Notice of Request for Information on the Department of Veterans Affairs; Cytotechnologists Standard of Practice, 31306-31308 [2023-10426]

Download as PDF lotter on DSK11XQN23PROD with NOTICES1 31306 Federal Register / Vol. 88, No. 94 / Tuesday, May 16, 2023 / Notices international-capital-tic-system-homepage/tic-forms-instructions/forms-shl. SUPPLEMENTARY INFORMATION: Definition: A U.S. person is any individual, branch, partnership, associated group, association, estate, trust, corporation, or other organization (whether or not organized under the laws of any State), and any government (including a foreign government, the United States Government, a State or local government, and any agency, corporation, financial institution, or other entity or instrumentality thereof, including a government-sponsored agency), who resides in the United States or is subject to the jurisdiction of the United States. Who Must Report: This mandatory survey is conducted under the authority of the International Investment and Trade in Services Survey Act (22 U.S.C. 3101 et seq.) and in accordance with 31 CFR 129. The panel for this survey is based primarily on the level of foreign resident holdings of U.S. securities reported on the June 2019 benchmark survey of foreign resident holdings of U.S. securities, and on the Aggregate Holdings of Long-Term Securities by U.S. and Foreign Residents (TIC SLT) report as of December 2022, and will consist mostly of the largest reporters. Entities required to report will be contacted individually by the Federal Reserve Bank of New York. Entities not contacted by the Federal Reserve Bank of New York have no reporting responsibilities. What to Report: This report will collect information on foreign resident holdings of U.S. securities, including equities, short-term debt securities (including selected money market instruments), and long-term debt securities. How to Report: Copies of the survey forms and instructions, which contain complete information on reporting procedures and definitions, may be obtained at the website address given above in the Summary, or by contacting the survey staff of the Federal Reserve Bank of New York at (212) 720–6300 or (646) 720–6300, email: SHLA.help@ ny.frb.org. The mailing address is: Federal Reserve Bank of New York, Data and Statistics Function, 6th Floor, 33 Liberty Street, New York, NY 10045– 0001. Inquiries can also be made to the Federal Reserve Board of Governors, at (202) 452–3476, or to Dwight Wolkow, at (202) 923–0518, or by email: comments2TIC@treasury.gov When to Report: Data should be submitted to the Federal Reserve Bank of New York, acting as fiscal agent for the Department of the Treasury, by August 31, 2023. VerDate Sep<11>2014 17:33 May 15, 2023 Jkt 259001 Paperwork Reduction Act Notice: This data collection has been approved by the Office of Management and Budget (OMB) in accordance with the Paperwork Reduction Act and assigned control number 1505–0123. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a valid control number assigned by OMB. The estimated average annual burden associated with this collection of information is 486 hours per report for the largest custodians of securities, and 110 hours per report for the largest issuers of securities that have data to report and are not custodians. Comments concerning the accuracy of this burden estimate and suggestions for reducing this burden should be directed to the Department of the Treasury, Office of International Affairs, Attention Administrator, International Portfolio Investment Data Reporting Systems, Room 1050, Washington, DC 20220, and to OMB, Attention Desk Officer for the Department of the Treasury, Office of Information and Regulatory Affairs, Washington, DC 20503. Dwight D. Wolkow, Administrator, International Portfolio Investment Data Reporting Systems. [FR Doc. 2023–10350 Filed 5–15–23; 8:45 am] BILLING CODE 4810–AK–P DEPARTMENT OF VETERANS AFFAIRS Notice of Request for Information on the Department of Veterans Affairs; Cytotechnologists Standard of Practice Department of Veterans Affairs. Request for information. AGENCY: ACTION: Cytotechnologists, also referred to as Cytologists, are certified laboratory professionals performing highly complex laboratory diagnostic testing on human specimens for diagnosis, treatment, or prevention of disease in the specialty of cytopathology. VA is requesting information to assist in developing a national standard of practice for VA Cytotechnologists. VA seeks comments on various topics to help inform VA’s development of this national standard of practice. DATES: Comments must be received on or before July 17, 2023. ADDRESSES: Comments must be submitted through www.regulations.gov. Except as provided below, comments received before the close of the SUMMARY: PO 00000 Frm 00089 Fmt 4703 Sfmt 4703 comment period will be available at www.regulations.gov for public viewing, inspection, or copying, including any personally identifiable or confidential business information that is included in a comment. We post the comments received before the close of the comment period on the following website as soon as possible after they have been received: https:// www.regulations.gov. VA will not post on Regulations.gov public comments that make threats to individuals or institutions or suggest that the commenter will take actions to harm the individual. VA encourages individuals not to submit duplicative comments. We will post acceptable comments from multiple unique commenters even if the content is identical or nearly identical to other comments. Any public comment received after the comment period’s closing date is considered late and will not be considered in a potential rulemaking. FOR FURTHER INFORMATION CONTACT: Ethan Kalett, Office of Regulations, Appeals and Policy (10BRAP), Veterans Health Administration, Department of Veterans Affairs, 810 Vermont Avenue NW, Washington, DC 20420, at 202– 461–0500. This is not a toll-free number. SUPPLEMENTARY INFORMATION: Authority Chapters 73 and 74 of 38 U.S.C. and 38 U.S.C. 303 authorize the Secretary to regulate the professional activities of VA health care professions to make certain that VA’s health care system provides safe and effective health care by qualified health care professionals to ensure the well-being of those Veterans who have borne the battle. On November 12, 2020, VA published an interim final rule confirming that VA health care professionals may practice their health care profession consistent with the scope and requirements of their VA employment, notwithstanding any State license, registration, certification, or other requirements that unduly interfere with their practice. 38 CFR 17.419; 85 FR 71838. Specifically, this rulemaking confirmed VA’s current practice of allowing VA health care professionals to deliver health care services in a State other than the health care professional’s State of licensure, registration, certification, or other State requirement, thereby enhancing beneficiaries’ access to critical VA health care services. The rulemaking also confirmed VA’s authority to establish national standards of practice for its health care professionals that would standardize a health care E:\FR\FM\16MYN1.SGM 16MYN1 Federal Register / Vol. 88, No. 94 / Tuesday, May 16, 2023 / Notices lotter on DSK11XQN23PROD with NOTICES1 professional’s practice in all VA medical facilities. The rulemaking explained that a national standard of practice describes the tasks and duties that a VA health care professional practicing in the health care profession may perform and may be permitted to undertake. Having a national standard of practice means that individuals from the same VA health care profession may provide the same type of tasks and duties regardless of the VA medical facility where they are located or the State license, registration, certification, or other State requirement they hold. We emphasized in the rulemaking and reiterate here that VA will determine, on an individual basis, that a health care professional has the necessary education, training and skills to perform the tasks and duties detailed in the national standard of practice and will only be able to perform such tasks and duties after they have been incorporated into the individual’s privileges, scope of practice, or functional statement. The rulemaking explicitly did not create any such national standards and directed that all national standards of practice would be subsequently created via policy. Need for National Standards of Practice As the Nation’s largest integrated health care system, it is critical that VA develops national standards of practice to ensure beneficiaries receive the same high-quality care regardless of where they enter the system and to ensure that VA health care professionals can efficiently meet the needs of beneficiaries when practicing within the scope of their VA employment. National standards are designed to increase beneficiaries’ access to safe and effective health care, thereby improving health outcomes. The importance of this initiative has been underscored by the Coronavirus Disease 2019 (COVID–19) pandemic. With an increased need for mobility in our workforce, including through VA’s Disaster Emergency Medical Personnel System, creating a uniform standard of practice better supports VA health care professionals who already frequently practice across State lines. In addition, the development of national standards of practice aligns with VA’s long-term deployment of a new electronic health record (EHR). National standards of practice are critical for optimal EHR implementation to enable the specific roles for each health care profession in EHR to be consistent across the Veterans Health Administration (VHA) and to support increased interoperability between VA and the Department of VerDate Sep<11>2014 17:33 May 15, 2023 Jkt 259001 Defense (DoD). DoD has historically standardized practice for certain health care professionals, and VHA closely partnered with DoD to learn from their experience. Process To Develop National Standards of Practice Consistent with 38 CFR 17.419, VA is developing national standards of practice through policy. There will be one overarching national standard of practice directive that will generally describe VHA’s policy and have each individual national standard of practice as an appendix to the directive. The directive and all appendices will be accessible on VHA Publications website at: https://vaww.va.gov/ vhapublications/ (internal) and https:// www.va.gov/vhapublications/ (external) once published. To develop these national standards, VA is using a robust, interactive process that is consistent with the guidance outlined in Executive Order (E.O.) 13132 to preempt State law. The process includes consultation with internal and external stakeholders, including State licensing boards, VA employees, professional associations, Veterans Service Organizations, labor partners and others. For each identified VA occupation, a workgroup comprised of health care professionals conducts State variance research to identify internal best practices that may not be authorized under every State license, certification, or registration, but would enhance the practice and efficiency of the profession throughout the agency. The workgroup is comprised of VA employees who are health care professionals in the identified occupation; they may consult with internal stakeholders at any point throughout the process. If a best practice is identified that is not currently authorized by every State, the workgroup determines what education, training and skills are required to perform such task or duty. The workgroup then drafts a proposed VA national standard of practice using the data gathered during the State variance research and incorporates internal stakeholder feedback to date. The proposed national standard of practice is internally reviewed, to include by an interdisciplinary workgroup consisting of representatives from Quality Management; Field Chief of Staff; Academic Affiliates; Field Chief Nursing Officer; Ethics; Workforce Management and Consulting; Surgery; Credentialing and Privileging; Field Chief Medical Office; and EHR Modernization. PO 00000 Frm 00090 Fmt 4703 Sfmt 4703 31307 Externally, the proposed national standard of practice is provided to our partners in DoD. In addition, VA labor partners are engaged informally as part of a pre-decisional collaboration. Consistent with E.O. 13132, a letter is sent to each State board and certifying organization that includes the proposed national standard and an opportunity to further discuss the national standard with VA. After the States and certifying organization have received notification, the proposed national standard of practice is published to the Federal Register for 60 days to obtain feedback from the public, including professional associations and unions. At the same time, the proposed national standard is published on an internal VA site to obtain feedback from VA employees. Feedback from State boards, professional associations, unions, VA employees and any other person or organization who informally provides comments through the Federal Register will be reviewed. VA will make appropriate revisions in light of the comments, including those that present evidence-based practice and alternatives that help VA meet our mission and goals, and that are better for Veterans or VA health care professionals. We will publish a collective response to all comments at https://www.va.gov/ standardsofpractice. After the national standard of practice is finalized, approved and published in VHA policy, VA will implement the tasks and duties authorized by that national standard of practice. Any tasks or duties included in the national standard will be incorporated into an individual health care professional’s privileges, scope of practice, or functional statement following any training and education necessary for the health care professional to perform those functions. Implementation of the national standard of practice may be phased in across all medical facilities, with limited exemptions for health care professionals as needed. National Standard for Cytotechnologists The proposed format for national standards of practice when there are State licenses and a national certification is as follows. The first paragraph provides general information about the profession and what the health care professionals can do. The second paragraph references the education and certification needed to practice this profession at VA. The third paragraph confirms that this profession follows the standard set by the national certifying body. A final statement explains that while VA only requires a E:\FR\FM\16MYN1.SGM 16MYN1 lotter on DSK11XQN23PROD with NOTICES1 31308 Federal Register / Vol. 88, No. 94 / Tuesday, May 16, 2023 / Notices national certification, some States also require licensure for this profession. The standard includes information on which States offer an exemption for Federal employees and where VA will preempt State laws, if applicable. We note that the proposed standards of practice do not contain an exhaustive list of every task and duty that each VA health care professional can perform. Rather, it is designed to highlight whether there are any areas of variance in how this profession can practice across States and how this profession will be able to practice within VA notwithstanding their State license, certification, registration and other requirements. VA qualification standards require Cytotechnologists to have an active, current, full and unrestricted Cytologist (CT) or Specialist in Cytology (SCT) certification from the American Society for Clinical Pathology. VA reviewed whether there are any alternative registrations, certifications, or State requirements that could be required for a Cytotechnologist and found that nine States require a license. Of those, six States exempt Federal employees from their State license requirements. The standards set forth in the licensure requirements for all nine States are consistent with what is permitted under the national certifications. Therefore, there is no variance in how Cytotechnologists practice in any State. VA proposes to adopt a standard of practice consistent with the national certifications; therefore, VA Cytotechnologists will continue to follow the same standard as set by their national certifications. The standard for the certifications can be found here: https://www.ascp.org/content/docs/ default-source/policy-statements/ascppdft-pp-personnelstandards.pdf?sfvrsn=2. Because the practice of Cytotechnologists is not changing, there will be no impact on the practice of this occupation when this national standard of practice is implemented. with pathologists to diagnose benign and infectious processes, precancerous lesions and malignant diseases. Cytotechnologists in VA possess the education and certification required by VA qualification standards, as more specifically described in VA Handbook 5005, Staffing, dated February 4, 2022. This national standard of practice confirms that Cytotechnologists practice according to the CT or SCT standards from the American Society for Clinical Pathology (ASCP) available at: www.ascp.org. As of March 2022, all Cytotechnologists in VA follow this national certification. Although VA only requires a certification, nine States require a State license in order to practice as a Cytotechnologist in that State: California, Florida, Hawaii, Louisiana, Montana, Nevada, New York, Tennessee and West Virginia. Of these, the following States exempt Federal employees from their State license requirements: Florida, Louisiana, Montana, New York, Tennessee and West Virginia. As of October 2022, there is no variance in how VA Cytotechnologists practice in any State. Proposed National Standard of Practice for Cytotechnologist Cytotechnologists are certified laboratory professionals performing highly complex laboratory diagnostic testing on human specimens for diagnosis, treatment, or prevention of disease in the specialty of cytopathology. Cytotechnologists are responsible for reporting the microscopic interpretation of normal gynecological cytology smear tests used to detect cervical cancer; providing preliminary interpretation of specimens from other body sites; and collaborating Denis McDonough, Secretary of Veterans Affairs, approved this document on April 14, 2023, and authorized the undersigned to sign and submit the document to the Office of the Federal Register for publication electronically as an official document of the Department of Veterans Affairs. VerDate Sep<11>2014 17:33 May 15, 2023 Jkt 259001 Request for Information 1. Are there any required trainings for the aforementioned practices that we should consider? 2. Are there any factors that would inhibit or delay the implementation of the aforementioned practices for VA health care professionals in any States? 3. Is there any variance in practice that we have not listed? 4. What should we consider when preempting conflicting State laws, regulations, or requirements regarding supervision of individuals working toward obtaining their license or unlicensed personnel? 5. Is there anything else you would like to share with us about this national standard of practice? Signing Authority Luvenia Potts, Regulation Development Coordinator, Office of Regulation Policy & Management, Office of General Counsel, Department of Veterans Affairs. [FR Doc. 2023–10426 Filed 5–15–23; 8:45 am] BILLING CODE 8320–01–P PO 00000 Frm 00091 Fmt 4703 Sfmt 4703 DEPARTMENT OF VETERANS AFFAIRS Notice of Request for Information on the Department of Veterans Affairs; Histopathology Technologists Standard of Practice Department of Veterans Affairs. Request for information. AGENCY: ACTION: The Department of Veterans Affairs (VA) is requesting information to assist in developing a national standard of practice for VA Histopathology Technologists. VA seeks comments on various topics to help inform VA’s development of this national standard of practice. DATES: Comments must be received on or before July 17, 2023. ADDRESSES: Comments must be submitted through www.regulations.gov. Except as provided below, comments received before the close of the comment period will be available at www.regulations.gov for public viewing, inspection, or copying, including any personally identifiable or confidential business information that is included in a comment. We post the comments received before the close of the comment period on the following website as soon as possible after they have been received: https:// www.regulations.gov. VA will not post on Regulations.gov public comments that make threats to individuals or institutions or suggest that the commenter will take actions to harm the individual. VA encourages individuals not to submit duplicative comments. We will post acceptable comments from multiple unique commenters even if the content is identical or nearly identical to other comments. Any public comment received after the comment period’s closing date is considered late and will not be considered in a potential rulemaking. FOR FURTHER INFORMATION CONTACT: Ethan Kalett, Office of Regulations, Appeals and Policy (10BRAP), Veterans Health Administration, Department of Veterans Affairs, 810 Vermont Avenue NW, Washington, DC 20420, 202–461– 0500. This is not a toll-free number. SUPPLEMENTARY INFORMATION: SUMMARY: Authority Chapters 73 and 74 of 38 U.S.C. and 38 U.S.C. 303 authorize the Secretary to regulate the professional activities of VA health care professions to make certain that VA’s health care system provides safe and effective health care by qualified health care professionals to ensure the well-being of those Veterans who have borne the battle. E:\FR\FM\16MYN1.SGM 16MYN1

Agencies

[Federal Register Volume 88, Number 94 (Tuesday, May 16, 2023)]
[Notices]
[Pages 31306-31308]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-10426]


=======================================================================
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DEPARTMENT OF VETERANS AFFAIRS


Notice of Request for Information on the Department of Veterans 
Affairs; Cytotechnologists Standard of Practice

AGENCY: Department of Veterans Affairs.

ACTION: Request for information.

-----------------------------------------------------------------------

SUMMARY: Cytotechnologists, also referred to as Cytologists, are 
certified laboratory professionals performing highly complex laboratory 
diagnostic testing on human specimens for diagnosis, treatment, or 
prevention of disease in the specialty of cytopathology. VA is 
requesting information to assist in developing a national standard of 
practice for VA Cytotechnologists. VA seeks comments on various topics 
to help inform VA's development of this national standard of practice.

DATES: Comments must be received on or before July 17, 2023.

ADDRESSES: Comments must be submitted through www.regulations.gov. 
Except as provided below, comments received before the close of the 
comment period will be available at www.regulations.gov for public 
viewing, inspection, or copying, including any personally identifiable 
or confidential business information that is included in a comment. We 
post the comments received before the close of the comment period on 
the following website as soon as possible after they have been 
received: https://www.regulations.gov. VA will not post on 
Regulations.gov public comments that make threats to individuals or 
institutions or suggest that the commenter will take actions to harm 
the individual. VA encourages individuals not to submit duplicative 
comments. We will post acceptable comments from multiple unique 
commenters even if the content is identical or nearly identical to 
other comments. Any public comment received after the comment period's 
closing date is considered late and will not be considered in a 
potential rulemaking.

FOR FURTHER INFORMATION CONTACT: Ethan Kalett, Office of Regulations, 
Appeals and Policy (10BRAP), Veterans Health Administration, Department 
of Veterans Affairs, 810 Vermont Avenue NW, Washington, DC 20420, at 
202-461-0500. This is not a toll-free number.

SUPPLEMENTARY INFORMATION:

Authority

    Chapters 73 and 74 of 38 U.S.C. and 38 U.S.C. 303 authorize the 
Secretary to regulate the professional activities of VA health care 
professions to make certain that VA's health care system provides safe 
and effective health care by qualified health care professionals to 
ensure the well-being of those Veterans who have borne the battle.
    On November 12, 2020, VA published an interim final rule confirming 
that VA health care professionals may practice their health care 
profession consistent with the scope and requirements of their VA 
employment, notwithstanding any State license, registration, 
certification, or other requirements that unduly interfere with their 
practice. 38 CFR 17.419; 85 FR 71838. Specifically, this rulemaking 
confirmed VA's current practice of allowing VA health care 
professionals to deliver health care services in a State other than the 
health care professional's State of licensure, registration, 
certification, or other State requirement, thereby enhancing 
beneficiaries' access to critical VA health care services. The 
rulemaking also confirmed VA's authority to establish national 
standards of practice for its health care professionals that would 
standardize a health care

[[Page 31307]]

professional's practice in all VA medical facilities.
    The rulemaking explained that a national standard of practice 
describes the tasks and duties that a VA health care professional 
practicing in the health care profession may perform and may be 
permitted to undertake. Having a national standard of practice means 
that individuals from the same VA health care profession may provide 
the same type of tasks and duties regardless of the VA medical facility 
where they are located or the State license, registration, 
certification, or other State requirement they hold. We emphasized in 
the rulemaking and reiterate here that VA will determine, on an 
individual basis, that a health care professional has the necessary 
education, training and skills to perform the tasks and duties detailed 
in the national standard of practice and will only be able to perform 
such tasks and duties after they have been incorporated into the 
individual's privileges, scope of practice, or functional statement. 
The rulemaking explicitly did not create any such national standards 
and directed that all national standards of practice would be 
subsequently created via policy.

Need for National Standards of Practice

    As the Nation's largest integrated health care system, it is 
critical that VA develops national standards of practice to ensure 
beneficiaries receive the same high-quality care regardless of where 
they enter the system and to ensure that VA health care professionals 
can efficiently meet the needs of beneficiaries when practicing within 
the scope of their VA employment. National standards are designed to 
increase beneficiaries' access to safe and effective health care, 
thereby improving health outcomes. The importance of this initiative 
has been underscored by the Coronavirus Disease 2019 (COVID-19) 
pandemic. With an increased need for mobility in our workforce, 
including through VA's Disaster Emergency Medical Personnel System, 
creating a uniform standard of practice better supports VA health care 
professionals who already frequently practice across State lines. In 
addition, the development of national standards of practice aligns with 
VA's long-term deployment of a new electronic health record (EHR). 
National standards of practice are critical for optimal EHR 
implementation to enable the specific roles for each health care 
profession in EHR to be consistent across the Veterans Health 
Administration (VHA) and to support increased interoperability between 
VA and the Department of Defense (DoD). DoD has historically 
standardized practice for certain health care professionals, and VHA 
closely partnered with DoD to learn from their experience.

Process To Develop National Standards of Practice

    Consistent with 38 CFR 17.419, VA is developing national standards 
of practice through policy. There will be one overarching national 
standard of practice directive that will generally describe VHA's 
policy and have each individual national standard of practice as an 
appendix to the directive. The directive and all appendices will be 
accessible on VHA Publications website at: https://vaww.va.gov/vhapublications/ (internal) and https://www.va.gov/vhapublications/ 
(external) once published.
    To develop these national standards, VA is using a robust, 
interactive process that is consistent with the guidance outlined in 
Executive Order (E.O.) 13132 to preempt State law. The process includes 
consultation with internal and external stakeholders, including State 
licensing boards, VA employees, professional associations, Veterans 
Service Organizations, labor partners and others. For each identified 
VA occupation, a workgroup comprised of health care professionals 
conducts State variance research to identify internal best practices 
that may not be authorized under every State license, certification, or 
registration, but would enhance the practice and efficiency of the 
profession throughout the agency. The workgroup is comprised of VA 
employees who are health care professionals in the identified 
occupation; they may consult with internal stakeholders at any point 
throughout the process. If a best practice is identified that is not 
currently authorized by every State, the workgroup determines what 
education, training and skills are required to perform such task or 
duty. The workgroup then drafts a proposed VA national standard of 
practice using the data gathered during the State variance research and 
incorporates internal stakeholder feedback to date.
    The proposed national standard of practice is internally reviewed, 
to include by an interdisciplinary workgroup consisting of 
representatives from Quality Management; Field Chief of Staff; Academic 
Affiliates; Field Chief Nursing Officer; Ethics; Workforce Management 
and Consulting; Surgery; Credentialing and Privileging; Field Chief 
Medical Office; and EHR Modernization.
    Externally, the proposed national standard of practice is provided 
to our partners in DoD. In addition, VA labor partners are engaged 
informally as part of a pre-decisional collaboration. Consistent with 
E.O. 13132, a letter is sent to each State board and certifying 
organization that includes the proposed national standard and an 
opportunity to further discuss the national standard with VA. After the 
States and certifying organization have received notification, the 
proposed national standard of practice is published to the Federal 
Register for 60 days to obtain feedback from the public, including 
professional associations and unions. At the same time, the proposed 
national standard is published on an internal VA site to obtain 
feedback from VA employees. Feedback from State boards, professional 
associations, unions, VA employees and any other person or organization 
who informally provides comments through the Federal Register will be 
reviewed. VA will make appropriate revisions in light of the comments, 
including those that present evidence-based practice and alternatives 
that help VA meet our mission and goals, and that are better for 
Veterans or VA health care professionals. We will publish a collective 
response to all comments at https://www.va.gov/standardsofpractice.
    After the national standard of practice is finalized, approved and 
published in VHA policy, VA will implement the tasks and duties 
authorized by that national standard of practice. Any tasks or duties 
included in the national standard will be incorporated into an 
individual health care professional's privileges, scope of practice, or 
functional statement following any training and education necessary for 
the health care professional to perform those functions. Implementation 
of the national standard of practice may be phased in across all 
medical facilities, with limited exemptions for health care 
professionals as needed.

National Standard for Cytotechnologists

    The proposed format for national standards of practice when there 
are State licenses and a national certification is as follows. The 
first paragraph provides general information about the profession and 
what the health care professionals can do. The second paragraph 
references the education and certification needed to practice this 
profession at VA. The third paragraph confirms that this profession 
follows the standard set by the national certifying body. A final 
statement explains that while VA only requires a

[[Page 31308]]

national certification, some States also require licensure for this 
profession. The standard includes information on which States offer an 
exemption for Federal employees and where VA will preempt State laws, 
if applicable.
    We note that the proposed standards of practice do not contain an 
exhaustive list of every task and duty that each VA health care 
professional can perform. Rather, it is designed to highlight whether 
there are any areas of variance in how this profession can practice 
across States and how this profession will be able to practice within 
VA notwithstanding their State license, certification, registration and 
other requirements.
    VA qualification standards require Cytotechnologists to have an 
active, current, full and unrestricted Cytologist (CT) or Specialist in 
Cytology (SCT) certification from the American Society for Clinical 
Pathology. VA reviewed whether there are any alternative registrations, 
certifications, or State requirements that could be required for a 
Cytotechnologist and found that nine States require a license. Of 
those, six States exempt Federal employees from their State license 
requirements. The standards set forth in the licensure requirements for 
all nine States are consistent with what is permitted under the 
national certifications. Therefore, there is no variance in how 
Cytotechnologists practice in any State.
    VA proposes to adopt a standard of practice consistent with the 
national certifications; therefore, VA Cytotechnologists will continue 
to follow the same standard as set by their national certifications. 
The standard for the certifications can be found here: https://www.ascp.org/content/docs/default-source/policy-statements/ascp-pdft-pp-personnel-standards.pdf?sfvrsn=2.
    Because the practice of Cytotechnologists is not changing, there 
will be no impact on the practice of this occupation when this national 
standard of practice is implemented.

Proposed National Standard of Practice for Cytotechnologist

    Cytotechnologists are certified laboratory professionals performing 
highly complex laboratory diagnostic testing on human specimens for 
diagnosis, treatment, or prevention of disease in the specialty of 
cytopathology. Cytotechnologists are responsible for reporting the 
microscopic interpretation of normal gynecological cytology smear tests 
used to detect cervical cancer; providing preliminary interpretation of 
specimens from other body sites; and collaborating with pathologists to 
diagnose benign and infectious processes, precancerous lesions and 
malignant diseases.
    Cytotechnologists in VA possess the education and certification 
required by VA qualification standards, as more specifically described 
in VA Handbook 5005, Staffing, dated February 4, 2022.
    This national standard of practice confirms that Cytotechnologists 
practice according to the CT or SCT standards from the American Society 
for Clinical Pathology (ASCP) available at: www.ascp.org. As of March 
2022, all Cytotechnologists in VA follow this national certification.
    Although VA only requires a certification, nine States require a 
State license in order to practice as a Cytotechnologist in that State: 
California, Florida, Hawaii, Louisiana, Montana, Nevada, New York, 
Tennessee and West Virginia. Of these, the following States exempt 
Federal employees from their State license requirements: Florida, 
Louisiana, Montana, New York, Tennessee and West Virginia. As of 
October 2022, there is no variance in how VA Cytotechnologists practice 
in any State.

Request for Information

    1. Are there any required trainings for the aforementioned 
practices that we should consider?
    2. Are there any factors that would inhibit or delay the 
implementation of the aforementioned practices for VA health care 
professionals in any States?
    3. Is there any variance in practice that we have not listed?
    4. What should we consider when preempting conflicting State laws, 
regulations, or requirements regarding supervision of individuals 
working toward obtaining their license or unlicensed personnel?
    5. Is there anything else you would like to share with us about 
this national standard of practice?

Signing Authority

    Denis McDonough, Secretary of Veterans Affairs, approved this 
document on April 14, 2023, and authorized the undersigned to sign and 
submit the document to the Office of the Federal Register for 
publication electronically as an official document of the Department of 
Veterans Affairs.

Luvenia Potts,
Regulation Development Coordinator, Office of Regulation Policy & 
Management, Office of General Counsel, Department of Veterans Affairs.
[FR Doc. 2023-10426 Filed 5-15-23; 8:45 am]
BILLING CODE 8320-01-P
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