Agency Information Collection Activities: Proposed Collection; Comment Request, 38292-38294 [2012-15615]
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Federal Register / Vol. 77, No. 124 / Wednesday, June 27, 2012 / Notices
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[FR Doc. 2012–15625 Filed 6–26–12; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve the proposed
information collection project: ‘‘Online
Application Order Form for Products
from the Healthcare Cost and Utilization
Project (HCUP).’’ In accordance with the
Paperwork Reduction Act, 44 U.S.C.
3501–3521, AHRQ invites the public to
comment on this proposed information
collection.
DATES: Comments on this notice must be
received by August 27, 2012.
ADDRESSES: Written comments should
be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by
email at doris.lefkowitz@AHRQ.hhs.gov.
Copies of the proposed collection
plans, data collection instruments, and
specific details on the estimated burden
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SUMMARY:
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can be obtained from the AHRQ Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
email at doris.lefkowitz@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
Proposed Project
Online Application Order Form for
Products From the Healthcare Cost and
Utilization Project (HCUP)
The Healthcare Cost and Utilization
Project (HCUP, pronounced ‘‘H-Cup’’) is
a vital resource helping AHRQ achieve
its research agenda, thereby furthering
its goal of improving the delivery of
health care in the United States. HCUP
is a family of health care databases and
related software tools and products
developed through a Federal-StateIndustry partnership and sponsored by
AHRQ. HCUP includes the largest
collection of longitudinal hospital care
data in the United States, with all-payer,
encounter-level information beginning
in 1988. The HCUP databases are annual
files that contain anonymous
information from hospital discharge
records for inpatient care and certain
components of outpatient care, such as
emergency care and ambulatory
surgeries. The project currently releases
a variety of databases created for
research use on a broad range of health
issues, including cost and quality of
health services, medical practice
patterns, access to health care programs,
and outcomes of treatments at the
national, State, and local market levels.
HCUP also produces a large number of
software tools to enhance the use of
administrative health care data for
research and public health use. Software
tools use information available from a
variety of sources to create new data
elements, often through sophisticated
algorithms, for use with the HCUP
databases.
HCUP’s objectives are to:
• Create and enhance a powerful
source of national, state, and all-payer
health care data.
• Produce a broad set of software
tools and products to facilitate the use
of HCUP and other administrative data.
• Enrich a collaborative partnership
with statewide data organizations (that
voluntarily participate in the project)
aimed at increasing the quality and use
of health care data.
• Conduct and translate research to
inform decision making and improve
health care delivery.
The HCUP releases six types of
databases for public research use:
(1) The Nationwide Inpatient Sample
(NIS) is the largest all-payer inpatient
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care database in the United States,
containing data from approximately 8
million hospital stays from roughly
1,000 hospitals; this approximates a 20percent stratified sample of U.S.
community hospitals. NIS data releases
are available for purchase from the
HCUP Central Distributor for data years
beginning in 1988.
(2) The Kids’ Inpatient Database (KID)
is the only all-payer inpatient care
database for children in the United
States. The KID was specifically
designed to permit researchers to study
a broad range of conditions and
procedures related to child health
issues. The KID contains a sample of
over 3 million discharges for children
age 20 and younger from more than
3,500 U.S. community hospitals.
(3) The Nationwide Emergency
Department Sample (NEDS) is the
largest all-payer ED database in the
United States. It is constructed to
capture information both on ED visits
that do not result in an admission and
on ED visits that result in an admission
to the same hospital. The NEDS
contains more than 25 million
unweighted records for ED visits at
about 1,000 U.S. community hospitals
and approximates a 20-percent stratified
sample of U.S. hospital-based EDs. Files
are available beginning with data year
2006.
(4) The State Inpatient Databases (SID)
contain the universe of inpatient
discharge abstracts from data
organizations in 46 States that currently
participate in the SID. Together, the SID
encompasses approximately 97 percent
of all U.S. community hospital
discharges. Most States that participate
in the SID make their data available for
purchase through the HCUP Central
Distributor. Files are available beginning
with data year 1990.
(5) The State Ambulatory Surgery
Databases (SASD) contain data from
ambulatory care encounters in hospitalaffiliated (and sometimes freestanding)
ambulatory surgery sites. Currently, 29
States participate in the SASD. Files are
available beginning with data year 1997.
(6) The State Emergency Department
Databases (SEDD) contain data from
hospital-affiliated emergency
department (ED) abstracts for visits that
do not result in a hospitalization.
Currently, 29 States participate in the
SEDD. Files are available beginning
with data year 1999.
To support AHRQ’s mission to
improve health care through scientific
research, HCUP databases and software
tools are disseminated to users outside
of the Agency through a mechanism
known as the HCUP Central Distributor.
The HCUP Central Distributor assists
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38293
Federal Register / Vol. 77, No. 124 / Wednesday, June 27, 2012 / Notices
qualified researchers to access uniform
research data across multiple states with
the use of one application process. The
HCUP databases disseminated through
the Central distributor are referred to as
‘‘restricted access public release files;’’
that is, they are publicly available, but
only under restricted conditions.
HCUP databases are released to
researchers outside of AHRQ after the
completion of required training and
submission of an application that
includes a signed HCUP Data Use
Agreement (DUA). In addition, before
restricted access public release statelevel databases are released, the user is
asked for a brief description of their
research to ensure that the planned use
is consistent with HCUP policies and
with the HCUP data use requirements.
Fees are set for databases released
through the HCUP Central Distributor
depending on the type of database. The
fee for sale of state-level data is
determined by each participating
Statewide Data Organization and
reimbursed to those organizations. This
project is being conducted by AHRQ
through its contractor and
subcontractor, Thomson Reuters and
Social & Scientific Systems, Inc.,
pursuant to AHRQ’s statutory authority
to conduct and support research on
healthcare and on systems for the
delivery of such care, including
activities with respect to the outcomes,
cost, cost-effectiveness, and use of
health care services and access to such
services. (42 U.S.C. 299a(a)(3).)
Method of Collection
This information collection request is
for the activities associated with
completing an online application form
to request HCUP data, not the collection
of health care data for HCUP databases.
The activities associated with the HCUP
online application include:
(1) HCUP Application Form. All
persons wanting access to the HCUP
databases must complete an application
package. Each unique database has a
unique application package. All
application packages are available for
downloading at https://www.hcupus.ahrq.gov/tech_assist/centdist.jsp.
(2) HCUP Data Use Agreement
Training. All persons wanting access to
the HCUP databases must complete this
online training course. The purpose of
the training is to emphasize the
importance of data protection, reduce
the risk of inadvertent violations, and
describe the individual’s responsibility
when using HCUP data. The training
course can be accessed and completed
online at https://www.hcup-us.ahrq.gov/
tech_assist/dua.jsp.
(3) HCUP Data Use Agreement (DUA).
All persons wanting access to the HCUP
databases must sign a data use
agreement. Each database has a unique
DUA; an example DUA for the
Nationwide Inpatient Sample database
is available at https://www.hcupus.ahrq.gov/team/NISDUA.jsp.
Information collected in the HCUP
Application Order Form will be used for
two purposes only:
1. Business Transaction: HCUP
databases and software are currently
delivered on disk and shipped to users
who have completed the application
process. Contact information is used for
shipping the data on disk (or any other
media used in the future). AHRQ policy
and current agreements with Statewide
Data Organizations contributing data to
HCUP prohibit providing access to the
data via the Internet or email.
2. Enforcement of the HCUP Data Use
Agreement (DUA): The HCUP DUA
contains several restrictions on use of
the data. Most of these restrictions have
been put in place to safeguard the
privacy of individuals and
establishments represented in the data.
For example, data users can only use the
data for research, analysis, and aggregate
statistical reporting and are prohibited
from attempting to identify any persons
in the data. Contact information on
HCUP Data Use Agreements is retained
in the event that a violation of the DUA
takes place.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated
annualized burden associated with the
applicants’ time to order any of the
HCUP databases. An estimated 1,200
persons will order HCUP data annually.
Each of these persons will complete an
application (10 minutes), the DUA
training (15 minutes) and a DUA
(5 minutes). The total burden is
estimated to be 600 hours annually.
Exhibit 2 shows the estimated
annualized cost burden associated with
the applicants’ time to order HCUP data.
The total cost burden is estimated to be
$21,408 annually.
EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Hours per
response
Total burden
hours
HCUP Application Form ..................................................................................
HCUP DUA Training ........................................................................................
HCUP DUA ......................................................................................................
1,200
1,200
1,200
1
1
1
0/60
15/60
5/60
200
300
100
Total ..........................................................................................................
3,600
na
na
600
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents
srobinson on DSK4SPTVN1PROD with NOTICES
Form name
Total burden
hours
Average
hourly wage
rate *
Total cost
burden
HCUP Application Form ..................................................................................
HCUP DUA Training ........................................................................................
HCUP DUA ......................................................................................................
1,200
1,200
1,200
200
300
100
$35.68
35.68
35.68
$7,136
10,704
3,568
Total ..........................................................................................................
3,600
600
na
21,408
* Based upon the mean of the average wages for Life Scientists, All Other (19–1099), National Compensation Survey: Occupational wages in
the United States May 2011, ‘‘U.S. Department of Labor, Bureau of Labor Statistics.’’
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Federal Register / Vol. 77, No. 124 / Wednesday, June 27, 2012 / Notices
Estimated Annual Costs to the Federal
Government
Exhibit 3 shows the estimated total
and annualized cost to process HCUP
database applications and maintain the
ordering system over the 3 years
covered by this information collection
request. It is estimated to cost $17,237
annually to operate and maintain the
ordering system.
Exhibit 3. Estimated Total and
Annualized Cost
Cost component
Total cost
Annualized
cost
Order Review ...........................................................................................................................................................
Monthly Updates—Product Catalog ........................................................................................................................
System Maintenance ...............................................................................................................................................
Customer Inquiries ...................................................................................................................................................
Management/Troubleshooting .................................................................................................................................
$14,493
1,857
13,820
4,483
17,058
$4,831
619
4,607
1,495
5,689
Total ..................................................................................................................................................................
51,711
17,237
Request for Comments
In accordance with the Paperwork
Reduction Act, comments on AHRQ’s
information collection are requested
with regard to any of the following: (a)
Whether the proposed collection of
information is necessary for the proper
performance of AHRQ healthcare
research and healthcare information
dissemination functions, including
whether the information will have
practical utility; (b) the accuracy of
AHRQ’s estimate of burden (including
hours and costs) of the proposed
collection(s) of information; (c) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(d) ways to minimize the burden of the
collection of information upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
Dated: June 19, 2012.
Carolyn M. Clancy,
Director.
[FR Doc. 2012–15615 Filed 6–26–12; 8:45 am]
BILLING CODE 4160–90–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
srobinson on DSK4SPTVN1PROD with NOTICES
Agency for Healthcare Research and
Quality
Notice of Meeting
the Agency’s Health Services Research
Initial Review Group Committee.
The subcommittee meeting will be
closed to the public in accordance with
the Federal Advisory Committee Act,
section 10(d) of 5 U.S.C., Appendix 2
and 5 U.S.C. 552b(c)(6). Grant
applications are to be reviewed and
discussed at this meeting. These
discussions are likely to involve
information concerning individuals
associated with the applications,
including assessments of their personal
qualifications to conduct their proposed
projects. This information is exempt
from mandatory disclosure under the
above-cited statutes.
Name of Subcommittee: Health Care
Research Training (2) Virtual Review.
Date: July 12, 2012 (Open from 1:00 p.m.
to 1:15 p.m. on July 12 and closed for
remainder of the meeting).
Place: Agency for Healthcare Research and
Quality, John Eisenberg Building, 540 Gaither
Road, OEREP Conference Room, Rockville,
MD 20850.
Contact Person: Anyone wishing to obtain
a roster of members, agenda or minutes of the
nonconfidential portions of the meeting
should contact Mrs. Bonnie Campbell,
Committee Management Officer, Office of
Extramural Research, Education and Priority
Populations, AHRQ, 540 Gaither Road, Suite
2000, Rockville, Maryland 20850, Telephone
(301) 427–1554.
Agenda items for these meetings are
subject to change as priorities dictate.
Dated: June 14, 2012.
Carolyn M. Clancy,
Director.
19:05 Jun 26, 2012
BILLING CODE 4160–90–M
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Agency for Healthcare Research and
Quality
Patient Safety Organizations: Delisting
for Cause for Medical Informatics
Agency for Healthcare Research
and Quality (AHRQ), HHS.
AGENCY:
ACTION:
Notice of Delisting.
AHRQ has delisted Medical
Informatics as a Patient Safety
Organization (PSO) due to its failure to
correct a deficiency. The Patient Safety
and Quality Improvement Act of 2005
(Patient Safety Act) authorizes the
listing of PSOs, which are entities or
component organizations whose
mission and primary activity is to
conduct activities to improve patient
safety and the quality of health care
delivery. HHS issued the Patient Safety
and Quality Improvement Final Rule
(Patient Safety Rule) to implement the
Patient Safety Act. AHRQ administers
the provisions of the Patient Safety Act
and Patient Safety Rule relating to the
listing and operation of PSOs.
SUMMARY:
The directories for both listed
and delisted PSOs are ongoing and
reviewed weekly by AHRQ. The
delisting was effective at 12:00 Midnight
ET (2400) on June 1, 2012.
DATES:
Both directories can be
accessed electronically at the following
HHS Web site: https://
www.pso.AHRQ.gov/.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
[FR Doc. 2012–15611 Filed 6–26–12; 8:45 am]
In accordance with section 10(d) of
the Federal Advisory Committee Act as
amended (5 U.S.C., Appendix 2), the
Agency for Healthcare Research and
Quality (AHRQ) announces this meeting
of scientific peer review groups. The
subcommittee listed below is a part of
VerDate Mar<15>2010
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Eileen Hogan, Center for Quality
Improvement and Patient Safety, AHRQ,
540 Gaither Road, Rockville, MD 20850;
Telephone (toll free): (866) 403–3697;
Telephone (local): (301) 427–1111; TTY
(toll free): (866) 438–7231; TTY (local):
(301) 427–1130; Email:
pso@AHRQ.hhs.qov.
SUPPLEMENTARY INFORMATION:
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]]>Agencies
[Federal Register Volume 77, Number 124 (Wednesday, June 27, 2012)]
[Notices]
[Pages 38292-38294]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-15615]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Agency for Healthcare Research and Quality, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the intention of the Agency for
Healthcare Research and Quality (AHRQ) to request that the Office of
Management and Budget (OMB) approve the proposed information collection
project: ``Online Application Order Form for Products from the
Healthcare Cost and Utilization Project (HCUP).'' In accordance with
the Paperwork Reduction Act, 44 U.S.C. 3501-3521, AHRQ invites the
public to comment on this proposed information collection.
DATES: Comments on this notice must be received by August 27, 2012.
ADDRESSES: Written comments should be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by email at
doris.lefkowitz@AHRQ.hhs.gov.
Copies of the proposed collection plans, data collection
instruments, and specific details on the estimated burden can be
obtained from the AHRQ Reports Clearance Officer.
FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427-1477, or by email at
doris.lefkowitz@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
Proposed Project
Online Application Order Form for Products From the Healthcare Cost and
Utilization Project (HCUP)
The Healthcare Cost and Utilization Project (HCUP, pronounced ``H-
Cup'') is a vital resource helping AHRQ achieve its research agenda,
thereby furthering its goal of improving the delivery of health care in
the United States. HCUP is a family of health care databases and
related software tools and products developed through a Federal-State-
Industry partnership and sponsored by AHRQ. HCUP includes the largest
collection of longitudinal hospital care data in the United States,
with all-payer, encounter-level information beginning in 1988. The HCUP
databases are annual files that contain anonymous information from
hospital discharge records for inpatient care and certain components of
outpatient care, such as emergency care and ambulatory surgeries. The
project currently releases a variety of databases created for research
use on a broad range of health issues, including cost and quality of
health services, medical practice patterns, access to health care
programs, and outcomes of treatments at the national, State, and local
market levels. HCUP also produces a large number of software tools to
enhance the use of administrative health care data for research and
public health use. Software tools use information available from a
variety of sources to create new data elements, often through
sophisticated algorithms, for use with the HCUP databases.
HCUP's objectives are to:
Create and enhance a powerful source of national, state,
and all-payer health care data.
Produce a broad set of software tools and products to
facilitate the use of HCUP and other administrative data.
Enrich a collaborative partnership with statewide data
organizations (that voluntarily participate in the project) aimed at
increasing the quality and use of health care data.
Conduct and translate research to inform decision making
and improve health care delivery.
The HCUP releases six types of databases for public research use:
(1) The Nationwide Inpatient Sample (NIS) is the largest all-payer
inpatient care database in the United States, containing data from
approximately 8 million hospital stays from roughly 1,000 hospitals;
this approximates a 20-percent stratified sample of U.S. community
hospitals. NIS data releases are available for purchase from the HCUP
Central Distributor for data years beginning in 1988.
(2) The Kids' Inpatient Database (KID) is the only all-payer
inpatient care database for children in the United States. The KID was
specifically designed to permit researchers to study a broad range of
conditions and procedures related to child health issues. The KID
contains a sample of over 3 million discharges for children age 20 and
younger from more than 3,500 U.S. community hospitals.
(3) The Nationwide Emergency Department Sample (NEDS) is the
largest all-payer ED database in the United States. It is constructed
to capture information both on ED visits that do not result in an
admission and on ED visits that result in an admission to the same
hospital. The NEDS contains more than 25 million unweighted records for
ED visits at about 1,000 U.S. community hospitals and approximates a
20-percent stratified sample of U.S. hospital-based EDs. Files are
available beginning with data year 2006.
(4) The State Inpatient Databases (SID) contain the universe of
inpatient discharge abstracts from data organizations in 46 States that
currently participate in the SID. Together, the SID encompasses
approximately 97 percent of all U.S. community hospital discharges.
Most States that participate in the SID make their data available for
purchase through the HCUP Central Distributor. Files are available
beginning with data year 1990.
(5) The State Ambulatory Surgery Databases (SASD) contain data from
ambulatory care encounters in hospital-affiliated (and sometimes
freestanding) ambulatory surgery sites. Currently, 29 States
participate in the SASD. Files are available beginning with data year
1997.
(6) The State Emergency Department Databases (SEDD) contain data
from hospital-affiliated emergency department (ED) abstracts for visits
that do not result in a hospitalization. Currently, 29 States
participate in the SEDD. Files are available beginning with data year
1999.
To support AHRQ's mission to improve health care through scientific
research, HCUP databases and software tools are disseminated to users
outside of the Agency through a mechanism known as the HCUP Central
Distributor. The HCUP Central Distributor assists
[[Page 38293]]
qualified researchers to access uniform research data across multiple
states with the use of one application process. The HCUP databases
disseminated through the Central distributor are referred to as
``restricted access public release files;'' that is, they are publicly
available, but only under restricted conditions.
HCUP databases are released to researchers outside of AHRQ after
the completion of required training and submission of an application
that includes a signed HCUP Data Use Agreement (DUA). In addition,
before restricted access public release state-level databases are
released, the user is asked for a brief description of their research
to ensure that the planned use is consistent with HCUP policies and
with the HCUP data use requirements. Fees are set for databases
released through the HCUP Central Distributor depending on the type of
database. The fee for sale of state-level data is determined by each
participating Statewide Data Organization and reimbursed to those
organizations. This project is being conducted by AHRQ through its
contractor and subcontractor, Thomson Reuters and Social & Scientific
Systems, Inc., pursuant to AHRQ's statutory authority to conduct and
support research on healthcare and on systems for the delivery of such
care, including activities with respect to the outcomes, cost, cost-
effectiveness, and use of health care services and access to such
services. (42 U.S.C. 299a(a)(3).)
Method of Collection
This information collection request is for the activities
associated with completing an online application form to request HCUP
data, not the collection of health care data for HCUP databases. The
activities associated with the HCUP online application include:
(1) HCUP Application Form. All persons wanting access to the HCUP
databases must complete an application package. Each unique database
has a unique application package. All application packages are
available for downloading at https://www.hcup-us.ahrq.gov/tech_assist/centdist.jsp.
(2) HCUP Data Use Agreement Training. All persons wanting access to
the HCUP databases must complete this online training course. The
purpose of the training is to emphasize the importance of data
protection, reduce the risk of inadvertent violations, and describe the
individual's responsibility when using HCUP data. The training course
can be accessed and completed online at https://www.hcup-us.ahrq.gov/tech_assist/dua.jsp.
(3) HCUP Data Use Agreement (DUA). All persons wanting access to
the HCUP databases must sign a data use agreement. Each database has a
unique DUA; an example DUA for the Nationwide Inpatient Sample database
is available at https://www.hcup-us.ahrq.gov/team/NISDUA.jsp.
Information collected in the HCUP Application Order Form will be
used for two purposes only:
1. Business Transaction: HCUP databases and software are currently
delivered on disk and shipped to users who have completed the
application process. Contact information is used for shipping the data
on disk (or any other media used in the future). AHRQ policy and
current agreements with Statewide Data Organizations contributing data
to HCUP prohibit providing access to the data via the Internet or
email.
2. Enforcement of the HCUP Data Use Agreement (DUA): The HCUP DUA
contains several restrictions on use of the data. Most of these
restrictions have been put in place to safeguard the privacy of
individuals and establishments represented in the data. For example,
data users can only use the data for research, analysis, and aggregate
statistical reporting and are prohibited from attempting to identify
any persons in the data. Contact information on HCUP Data Use
Agreements is retained in the event that a violation of the DUA takes
place.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annualized burden associated with the
applicants' time to order any of the HCUP databases. An estimated 1,200
persons will order HCUP data annually. Each of these persons will
complete an application (10 minutes), the DUA training (15 minutes) and
a DUA (5 minutes). The total burden is estimated to be 600 hours
annually.
Exhibit 2 shows the estimated annualized cost burden associated
with the applicants' time to order HCUP data. The total cost burden is
estimated to be $21,408 annually.
Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of
Form name Number of responses per Hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
HCUP Application Form........................... 1,200 1 0/60 200
HCUP DUA Training............................... 1,200 1 15/60 300
HCUP DUA........................................ 1,200 1 5/60 100
---------------------------------------------------------------
Total....................................... 3,600 na na 600
----------------------------------------------------------------------------------------------------------------
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Average
Form name Number of Total burden hourly wage Total cost
respondents hours rate * burden
----------------------------------------------------------------------------------------------------------------
HCUP Application Form........................... 1,200 200 $35.68 $7,136
HCUP DUA Training............................... 1,200 300 35.68 10,704
HCUP DUA........................................ 1,200 100 35.68 3,568
---------------------------------------------------------------
Total....................................... 3,600 600 na 21,408
----------------------------------------------------------------------------------------------------------------
* Based upon the mean of the average wages for Life Scientists, All Other (19-1099), National Compensation
Survey: Occupational wages in the United States May 2011, ``U.S. Department of Labor, Bureau of Labor
Statistics.''
[[Page 38294]]
Estimated Annual Costs to the Federal Government
Exhibit 3 shows the estimated total and annualized cost to process
HCUP database applications and maintain the ordering system over the 3
years covered by this information collection request. It is estimated
to cost $17,237 annually to operate and maintain the ordering system.
Exhibit 3. Estimated Total and Annualized Cost
------------------------------------------------------------------------
Annualized
Cost component Total cost cost
------------------------------------------------------------------------
Order Review............................ $14,493 $4,831
Monthly Updates--Product Catalog........ 1,857 619
System Maintenance...................... 13,820 4,607
Customer Inquiries...................... 4,483 1,495
Management/Troubleshooting.............. 17,058 5,689
-------------------------------
Total............................... 51,711 17,237
------------------------------------------------------------------------
Request for Comments
In accordance with the Paperwork Reduction Act, comments on AHRQ's
information collection are requested with regard to any of the
following: (a) Whether the proposed collection of information is
necessary for the proper performance of AHRQ healthcare research and
healthcare information dissemination functions, including whether the
information will have practical utility; (b) the accuracy of AHRQ's
estimate of burden (including hours and costs) of the proposed
collection(s) of information; (c) ways to enhance the quality, utility,
and clarity of the information to be collected; and (d) ways to
minimize the burden of the collection of information upon the
respondents, including the use of automated collection techniques or
other forms of information technology.
Comments submitted in response to this notice will be summarized
and included in the Agency's subsequent request for OMB approval of the
proposed information collection. All comments will become a matter of
public record.
Dated: June 19, 2012.
Carolyn M. Clancy,
Director.
[FR Doc. 2012-15615 Filed 6-26-12; 8:45 am]
BILLING CODE 4160-90-M
