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AGENCY:
Agency for Healthcare Research and Quality (AHRQ), Department of Health and Human Services (HHS).
ACTION:
Notice.
SUMMARY:
This notice announces the intention of AHRQ to request that the Office of Management and Budget (OMB) approve the proposed information collection project “Patient Safety Organization Certification for Initial Listing and Related Forms, Patient Safety Confidentiality Complaint Form, and Common Formats .”
This proposed information collection was previously published in the Federal Register on February 26, 2018 and allowed 60 days for public comment. AHRQ did not receive any substantive comments.
DATES:
Comments on this notice must be received by July 5, 2018.
ADDRESSES:
Written comments should be submitted to: AHRQ's OMB Desk Officer by fax at (202) 395-6974 (attention: AHRQ's desk officer) or by email at OIRA_submission@omb.eop.gov (attention: AHRQ's desk officer).
Start Further InfoFOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports Clearance Officer, (301) 427-1477, or by email at doris.lefkowitz@AHRQ.hhs.gov.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
Proposed Project
Patient Safety Organization Certification for Initial Listing and Related Forms, Patient Safety Confidentiality Complaint Form, and Common Formats
In accordance with the Paperwork Reduction Act, 44 U.S.C. 3501-3521, AHRQ invites the public to comment on this proposed information collection. The Patient Safety and Quality Improvement Act of 2005 (Patient Safety Act), signed into law on July 29, 2005, was enacted in response to growing concern about quality and patient safety in the United States and the Institute of Medicine's 1999 report, To Err is Human: Building a Safer Health System. The goal of the statute is to create a national learning system by providing for the voluntary formation of Patient Safety Organizations (PSOs). By analyzing substantial amounts of information across multiple institutions, PSOs are able to identify patterns of failures and propose quality and safety improvements. The Patient Safety Act signifies the Federal Government's commitment to fostering and creating an environment in which the causes of health care risks and hazards can be thoroughly and honestly examined and discussed without fear of penalties and liabilities.
In order to implement the Patient Safety Act, HHS issued the Patient Safety and Quality Improvement Final Rule (Patient Safety Rule) which became effective on January 19, 2009. The Patient Safety Rule establishes a framework for the reporting of quality and patient safety information—by hospitals, doctors, nurses, pharmacists, and other providers—to PSOs, on a privileged and confidential basis, for aggregation and analysis. In addition, the Patient Safety Rule outlines the requirements that entities must meet to become and remain listed as PSOs and the process by which the Secretary of HHS (Secretary) will accept certifications and list PSOs.
When specific statutory requirements are met, the information collected and the analyses and deliberations regarding the information receive confidentiality and privilege protections under this legislation. The Secretary delegated authority to the Director of the Office for Civil Rights (OCR) to enforce the confidentiality protections of the Patient Safety Act (Federal Register, Vol. 71, No. 95, May 17, 2006, p. 28701-2). OCR is responsible for enforcing confidentiality protections regarding patient safety work product (PSWP), which may include: Patient-,provider-, and reporter-identifying information that is collected, created, or used for or by PSOs for patient safety and quality activities. Civil money penalties may be imposed for knowing or reckless impermissible disclosures of PSWP. AHRQ implements and administers the rest of the statute's provisions.
Pursuant to the Patient Safety Rule, an entity that seeks to be listed as a PSO by the Secretary must certify that it meets certain requirements and, upon listing, would meet other criteria (42 CFR 3.102). To remain listed for renewable three-year periods, a PSO must re-certify that it meets these obligations and would continue to meet them while listed. The Patient Safety Act and Patient Safety Rule also impose other obligations discussed below that a PSO must meet to remain listed. In accordance with the requirements of the Patient Safety Rule (see, e.g., 42 CFR 3.102(a)(1), 3.102(b)(2)(i)(E), 3.102(d)(1), and 3.112), the entities seeking to be listed and to remain listed must complete the proposed forms, in order to attest to compliance with statutory criteria and the corresponding regulatory requirements.
Method of Collection
With this submission, AHRQ is requesting approval of the following proposed administrative forms:
1. PSO Certification for Initial Listing Form. This form, containing certifications of eligibility and a capacity and intention to comply with statutory criteria and regulatory requirements, is to be completed, in accordance with 42 U.S.C. 299b-24(a)(1) and the corresponding regulatory provisions, by an entity seeking to be listed by the Secretary as a PSO for an initial three-year period.
2. PSO Certification for Continued Listing Form. In accordance with 42 U.S.C. 299b-24(a)(2) and the corresponding regulatory provisions, this form is to be completed by a listed PSO seeking continued listing as a PSO by the Secretary for each successive three-year period.
3. PSO Two Bona Fide Contracts Requirement Certification Form. To remain listed, a PSO must meet a statutory requirement in 42 U.S.C. 299b-24(b)(1)(C) that it has bona fide contracts with more than one provider, within successive 24-month periods, beginning with the date of the PSO's initial listing, for the purpose of receiving and reviewing patient safety work product. This form is to be used by a PSO to certify whether it has met this statutory requirement and the corresponding regulatory provisions.
4. PSO Disclosure Statement Form. This form provides detailed instructions to a PSO regarding the disclosure statement it must submit and provides for the required certification of the statement's accuracy by the PSO in accordance with the 42 U.S.C. 299b-24(b)(1)(E) whereby the entity shall fully disclose: (i) Any financial, reporting, or contractual relationship between the entity and any provider that contracts with the PSO; and (ii) if applicable, the fact that the PSO is not managed, not controlled, and operated independently from any provider that contracts with the PSO. In accordance with the Patient Safety Act and the Patient Safety Rule, the Secretary is required to review each such report and make public findings as to whether a PSO can fairly and accurately carry out its patient safety activities.
5. PSO Profile Form. This form gathers information on the type of providers and settings with which PSOs are working to conduct patient safety activities in order to improve patient safety. It is designed to collect a minimum level of information necessary to develop aggregate data relating to the Patient Safety Act. This information will be included in AHRQ's annual quality report, required by 42 U.S.C. 299b-2(b)(2).
6. PSO Change of Listing Information Form. The Secretary is required under 42 U.S.C. 299b-24(d) to maintain a publicly available list of PSOs. Under the Patient Safety Rule, that list includes, among other Start Printed Page 25669information, each PSO's current contact information. The Patient Safety Rule, at 42 CFR 3.102(a)(1)(vi), also requires that, during its period of listing, a PSO must promptly notify the Secretary of any changes in the accuracy of the information submitted for listing.
7. PSO Voluntary Relinquishment Form. A PSO may choose to voluntarily relinquish its status as a PSO for any reason. Pursuant to 42 CFR 3.108(c)(2), in order for the Secretary to accept a PSO's notification of voluntary relinquishment, the notice must contain certain attestations and future contact information. This form provides an efficient manner for a PSO seeking voluntary relinquishment to provide all of the required information.
AHRQ will use these forms to obtain information necessary to carry out its authority to implement the Patient Safety Act and Patient Safety Rule. This includes obtaining initial and subsequent certifications from entities seeking to be or remain listed as PSOs and for making the statutorily-required determinations prior to and during an entity's period of listing as a PSO. This information is used by the PSO Program Office housed in AHRQ's Center for Quality Improvement and Patient Safety.
OCR is requesting approval of the following administrative form:
Patient Safety Confidentiality Complaint Form. The purpose of this collection is to allow OCR to collect the minimum information needed from individuals filing patient safety confidentiality complaints with OCR so that there is a basis for initial processing of those complaints.
OCR will use the Patient Safety Confidentiality Complaint Form to collect information for the initial assessment of an incoming complaint. The form is modeled on OCR's form for complaints alleging violation of the privacy of protected health information. Use of the form is voluntary. It may help a complainant provide the essential information. Alternatively, a complainant may choose to submit a complaint in the form of a letter or electronically. An individual who needs help to submit a complaint in writing may call OCR for assistance.
The forms described above, other than the PSO Voluntary Relinquishment Form, are revised collection instruments that were previously approved by OMB in 2008, 2011, and 2014.
In addition, AHRQ is requesting approval for a set of common definitions and reporting formats (hereafter Common Formats). AHRQ coordinates the development of the Common Formats, as authorized by 42 U.S.C. 299b-23(b), that allow PSOs and providers to voluntarily collect and submit standardized information regarding patient safety events to ensure that data collected by PSOs and other entities have comparable clinical meaning. The Common Formats facilitate aggregation of comparable data at local, PSO, regional and national levels.
Estimated Annual Respondent Burden
The information collection forms that are the subject of this notice will be implemented at different times and frequencies due to the voluntary nature of: Seeking listing and remaining listed as a PSO, filing an OCR Patient Safety Confidentiality Complaint Form, and using the Common Formats. The burden estimates are based on the average of the forms submissions received over the past three years.
Exhibit 1 shows the estimated annualized burden hours for the respondent to provide the requested information, and Exhibit 2 shows the estimated annualized cost burden associated with the respondents' time to provide the requested information. The total burden hours are estimated to be 100,724.88 hours annually and the total cost burden is estimated to be $3,833,588.92 annually.
PSO Certification for Initial Listing Form: The average annual burden for the collection of information requested by the certification form for initial listing is based upon a total average estimate of 16 respondents per year and an estimated time of 18 hours per response. The estimated response number not only includes submissions by entities subsequently listed as PSOs, but also entities that submit an initial listing form that do not become a PSO. After submitting a PSO Certification for Initial Listing Form, an entity may withdraw its form or submit a revised form, particularly after receiving technical assistance from AHRQ. In addition, AHRQ, on behalf of the Secretary, may deny listing if an entity does not meet the requirements of the Patient Safety Act and Patient Safety Rule.
PSO Certification for Continued Listing Form: The average annual burden for the collection of information requested by the certification form for continued listing has an estimated time of eight hours per response and 21 responses annually. The PSO Certification for Continued Listing Form must be completed by any interested PSO at least 75 days before the end of its current three-year listing period.
PSO Two Bona Fide Contracts Requirement Certification Form: The average annual burden for the collection of information requested by the PSO Two Bona Fide Contract Certification Form is based upon an estimate of 42 respondents per year and an estimated one hour per response. This collection of information takes place at least every 24 months when the PSO notifies the Secretary that it has entered into two contracts with providers.
PSO Disclosure Statement Form: Because only a small percentage of PSOs will need to file a Disclosure Statement Form, the average burden for the collection of information requested by the disclosure form is based upon an estimate of three respondents per year and estimated three hours per response. This information collection takes place within 45 days of when a PSO begins having any of the specified types of additional relationships with a provider with which it has a contract to carry out patient safety activities.
PSO Profile Form: The overall annual burden for the collection of information requested by the PSO Profile Form is based upon an estimate of 70 respondents per year and an estimated three hours per response. The collection of information takes place annually, with newly listed PSOs initially requested to submit the form in the calendar year after their listing by the Secretary.
Change of Listing Information Form: The average annual burden for the collection of information requested by the PSO Change of Listing Information Form is based upon an estimate of 61 respondents per year and an estimated time of five minutes per response. This collection of information takes place on an ongoing basis as needed when there are changes to the PSO's listing information.
OCR Patient Safety Confidentiality Complaint Form: The overall annual burden estimate of one third of an hour for the collection of information requested by the form is based on an estimate of one respondent per year and an estimated 20 minutes per response; the estimate of one form is provided due to the fact that no submissions have been received. OCR's information collection using this form will not begin until after there is an allegation of a violation of the confidentiality protections of PSWP.
PSO Voluntary Relinquishment Form: The average annual burden for the collection of information requested by the PSO Voluntary Relinquishment Form is based upon a total average estimate of five respondents per year and an estimated time of five minutes per response.
Common Formats: AHRQ estimates that 5% FTE of a patient safety manager at a facility will be spent to administer Start Printed Page 25670the Common Formats, which is approximately 100 hours a year. The use of the Common Formats by PSOs and other entities is voluntary and is on an ongoing basis. This estimate of the number of respondents is based on the feedback that AHRQ has received during meetings and technical assistance calls from PSOs and other entities that have been utilizing the Common Formats. As the network for patient safety databases (NPSD) becomes operational, AHRQ will revise the estimate based on actual submissions.
Exhibit 1—Estimated Annualized Burden Hours
Form Number of respondents Number of responses per respondent Hours per response Total burden hours PSO Certification for Initial Listing Form 16 1 18 288 PSO Certification for Continued Listing Form 21 1 8 168 PSO Two Bona Fide Contracts Requirement Form 42 1 1 42 PSO Disclosure Statement Form 3 1 3 9 PSO Profile Form 70 1 3 210 PSO Change of Listing Information 61 1 05/60 5.08 OCR Patient Safety Confidentiality Complaint Form 1 1 20/60 0.33 PSO Voluntary Relinquishment Form 5 1 30/60 2.50 Common Formats 1,000 1 100 100,000 Total NA NA 100,724.91 Exhibit 2—Estimated Annualized Cost Burden
Form Number of respondents Total burden hours Average hourly wage rate * Total cost PSO Certification for Initial Listing Form 16 288 $38.06 $10,961.28 PSO Certification for Continued Listing Form 21 168 38.06 6,394.08 PSO Two Bona Fide Contracts Requirement Form 42 42 38.06 1,598.52 PSO Disclosure Statement Form 3 9 38.06 342.54 PSO Profile Form 70 210 38.06 7,992.60 PSO Change of Listing Form 61 5.08 38.06 193.34 OCR Patient Safety Confidentiality Complaint Form 1 0.33 38.06 12.55 PSO Voluntary Relinquishment Form 5 2.50 38.06 95.15 Common Formats 1,000 100,000 38.06 3,806,000.00 Total 3,833,590.06 * Based upon the mean of the hourly average wages for health care practitioner and technical occupations, 29-0000, National Compensation Survey, May 2016, “U.S. Department of Labor, Bureau of Labor Statistics.” https://www.bls.gov/oes/current/oes290000.htm. Request for Comments
In accordance with the Paperwork Reduction Act, comments on AHRQ's information collection are requested with regard to any of the following: (a) Whether the proposed collection of information is necessary for the proper performance of AHRQ functions, including whether the information will have practical utility, and; for OCR's enforcement of confidentiality; (b) the accuracy of AHRQ's estimate of burden (including hours and costs) of the proposed collection(s) 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 upon the respondents, including the use of automated collection techniques or other forms of information technology.
Comments submitted in response to this notice will be summarized and included in the Agency's subsequent request for OMB approval of the proposed information collection. All comments will become a matter of public record.
Start SignatureFrancis D. Chesley, Jr.,
Acting Deputy Director.
[FR Doc. 2018-11926 Filed 6-1-18; 8:45 am]
BILLING CODE 4160-90-P
Document Information
- Published:
- 06/04/2018
- Department:
- Agency for Healthcare Research and Quality
- Entry Type:
- Notice
- Action:
- Notice.
- Document Number:
- 2018-11926
- Dates:
- Comments on this notice must be received by July 5, 2018.
- Pages:
- 25668-25670 (3 pages)
- PDF File:
- 2018-11926.pdf
- Supporting Documents:
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- » Supplemental Evidence and Data Request: Platelet-Rich Plasma for Wound Care in the Medicare Population
- » Agency Information Collection Activities; Proposals, Submissions, and Approvals
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