# Agency Information Collection Activities: Submission to OMB for Review and Approval; Public Comment Request; Data System for Organ Procurement and Transplantation Network, OMB No. 0915-0157-Revision

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URL: https://www.frixlaw.com/law-library/documents/fr%3A2022-00239

## Record

- **Collection:** Federal Register
- **Document type:** Notice
- **Published:** January 10, 2022
- **Citation:** 87 FR 1151

## Text

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Submission to OMB for Review and Approval; Public Comment Request; Data System for Organ Procurement and Transplantation Network, OMB No. 0915-0157—Revision

AGENCY:

Health Resources and Services Administration (HRSA), Department of Health and Human Services.

ACTION:

Notice.

SUMMARY:

In compliance with the Paperwork Reduction Act of 1995, HRSA has submitted an Information Collection Request (ICR) to the Office of Management and Budget (OMB) for review and approval. Comments submitted during the first public review of this ICR will be provided to OMB. OMB will accept further comments from the public during the review and approval period. OMB may act on HRSA's ICR only after the 30-day comment period for this notice has closed.

DATES:

Comments on this ICR should be received no later than February 9, 2022.

ADDRESSES:

Written comments and recommendations for the proposed information collection should be sent within 30 days of publication of this notice to
www.reginfo.gov/public/do/PRAMain.
Find this particular information collection by selecting “Currently under Review—Open for Public Comments” or by using the search function.

FOR FURTHER INFORMATION CONTACT:

To request a copy of the clearance requests submitted to OMB for review, email Samantha Miller, the acting HRSA Information Collection Clearance Officer at
paperwork@hrsa.gov
or call (301) 443-9094.

SUPPLEMENTARY INFORMATION:

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 Act requires that the Secretary, by contract, provide for the establishment and operation of a private, non-profit entity: The Organ Procurement and Transplantation Network (OPTN). The data collected pursuant to the OPTN's regulatory authority in 42 CFR 121.11 of the OPTN Final Rule will be collected through OMB-approved data collection forms. Therefore, data approved for collection by the OPTN Board of Directors are submitted by HRSA for OMB approval under the Paperwork Reduction Act of 1995.

A 60-day notice was published in the
Federal Register
, 86 FR 48743 (Aug. 31, 2021). One comment was received. The commenter supported the necessity and utility of the proposed information collection and the use of automated collection techniques. The commenter recommended that HRSA account for anticipated increased staff hours and recommended emphasizing collecting data pertaining to race, ethnicity, social determinants of health, and any other characteristics that will help achieve equity in organ donation and transplantation. HRSA appreciates all feedback, and we will continue to review and evaluate all data collection efforts going forward in consultation with the OPTN.

The 60-day notice proposed data collection changes to existing data collection forms related to Vascularized Composite Allograft (VCA) transplantation, to implement policies approved by the OPTN Board of Directors. The OPTN expects to make additional changes to these VCA data collection forms in the near future so implementation of data collection changes has been postponed. These data collection changes are not included in this 30-day notice and will be included for review in a future submission.

Need and Proposed Use of the Information:
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.

This is a request to revise the current OPTN data collection associated with an individual's clinical characteristics at the time of registration, transplant, and follow-up after the transplant to include data collection forms in the OPTN Organ Labeling, Packaging, and Tracking System, the OPTN Kidney Paired Donation Pilot Program (KPDPP), and the OPTN Patient Safety Reporting Portal (PSRP). This revision also includes OPTN Board of Directors-approved changes to the existing OMB data collection forms. These specific data elements of the OPTN data system are collected from transplant hospitals, organ procurement organizations, and histocompatibility laboratories. The information is used to (1) facilitate organ placement and match donor organs with recipients; (2) monitor compliance of member organizations with Federal laws and regulations and with OPTN requirements; (3) review and report periodically to the public on the status of organ donation and transplantation in the United States; (4) provide data to researchers and government agencies to study the scientific and clinical status of organ transplantation; (5) perform transplantation-related public health surveillance including the possible transmission of donor disease.

HRSA is submitting the following changes to improve the OPTN organ matching and allocation process and improve OPTN member compliance with OPTN requirements. All of these proposed changes have been approved by the OPTN Board of Directors.

(1) Adding data collection forms for the OPTN Organ Labeling, Packaging, and Tracking System to the existing OMB-approved Data System for Organ Procurement and Transplantation Network. The system has two forms that are used through mobile and web-based applications to ensure the correct organ is transplanted into the correct patient, minimize labeling and transport errors, accelerate organ information transfer, and capture data regarding organ procurement. OPTN Organ Labeling, Packaging and Tracking System is comprised of two data collection forms: Organ labeling and packaging, and organ tracking and validating.

(2) Adding data collection forms for the OPTN KPDPP to the existing OMB-approved Data System for Organ Procurement and Transplantation Network. Kidney paired donation is a transplant option for those patients waiting for a kidney transplant who have a willing living donor who is medically able but cannot donate a kidney to their intended candidate because they are incompatible. OPTN KPDPP matches living donors, and their intended candidates with other living donors or intended candidate pairs when the living donors cannot donate to the person(s) they initially hoped would receive their kidney. OPTN KPDPP is comprised of three data collection forms: Candidate registration, donor registration, and match offer management.

(3) Adding data collection forms in the OPTN PSRP to the existing OMB-approved Data System for Organ Procurement and Transplantation Network. OPTN PSRP allows the OPTN to collect reports on any event or process variance that could cause concerns from transplantation, donation, safety, or quality perspective. OPTN PSRP is comprised of four data collection forms: Disease transmission event, living donor event, safety situation, and potential disease transmission.

(4) Adding a request to unlock form

(5) Additional revisions to existing data collection forms were made based on the OPTN Board of Directors-approved changes to improve organ matching, allocation, and OPTN policy compliance.

Likely Respondents:
Transplant programs, Organ Procurement Organizations, and Histocompatibility Laboratories.

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; to 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; to train personnel and to be able to respond to a collection of information; to search data sources; to complete and review the collection of information; and to transmit or otherwise disclose the information. The total annual burden hours estimated for this ICR are summarized in the table below.

The total burden hours in the OMB inventory increased by 4,337 hours from the previously OMB-approved data collection package from August 25, 2020. This increase is due to including new data collection forms and additional data to existing data collection forms. However, the total burden hours of this request is less than the total burden hours presented in the 60-day notice, because of the removal of the proposed data collection changes associated with implementing the “Modify Data Collection on VCA Living Donors” and “Programming VCA Allocation in UNet” policies.

Total Estimated Annualized Burden—Hours

Form name

Number of
respondents

Number of
responses per
respondent *

Total
responses

Average
burden per
response
(in hours)

Total burden
hours

Deceased Donor Registration
57
188.26
10,731
1.10
11,804

Living Donor Registration
300
22.85
6,855
1.80

a
12,339

Living Donor Follow-up
300
62.23
18,669
1.30

b
24,270

Donor Histocompatibility
147
123.99
18,226
0.20
3,645

Recipient Histocompatibility
147
225.10
33,090
0.40
13,236

Heart Candidate Registration
140
33.69
4,717
0.90
4,245

Heart Recipient Registration
140
24.33
3,406
1.20
4,087

Heart Follow Up (6 Month)
140
22.01
3,081
0.40
1,232

Heart Follow Up (1-5 Year)
140
90.61
12,685
0.90
11,417

Heart Follow Up (Post 5 Year)
140
153.97
21,556
0.50
10,778

Heart Post-Transplant Malignancy Form
140
12.77
1,788
0.90
1,609

Lung Candidate Registration
71
45.21
3,210
0.90
2,889

Lung Recipient Registration
71
35.66
2,532
1.20
3,038

Lung Follow Up (6 Month)
71
32.35
2,297
0.50
1,148

Lung Follow Up (1-5 Year)
71
118.85
8,438
1.10
9,282

Lung Post-Transplant Malignancy Form
71
19.72
1,400
0.40
560

Heart/Lung Candidate Registration
69
0.97
67
1.10
74

Heart/Lung Recipient Registration
69
0.46
32
1.30
42

Heart/Lung Follow Up (6 Month)
69
0.45
31
0.80
25

Heart/Lung Follow Up (1-5 Year)
69
1.14
79
1.10
87

Heart/Lung Follow Up (Post 5 Year)
69
3.30
228
0.60
137

Heart/Lung Post-Transplant Malignancy Form
69
0.30
21
0.40
8

Liver Candidate Registration
146
90.29
13,182
0.80
10,546

Liver Recipient Registration
146
56.55
8,256
1.20
9,907

Liver Follow-up (6 Month-5 Year)
146
266.57
38,919
1.00
38,919

Liver Follow-up (Post 5 Year)
146
316.61
46,225
0.50
23,113

Liver Recipient Explant Pathology Form
146
10.58
1,545
0.60
927

Liver Post-Transplant Malignancy
146
16.35
2,387
0.80
1,910

Intestine Candidate Registration
20
6.95
139
1.30
181

Intestine Recipient Registration
20
5.20
104
1.80
187

Intestine Follow Up (6 Month-5 Year)
20
26.20
524
1.50
786

Intestine Follow Up (Post 5 Year)
20
37.20
744
0.40
298

Intestine Post-Transplant Malignancy Form
20
2.10
42
1.00
42

Kidney Candidate Registration
237
168.77
39,998
0.80
31,998

Kidney Recipient Registration
237
89.43
21,195
1.20
25,434

Kidney Follow-up (Post 5 Year)
237
449.40
106,508
0.50
53,254

Kidney Post-Transplant Malignancy Form
237
22.64
5,366
0.80
4,292

Pancreas Candidate Registration
133
2.77
368
0.60
221

Pancreas Recipient Registration
133
1.46
194
1.20
233

Pancreas Follow-up (6 Month-5 Year)
133
7.87
1,047
0.50
524

Pancreas Follow-up (Post 5 Year)
133
15.93
2,119
0.50
1,060

Pancreas Post-Transplant Malignancy Form
133
0.73
97
0.60
58

Kidney/Pancreas Candidate Registration
133
9.75
1,297
0.60
778

Kidney/Pancreas Recipient Registration
133
7.73
1,028
1.20
1,234

Kidney/Pancreas Follow-up (6 Month-5 Year)
133
32.80
4,362
0.50
2,181

Kidney/Pancreas Follow-up (Post 5 Year)
133
57.80
7,687
0.60
4,612

Kidney/Pancreas Post-Transplant Malignancy Form
133
2.20
293
0.40
117

VCA Candidate Registration
27
0.89
24
0.40
10

VCA Recipient Registration
27
1.59
43
1.30

c
56

VCA Recipient Follow Up
27
0.67
18
1.00

d
18

Organ Labeling and Packaging System
57
208.25
11,870
0.18
2,137

Organ Tracking and Validating System
34
169.06
5,748
0.08
460

Kidney Paired Donation Candidate Registration
160
1.38
221
0.29
64

Kidney Paired Donation Donor Registration
160
1.46
234
1.07
250

Kidney Paired Donation Match Offer Management
160
1.51
242
0.67
162

Living Donor Event
251
0.12
30
0.56
17

Safety Situation
450
0.48
216
0.56
121

Potential Disease Transmission Report
57
6.88
392
1.27
498

Request to Unlock Form
450
39.22
17,649
0.02
353

Total
8,290

604,519

430,267

* The Number of Reponses per Respondent was calculated by dividing the Total Responses by the Number of Respondents and rounding to the nearest tenth.

a

b

c

d
Total burden hours in these forms decreased from estimates provided in the 60-day Notice due to the removal of the proposed data collection changes associated with implementing the “Modify Data Collection on VCA Living Donors” and “Programming VCA Allocation in UNet” policies.

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.

Maria G. Button,
Director, Executive Secretariat.

[FR Doc. 2022-00239 Filed 1-7-22; 8:45 am]
BILLING CODE 4165-15-P

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Source: Frix Law Library, https://www.frixlaw.com/law-library/documents/fr%3A2022-00239. Public record. Not legal advice.