Agency Information Collection Activities: Proposed Collection: Public Comment Request, 53203-53204 [2014-21283]
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53203
Federal Register / Vol. 79, No. 173 / Monday, September 8, 2014 / Notices
the Administration for Children and
Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2014–21318 Filed 9–5–14; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request
Health Resources and Services
Administration, HHS.
ACTION: Notice.
AGENCY:
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects (Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995), the
Health Resources and Services
Administration (HRSA) announces
plans to submit an Information
Collection Request (ICR), described
below, to the Office of Management and
Budget (OMB). Prior to submitting the
ICR to OMB, HRSA seeks comments
from the public regarding the burden
estimate, below, or any other aspect of
the ICR.
DATES: Comments on this Information
Collection Request must be received
within 60 days of this notice.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
SUMMARY:
Officer, Room 10–29, Parklawn
Building, 5600 Fishers Lane, Rockville,
MD 20857.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call the HRSA Information Collection
Clearance Officer at (301) 443–1984.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
information request collection title for
reference.
Information Collection Request Title:
Data System for Organ Procurement and
Transplantation Network
OMB No.: 0915–0157—Revision
Abstract: Section 372 of the Public
Health Service (PHS) Act requires that
the Secretary, by contract, provide for
the establishment and operation of an
Organ Procurement and Transplantation
Network (OPTN). This is a request for
revisions to current OPTN data
collection forms associated with donor
organ procurement and an individual’s
clinical characteristics at the time of
registration, transplant, and follow-up
after the transplant. Data for the OPTN
data system are collected from
transplant hospitals, organ procurement
organizations, and tissue-typing
laboratories. The information is used to
indicate the disease severity of
transplant candidates, to monitor
compliance of member organizations
with OPTN rules and requirements, and
to report periodically on the clinical and
scientific status of organ donation and
transplantation in this country. Data are
used to develop transplant, donation,
Number of
respondents
rmajette on DSK2TPTVN1PROD with NOTICES
Section/activity
Deceased Donor Registration ..............................................
Living Donor Registration ....................................................
Living Donor Follow-up ........................................................
Donor Histocompatibility ......................................................
Recipient Histocompatibility .................................................
Heart Candidate Registration ..............................................
Heart Recipient Registration ................................................
Heart Follow Up (6 Month) ..................................................
Heart Follow Up (1–5 Year) .................................................
Heart Follow Up (Post 5 Year) ............................................
Heart Post-Transplant Malignancy Form .............................
Lung Candidate Registration ...............................................
Lung Recipient Registration .................................................
Lung Follow Up (6 Month) ...................................................
Lung Follow Up (1–5 Year) .................................................
Lung Follow Up (Post 5 Year) .............................................
Lung Post-Transplant Malignancy Form ..............................
Heart/Lung Candidate Registration .....................................
Heart/Lung Recipient Registration .......................................
Heart/Lung Follow Up (6 Month) .........................................
Heart/Lung Follow Up (1–5 Year) ........................................
Heart/Lung Follow Up (Post 5 Year) ...................................
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Average
number of
responses per
respondent
58
290
290
151
151
131
131
131
131
131
131
64
64
64
64
64
64
63
63
63
63
63
Fmt 4703
Sfmt 4703
and allocation policies, to determine
whether institutional members are
complying with policy, to determine
member-specific performance, to ensure
patient safety and to fulfill the
requirements of the OPTN Final Rule.
The practical utility of the data
collection is further enhanced by
requirements that the OPTN data must
be made available, consistent with
applicable laws, for use by OPTN
members, the Scientific Registry of
Transplant Recipients, the Department
of Health and Human Services, and
members of the public for evaluation,
research, patient information, and other
important purposes.
Likely Respondents: Transplant
programs, organ procurement
organizations, histocompatibility
laboratories, medical and scientific
organizations, and public organizations.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose or provide the information
requested. This includes the time
needed to: review instructions; develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; train
personnel to respond to a request for
collection of information; search data
sources; complete and review the
collection of information; and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this Information
Collection Request are summarized in
the table below.
Total
number of
responses
158.2
20.6
60.7
96.7
173.5
30.5
19.3
17.0
73.9
115.2
11.0
39.6
30.0
26.2
99.4
65.6
1.5
0.7
0.3
0.3
1.5
3.1
E:\FR\FM\08SEN1.SGM
9174
5984
17610
14598
26199
3991
2525
2229
9683
15091
1447
2534
1923
1677
6364
4201
99
46
21
20
97
194
08SEN1
Average
burden per
response
(in hours)
1.1
1.8
1.3
0.2
0.4
0.9
1.4
0.4
0.9
0.5
0.9
0.9
1.4
0.5
1.1
0.6
0.4
1.1
1.4
0.8
1.1
0.6
Total
burden hours
10091.4
10771.2
22893.0
2919.6
10479.6
3591.9
3535.0
891.6
8714.7
7545.5
1302.3
2280.6
2692.2
838.5
7000.4
2520.6
39.6
50.6
29.4
16
106.7
116.4
53204
Federal Register / Vol. 79, No. 173 / Monday, September 8, 2014 / Notices
Number of
respondents
Section/activity
Average
number of
responses per
respondent
Total
number of
responses
Average
burden per
response
(in hours)
Total
burden hours
Heart/Lung Post-Transplant Malignancy Form ....................
Liver Candidate Registration ...............................................
Liver Recipient Registration .................................................
Liver Follow-up (6 Month–5 Year) .......................................
Liver Follow-up (Post 5 Year) ..............................................
Liver Recipient Explant Pathology Form .............................
Liver Post-Transplant Malignancy .......................................
Intestine Candidate Registration ..........................................
Intestine Recipient Registration ...........................................
Intestine Follow Up (6 Month–5 Year) .................................
Intestine Follow Up (Post 5 Year) .......................................
Intestine Post-Transplant Malignancy Form ........................
Kidney Candidate Registration ............................................
Kidney Recipient Registration ..............................................
Kidney Follow-Up (6 Month–5 Year) ...................................
Kidney Follow-up (Post 5 Year) ...........................................
Kidney Post-Transplant Malignancy Form ...........................
Pancreas Candidate Registration ........................................
Pancreas Recipient Registration .........................................
Pancreas Follow-up (6 Month–5 Year) ................................
Pancreas Follow-up (Post 5 Year) ......................................
Pancreas Post-Transplant Malignancy Form ......................
Kidney/Pancreas Candidate Registration ............................
Kidney/Pancreas Recipient Registration .............................
Kidney/Pancreas Follow-up (6 Month–5 Year) ....................
Kidney/Pancreas Follow-up (Post 5 Year) ..........................
Kidney/Pancreas Post-Transplant Malignancy Form ..........
VCA Candidate Registration ................................................
VCA Recipient Registration .................................................
VCA Recipient Follow Up ....................................................
63
135
135
135
135
135
135
41
41
41
41
41
233
233
233
233
233
134
134
134
134
134
134
134
134
134
134
9
9
9
0.2
89.2
47.8
231.1
256.5
12.3
13.2
4.4
2.7
13.3
13.5
0.6
162.6
72.5
379.5
346.7
18.1
3.6
1.9
10.4
13.5
0.8
9.6
5.7
33.6
48.2
1.6
1.7
1.7
1.7
12
12048
6457
31194
34622
1665
1786
182
109
547
553
25
37880
16904
88422
80770
4213
479
259
1398
1804
108
1280
760
4509
6465
211
15
15
15
0.4
0.8
1.3
1
0.5
0.6
0.8
1.3
1.8
1.5
0.4
1.0
0.8
1.3
0.9
0.5
0.8
0.9
1.1
1.0
0.5
0.6
0.9
1.1
1.0
0.6
0.4
0.4
1.3
1.0
4.8
9638.4
8394.1
31194.0
17311.0
999.0
1428.8
236.6
196.2
820.5
221.2
25.0
30304.0
21975.2
79579.8
40385.0
3370.4
431.1
284.9
1398.0
902.0
64.8
1152.0
836.0
4509.0
3879.0
84.4
6.0
19.5
15.0
Total ..............................................................................
*453
........................
460414
........................
358092.5
* Total number of OPTN member institutions as of 6/6/2014. Number of respondents for transplant candidate or recipient forms based on number of organ specific programs associated with each form.
HRSA specifically requests comments
on (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.
Dated: August 29, 2014.
Jackie Painter,
Acting Director, Division of Policy and
Information Coordination.
[FR Doc. 2014–21283 Filed 9–5–14; 8:45 am]
rmajette on DSK2TPTVN1PROD with NOTICES
BILLING CODE 4165–15–P
VerDate Mar<15>2010
15:14 Sep 05, 2014
Jkt 232001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Service
Administration
Advisory Committee on
Interdisciplinary, Community-Based
Linkages; Notice of Meeting
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), notice is hereby given
of the following meeting:
Name: Advisory Committee on
Interdisciplinary, Community-Based
Linkages (ACICBL).
Dates and Times: September 10, 2014
(8:30 a.m.–5:30 p.m.) and September 11,
2014 (8:30 a.m.–4:00 p.m.).
Place: In-Person Meeting, Webinar,
and Conference Call Format.
Status: The meeting will be open to
the public.
Purpose: The members of the ACICBL
will continue discussions to develop the
legislatively mandated 14th Annual
Report to the Secretary of Health and
Human Services and Congress. The
Committee members have chosen the
working topic: Rethinking Complex
Care: Preparing the Health Care
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
Workforce to Foster Person-Centered
Care.
Agenda: The ACICBL agenda includes
an opportunity for members to consult
with experts in the area of complex care
and to further discuss and develop a
plan for developing the 14th Annual
Report. The agenda will be available 2
days prior to the meeting on the HRSA
Web site at https://www.hrsa.gov/
advisorycommittees/bhpradvisory/
acicbl/acicbl.html. Agenda items are
subject to change as priorities dictate.
The Committee has invited Anand K.
Parekh, Deputy Assistant Secretary for
Health, U.S. Department of Health &
Human Services; Tara A. Cortes,
Executive Director, The Hartford
Institute for Geriatric Nursing and
Professor, NYU College of Nursing;
Kimberly Lochner, Centers For
Medicare & Medicaid Services, Office of
Information Products and Data Analysis;
Mark Sciegaj, Associate Professor of
Health Policy and Administration,
College of Health and Human
Development, Pennsylvania State
University; and Michael J. Barry,
President, Informed Medical Decisions
Foundation, to provide expertise in the
areas of person-centered care, chronic
E:\FR\FM\08SEN1.SGM
08SEN1
]]>Agencies
[Federal Register Volume 79, Number 173 (Monday, September 8, 2014)]
[Notices]
[Pages 53203-53204]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-21283]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request
AGENCY: Health Resources and Services Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement for opportunity for public
comment on proposed data collection projects (Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995), the Health Resources and Services
Administration (HRSA) announces plans to submit an Information
Collection Request (ICR), described below, to the Office of Management
and Budget (OMB). Prior to submitting the ICR to OMB, HRSA seeks
comments from the public regarding the burden estimate, below, or any
other aspect of the ICR.
DATES: Comments on this Information Collection Request must be received
within 60 days of this notice.
ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance Officer, Room 10-29, Parklawn
Building, 5600 Fishers Lane, Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
draft instruments, email paperwork@hrsa.gov or call the HRSA
Information Collection Clearance Officer at (301) 443-1984.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the information request collection title
for reference.
Information Collection Request Title: Data System for Organ
Procurement and Transplantation Network
OMB No.: 0915-0157--Revision
Abstract: Section 372 of the Public Health Service (PHS) Act
requires that the Secretary, by contract, provide for the establishment
and operation of an Organ Procurement and Transplantation Network
(OPTN). This is a request for revisions to current OPTN data collection
forms associated with donor organ procurement and an individual's
clinical characteristics at the time of registration, transplant, and
follow-up after the transplant. Data for the OPTN data system are
collected from transplant hospitals, organ procurement organizations,
and tissue-typing laboratories. The information is used to indicate the
disease severity of transplant candidates, to monitor compliance of
member organizations with OPTN rules and requirements, and to report
periodically on the clinical and scientific status of organ donation
and transplantation in this country. Data are used to develop
transplant, donation, and allocation policies, to determine whether
institutional members are complying with policy, to determine member-
specific performance, to ensure patient safety and to fulfill the
requirements of the OPTN Final Rule. The practical utility of the data
collection is further enhanced by requirements that the OPTN data must
be made available, consistent with applicable laws, for use by OPTN
members, the Scientific Registry of Transplant Recipients, the
Department of Health and Human Services, and members of the public for
evaluation, research, patient information, and other important
purposes.
Likely Respondents: Transplant programs, organ procurement
organizations, histocompatibility laboratories, medical and scientific
organizations, and public organizations.
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose or provide the
information requested. This includes the time needed to: review
instructions; develop, acquire, install and utilize technology and
systems for the purpose of collecting, validating and verifying
information, processing and maintaining information, and disclosing and
providing information; train personnel to respond to a request for
collection of information; search data sources; complete and review the
collection of information; and to transmit or otherwise disclose the
information. The total annual burden hours estimated for this
Information Collection Request are summarized in the table below.
----------------------------------------------------------------------------------------------------------------
Average Average
Number of number of Total number burden per Total burden
Section/activity respondents responses per of responses response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Deceased Donor Registration..... 58 158.2 9174 1.1 10091.4
Living Donor Registration....... 290 20.6 5984 1.8 10771.2
Living Donor Follow-up.......... 290 60.7 17610 1.3 22893.0
Donor Histocompatibility........ 151 96.7 14598 0.2 2919.6
Recipient Histocompatibility.... 151 173.5 26199 0.4 10479.6
Heart Candidate Registration.... 131 30.5 3991 0.9 3591.9
Heart Recipient Registration.... 131 19.3 2525 1.4 3535.0
Heart Follow Up (6 Month)....... 131 17.0 2229 0.4 891.6
Heart Follow Up (1-5 Year)...... 131 73.9 9683 0.9 8714.7
Heart Follow Up (Post 5 Year)... 131 115.2 15091 0.5 7545.5
Heart Post-Transplant Malignancy 131 11.0 1447 0.9 1302.3
Form...........................
Lung Candidate Registration..... 64 39.6 2534 0.9 2280.6
Lung Recipient Registration..... 64 30.0 1923 1.4 2692.2
Lung Follow Up (6 Month)........ 64 26.2 1677 0.5 838.5
Lung Follow Up (1-5 Year)....... 64 99.4 6364 1.1 7000.4
Lung Follow Up (Post 5 Year).... 64 65.6 4201 0.6 2520.6
Lung Post-Transplant Malignancy 64 1.5 99 0.4 39.6
Form...........................
Heart/Lung Candidate 63 0.7 46 1.1 50.6
Registration...................
Heart/Lung Recipient 63 0.3 21 1.4 29.4
Registration...................
Heart/Lung Follow Up (6 Month).. 63 0.3 20 0.8 16
Heart/Lung Follow Up (1-5 Year). 63 1.5 97 1.1 106.7
Heart/Lung Follow Up (Post 5 63 3.1 194 0.6 116.4
Year)..........................
[[Page 53204]]
Heart/Lung Post-Transplant 63 0.2 12 0.4 4.8
Malignancy Form................
Liver Candidate Registration.... 135 89.2 12048 0.8 9638.4
Liver Recipient Registration.... 135 47.8 6457 1.3 8394.1
Liver Follow-up (6 Month-5 Year) 135 231.1 31194 1 31194.0
Liver Follow-up (Post 5 Year)... 135 256.5 34622 0.5 17311.0
Liver Recipient Explant 135 12.3 1665 0.6 999.0
Pathology Form.................
Liver Post-Transplant Malignancy 135 13.2 1786 0.8 1428.8
Intestine Candidate Registration 41 4.4 182 1.3 236.6
Intestine Recipient Registration 41 2.7 109 1.8 196.2
Intestine Follow Up (6 Month-5 41 13.3 547 1.5 820.5
Year)..........................
Intestine Follow Up (Post 5 41 13.5 553 0.4 221.2
Year)..........................
Intestine Post-Transplant 41 0.6 25 1.0 25.0
Malignancy Form................
Kidney Candidate Registration... 233 162.6 37880 0.8 30304.0
Kidney Recipient Registration... 233 72.5 16904 1.3 21975.2
Kidney Follow-Up (6 Month-5 233 379.5 88422 0.9 79579.8
Year)..........................
Kidney Follow-up (Post 5 Year).. 233 346.7 80770 0.5 40385.0
Kidney Post-Transplant 233 18.1 4213 0.8 3370.4
Malignancy Form................
Pancreas Candidate Registration. 134 3.6 479 0.9 431.1
Pancreas Recipient Registration. 134 1.9 259 1.1 284.9
Pancreas Follow-up (6 Month-5 134 10.4 1398 1.0 1398.0
Year)..........................
Pancreas Follow-up (Post 5 Year) 134 13.5 1804 0.5 902.0
Pancreas Post-Transplant 134 0.8 108 0.6 64.8
Malignancy Form................
Kidney/Pancreas Candidate 134 9.6 1280 0.9 1152.0
Registration...................
Kidney/Pancreas Recipient 134 5.7 760 1.1 836.0
Registration...................
Kidney/Pancreas Follow-up (6 134 33.6 4509 1.0 4509.0
Month-5 Year)..................
Kidney/Pancreas Follow-up (Post 134 48.2 6465 0.6 3879.0
5 Year)........................
Kidney/Pancreas Post-Transplant 134 1.6 211 0.4 84.4
Malignancy Form................
VCA Candidate Registration...... 9 1.7 15 0.4 6.0
VCA Recipient Registration...... 9 1.7 15 1.3 19.5
VCA Recipient Follow Up......... 9 1.7 15 1.0 15.0
-------------------------------------------------------------------------------
Total....................... *453 .............. 460414 .............. 358092.5
----------------------------------------------------------------------------------------------------------------
* Total number of OPTN member institutions as of 6/6/2014. Number of respondents for transplant candidate or
recipient forms based on number of organ specific programs associated with each form.
HRSA specifically requests comments on (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.
Dated: August 29, 2014.
Jackie Painter,
Acting Director, Division of Policy and Information Coordination.
[FR Doc. 2014-21283 Filed 9-5-14; 8:45 am]
BILLING CODE 4165-15-P
