form Number:
CMS–10102 (OCN: 0938–0981);
Frequency: Occasionally; Affected
Public: Individuals or Households,
Private Sector—Business or other forprofits and not-for-profit institutions.
Number of Respondents: 2,713,812;
Total Annual Responses: 2,713,812;
E:\FR\FM\27APN1.SGM
27APN1
mstockstill on DSK4VPTVN1PROD with NOTICES
Federal Register / Vol. 77, No. 82 / Friday, April 27, 2012 / Notices
Total Annual Hours: 365,136. (For
policy questions regarding this
collection contact William Lehrman at
410–786–1037. For all other issues call
410–786–1326.)
2. Type of Information Collection
Request: Reinstatement with change of a
previously approved collection; Title of
Information Collection: Site
Investigation for Durable Medical
Equipment (DME) Suppliers ; Use: CMS
is mandated to identify and implement
measures to prevent fraud and abuse in
the Medicare program. To meet this
challenge, CMS has moved forward to
improve the quality of the process for
enrolling suppliers into the Medicare
program by establishing a uniform
application for enumerating suppliers of
durable medical equipment, prosthetics,
orthotics, and supplies (DMEPOS).
Implementation of enhanced procedures
for verifying the enrollment information
has also improved the enrollment
process. As part of this process,
verification of compliance with supplier
standards is necessary. The site
investigation form has been used in the
past to aid the Medicare contractor (the
National Supplier Clearinghouse and/or
its subcontractors) in verifying
compliance with the required supplier
standards found in 42 CFR 424.57(c).
The primary function of the site
investigation form is to provide a
standardized, uniform tool to gather
information from a DMEPOS supplier
that tells us whether it meets certain
qualifications to be a DMEPOS supplier
(as found in 42 CFR 424.57(c)) and
where it practices or renders its
services.
This site investigation form collects
the same information as its predecessor,
with the exception of one new yes/no
question under the ‘‘Records and
Telephone’’ section (question 11(a))
used to verify if the DMEPOS supplier
maintains physician ordering/referring
records for the supplies and/or services
it renders to Medicare beneficiaries (if
applicable). This information is required
by section 1833(q) of the Social Security
Act (the Act) which states that all
physicians and non-physician
practitioners that meet the definitions at
section 1861(r) and 1842(b)(18)(C) of the
Act, be uniquely identified for all claims
for services that are ordered or referred.
Other information collected on this site
investigation remains unchanged, but
has been reformatted for greater
functionality. Form Number: CMS–R–
263 (OCN: 0938–0749); Frequency:
Once; Affected Public: Private Sector—
Business or other for-profits and not-forprofit institutions; Number of
Respondents: 30,000; Total Annual
Responses: 30,000; Total Annual Hours:
VerDate Mar<15>2010
17:44 Apr 26, 2012
Jkt 226001
15,000. (For policy questions regarding
this collection contact Kimberly
McPhillips at 410–786–5374. For all
other issues call 410–786–1326.)
3. Type of Information Collection
Request: Revision of a currently
approved collection;
Title of Information Collection:
Medicare Registration Application; Use:
The CMS 855O allows a physician to
receive a Medicare identification
number (without being approved for
billing privileges) for the sole purpose of
ordering and referring Medicare
beneficiaries to Medicare approved
providers and suppliers. This new
Medicare registration application form
allows physicians who do not provide
services to Medicare beneficiaries to be
given a Medicare identification number
without having to supply all the data
required for the submission of Medicare
claims. It also allows the Medicare
program to identify ordering and
referring physicians without having to
validate the amount of data necessary to
determine claims payment eligibility
(such as banking information), while
continuing to identify the physician’s
credentials as valid for ordering and
referring purposes. Since the physicians
and non-physician practitioners
submitting this application are not
enrolling in Medicare to submit claims
but are only registering with Medicare
as eligible to order and refer, CMS
believes changing the title from
Medicare Enrollment Application to
Medicare Registration Application
better captures the actual purpose of
this form.
Where appropriate, CMS has changed
all references to enrollment or enrolling
to registration and registering and
Medicare billing number to National
Provider Identifier. CMS also added a
check box to allow physicians and nonphysician practitioners to withdraw
from the ordering and referring registry.
A section to collect information on
professional certifications was added for
those practitioners who are not
professionally licensed. Editorial and
formatting corrections were made in
response to prior comments received
during the approval of the current
version of this application. Other minor
editorial and formatting corrections
were made to better clarify the purpose
of this application. Form Number:
CMS–855(O) (OCN: 0938–1135);
Frequency: Occasionally; Affected
Public: Individuals; Number of
Respondents: 48,500; Total Annual
Responses: 48,500; Total Annual Hours:
24,125. (For policy questions regarding
this collection contact Kimberly
McPhillips at 410–786–5374. For all
other issues call 410–786–1326.)
PO 00000
Frm 00063
Fmt 4703
Sfmt 4703
25183
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 by the OMB desk officer at
the address below, no later than 5 p.m.
on May 29, 2012.
OMB, Office of Information and
Regulatory Affairs, Attention: CMS Desk
Officer, Fax Number: (202) 395–6974,
Email: OIRA_submission@omb.eop.gov.
Dated: April 24, 2012.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–10225 Filed 4–26–12; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0001]
Circulatory System Devices Panel of
the Medical Devices 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.
Name of Committee: Circulatory System
Devices Panel of the Medical Devices
Advisory Committee.
General Function of the Committee: To
provide advice and recommendations to the
Agency on FDA’s regulatory issues.
Date and Time: The meeting will be held
on June 13, 2012, from 8 a.m. to 6 p.m.
Location: Hilton Washington DC North/
Gaithersburg, Salons A, B, C, and D, 620
Perry Pkwy., Gaithersburg, MD 20877. The
hotel telephone number is 301–977–8900.
Contact Person: Jamie Waterhouse, Center
for Devices and Radiological Health, Food
and Drug Administration, 10903 New
Hampshire Ave., Silver Spring, MD 20993, or
FDA Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington, DC area), and follow the
prompts to the desired center or product
E:\FR\FM\27APN1.SGM
27APN1
Agencies
[Federal Register Volume 77, Number 82 (Friday, April 27, 2012)]
[Notices]
[Pages 25182-25183]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-10225]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier CMS-10102, CMS-R-263 and CMS-855(O)]
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 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: Revision of a currently
approved collection;
Title of Information Collection: National Implementation of
Hospital Consumer Assessment of Healthcare Providers and Systems
(HCAHPS); Use: The HCAHPS (Hospital Consumer Assessment of Healthcare
Providers and Systems) survey is the first national, standardized,
publicly reported survey of patients' perspectives of hospital care.
HCAHPS (pronounced ``H-caps''), also known as the CAHPS[supreg]
Hospital Survey, is a survey instrument and data collection methodology
for measuring patients' perceptions of their hospital experience. While
many hospitals have collected information on patient satisfaction for
their own internal use, until HCAHPS there was no national standard for
collecting and publicly reporting information about patient experience
of care that allowed valid comparisons to be made across hospitals
locally, regionally and nationally.
Three broad goals have shaped HCAHPS. First, the survey is designed
to produce data about patients' perspectives of care that allow
objective and meaningful comparisons of hospitals on topics that are
important to consumers. Second, public reporting of the survey results
creates new incentives for hospitals to improve quality of care. Third,
public reporting serves to enhance accountability in health care by
increasing transparency of the quality of hospital care provided in
return for the public investment. With these goals in mind, the Centers
for Medicare & Medicaid Services (CMS) has taken substantial steps to
assure that the survey is credible, useful, and practical. Hospitals
implement HCAHPS under the auspices of the Hospital Quality Alliance
(HQA), a private/public partnership that includes major hospital and
medical associations, consumer groups, measurement and accrediting
bodies, government, and other groups that share an interest in
improving hospital quality. Both the HQA and the National Quality Forum
have endorsed HCAHPS.
The enactment of the Deficit Reduction Act of 2005 created an
additional incentive for acute care hospitals to participate in HCAHPS.
Since July 2007, hospitals subject to the Inpatient Prospective Payment
System (IPPS) annual payment update provisions (``subsection (d)
hospitals'') must collect and submit HCAHPS data in order to receive
their full IPPS annual payment update. IPPS hospitals that fail to
publicly report the required quality measures, which include the HCAHPS
survey, may receive an annual payment update that is reduced by 2.0
percentage points. Non-IPPS hospitals, such as Critical Access
Hospitals, may voluntarily participate in HCAHPS.
The Patient Protection and Affordable Care Act of 2010 (Pub. L.
111-148) includes HCAHPS among the measures to be used to calculate
value-based incentive payments in the Hospital Value-Based Purchasing
program, beginning with discharges in October 2012.
Currently the HCAHPS survey asks discharged patients 27 questions
about their recent hospital stay. The survey contains 18 core questions
about critical aspects of patients' hospital experiences (communication
with nurses and doctors, the responsiveness of hospital staff, the
cleanliness and quietness of the hospital environment, pain management,
communication about medicines, discharge information, overall rating of
hospital, and would they recommend the hospital). The survey also
includes four items to direct patients to relevant questions, three
items to adjust for the mix of patients across hospitals, and two items
that support Congressionally-mandated reports.
This revision is being submitted in order to add five new items to
the survey: three items that comprise a Care Transitions composite; one
item that asks whether the patient was admitted through the emergency
room; and one item that asks about the patient's overall mental health.
This marks the first addition of items to the HCAHPS Survey since its
national implementation in 2006. Form Number: CMS-10102 (OCN: 0938-
0981); Frequency: Occasionally; Affected Public: Individuals or
Households, Private Sector--Business or other for-profits and not-for-
profit institutions. Number of Respondents: 2,713,812; Total Annual
Responses: 2,713,812;
[[Page 25183]]
Total Annual Hours: 365,136. (For policy questions regarding this
collection contact William Lehrman at 410-786-1037. For all other
issues call 410-786-1326.)
2. Type of Information Collection Request: Reinstatement with
change of a previously approved collection; Title of Information
Collection: Site Investigation for Durable Medical Equipment (DME)
Suppliers ; Use: CMS is mandated to identify and implement measures to
prevent fraud and abuse in the Medicare program. To meet this
challenge, CMS has moved forward to improve the quality of the process
for enrolling suppliers into the Medicare program by establishing a
uniform application for enumerating suppliers of durable medical
equipment, prosthetics, orthotics, and supplies (DMEPOS).
Implementation of enhanced procedures for verifying the enrollment
information has also improved the enrollment process. As part of this
process, verification of compliance with supplier standards is
necessary. The site investigation form has been used in the past to aid
the Medicare contractor (the National Supplier Clearinghouse and/or its
subcontractors) in verifying compliance with the required supplier
standards found in 42 CFR 424.57(c). The primary function of the site
investigation form is to provide a standardized, uniform tool to gather
information from a DMEPOS supplier that tells us whether it meets
certain qualifications to be a DMEPOS supplier (as found in 42 CFR
424.57(c)) and where it practices or renders its services.
This site investigation form collects the same information as its
predecessor, with the exception of one new yes/no question under the
``Records and Telephone'' section (question 11(a)) used to verify if
the DMEPOS supplier maintains physician ordering/referring records for
the supplies and/or services it renders to Medicare beneficiaries (if
applicable). This information is required by section 1833(q) of the
Social Security Act (the Act) which states that all physicians and non-
physician practitioners that meet the definitions at section 1861(r)
and 1842(b)(18)(C) of the Act, be uniquely identified for all claims
for services that are ordered or referred. Other information collected
on this site investigation remains unchanged, but has been reformatted
for greater functionality. Form Number: CMS-R-263 (OCN: 0938-0749);
Frequency: Once; Affected Public: Private Sector--Business or other
for-profits and not-for-profit institutions; Number of Respondents:
30,000; Total Annual Responses: 30,000; Total Annual Hours: 15,000.
(For policy questions regarding this collection contact Kimberly
McPhillips at 410-786-5374. For all other issues call 410-786-1326.)
3. Type of Information Collection Request: Revision of a currently
approved collection;
Title of Information Collection: Medicare Registration Application;
Use: The CMS 855O allows a physician to receive a Medicare
identification number (without being approved for billing privileges)
for the sole purpose of ordering and referring Medicare beneficiaries
to Medicare approved providers and suppliers. This new Medicare
registration application form allows physicians who do not provide
services to Medicare beneficiaries to be given a Medicare
identification number without having to supply all the data required
for the submission of Medicare claims. It also allows the Medicare
program to identify ordering and referring physicians without having to
validate the amount of data necessary to determine claims payment
eligibility (such as banking information), while continuing to identify
the physician's credentials as valid for ordering and referring
purposes. Since the physicians and non-physician practitioners
submitting this application are not enrolling in Medicare to submit
claims but are only registering with Medicare as eligible to order and
refer, CMS believes changing the title from Medicare Enrollment
Application to Medicare Registration Application better captures the
actual purpose of this form.
Where appropriate, CMS has changed all references to enrollment or
enrolling to registration and registering and Medicare billing number
to National Provider Identifier. CMS also added a check box to allow
physicians and non-physician practitioners to withdraw from the
ordering and referring registry. A section to collect information on
professional certifications was added for those practitioners who are
not professionally licensed. Editorial and formatting corrections were
made in response to prior comments received during the approval of the
current version of this application. Other minor editorial and
formatting corrections were made to better clarify the purpose of this
application. Form Number: CMS-855(O) (OCN: 0938-1135); Frequency:
Occasionally; Affected Public: Individuals; Number of Respondents:
48,500; Total Annual Responses: 48,500; Total Annual Hours: 24,125.
(For policy questions regarding this collection contact Kimberly
McPhillips at 410-786-5374. For all other issues call 410-786-1326.)
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 by the OMB desk
officer at the address below, no later than 5 p.m. on May 29, 2012.
OMB, Office of Information and Regulatory Affairs, Attention: CMS
Desk Officer, Fax Number: (202) 395-6974, Email: OIRA_submission@omb.eop.gov.
Dated: April 24, 2012.
Martique Jones,
Director, Regulations Development Group, Division B, Office of
Strategic Operations and Regulatory Affairs.
[FR Doc. 2012-10225 Filed 4-26-12; 8:45 am]
BILLING CODE 4120-01-P