0937-0166 sterilization8-25

0937-0166 sterilization8-25.doc

42 C.F.R. Subpart B: Sterilization of Persons in Federally Assisted Family Planning Projects

OMB: 0937-0166

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Supporting Statement for Information Collection Requirements

Contained the Public Health Service (PHS)

Sterilization of Persons in Federally Assisted Family Planning Projects

42 CFR Part 50, subpart B



A. Justification


1. Circumstances Making the Collection Necessary


In order to comply with the Paperwork Reduction Act of 1995, the Office of Population Affairs (OPA), Department of Health and Human Services (DHHS), requests that the Office of Management and Budget (OMB) approve for three years from approval date, the "Consent for Sterilization Form.” Approval for the PHS information collection requirement contained in the sterilization consent form has been given under OMB number 0937-0166.


This is a request for an extension of a currently approved collection for the disclosure and record-keeping requirements codified at 42 CFR part 50, subpart B, “Sterilization of Persons in Federally Assisted Family Planning Projects.” The Sterilization Consent Form has been revised to reflect a new expiration date.


These rules prescribe the requirements for sterilizations funded under the various PHS programs administered by the Department of Health and Human Services (HHS). Included with the portion of the rules pertaining to those programs administered by the PHS, as part of the appendix to subpart B, is a copy of the required sterilization consent form. The requirements apply when sterilization procedures are carried out by programs or projects funded by the PHS, under grant or contract. The requirements are as follows:


42 CFR 50.204 - Disclosure - Specifies information that must be provided to the individual in order to constitute informed consent.


42 CFR 50.205 and 50.208 - Record-keeping - Specifies the consent form that must be used, signatures and certifications required and record retention requirements.


The requirements of the regulation result from several tragic incidents of sterilization abuse under Federal family planning programs that were brought to the Department's attention in 1973 (Relf v. Wienberger). In 1978, HHS published in the Federal Register, final rules prescribing the requirements for sterilizations funded under various health programs administered by the Department. The Department funds family planning services, including sterilizations, under several Federal statutes. The sterilization consent regulations set forth the procedures to be followed and information to be provided in order to assure informed consent. In brief, the regulation allows Federal funding of sterilizations only in cases where the individual requesting the procedure is at least 21 years of age, mentally competent and has given informed consent at least 72 hours before the sterilization was performed. The regulations require a 30-day (but not more than 180 days) waiting period, prohibit Federal funding of sterilizations of mentally incompetent individuals unless he or she had been declared competent for purposes which include the ability to consent to sterilization, and prohibit sterilizations for institutionalized persons.


The consent form provides information to assure voluntary and informed consent to persons undergoing sterilization in programs for health services which are supported by federal financial assistance administered by the PHS. The consent form provides additional procedural protection to the individual, and the regulation requires that the consent form be either a copy of the form that is appended to the PHS regulation or another similar consent form approved by the Secretary. In 2003, the PHS sterilization consent form was revised to conform to OMB government-wide standards for the collection of race/ethnicity data and to incorporate the PRA burden statement as part of the consent form. In 2006, OMB approved an extension of the information collection. Section 301 of the Public Health Service Act (42 U.S.C. 241).


2. Purpose and Use of Information


Consent forms are signed by individuals undergoing a federally funded sterilization procedure and certified by necessary medical authorities. Forms are incorporated into the patient's medical records and the agency's records. Through periodic site audits and visits, PHS staff review completed consent forms to determine compliance with the regulation. Thus, the purpose of the consent form is twofold. First, it serves as a mechanism to ensure that a person receives information about sterilization and voluntarily consents to the procedure. Second, it facilitates compliance monitoring.


Payments are disallowed for violations of the sterilization regulations requirements. In instances where widespread abuses are observed, a PHS program may be defunded. Examples of potential violations include disregard of mandatory waiting periods or the minimum age limit; sterilizations of mentally incompetent individuals; or lack of informed consent by the patient.


  1. Use of Improved Technology and Burden Reduction


This regulation in no way prescribes how the facility should prepare to maintain records. The programs are free to take advantage of any technological advance which they find appropriate for their needs.


4. Efforts to Identify Duplication and Use of Similar Information


These are unique requirements which are specified in a way so as not to duplicate existing program or agency policy. The procedures required to assure informed consent are carried out once for each case of sterilization. No other forms unique to sterilization are required by the PHS agencies. The information obtained on the consent form is required by regulation, and is not collected by any other source.


5. Impact on Small Business or Other Small Entities


All federally funded public health programs are required to follow the regulations regardless of their size. The consent form protects the individual by ensuring that he/she is aware of the risks, benefits, alternatives and consequences of sterilization. The burden cannot be reduced for small organizations without violating or failing to properly ensure the rights of individuals seeking sterilization.


6. Consequences of Less Frequent Collection


The disclosure requirements and consent form are used on a single time basis of individuals seeking sterilization involving PHS Federal financial participation.


7. Special Circumstances Relating to the Guidelines of 5 CFR 1320.5


These requirements comply with all general information collection guidelines.


8. Comments in Response to Federal Register Notice/Outside Consultation


A 60-day Federal Register Notice was published in the Federal Register on July 2, 2015, vol. 80, Number 127; p. 38217-38218. There were no public comments.


9. Explanation of any Payment/Gift to Respondents


No payment is made to respondents.


10. Assurance of Confidentiality Provided to Respondents


The medical records maintained by agencies will be kept private to the extent allowed by law. Information may be disclosed only in summary, statistical or other form which does not identify particular individuals.


11. Justification of Sensitive Questions


The regulations require only disclosure of information to individuals seeking the sterilization operation and informed consent of such individuals, not responses to sensitive questions.


12. Estimates of Annualized Burden Hours

Sterilizations comprise about two percent of approximately five million family planning service patients (100,000 sterilizations). From discussion with providers, practitioners, PHS staff and others, it is estimated that approximately one hour is necessary to inform the individual of the sterilization procedures and his/her rights.

Therefore, the annual collection burden is: 1 hour/patient x 100,000 = 100,000 hours.


In addition to disclosure, we estimate fifteen minutes per patient for record-keeping (i.e., filing and necessary documentation).

Therefore, the annual record-keeping burden is 15 minutes x 100,000 records = 25,000 hours.


The total annual burden which appears in the information collection budget is 125,000 hours.


Estimated Annualized Burden Hours


Type of Respondent

Information Collection

Number of Respondents

Number of Responses per Respondent

Average Burden per Response

Total Hours

Citizens Seeking Sterilization


Information Disclosure for Sterilization Consent Form

100,000

1

1

100,000

Citizens Seeking Sterilization


Record-keeping for Sterilization Consent Form

100,000

1

15/60

25,000

Total





125,000


Estimated Annualized Cost


Type of Respondent

Information Collection

Total Burden Hours

Hourly Wage Rate


Total Respondent Costs

Citizens Seeking Sterilization

Information Disclosure

100,000

$10.00


$1,000,000

Citizens Seeking Sterilization

Record-keeping

25,000

$10.00

$250,000

Total




$1,250,000



13. Estimates of Other Total Annual Cost Burden to Respondents or Record-keepers/Capital Costs


No start-up costs required. Clinicians will not need new information to utilize this form.


14. Annualized Costs to the Federal Government


Estimated Annualized Cost to the Federal Government


Number of Title X Grantees

Number Chart Audits per Grantee

Total Number Chart Audits

Number Hours to Complete One Chart Audit

Cost per Chart Audit

Total Federal Annual Cost


88

8

704

2

$15.00

$21,120.00


We estimate the Federal cost to be the following:


8 chart audits annually x 88 grantees = 704 audits

704 chart audits x 2 hours to complete = 1,408 hours

Total Federal annual cost = 1,408 hours @ $15.00/hour = $21,100.00.


15. Explanation for Program Changes or Adjustments


This is an ongoing collection of information. This collection burden has not changed from the burden shown in the current inventory. Therefore, this is a request for a renewal without changes. The only revision to the form is based on the new date that will allow the extension of the form so it will not expire for three years.


16. Plans for Tabulation and Publication and Project Time Schedule


This information is not tabulated or published.


17. Display of Expiration Date for OMB Approval


The expiration date will be displayed on the information collection item.


  1. Exceptions to the Certification Statement


Not applicable. There are no exceptions to the certification.


B. Collection of Information Employing Statistical Methods


Statistical methods are not used in this activity.






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File Typeapplication/msword
File TitleSupporting Statement for Information Collection Requirements
Authorpamela.kania
Last Modified ByWindows User
File Modified2015-10-21
File Created2015-10-21

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