Agency Information Collection Activities: Submission for OMB Review; Comment Request, 12191-12192 [2021-04274]
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Federal Register / Vol. 86, No. 39 / Tuesday, March 2, 2021 / Notices
confidential; marketing materials; study
types not included in the review; or
information on indications not included
in the review cannot be used by the EPC
Program. This is a voluntary request for
information, and all costs for complying
with this request must be borne by the
submitter.
The draft of this review will be posted
on AHRQ’s EPC Program website and
available for public comment for a
period of 4 weeks. If you would like to
be notified when the draft is posted,
please sign up for the email list at:
https://
www.effectivehealthcare.ahrq.gov/
email-updates.
The systematic review will answer the
following questions. This information is
provided as background. AHRQ is not
requesting that the public provide
answers to these questions.
Key Questions (KQs)
KQ 1. What is the effectiveness of
provider-to-provider telehealth for rural
patients?
a. What is the impact of provider-toprovider telehealth on rural patient and
population outcomes?
b. What is the impact of provider-toprovider telehealth on healthcare
providers?
c. What is the impact of provider-toprovider telehealth on private and
public (ex. CMS, TriCare, VA, etc.)
payers?
d. What adverse events or unintended
consequences are associated with
provider-to-provider telehealth for rural
patients?
e. What are the methodological
weaknesses of the identified
effectiveness studies of provider-toprovider telehealth for rural patients
and what improvements in study design
(e.g., focus on relevant comparisons and
outcomes) might increase the impact of
future research?
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KQ 2. What is the effectiveness of
implementation strategies for providerto-provider telehealth in rural areas?
a. What is the uptake of different
types of provider-to-provider telehealth
in rural areas?
Æ Who are the current patients,
providers, and payers engaged in
provider-to-provider telehealth in rural
areas?
Æ What factors affect whether
provider-to-provider telehealth in rural
areas can be sustained?
b. Which barriers and facilitators
impact adoption and implementation of
provider-to-provider telehealth in rural
areas?
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c. Which strategies are effective in
sustaining provider-to-provider
telehealth in rural areas?
d. What are the methodological
weaknesses of the identified studies of
implementation and sustainability of
provider-to-provider telehealth in rural
areas and what improvements in study
design (e.g., focus on relevant
comparisons and outcomes) might
increase the impact of future research?
Populations, Interventions,
Comparators, Outcomes, Settings
• Population(s)
Æ Rural individual patients, patient
families/care partners, and patient
populations.
Æ Healthcare providers (individuals
and organizations) who provide health
care services to rural patients or
populations.
• Providers include any profession or
occupation providing formal, paid
services.
• Family or informal care partners are
not considered providers.
Æ Payers who pay for healthcare
services for rural patients or
populations.
• Interventions
Æ Provider-to-provider telehealth
defined as: Any telecommunications
facilitated interaction among, or support
for, healthcare professionals designed to
improve access, quality of care, or
health outcomes for rural patients and
populations.
• Comparators
Æ KQ1: Other telehealth facilitated
care (not provider-to-provider), usual
(in-person) provider-to-provider
supports, no interaction or no care.
Æ KQ2: Different strategies for
dissemination, implementation, or
spread; no strategies; time periods prior
to implementation.
• Outcomes
Æ KQ1: Clinical outcomes for the
identified conditions (patient-reported
outcomes, mortality, morbidity, such as
function, illness recovery, infection);
Economic outcomes such as return on
investment, cost, volume of visits, and
resource use, including length of stay
and readmissions; Intermediate
Outcomes; Patient satisfaction, behavior
(such as care-seeking and compliance),
and decisions such as completion of
treatment, or satisfaction with less travel
to access healthcare; Provider
satisfaction, behavior, and decisions
such as choice of treatment or antibiotic
stewardship; Access measures and
indicators including but not limited to
time to diagnosis or time to treatment.
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12191
Æ KQ2: Indicators and measures of
uptake (e.g., rates of use, timing to
implementation) and characteristics of
users; categories and descriptors of
barriers and facilitators; categories and
descriptors of strategies.
• Settings
Æ Outpatient (primary care and
specialty care), inpatient, prehospital
and emergency care, post-acute and
long-term care.
Æ Civilian, Veterans Administration,
or military.
Æ Health care and non-healthcare
settings where health services are
delivered including in the home.
Æ U.S. relevant settings [Note that
studies from countries with significantly
different healthcare systems and fewer
resources (e.g., low-income countries)
are excluded.]
Dated: February 24, 2021.
Marquita Cullom,
Associate Director.
[FR Doc. 2021–04187 Filed 3–1–21; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10175]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility, and clarity of the
information to be collected, and the use
SUMMARY:
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12192
Federal Register / Vol. 86, No. 39 / Tuesday, March 2, 2021 / Notices
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
Comments on the collection(s) of
information must be received by the
OMB desk officer by April 1, 2021.
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 30-day Review—Open
for Public Comments’’ or by using the
search function.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ website address at
website address at: https://
www.cms.gov/Regulations-andGuidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
DATES:
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. The term ‘‘collection of
information’’ is defined in 44 U.S.C.
3502(3) and 5 CFR 1320.3(c) and
includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Certification
Statement for Electronic File
Interchange Organizations (EFIOs) that
submit National Provider Identifier
(NPI) data to the National Plan and
Provider Enumeration System (NPPES);
Use: the EFI process allows
organizations to submit NPI application
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SUPPLEMENTARY INFORMATION:
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information on large numbers of
providers in a single file. Once it has
obtained and formatted the necessary
provider data, the EFIO can
electronically submit the file to NPPES
for processing. As each file can contain
up to approximately 25,000 records, or
provider applications, the EFI process
greatly reduces the paperwork and
overall administrative burden associated
with enumerating providers. It is
essential to collect this information from
the EFIO to ensure that the EFIO
understands its legal responsibilities as
an EFIO and attests that it has the
authority to act on behalf of the
providers for whom it is submitting
data. In short, the certification
statement, which must be signed by an
authorized official of the EFIO, serves as
a safeguard against EFIOs attempting to
obtain NPIs for illicit or inappropriate
purposes. Form Number: CMS–10175
(OMB control number 0938–0984);
Frequency: Once, Annually; Affected
Public: Private Sector, State, Business,
and Not-for Profits; Number of
Respondents: 32; Number of Responses:
32; Total Annual Hours: 8. (For
questions regarding this collection
contact DaVona Boyd at 410–786–7483.)
Dated: February 25, 2021.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2021–04274 Filed 3–1–21; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–10054 and CMS–
10632]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
SUMMARY:
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60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
the necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions,
the accuracy of the estimated burden,
ways to enhance the quality, utility, and
clarity of the information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
May 3, 2021.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number, Room C4–26–05, 7500
Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ website address at
https://www.cms.gov/Regulations-andGuidance/Legislation/
PaperworkReductionActof1995/PRAListing.html
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10054 New Technology Services
for Ambulatory Payment
Classifications under the Outpatient
Prospective Payment System
CMS–10632 Evaluating Coverage to
Care in Communities
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Agencies
[Federal Register Volume 86, Number 39 (Tuesday, March 2, 2021)]
[Notices]
[Pages 12191-12192]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-04274]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10175]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. Under the Paperwork Reduction
Act of 1995 (PRA), federal agencies are required to publish notice in
the Federal Register concerning each proposed collection of
information, including each proposed extension or reinstatement of an
existing collection of information, and to allow a second opportunity
for public comment on the notice. Interested persons are invited to
send comments regarding the burden estimate or any other aspect of this
collection of information, including the necessity and utility of the
proposed information collection for the proper performance of the
agency's functions, the accuracy of the estimated burden, ways to
enhance the quality, utility, and clarity of the information to be
collected, and the use
[[Page 12192]]
of automated collection techniques or other forms of information
technology to minimize the information collection burden.
DATES: Comments on the collection(s) of information must be received by
the OMB desk officer by April 1, 2021.
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 30-day Review--
Open for Public Comments'' or by using the search function.
To obtain copies of a supporting statement and any related forms
for the proposed collection(s) summarized in this notice, you may make
your request using one of following:
1. Access CMS' website address at website address at: https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786-4669.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. The term ``collection of
information'' is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and
includes agency requests or requirements that members of the public
submit reports, keep records, or provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires
federal agencies to publish a 30-day notice in the Federal Register
concerning each proposed collection of information, including each
proposed extension or reinstatement of an existing collection of
information, before submitting the collection to OMB for approval. To
comply with this requirement, CMS is publishing this notice that
summarizes the following proposed collection(s) of information for
public comment:
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Certification
Statement for Electronic File Interchange Organizations (EFIOs) that
submit National Provider Identifier (NPI) data to the National Plan and
Provider Enumeration System (NPPES); Use: the EFI process allows
organizations to submit NPI application information on large numbers of
providers in a single file. Once it has obtained and formatted the
necessary provider data, the EFIO can electronically submit the file to
NPPES for processing. As each file can contain up to approximately
25,000 records, or provider applications, the EFI process greatly
reduces the paperwork and overall administrative burden associated with
enumerating providers. It is essential to collect this information from
the EFIO to ensure that the EFIO understands its legal responsibilities
as an EFIO and attests that it has the authority to act on behalf of
the providers for whom it is submitting data. In short, the
certification statement, which must be signed by an authorized official
of the EFIO, serves as a safeguard against EFIOs attempting to obtain
NPIs for illicit or inappropriate purposes. Form Number: CMS-10175 (OMB
control number 0938-0984); Frequency: Once, Annually; Affected Public:
Private Sector, State, Business, and Not-for Profits; Number of
Respondents: 32; Number of Responses: 32; Total Annual Hours: 8. (For
questions regarding this collection contact DaVona Boyd at 410-786-
7483.)
Dated: February 25, 2021.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2021-04274 Filed 3-1-21; 8:45 am]
BILLING CODE 4120-01-P