Skip to Content


Agency Information Collection Activities: Proposed Collection: Comment Request

Document Details

Information about this document as published in the Federal Register.

Published Document

This document has been published in the Federal Register. Use the PDF linked in the document sidebar for the official electronic format.

Start Preamble

In compliance with the requirement for opportunity for public comment on proposed data collection projects (44 U.D.C. 3506(c)(2)(A)), the Health Resources and Services Administration (HRSA) publishes periodic summaries of proposed projects being developed for submission to OMB under the Paperwork Reduction Act of 1995. To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, call the HRSA Reports Clearance Officer on (301) 443-1129.

Comments are invited on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency's estimate of the burden of the proposed collection 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 on respondents, including through the use of automated collection techniques or other forms of information technology.

Proposed Project: Data System for Organ Procurement and Transplantation Network and Associated Forms (OMB No. 0915-0157): Revision

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). The OPTN, among other responsibilities, operates and maintains a national waiting list of individuals requiring organ transplants, maintains a computerized system for matching donor organs with transplant candidates on the waiting list, and operates a 24-hour system to facilitate matching organs with individuals included in the list.

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 if institutional members are complying with policy, to determine member specific performance, to ensure patient safety when no alternative sources of data exist 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 others for evaluation, research, patient information, and other important purposes.

Revisions in the 26 data collection forms are intended to implement approved reduction in data collection for candidates and recipients, to provide additional information specific to pediatric patients, and to clarify existing questions. Start Printed Page 10227

Estimates of Annualized Hour Burden

FormNumber of respondentsResponses per respondentsTotal responsesHours per responseTotal burden hours
Deceased Donor Registration5821512,4700.42005,237.4000
Death referral data581269610.00006,960.0000
Living Donor Registration711107,1100.41002,915.1000
Living Donor Follow-up7111812,7980.33004,223.3400
Donor Histocompatibility1549514,6300.0600877.8000
Recipient Histocompatibility15417226,4880.11002,913.6800
Heart Candidate Registration135233,1050.2800869.4000
Lung Candidate Registration67271,8090.2800506.5200
Heart/Lung Candidate Registration591590.280016.5200
Thoracic Registration135273,6450.44001,603.8000
Thoracic Follow-up13522930,9150.413012,767.8950
Kidney Candidate Registration25013333,2500.28009,310.0000
Kidney Registration2506917,2500.44007,590.0000
Kidney Follow-up250544136,0000.333245,315.2000
Liver Candidate Registration1258911,1250.28003,115.0000
Liver Registration125546,7500.40002,700.0000
Liver Follow-up12538347,8750.333615,971.1000
Kidney/Pancreas Candidate Registration146121,7520.2800490.5600
Kidney/Pancreas Registration14671,0220.5300541.6600
Kidney/Pancreas Follow-up146659,4900.50274,770.6230
Pancreas Candidate Registration14671,0220.2800286.1600
Pancreas Registration14634380.4400192.7200
Pancreas Follow-up146233,3580.41331,387.8614
Intestine Candidate Registration4583600.240086.4000
Intestine Registration4541800.530095.4000
Intestine Follow-up45177650.5059387.0135
Post Transplant Malignancy71164,2660.0800341.2800

Send comments to Susan G. Queen, PhD, HRSA Reports Clearance Officer, Room 10-33, Parklawn Building, 5600 Fishers Lane, Rockville, MD 20857. Written comments should be received within 60 days of this notice.

Start Signature

Dated: February 27, 2007.

Alexandra Huttinger,

Acting Director, Division of Policy Review and Coordination.

End Signature End Preamble

[FR Doc. E7-3918 Filed 3-6-07; 8:45 am]