[Federal Register: May 8, 2007 (Volume 72, Number 88)]
[Notices]
[Page 26136-26137]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr08my07-76]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources and Services Administration
(HRSA) publishes abstracts of information collection requests under
review by the Office of Management and Budget (OMB), in compliance with
the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). To request
a copy of the clearance requests submitted to OMB for review, call the
HRSA Reports Clearance Office at (301) 443-1129.
The following request has been submitted to the Office of
Management and Budget for review under the Paperwork Reduction Act of
1995:
[[Page 26137]]
Proposed Project: The Stem Cell Therapeutic Outcomes Database--(New)
The Stem Cell Therapeutic and Research Act of 2005 establishes the
C.W. Bill Young Cell Transplantation Program and provides for the
collection and maintenance of human blood stem cells for the treatment
of patients and for research. The Health Resources and Services
Administration's (HRSA), Healthcare Systems Bureau (HSB), is
establishing the Stem Cell Therapeutic Outcomes Database as one
component of the C.W. Bill Young Cell Transplantation Program.
Operation of this database necessitates certain reporting requirements
in order to perform the functions related to hematopoietic stem cell
transplantation under contract to HHS. The Act requires the Secretary
to contract for the collection and maintenance of information related
to patients who have received stem cell therapeutic products and to do
so using a standardized, electronic format. Data will be collected from
transplant centers in a manner similar to the data collection
activities historically conducted by the Medical College of Wisconsin's
Center for International Blood and Marrow Transplant Research (CIBMTR)
and will be used for ongoing analysis of transplant outcomes. HRSA will
use the information in order to carry out its statutory
responsibilities. Information is needed to monitor the clinical status
of transplantation, and to provide the Secretary with an annual report
of transplant center-specific survival data.
The estimate of burden is as follows:
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Estimated
Form number of Responses per Total Hours per Total burden
respondents respondent Responses response hours
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Baseline Pre-TED (Transplant 225 32 7,200 0.85 6,120
Essential Data)................
Product Form (includes Infusion, 225 14 3,150 1.5 4,725
HLA, and Infectious Disease
Marker inserts)................
100-Day Post-TED................ 225 32 7,200 0.85 6,120
6-Month Post-TED................ 225 23 5,175 1.00 5,175
12-Month Post-TED............... 225 20 4,500 1.00 4,500
Annual Post-TED................. 225 16 3,600 1.50 5,400
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Total....................... 225 .............. 30,825 .............. 32,040
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The Pre-TED, Product Form, 100-Day Post-TED, 6-Month Post-TED, and 12-Month Post-TED will be collected on all
patients during their first year of transplant. In subsequent years, patient outcomes will be reported on the
Annual Post-TED form. There will be a gradual increase in the cumulative reporting burden over time
commensurate with the number of survivors for which transplant centers must submit an Annual Post-TED.
Written comments and recommendations concerning the proposed
information collection should be sent within 30 days of this notice to:
Karen Matsuoka, Human Resources and Housing Branch, Office of
Management and Budget, New Executive Office Building, Room 10235,
Washington, DC 20503.
Dated: May 2, 2007.
Caroline Lewis,
Associate Administrator for Management.
[FR Doc. E7-8799 Filed 5-7-07; 8:45 am]
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